@misc{TremblayBlancoRey2015,
  author    = {Tremblay, Jean Christophe and Blanco-Rey, Maria},
  title     = {Manipulating interfacial hydrogens at palladium via STM},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-99511},
  pages     = {11},
  year      = {2015},
  abstract  = {In this contribution, we provide a detailed dynamical analysis of the interfacial hydrogen migration mediated by scanning tunneling microscopy (STM). Contributions from the STM-current and from the non-adiabatic couplings are taken into account using only first principle models. The slight asymmetry of the tunnelling rates with respect to the potential bias sign inferred from experimental observations is reproduced by weighting the contributions of the metal acceptor-donor states for the propagation of the impinging electrons. The quasi-thermal inelastic collision mechanism is treated perturbatively. The influence of hydrogen pre-coverage is also investigated using new potential energy surfaces obtained from periodic density functional theory calculations. Fully quantum dynamical simulations of the system evolution are performed by solving the Pauli master equation, providing insight into the reaction mechanism of STM manipulation of subsurface hydrogens. It is observed that the hydrogen impurity favors resurfacing over occupation of the bulk and subsurface sites whenever possible. The present simulations give strong indication that the experimentally observed protuberances after STM-excitation are due to hydrogen accumulating in the vicinity of the surface.},
  language  = {en}
}
@article{Schmidt2015,
  author    = {Schmidt, Joachim},
  title     = {Die Arbeit bei irreversibler Druck-Volumen-{\"A}nderung},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-74931},
  year      = {2015},
  abstract  = {For the calculation of the work in an irreversible pressure-volume change, we propose approxima-tions, which in contrast to the usual representation in the literature reflect the work performed during expansion and compression symmetrically. The calculations are based on the Reversible-Share-Theorem: Is used the force to overcome for calculating the work, so it captures only the configurational reversible work share.},
  language  = {de}
}
@article{SchmidtBechmann2014,
  author    = {Schmidt, Joachim and Bechmann, Wolfgang},
  title     = {Zur Anwendung des Skalarprodukts von Kraft und Weg auf reversible Prozesse (Druck-Volumen-{\"A}nderung, Dehnung, Elektrostatische Wechselwirkung, Hub)},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-69732},
  year      = {2014},
  abstract  = {Wir schlagen einen allgemein anwendbaren Algorithmus vor, der unter Verwendung des Skalarprodukts von Kraft und Weg zum richtigen Vorzeichen in den Gleichungen f{\"u}r die Arbeit und die Potentielle Energie bei reversiblen Prozessen (Druck-Volumen-{\"A}nderung, Dehnung, Elektrostatische Wechselwirkung, Hub)f{\"u}hrt. Wir zeigen, dass es dabei m{\"o}glich ist, systemimmanente oder externe Kr{\"a}fte zu benutzen. Wir zeigen, dass bei Verwendung von systemimmanenten Kr{\"a}ften das Skalarprodukt mit negativem Vorzeichen anzusetzen ist. Zudem ist es sehr wichtig, n{\"o}tige Vorzeichenwechsel bei den einzelnen Schritten zu beachten. Wir betonen dies, weil gelegentlich {\"u}bersehen wird, dass ein Vorzeichenwechsel n{\"o}tig ist, wenn das Wegdifferential ds durch das H{\"o}hendifferential dh beziehungsweise durch das Abstandsdifferential dx oder dr ersetzt werden muss.},
  language  = {de}
}
@misc{Metzke2013,
  type      = {Master Thesis},
  author    = {Metzke, Sarah},
  title     = {Synthesis and characterization of transition metal nitrides and carbides for catalysis and electrochemistry application},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-69835},
  school      = {Universit{\"a}t Potsdam},
  year      = {2013},
  abstract  = {It was the goal of this work to explore two different synthesis pathways using green chemistry. The first part of this thesis is focusing on the use of the urea-glass route towards single phase manganese nitride and manganese nitride/oxide nano-composites embedded in carbon, while the second part of the thesis is focusing on the use of the "saccharide route" (namely cellulose, sucrose, glucose and lignin) towards metal (Ni0), metal alloy (Pd0.9Ni0.1, Pd0.5Ni0.5, Fe0.5Ni0.5, Cu0.5Ni0.5 and W0.15Ni0.85) and ternary carbide (Mn0.75Fe2.25C) nanoparticles embedded in carbon. In the interest of battery application, MnN0.43 nanoparticles surrounded by a graphitic shell and embedded in carbon with a high surface area (79 m^2/g) were synthesized, following a previously set route.The comparison of the material characteristics before and after the discharge showed no remarkable difference in terms of composition and just slight differences in the morphological point of view, meaning the particles are stable but agglomerate. The graphitic shell is contributing to the resistance of the material and leads to a fine cyclic stability over 140 cycles of 230 mAh/g after the first charge/discharge and coulombic efficiencies close to 100\%. Due to the low voltage towards Li/Li+ and the low polarization, it might be an attractive anode material for lithium ion batteries. However, the capacity is still noticeably lower than the theoretical value for MnN0.43. A mixture of MnN0.43 and MnO nanoparticles embedded in carbon (surface area 93 m^2/g) was able to improve the cyclic stability to over 160 cycles giving a capacity of 811 mAh/g, which is considerably higher than the capacity of the conventional material graphite (372 mAh/g). This nano-composite seems to agglomerate less during the process of discharge. Interestingly, although the capacity is much higher than of the single phase manganese nitride, the nano-composite seems to only contain MnN0.43 nanoparticles after the process of discharge with no oxide phase to be found. Concerning catalysis application, different metal, metal alloy, and metal carbide nanoparticles were synthesized using the saccharide route. At first, systems that were already investigated before, being Pd0.9Ni0.1, Pd0.5Ni0.5, Fe0.5Ni0.5 and Mn0.75Fe2.25C using cellulose as the carbon source were prepared and tested in an alkylation reaction of toluene with benzylchloride. Unexpectedly, the metal alloys did not show any catalytic activity, but the ternary carbide Mn0.75Fe2.25C showed fine catalytic activity of 98\% conversion after 9 hour reaction time (110 °C). In a second step, the saccharide route was modified towards other carbon sources and carbon to metal ratios in order to improve the homogeneity of the samples and accessibility of the particle surfaces. The used carbon sources sucrose and glucose are similar in their basic structure of carbohydrates, but reducing the (polymeric) chain length. Indeed, the cellulose could be successfully replaced by sucrose and glucose. A lower carbon to metal ratio was found to influence the size, homogeneity and accessibility (as evidenced by TEM) of the samples. Since sucrose is an aliment, glucose is the better choice as a carbon source. Using glucose, the synthesis of Cu0.5Ni0.5 and W0.15Ni0.85 nano-composites was also possible, although the later was never obtained as pure phase. These alloy nano-composites were tested, along with nickel0 nanoparticles also prepared with glucose and on their catalytic activity towards the reduction of phenylacetylene. The results obtained let believe that any (poly) saccharide, including lignin, could be used as carbon source. The nickel0 nano-composites prepared with lignin as a carbon source were tested along with those prepared with cellulose and sucrose for their catalytic activity in the transfer hydrogenation of nitrobenzene (results compared with exposed nickel nanoparticles and nickel supported on carbon) leading to very promising results. Based on the urea-glass route and the saccharide route, simple equipment and transition metals, it was possible to have a one-pot synthesize with scale-up possibilities towards new material that can be applied in catalysis and battery systems.},
  language  = {en}
}
@phdthesis{Suetterlin2013,
  author    = {S{\"u}tterlin, Martin},
  title     = {New inverse hydogel opals as protein responsive sensors},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-70179},
  school      = {Universit{\"a}t Potsdam},
  year      = {2013},
  abstract  = {In this work, the development of temperature- and protein-responsive sensor materials based on biocompatible, inverse hydrogel opals (IHOs) is presented. With these materials, large biomolecules can be specifically recognised and the binding event visualised. The preparation of the IHOs was performed with a template process, for which monodisperse silica particles were vertically deposited onto glass slides as the first step. The obtained colloidal crystals with a thickness of 5 μm displayed opalescent reflections because of the uniform alignment of the colloids. As a second step, the template was embedded in a matrix consisting of biocompatible, thermoresponsive hydrogels. The comonomers were selected from the family of oligo(ethylene glycol)methacrylates. The monomer solution was injected into a polymerisation mould, which contained the colloidal crystals as a template. The space in-between the template particles was filled with the monomer solution and the hydrogel was cured via UV-polymerisation. The particles were chemically etched, which resulted in a porous inner structure. The uniform alignment of the pores and therefore the opalescent reflection were maintained, so these system were denoted as inverse hydrogel opals. A pore diameter of several hundred nanometres as well as interconnections between the pores should facilitate a diffusion of bigger (bio)molecules, which was always a challenge in the presented systems until now. The copolymer composition was chosen to result in a hydrogel collapse over 35 °C. All hydrogels showed pronounced swelling in water below the critical temperature. The incorporation of a reactive monomer with hydroxyl groups ensured a potential coupling group for the introduction of recognition units for analytes, e.g. proteins. As a test system, biotin as a recognition unit for avidin was coupled to the IHO via polymer-analogous Steglich esterification. The amount of accessible biotin was quantified with a colorimetric binding assay. When avidin was added to the biotinylated IHO, the wavelength of the opalescent reflection was significantly shifted and therefore the binding event was visualised. This effect is based on the change in swelling behaviour of the hydrogel after binding of the hydrophilic avidin, which is amplified by the thermoresponsive nature of the hydrogel. A swelling or shrinking of the pores induces a change in distance of the crystal planes, which are responsible for the colour of the reflection. With these findings, the possibility of creating sensor materials or additional biomolecules in the size range of avidin is given.},
  language  = {en}
}
@phdthesis{Salffner2013,
  author    = {Salffner, Katharina},
  title     = {Entwicklung eines breitbandigen Cavity-Ring-Down-Spektrometers unter Verwendung nahinfraroter, inkoh{\"a}renter Strahlung},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-68952},
  school      = {Universit{\"a}t Potsdam},
  year      = {2013},
  abstract  = {In der vorliegenden Arbeit werden verschiedene Spektrometer f{\"u}r die Analyse von Gasen bzw. Gasgemischen vorgestellt und deren Design, Aufbau, Charakterisierung und Optimierung beschrieben. Das Resultat der Optimierung und Weiterentwicklungen ist ein spektral breitbandiges Cavity-Ring-Down-Spektrometer (CRD-Spektrometer). Ausgangspunkt der hier vorgestellten Arbeit ist ein Spektrometer auf Basis klassischer Absorptionsspektroskopie in einer Multireflexionszelle. F{\"u}r dieses Spektrometer wurde als Strahlquelle ein Superkontinuumlaser verwendet. Der Vorteil dieses Spektrometers liegt in seiner Kompaktheit. Mit diesem Spektrometer wurden Absorptionsspektren von mehreren Reingasen und einem Gasgemisch {\"u}ber einen Wellenl{\"a}ngenbereich von 1500 nm - 1700 nm aufgenommen. Der qualitative Vergleich mit zu erwartenden Spektren, welche auf der HITRAN-Datenbank basieren, zeigte eine gute {\"U}bereinstimmung. Die quantitative Interpretierbarkeit der Daten war jedoch stark eingeschr{\"a}nkt aufgrund des hohen zuf{\"a}lligen und systematischen Fehlers der Messungen. Als Konsequenz aus der als nicht zufriedenstellend bewerteten quantitativen Interpretierbarkeit der Daten wurde eine alternative Messmethode gesucht, welche eine h{\"o}here Sensitivit{\"a}t und Genauigkeit erm{\"o}glicht. Die Wahl fiel auf die Cavity-Ring-Down-Spektroskopie, eine resonatorgest{\"u}tzte Variante der Absorptionsspektroskopie. Wesentliche Vorteile dieser Technik sind a) die Unabh{\"a}ngigkeit von Leistungsschwankungen der Strahlquelle, b) ein effektiver Absorptionsweg von bis zu mehreren Kilometern, welcher sich unmittelbar auf die Sensitivit{\"a}t der Messungen auswirkt, c) die Ermittlung absoluter Absorberkonzentrationen, ohne die Notwendigkeit einer Kalibrierung oder den Vergleich mit einer Referenzzelle und d) die Vernachl{\"a}ssigbarkeit von Absorptionen außerhalb des Resonators. Als notwendiger Zwischenschritt auf dem Weg zu einem breitbandigen CRD-Spektrometer wurde zun{\"a}chst ein monochromatisches CRD-Spektrometer designt, aufgebaut und charakterisiert. F{\"u}r die effektive Einkopplung von Strahlungsenergie in einen Resonator ist die Anpassung der Strahlparameter an die Mode des Resonators notwendig. Voraussetzung dieser Anpassung ist die Kenntnis der Strahlparameter, welche experimentell ermittelt wurden. Im Laufe des Aufbaus des Spektrometers ergab sich, dass trotz der Modenanpassung die Einkopplung der Strahlungsenergie in den Resonator gest{\"o}rt wurde. Daraufhin wurden systematisch m{\"o}gliche Ursachen dieser St{\"o}rung untersucht und das Spektrometer optimiert. Mit diesem optimierten Spektrometer wurden Spektren gemessen, welche sowohl qualitativ als auch quantitativ gut mit den zu erwartenden Spektren {\"u}bereinstimmen. Als Nachweisgrenze dieses Spektrometers wurde ein Wert f{\"u}r den Absorptionskoeffizienten alpha von 10^-8 cm-1 bestimmt. Mit dem monochromatischen CRD-Spektrometer war es zudem m{\"o}glich, isotopenspezifische Messungen durchzuf{\"u}hren. F{\"u}r das breitbandige Spektrometer wurde als Strahlquelle eine ASE-Diode (amplified spontaneous emission) verwendet. Dabei handelt es sich um eine inkoh{\"a}rente Strahlquelle. Mittels Messungen nach dem Prinzip der Cavity-Enhanced-Absorptionsspektroskopie wurde die generelle Funktionalit{\"a}t des resonatorgest{\"u}tzten Spektrometers {\"u}berpr{\"u}ft. Anschließend wurden die wellenl{\"a}ngenabh{\"a}ngigen Abklingsignale des leeren und des mit einem CO2-Luft-Gemisch gef{\"u}llten Resonators gemessen und ebenfalls mit den zu erwartenden Spektren verglichen. Qualitativ stimmen die experimentellen Spektren gut mit den zu erwartenden Spektren {\"u}berein. F{\"u}r die quantitative Interpretation der Daten wurde ein spezieller Algorithmus entwickelt, der die spektrale Aufl{\"o}sung des Systems ber{\"u}cksichtigt. Mit dem vorgestellten Spektrometer ist so die qualitative und quantitative Interpretation der Spektren m{\"o}glich. Die Nachweisgrenze des breitbandigen Cavity-Ring-Down-Spektrometers wurde zu einem Wert von alpha = 8x10^-7 cm-1 bestimmt. Der systematischen und der zuf{\"a}llige Fehler der Messungen lagen bei Werten von ca. 1\%. Bei diesem Spektrometer handelt es sich um einen Prototyp. Mittels Optimierung des Systems lassen sich sowohl der Wert der Nachweisgrenze als auch die Fehler der Messungen verbessern.},
  language  = {de}
}
@phdthesis{Glatzel2013,
  author    = {Glatzel, Stefan},
  title     = {Cellulose based transition metal nano-composites : structuring and development},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-64678},
  school      = {Universit{\"a}t Potsdam},
  year      = {2013},
  abstract  = {Cellulose is the most abundant biopolymer on earth. In this work it has been used, in various forms ranging from wood to fully processed laboratory grade microcrystalline cellulose, to synthesise a variety of metal and metal carbide nanoparticles and to establish structuring and patterning methodologies that produce highly functional nano-hybrids. To achieve this, the mechanisms governing the catalytic processes that bring about graphitised carbons in the presence of iron have been investigated. It was found that, when infusing cellulose with an aqueous iron salt solution and heating this mixture under inert atmosphere to 640 °C and above, a liquid eutectic mixture of iron and carbon with an atom ratio of approximately 1:1 forms. The eutectic droplets were monitored with in-situ TEM at the reaction temperature where they could be seen dissolving amorphous carbon and leaving behind a trail of graphitised carbon sheets and subsequently iron carbide nanoparticles. These transformations turned ordinary cellulose into a conductive and porous matrix that is well suited for catalytic applications. Despite these significant changes on the nanometre scale the shape of the matrix as a whole was retained with remarkable precision. This was exemplified by folding a sheet of cellulose paper into origami cranes and converting them via the temperature treatment in to magnetic facsimiles of those cranes. The study showed that the catalytic mechanisms derived from controlled systems and described in the literature can be transferred to synthetic concepts beyond the lab without loss of generality. Once the processes determining the transformation of cellulose into functional materials were understood, the concept could be extended to other metals and metal-combinations. Firstly, the procedure was utilised to produce different ternary iron carbides in the form of MxFeyC (M = W, Mn). None of those ternary carbides have thus far been produced in a nanoparticle form. The next part of this work encompassed combinations of iron with cobalt, nickel, palladium and copper. All of those metals were also probed alone in combination with cellulose. This produced elemental metal and metal alloy particles of low polydispersity and high stability. Both features are something that is typically not associated with high temperature syntheses and enables to connect the good size control with a scalable process. Each of the probed reactions resulted in phase pure, single crystalline, stable materials. After showing that cellulose is a good stabilising and separating agent for all the investigated types of nanoparticles, the focus of the work at hand is shifted towards probing the limits of the structuring and pattering capabilities of cellulose. Moreover possible post-processing techniques to further broaden the applicability of the materials are evaluated. This showed that, by choosing an appropriate paper, products ranging from stiff, self-sustaining monoliths to ultra-thin and very flexible cloths can be obtained after high temperature treatment. Furthermore cellulose has been demonstrated to be a very good substrate for many structuring and patterning techniques from origami folding to ink-jet printing. The thereby resulting products have been employed as electrodes, which was exemplified by electrodepositing copper onto them. Via ink-jet printing they have additionally been patterned and the resulting electrodes have also been post functionalised by electro-deposition of copper onto the graphitised (printed) parts of the samples. Lastly in a preliminary test the possibility of printing several metals simultaneously and thereby producing finely tuneable gradients from one metal to another have successfully been made. Starting from these concepts future experiments were outlined. The last chapter of this thesis concerned itself with alternative synthesis methods of the iron-carbon composite, thereby testing the robustness of the devolved reactions. By performing the synthesis with partly dissolved scrap metal and pieces of raw, dry wood, some progress for further use of the general synthesis technique were made. For example by using wood instead of processed cellulose all the established shaping techniques available for wooden objects, such as CNC milling or 3D prototyping, become accessible for the synthesis path. Also by using wood its intrinsic well defined porosity and the fact that large monoliths are obtained help expanding the prospect of using the composite. It was also demonstrated in this chapter that the resulting material can be applied for the environmentally important issue of waste water cleansing. Additionally to being made from renewable resources and by a cheap and easy one-pot synthesis, the material is recyclable, since the pollutants can be recovered by washing with ethanol. Most importantly this chapter covered experiments where the reaction was performed in a crude, home-built glass vessel, fuelled - with the help of a Fresnel lens - only by direct concentrated sunlight irradiation. This concept carries the thus far presented synthetic procedures from being common laboratory syntheses to a real world application. Based on cellulose, transition metals and simple equipment, this work enabled the easy one-pot synthesis of nano-ceramic and metal nanoparticle composites otherwise not readily accessible. Furthermore were structuring and patterning techniques and synthesis routes involving only renewable resources and environmentally benign procedures established here. Thereby it has laid the foundation for a multitude of applications and pointed towards several future projects reaching from fundamental research, to application focussed research and even and industry relevant engineering project was envisioned.},
  language  = {en}
}
@phdthesis{Mondal2013,
  author    = {Mondal, Suvendu Sekhar},
  title     = {Design of isostructural metal-imidazolate frameworks : application for gas storage},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-69692},
  school      = {Universit{\"a}t Potsdam},
  year      = {2013},
  abstract  = {The sharply rising level of atmospheric carbon dioxide resulting from anthropogenic emissions is one of the greatest environmental concerns facing our civilization today. Metal-organic frameworks (MOFs) are a new class of materials that constructed by metal-containing nodes bonded to organic bridging ligands. MOFs could serve as an ideal platform for the development of next generation CO2 capture materials owing to their large capacity for the adsorption of gases and their structural and chemical tunability. The ability to rationally select the framework components is expected to allow the affinity of the internal pore surface toward CO2 to be precisely controlled, facilitating materials properties that are optimized for the specific type of CO2 capture to be performed (post-combustion capture, precombustion capture, or oxy-fuel combustion) and potentially even for the specific power plant in which the capture system is to be installed. For this reason, significant effort has been made in recent years in improving the gas separation performance of MOFs and some studies evaluating the prospects of deploying these materials in real-world CO2 capture systems have begun to emerge. We have developed six new MOFs, denoted as IFPs (IFP-5, -6, -7, -8, -9, -10, IFP = Imidazolate Framework Potsdam) and two hydrogen-bonded molecular building block (MBB, named as 1 and 2 for Zn and Co based, respectively) have been synthesized, characterized and applied for gas storage. The structure of IFP possesses 1D hexagonal channels. Metal centre and the substituent groups of C2 position of the linker protrude into the open channels and determine their accessible diameter. Interestingly, the channel diameters (range : 0.3 to 5.2 {\AA}) for IFP structures are tuned by the metal centre (Zn, Co and Cd) and substituent of C2 position of the imidazolate linker. Moreover hydrogen bonded MBB of 1 and 2 is formed an in situ functionalization of a ligand under solvothermal condition. Two different types of channels are observed for 1 and 2. Materials contain solvent accessible void space. Solvent could be easily removed by under high vacuum. The porous framework has maintained the crystalline integrity even without solvent molecules. N2, H2, CO2 and CH4 gas sorption isotherms were performed. Gas uptake capacities are comparable with other frameworks. Gas uptake capacity is reduced when the channel diameter is narrow. For example, the channel diameter of IFP-5 (channel diameter: 3.8 {\AA}) is slightly lower than that of IFP-1 (channel diameter: 4.2 {\AA}); hence, the gas uptake capacity and Brunauer-Emmett-Teller (BET) surface area are slightly lower than IFP-1. The selectivity does not depend only on the size of the gas components (kinetic diameter: CO2 3.3 {\AA}, N2 3.6 {\AA} and CH4 3.8 ) but also on the polarizability of the surface and of the gas components. IFP-5 and-6 have the potential applications for the separation of CO2 and CH4 from N2-containing gas mixtures and CO2 and CH4 containing gas mixtures. Gas sorption isotherms of IFP-7, -8, -9, -10 exhibited hysteretic behavior due to flexible alkoxy (e.g., methoxy and ethoxy) substituents. Such phenomenon is a kind of gate effects which is rarely observed in microporous MOFs. IFP-7 (Zn-centred) has a flexible methoxy substituent. This is the first example where a flexible methoxy substituent shows the gate opening behavior in a MOF. Presence of methoxy functional group at the hexagonal channels, IFP-7 acted as molecular gate for N2 gas. Due to polar methoxy group and channel walls, wide hysteretic isotherm was observed during gas uptake. The N2 The estimated BET surface area for 1 is 471 m2 g-1 and the Langmuir surface area is 570 m2 g-1. However, such surface area is slightly higher than azolate-based hydrogen-bonded supramolecular assemblies and also comparable and higher than some hydrogen-bonded porous organic molecules.},
  language  = {en}
}
@phdthesis{Kroener2013,
  author    = {Kr{\"o}ner, Dominik},
  title     = {Analysis and control of light-induced processes in molecules: Electron and nuclear quantum dynamics for aspects of stereoisomerism and spectroscopy},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-70477},
  school      = {Universit{\"a}t Potsdam},
  year      = {2013},
  abstract  = {The habilitation thesis covers theoretical investigations on light-induced processes in molecules. The study is focussed on changes of the molecular electronic structure and geometry, caused either by photoexcitation in the event of a spectroscopic analysis, or by a selective control with shaped laser pulses. The applied and developed methods are predominantly based on quantum chemistry as well as on electron and nuclear quantum dynamics, and in parts on molecular dynamics. The studied scientific problems deal with stereoisomerism and the question of how to either switch or distinguish chiral molecules using laser pulses, and with the essentials for the simulation of the spectroscopic response of biochromophores, in order to unravel their photophysics. The accomplished findings not only explain experimental results and extend existing approaches, but also contribute significantly to the basic understanding of the investigated light-driven molecular processes. The main achievements can be divided in three parts: First, a quantum theory for an enantio- and diastereoselective or, in general, stereoselective laser pulse control was developed and successfully applied to influence the chirality of molecular switches. The proposed axially chiral molecules possess different numbers of "switchable" stable chiral conformations, with one particular switch featuring even a true achiral "off"-state which allows to enantioselectively "turn on" its chirality. Furthermore, surface mounted chiral molecular switches with several well-defined orientations were treated, where a newly devised highly flexible stochastic pulse optimization technique provides high stereoselectivity and efficiency at the same time, even for coupled chirality-changing degrees of freedom. Despite the model character of these studies, the proposed types of chiral molecular switches and, all the more, the developed basic concepts are generally applicable to design laser pulse controlled catalysts for asymmetric synthesis, or to achieve selective changes in the chirality of liquid crystals or in chiroptical nanodevices, implementable in information processing or as data storage. Second, laser-driven electron wavepacket dynamics based on ab initio calculations, namely time-dependent configuration interaction, was extended by the explicit inclusion of magnetic field-magnetic dipole interactions for the simulation of the qualitative and quantitative distinction of enantiomers in mass spectrometry by means of circularly polarized ultrashort laser pulses. The developed approach not only allows to explain the origin of the experimentally observed influence of the pulse duration on the detected circular dichroism in the ion yield, but also to predict laser pulse parameters for an optimal distinction of enantiomers by ultrashort shaped laser pulses. Moreover, these investigations in combination with the previous ones provide a fundamental understanding of the relevance of electric and magnetic interactions between linearly or non-linearly polarized laser pulses and (pro-)chiral molecules for either control by enantioselective excitation or distinction by enantiospecific excitation. Third, for selected light-sensitive biological systems of central importance, like e.g. antenna complexes of photosynthesis, simulations of processes which take place during and after photoexcitation of their chromophores were performed, in order to explain experimental (spectroscopic) findings as well as to understand the underlying photophysical and photochemical principles. In particular, aspects of normal mode mixing due to geometrical changes upon photoexcitation and their impact on (time-dependent) vibronic and resonance Raman spectra, as well as on intramolecular energy redistribution were addressed. In order to explain unresolved experimental findings, a simulation program for the calculation of vibronic and resonance Raman spectra, accounting for changes in both vibrational frequencies and normal modes, was created based on a time-dependent formalism. In addition, the influence of the biochemical environment on the electronic structure of the chromophores was studied by electrostatic interactions and mechanical embedding using hybrid quantum-classical methods. Environmental effects were found to be of importance, in particular, for the excitonic coupling of chromophores in light-harvesting complex II. Although the simulations for such highly complex systems are still restricted by various approximations, the improved approaches and obtained results have proven to be important contributions for a better understanding of light-induced processes in biosystems which also adds to efforts of their artificial reproduction.},
  language  = {en}
}
@phdthesis{Lemke2013,
  author    = {Lemke, Karina},
  title     = {Abtrennung und Charakterisierung von Polyelektrolyt-modifizierten Nanopartikeln},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-68133},
  school      = {Universit{\"a}t Potsdam},
  year      = {2013},
  abstract  = {Gegenstand der Dissertation ist die gr{\"o}ßen- und eigenschaftsoptimierte Synthese und Charakterisierung von anorganischen Nanopartikeln in einer geeigneten Polyelektrolytmodifizierten Mikroemulsion. Das Hauptziel bildet dabei die Auswahl einer geeigneten Mikroemulsion, zur Synthese von kleinen, stabilen, reproduzierbaren Nanopartikeln mit besonderen Eigenschaften. Die vorliegende Arbeit wurde in zwei Haupteile gegliedert. Der erste Teil befasst sich mit der Einmischung von unterschiedlichen Polykationen (lineares Poly (diallyldimethylammoniumchlorid) (PDADMAC) und verzweigtes Poly (ethylenimin) (PEI)) in verschiedene, auf unterschiedlichen Tensiden (CTAB - kationisch, SDS - anionisch, SB - zwitterionisch) basierenden, Mikroemulsionssysteme. Dabei zeigt sich, dass das Einmischen der Polykationen in die Wassertr{\"o}pfchen der Wasser-in-{\"O}l (W/O) Mikroemulsion prinzipiell m{\"o}glich ist. Der Einfluss der verschiedenen Polykationen auf das Phasenverhalten der W/O Mikroemulsion ist jedoch sehr unterschiedlich. In Gegenwart des kationischen Tensids f{\"u}hren die repulsiven Wechselwirkungen mit den Polykationen zu einer Destabilisierung des Systems, w{\"a}hrend die ausgepr{\"a}gten Wechselwirkungen mit dem anionischen Tensid in einer deutlichen Stabilisierung des Systems resultieren. F{\"u}r das zwitterionische Tensid f{\"u}hren die moderaten Wechselwirkungen mit den Polykationen zu einer partiellen Stabilisierung. Der zweite Teil der Arbeit besch{\"a}ftigt sich mit dem Einsatz der unterschiedlichen, Polyelektrolyt- modifizierten Mikroemulsionen als Templatphase f{\"u}r die Herstellung verschiedener, anorganischer Nanopartikel. Die CTAB-basierte Mikroemulsion erweist sich dabei als ungeeignet f{\"u}r die Herstellung von CdS Nanopartikeln, da zum einen nur eine geringe Toleranz gegen{\"u}ber den Reaktanden vorhanden ist (Destabilisierungseffekt) und zum anderen das Partikelwachstum durch den Polyelektrolyt-Tensid-Film nicht ausreichend begrenzt wird. Zudem zeigt sich, dass eine Abtrennung der Partikel aus der Mikroemulsion nicht m{\"o}glich ist. Die SDS-basierten Mikroemulsionen, erweisen sich als geeignete Templatphase zur Synthese kleiner anorganischer Nanopartikel (3 - 20 nm). Sowohl CdS Quantum Dots, als auch Gold Nanopartikel konnten erfolgreich in der Mikroemulsion synthetisiert werden, wobei das verzweigte PEI einen interessanten Templat-Effekt in der Mikroemulsion hervorruft. Als deutlicher Nachteil der SDS-basierten Mikroemulsionen offenbaren sich die starken Wechselwirkungen zwischen dem Tensid und den Polyelektrolyten w{\"a}hrend der Aufarbeitung der Nanopartikel aus der Mikroemulsion. Dabei erweist sich die Polyelektrolyt-Tensid-Komplexbildung als hinderlich f{\"u}r die Redispergierung der CdS Quantum Dots in Wasser, so dass Partikelaggregation einsetzt. Die SB-basierten Mikroemulsionen erweisen sich als g{\"u}nstige Templatphase f{\"u}r die Bildung von gr{\"o}ßen- und eigenschaftenoptimierten Nanopartikeln (< 4 nm), wobei insbesondere eine Modifizierung mit PEI als ideal betrachtet werden kann. In Gegenwart des verzweigten PEI gelang es erstmals ultrakleine, fluoreszierende Gold Cluster (< 2 nm) in einer SB-basierten Mikroemulsion als Templatphase herzustellen. Als besonderer Vorteil der SB-basierten Mikroemulsion zeigen sich die moderaten Wechselwirkungen zwischen dem zwitterionischen Tensid und den Polyelektrolyten, welche eine anschließende Abtrennung der Partikel aus der Mikroemulsion unter Erhalt der Gr{\"o}ße und ihrer optischen Eigenschaften erm{\"o}glichen. In der redispergierten w{\"a}ssrigen L{\"o}sung gelang somit eine Auftrennung der PEI-modifizierten Partikel mit Hilfe der asymmetrischer Fluss Feldflussfraktionierung (aF FFF). Die gebildeten Nanopartikel zeigen interessante optische Eigenschaften und k{\"o}nnen zum Beispiel erfolgreich zur Modifizierung von Biosensoren eingesetzt werden.},
  language  = {de}
}
@phdthesis{Winkler2013,
  author    = {Winkler, Henning},
  title     = {Synthese von thermoplastisch verarbeitbaren Fetts{\"a}ure-Acylderivaten der St{\"a}rke und Proteine},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-71089},
  school      = {Universit{\"a}t Potsdam},
  year      = {2013},
  abstract  = {In den vergangenen Jahren wurden stetig wachsende Produktionskapazit{\"a}ten von Biokunststoffen aus nachwachsenden Rohstoffe nverzeichnet. Trotz großer Produktionskapazit{\"a}ten und einem geeigneten Eigenschaftsprofil findet St{\"a}rke nur als hydrophile, mit Weichmachern verarbeitete thermoplastische St{\"a}rke (TPS) in Form von Blends mit z. B. Polyestern Anwendung. Gleiches gilt f{\"u}r Kunststoffe auf Proteinbasis. Die vorliegende Arbeit hat die Entwicklung von Biokunststoffen auf St{\"a}rkebasis zum Ziel, welche ohne externe Weichmacher thermoplastisch verarbeitbar und hydrophob sind sowie ein mechanisches Eigenschaftsprofil aufweisen, welches ein Potenzial zur Herstellung von Materialien f{\"u}r eine Anwendung als Verpackungsmittel bietet. Um die Rohstoffbasis f{\"u}r Biokunststoffe zu erweitern, soll das erarbeitete Konzept auf zwei industriell verf{\"u}gbare Proteintypen, Zein und Molkenproteinisolat (WPI), {\"u}bertragen werden. Als geeignete Materialklasse wurden Fetts{\"a}ureester der St{\"a}rke herausgearbeitet. Zun{\"a}chst fand ein Vergleich der S{\"a}urechlorid-Veresterung und der Umesterung von Fetts{\"a}urevinylestern statt, woraus letztere als geeignetere Methode hervorging. Durch Variation der Reaktionsparameter konnte diese optimiert und auf eine Serie der Fetts{\"a}urevinylester von Butanoat bis Stearat f{\"u}r DS-Werte bis zu 2,2-2,6 angewandt werden. M{\"o}glich war somit eine systematische Studie unter Variation der veresterten Fetts{\"a}ure sowie des Substitutionsgrades (DS). S{\"a}mtliche Produkte mit einem DS ab 1,5 wiesen eine ausgpr{\"a}gte L{\"o}slichkeit in organischen L{\"o}sungsmitteln auf wodurch sowohl die Aufnahme von NMR-Spektren als auch Molmassenbestimmung mittels Gr{\"o}ßenausschlusschromatographie mit gekoppelter Mehrwinkel-Laserlichtstreuung (GPC-MALLS) m{\"o}glich waren. Durch dynamische Lichtstreuung (DLS) wurde das L{\"o}slichkeitsverhalten veranschaulicht. S{\"a}mtliche Produkte konnten zu Filmen verarbeitet werden, wobei Materialien mit DS 1,5-1,7 hohe Zugfestigkeiten (bis zu 42 MPa) und Elastizit{\"a}tsmodule (bis 1390 MPa) aufwiesen. Insbesondere St{\"a}rkehexanoat mit DS <2 sowie St{\"a}rkebutanoat mit DS >2 hatten ein mechanisches Eigenschaftsprofil, welches insbesondere in Bezug auf die Festigkeit/Steifigkeit vergleichbar mit Verpackungsmaterialien wie Polyethylen war (Zugfestigkeit: 15-32 MPa, E-Modul: 300-1300 MPa). Zugfestigkeit und Elastizit{\"a}tsmodul nahmen mit steigender Kettenl{\"a}nge der veresterten Fetts{\"a}ure ab. Ester l{\"a}ngerkettiger Fetts{\"a}uren (C16-C18) waren spr{\"o}de. {\"U}ber Weitwinkel-R{\"o}ntgenstreuung (WAXS) und Infrarotspektroskopie (ATR-FTIR) konnte der Verlauf der Festigkeiten mit einer zunehmenden Distanz der St{\"a}rke im Material begr{\"u}ndet werden. Es konnten von DS und Kettenl{\"a}nge abh{\"a}ngige Glas{\"u}berg{\"a}nge detektiert werden, die kristallinen Strukturen der langkettigen Fetts{\"a}uren zeigten einen Schmelzpeak. Die Hydrophobie der Filme wurde anhand von Kontaktwinkeln >95° gegen Wasser dargestellt. Blends mit biobasierten Polyterpenen sowie den in der Arbeit hergestellten Zein-Acylderivaten erm{\"o}glichten eine weitere Verbesserung der Zugfestigkeit bzw. des Elastizit{\"a}tsmoduls hochsubstituierter Produkte. Eine thermoplastische Verarbeitung mittels Spritzgießen war sowohl f{\"u}r Produkte mit hohem als auch mittlerem DS-Wert ohne jeglichen Zusatz von Weichmachern m{\"o}glich. Es entstanden homogene, transparente Pr{\"u}fst{\"a}be. Untersuchungen der H{\"a}rte ergaben auch hier f{\"u}r St{\"a}rkehexanoat und -butanoat mit Polyethylen vergleichbare Werte. Ausgew{\"a}hlte Produkte wurden zu Fasern nach dem Schmelzspinnverfahren verarbeitet. Hierbei wurden insbesondere f{\"u}r hochsubstituierte Derivate homogenen Fasern erstellt, welche im Vergleich zur Gießfolie signifikant h{\"o}here Zugfestigkeiten aufwiesen. St{\"a}rkeester mit mittlerem DS ließen sich ebenfalls verarbeiten. Zun{\"a}chst wurden f{\"u}r eine {\"U}bertragung des Konzeptes auf die Proteine Zein und WPI verschiedene Synthesemethoden verglichen. Die Veresterung mit S{\"a}urechloriden ergab hierbei die h{\"o}chsten Werte. Im Hinblick auf eine gute L{\"o}slichkeit in organischen L{\"o}sungsmitteln wurde f{\"u}r WPI die Veresterung mit carbonyldiimidazol (CDI)-aktivierten Fetts{\"a}uren in DMSO und f{\"u}r Zein die Veresterung mit S{\"a}u-rechloriden in Pyridin bevorzugt. Es stellte sich heraus, dass acyliertes WPI zwar hydrophob, jedoch ohne Weichmacher nicht thermoplastisch verarbeitet werden konnte. Die Erstellung von Gießfolien f{\"u}hrte zu Spr{\"o}dbruchverhalten. Unter Zugabe der biobasierten {\"O}ls{\"a}ure wurde die Anwendung von acyliertem WPI als thermoplastischer Filler z. B. in Blends mit St{\"a}rkeestern dargestellt. Im Gegensatz hierzu zeigte acyliertes Zein Glas{\"u}berg{\"a}nge <100 °C bei ausreichender Stabilit{\"a}t (150-200 °C). Zeinoleat konnte ohne Weichmacher zu einer transparenten Gießfolie verarbeitet werden. S{\"a}mtliche Derivate erwiesen sich als ausgepr{\"a}gt hydrophob. Zeinoleat konnte {\"u}ber das Schmelzspinnverfahren zu thermoplastischen Fasern verarbeitet werden.},
  language  = {de}
}
@misc{JeličićFriedrichJeremićetal.2009,
  author    = {Jeličić, Aleksandra and Friedrich, Alwin and Jeremić, Katarina and Siekmeyer, Gerd and Taubert, Andreas},
  title     = {Polymer hydrogel/polybutadiene/iron oxide nanoparticle hybrid actuators for the characterization of NiTi implants},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-48589},
  year      = {2009},
  abstract  = {One of the main issues with the use of nickel titanium alloy (NiTi) implants in cardiovascular implants (stents) is that these devices must be of very high quality in order to avoid subsequent operations due to failing stents. For small stents with diameters below ca. 2 mm, however, stent characterization is not straightforward. One of the main problems is that there are virtually no methods to characterize the interior of the NiTi tubes used for fabrication of these tiny stents. The current paper reports on a robust hybrid actuator for the characterization of NiTi tubes prior to stent fabrication. The method is based on a polymer/hydrogel/magnetic nanoparticle hybrid material and allows for the determination of the inner diameter at virtually all places in the raw NiTi tubes. Knowledge of the inner structure of the raw NiTi tubes is crucial to avoid regions that are not hollow or regions that are likely to fail due to defects inside the raw tube. The actuator enables close contact of a magnetic polymer film with the inner NiTi tube surface. The magnetic signal can be detected from outside and be used for a direct mapping of the tube interior. As a result, it is possible to detect critical regions prior to expensive and slow stent fabrication processes.},
  language  = {en}
}
@misc{OliveiraJrGueddariMoerschbacheretal.2008,
  author    = {Oliveira Jr, E. N. and Gueddari, Nour E. El and Moerschbacher, Bruno M. and Peter, Martin and Franco, Telma},
  title     = {Growth of phytopathogenic fungi in the presence of partially acetylated chitooligosaccharides},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-42646},
  year      = {2008},
  abstract  = {Four phytopathogenic fungi were cultivated up to six days in media containing chitooligosaccharide mixtures differing in average DP and FA. The three different mixtures were named Q3 (which contained oligosaccharides ofDP2-DP10, withDP2-DP7 asmain components), Q2 (which contained oligosaccharides of DP2-DP12, with DP2-DP10 as main components) and Q1 (which derived from Q2 and contained oligomers of DP5-DP8 with hexamer and a heptamer as the main components). The novel aspect of this work is the description of the effect of mixtures of oligosaccharides with different and known composition on fungal growth rates. The growth rate of Alternaria alternata and Rhizopus stolonifer was initially inhibited by Q3 and Q2 at higher concentrations. Q1 had a growth stimulating effect on these two fungi. Growth of Botrytis cinerea was inhibited by Q3 and Q2, while Q1 had no effect on the growth of this fungus. Growth of Penicillium expansum was only slightly inhibited by higher concentrations of sample Q3, while Q2 and Q1 had no effect. The inhibition of growth rates or their resistance toward chitooligosaccharides correlated with the absence or presence of chitinolytic enzymes in the culture media, respectively.},
  language  = {en}
}
@misc{BringmannMutanyattaComarMaksimenkaetal.2008,
  author    = {Bringmann, Gerhard and Mutanyatta-Comar, Joan and Maksimenka, Katja and Wanjohi, John M. and Heydenreich, Matthias and Brun, Reto and M{\"u}ller, Werner E. G. and Peter, Martin and Midiwo, Jacob O. and Yenesew, Abiy},
  title     = {Joziknipholones A and B : the First Dimeric Phenylanthraquinones, from the Roots of Bulbine frutescens},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-42638},
  year      = {2008},
  abstract  = {From the roots of the African plant Bulbine frutescens (Asphodelaceae), two unprecedented novel dimeric phenylanthraquinones, named joziknipholones A and B, possessing axial and centrochirality, were isolated, together with six known compounds. Structural elucidation of the new metabolites was achieved by spectroscopic and chiroptical methods, by reductive cleavage of the central bond between the monomeric phenylanthraquinone and -anthrone portions with sodium dithionite, and by quantum chemical CD calculations. Based on the recently revised absolute axial configuration of the parent phenylanthraquinones, knipholone and knipholone anthrone, the new dimers were attributed to possess the P-configuration (i.e., with the acetyl portions below the anthraquinone plane) at both axes in the case of joziknipholone A, whereas in joziknipholone B, the knipholone part was found to be M-configured. Joziknipholones A and B are active against the chloroquine resistant strain K1 of the malaria pathogen, Plasmodium falciparum, and show moderate activity against murine leukemic lymphoma L5178y cells.},
  language  = {en}
}
@misc{TsukamotoHeabelValencaetal.2008,
  author    = {Tsukamoto, Junko and Heabel, Sophie and Valenca, Gustavo P. and Peter, Martin and Franco, Telma},
  title     = {Enzymatic direct synthesis of acrylic acid esters of mono- and disaccharides},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-42652},
  year      = {2008},
  abstract  = {BACKGROUND: There is an increased need to replace materials derived from fossil sources by renewables. Sugar-cane derived carbohydrates are very abundant in Brazil and are the cheapest sugars available in the market, with more than 400 million tons of sugarcane processed in the year 2007. The objective of this work was to study the preparation of sugar acrylates from free sugars and free acrylic acid, thus avoiding the previous preparation of protected sugar derivatives, such as glycosides, or activated acrylates, such as vinyl acrylate. RESULTS: Lipase catalyzed esterification of three mono- and two disaccharides with acrylic acid, in the presence or absence of molecular sieves was investigated. The reactions were monitored by high-performance liquid chromatography (HPLC) and the products were analyzed by matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry. The main products are mono- and diacrylates, while higher esters are formed as minor products. The highest conversion to sugar acrylates was observed for the D-glucose and D-fructose, followed by D-xylose and D-maltose. Molecular sieves had no pronounced effect on the conversion CONCLUSIONS: A feasible method is described to produce and to characterize sugar acrylates, including those containing more than two acrylate groups. The process for production of these higher esters could potentially be optimized further to produce molecules for cross-linking in acrylate polymerization and other applications. The direct enzymatic esterification of free carbohydrates with acrylic acid is unprecedented.},
  language  = {en}
}
@misc{SchaeferBungNest2008,
  author    = {Sch{\"a}fer-Bung, Boris and Nest, Mathias},
  title     = {Correlated dynamics of electrons with reduced two-electron density matrices},
  issn      = {1866-8372},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-41774},
  year      = {2008},
  abstract  = {We present an approach to the correlated dynamics of many-electron systems. We show, that the twoelectron reduced density matrix (2RDM) can provide a suitable description of the real time evolution of a system. To achieve this, the hierarchy of equations of motion must be truncated in a practical way. Also, the computational effort, given that the 2RDM is represented by products of two-electron determinants, is discussed, and numerical model calculations are presented.},
  language  = {en}
}
@phdthesis{Frankovitch2007,
  author    = {Frankovitch, Christine Marie},
  title     = {Optical methods for monitoring biological parameters of phototropic microorganisms during cultivation},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-15403},
  school      = {Universit{\"a}t Potsdam},
  year      = {2007},
  abstract  = {Phototropic microalgae have a large potential for producing valuable substances for the feed, food, cosmetics, pigment, bioremediation, and pharmacy industries as well as for biotechnological processes. Today it is estimated that the microalgal aquaculture worldwide production is 5000 tons of dry matter per year (not taking into account processed products) making it an approximately \$1.25 billion U.S. per year industry. In this work, several spectroscopic techniques were utilized for the investigation of microalgae cells. Specifically, photondensity wave spectroscopy was applied as a technique for the on-line observation of the culture. For effective evaluation of the photosynthetic growth processes, fast and non-invasive sensor systems that analyze the relevant biological and technical process parameters are preferred. Traditionally, the biomass in a photobioreactor is quantified with the help of turbidimetry measurements, which require extensive calibration. Another problem frequently encountered when using spectral analysis for investigating solutions is that samples of interest are often undiluted and highly scattering and do not adhere to Beer-Lambert's law. Due to the fluorescence properties of chlorophyll, fluorescence spectroscopy techniques including fluorescence lifetime imaging and single photon counting could be applied to provide images of the cells as well as determine the effects of excitation intensity on the fluorescence lifetime, which is an indicator of the condition of the cell. A photon density wave is a sinusoidally intensity-modulated optical wave stemming from a point-source of light, which propagates through diffuse medium and exhibits amplitude and phase variations. Light propagation though strongly scattering media can be described by the P1 approximation to the Boltzmann transport equation. Photon density wave spectroscopy enables the ability to differentiate between scattered and absorbed light, which is desired so that an independent determination of the reduced scattering and absorption coefficients can be made. The absorption coefficient is related to the pigment content in the cells, and the reduced scattering coefficient can be used to characterize physical and morphological properties of the medium and was here applied for the determination of the average cell size.},
  language  = {en}
}
@misc{HildebrandtCharbonniereZiesseletal.2006,
  author    = {Hildebrandt, Nico and Charbonni{\`e}re, Lo{\"i}c J. and Ziessel, Raymond F. and L{\"o}hmannsr{\"o}ben, Hans-Gerd},
  title     = {Quantum dots as resonance energy transfer acceptors for monitoring biological interactions},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-12213},
  year      = {2006},
  abstract  = {Quantum dots (QDs) are common as luminescing markers for imaging in biological applications because their optical properties seem to be inert against their surrounding solvent. This, together with broad and strong absorption bands and intense, sharp tuneable luminescence bands, makes them interesting candidates for methods utilizing Forster Resonance Energy Transfer (FRET), e. g. for sensitive homogeneous fluoroimmunoassays (FIA). In this work we demonstrate energy transfer from Eu3+-trisbipyridin (Eu-TBP) donors to CdSe-ZnS-QD acceptors in solutions with and without serum. The QDs are commercially available CdSe-ZnS core-shell particles emitting at 655 nm (QD655). The FRET system was achieved by the binding of the streptavidin conjugated donors with the biotin conjugated acceptors. After excitation of Eu-TBP and as result of the energy transfer, the luminescence of the QD655 acceptors also showed lengthened decay times like the donors. The energy transfer efficiency, as calculated from the decay times of the bound and the unbound components, amounted to 37\%. The Forster-radius, estimated from the absorption and emission bands, was ca. 77{\AA}. The effective binding ratio, which not only depends on the ratio of binding pairs but also on unspecific binding, was obtained from the donor emission dependent on the concentration. As serum promotes unspecific binding, the overall FRET efficiency of the assay was reduced. We conclude that QDs are good substitutes for acceptors in FRET if combined with slow decay donors like Europium. The investigation of the influence of the serum provides guidance towards improving binding properties of QD assays.},
  language  = {en}
}
@misc{SchmaelzlinWalzKlimantetal.2006,
  author    = {Schm{\"a}lzlin, Elmar and Walz, Bernd and Klimant, Ingo and Schewe, Bettina and L{\"o}hmannsr{\"o}ben, Hans-Gerd},
  title     = {Monitoring hormone-induced oxygen consumption in the salivary glands of the blowfly, Calliphora vicina, by use of luminescent microbeads},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-12206},
  year      = {2006},
  abstract  = {The salivary glands of the blowfly were injected with luminescent oxygen-sensitive microbeads. The changes in oxygen content within individual gland tubules during hormone-induced secretory activity were quantified. The measurements are based on an upgraded phase-modulation technique, where the phase shift of the sensor phosphorescence is determined independently from concentration and background signals. We show that the combination of a lock-in amplifier with a fluorescence microscope results in a convenient setup to measure oxygen concentrations within living animal tissues at the cellular level.},
  language  = {en}
}
@misc{EngelhardKumkeLoehmannsroeben2006,
  author    = {Engelhard, Sonja and Kumke, Michael Uwe and L{\"o}hmannsr{\"o}ben, Hans-Gerd},
  title     = {OPQS - optical process and quality sensing : exemplary applications in the beerbrewing and polyurethane foaming processes},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-12191},
  year      = {2006},
  abstract  = {Optical methods play an important role in process analytical technologies (PAT). Four examples of optical process and quality sensing (OPQS) are presented, which are based on three important experimental techniques: near-infrared absorption, luminescence quenching, and a novel method, photon density wave (PDW) spectroscopy. These are used to evaluate four process and quality parameters related to beer brewing and polyurethane (PU) foaming processes: the ethanol content and the oxygen (O2) content in beer, the biomass in a bioreactor, and the cellular structures of PU foam produced in a pilot production plant.},
  language  = {en}
}
@misc{LoehmannsroebenBeckHildebrandtetal.2006,
  author    = {L{\"o}hmannsr{\"o}ben, Hans-Gerd and Beck, Michael and Hildebrandt, Niko and Schm{\"a}lzlin, Elmar and van Dongen, Joost T.},
  title     = {New challenges in biophotonics : laser-based fluoroimmuno analysis and in-vivo optical oxygen monitoring},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-10120},
  year      = {2006},
  abstract  = {Two examples of our biophotonic research utilizing nanoparticles are presented, namely laser-based fluoroimmuno analysis and in-vivo optical oxygen monitoring. Results of the work include significantly enhanced sensitivity of a homogeneous fluorescence immunoassay and markedly improved spatial resolution of oxygen gradients in root nodules of a legume species.},
  subject      = {Sauerstoff},
  language  = {en}
}
@misc{LauSalffnerLoehmannsroeben2006,
  author    = {Lau, Steffen and Salffner, Katharina and L{\"o}hmannsr{\"o}ben, Hans-Gerd},
  title     = {Isotopic resolution of carbon monoxide and carbon dioxide by NIR diode laser spectroscopy},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-10135},
  year      = {2006},
  abstract  = {Near-infrared (NIR) absorption spectroscopy with tunable diode lasers allows the simultaneous detection of the three most important isotopologues of carbon dioxide (<SUP>12</SUP>CO<SUB>2</SUB>, <SUP>13</SUP>CO<SUB>2</SUB>, <SUP>12</SUP>C<SUP>18</SUP>O<SUP>16</SUP>O) and carbon monoxide (<SUP>12</SUP>CO, <SUP>13</SUP>CO, <SUP>12</SUP>C<SUP>18</SUP>O). The flexible and compact fiber-optic tunable diode laser absorption spectrometer (TDLAS) allows selective measurements of CO<SUB>2</SUB> and CO with high isotopic resolution without sample preparation since there is no interference with water vapour. For each species, linear calibration plots with a dynamic range of four orders of magnitude and detection limits (LOD) in the range of a few ppm were obtained utilizing wavelength modulation spectroscopy (WMS) with balanced detection in a Herriott-type multipass cell. The high performance of the apparatus is illustrated by fill-evacuation-refill cycles.},
  subject      = {Isotop},
  language  = {en}
}
@misc{NiederkruegerSalbBecketal.2006,
  author    = {Niederkr{\"u}ger, Matthias and Salb, Christian and Beck, Michael and Hildebrandt, Niko and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Marowsky, Gerd},
  title     = {Improvement of a fluorescence immunoassay with a compact diode-pumped solid state laser at 315 nm},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-10150},
  year      = {2006},
  abstract  = {We demonstrate the improvement of fluorescence immunoassay (FIA) diagnostics in deploying a newly developed compact diode-pumped solid state (DPSS) laser with emission at 315 nm. The laser is based on the quasi-three-level transition in Nd:YAG at 946 nm. The pulsed operation is either realized by an active Q-switch using an electro-optical device or by introduction of a Cr<SUP>4+</SUP>:YAG saturable absorber as passive Q-switch element. By extra-cavity second harmonic generation in different nonlinear crystal media we obtained blue light at 473 nm. Subsequent mixing of the fundamental and the second harmonic in a β-barium-borate crystal provided pulsed emission at 315 nm with up to 20 μJ maximum pulse energy and 17 ns pulse duration. Substitution of a nitrogen laser in a FIA diagnostics system by the DPSS laser succeeded in considerable improvement of the detection limit. Despite significantly lower pulse energies (7 μJ DPSS laser versus 150 μJ nitrogen laser), in preliminary investigations the limit of detection was reduced by a factor of three for a typical FIA.},
  subject      = {Immunoassay},
  language  = {en}
}
@misc{BeckHildebrandtLoehmannsroeben2006,
  author    = {Beck, Michael and Hildebrandt, Niko and L{\"o}hmannsr{\"o}ben, Hans-Gerd},
  title     = {Quantum dots as acceptors in FRET-assays containing serum},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-9504},
  year      = {2006},
  abstract  = {Quantum dots (QDs) are common as luminescing markers for imaging in biological applications because their optical properties seem to be inert against their surrounding solvent. This, together with broad and strong absorption bands and intense, sharp tuneable luminescence bands, makes them interesting candidates for methods utilizing F{\"o}rster Resonance Energy Transfer (FRET), e. g. for sensitive homogeneous fluoroimmunoassays (FIA). In this work we demonstrate energy transfer from Eu<SUP>3+</SUP>-trisbipyridin (Eu-TBP) donors to CdSe-ZnS-QD acceptors in solutions with and without serum. The QDs are commercially available CdSe-ZnS core-shell particles emitting at 655 nm (QD655). The FRET system was achieved by the binding of the streptavidin conjugated donors with the biotin conjugated acceptors. After excitation of Eu-TBP and as result of the energy transfer, the luminescence of the QD655 acceptors also showed lengthened decay times like the donors. The energy transfer efficiency, as calculated from the decay times of the bound and the unbound components, amounted to 37\%. The F{\"o}rster-radius, estimated from the absorption and emission bands, was ca. 77 {\AA}. The effective binding ratio, which not only depends on the ratio of binding pairs but also on unspecific binding, was obtained from the donor emission dependent on the concentration. As serum promotes unspecific binding, the overall FRET efficiency of the assay was reduced. We conclude that QDs are good substitutes for acceptors in FRET if combined with slow decay donors like Europium. The investigation of the influence of the serum provides guidance towards improving binding properties of QD assays.},
  subject      = {Quantenpunkt},
  language  = {en}
}
@misc{SchulerLipmanSteinbachetal.2005,
  author    = {Schuler, Benjamin and Lipman, Everett A. and Steinbach, Peter J. and Kumke, Michael Uwe and Eaton, William A.},
  title     = {Polyproline and the "spectroscopic ruler" revisited with single-molecule fluorescence},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-12229},
  year      = {2005},
  abstract  = {To determine whether F{\"o}rster resonance energy transfer (FRET) measurements can provide quantitative distance information in single-molecule fluorescence experiments on polypeptides, we measured FRET efficiency distributions for donor and acceptor dyes attached to the ends of freely diffusing polyproline molecules of various lengths. The observed mean FRET efficiencies agree with those determined from ensemble lifetime measurements but differ considerably from the values expected from F{\"o}rster theory, with polyproline treated as a rigid rod. At donor-acceptor distances much less than the F{\"o}rster radius R0, the observed efficiencies are lower than predicted, whereas at distances comparable to and greater than R0, they are much higher. Two possible contributions to the former are incomplete orientational averaging during the donor lifetime and, because of the large size of the dyes, breakdown of the point-dipole approximation assumed in F{\"o}rster theory. End-to-end distance distributions and correlation times obtained from Langevin molecular dynamics simulations suggest that the differences for the longer polyproline peptides can be explained by chain bending, which considerably shortens the donor-acceptor distances.},
  language  = {en}
}
@misc{LemkeFernandezTrujilloLoehmannsroeben2005,
  author    = {Lemke, Matthias and Fern{\´a}ndez-Trujillo, Rebeca and L{\"o}hmannsr{\"o}ben, Hans-Gerd},
  title     = {In-situ LIF analysis of biological and petroleum-based hydraulic oils on soil},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-12268},
  year      = {2005},
  abstract  = {Absorption and fluorescence properties of 4 hydraulic oils (3 biological and 1 petroleum-based) were investigated. In-situ LIF (laser-induced fluorescence) analysis of the oils on a brown sandy loam soil was performed. With calibration, quantitative detection was achieved. Estimated limits of detection were below ca. 500 mg/kg for the petroleum-based oil and ca. 2000 mg/kg for one biological oil. A semi-quantitative classification scheme is proposed for monitoring of the biological oils. This approach was applied to investigate the migration of a biological oil in soil-containing compartments, namely a soil column and a soil bed.},
  language  = {en}
}
@phdthesis{Maltseva2005,
  author    = {Maltseva, Elena},
  title     = {Model membrane interactions with ions and peptides at the air/water interface},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-5670},
  school      = {Universit{\"a}t Potsdam},
  year      = {2005},
  abstract  = {The interactions between peptides and lipids are of fundamental importance in the functioning of numerous membrane-mediated biochemical processes including antimicrobial peptide action, hormone-receptor interactions, drug bioavailability across the blood-brain barrier and viral fusion processes. Alteration of peptide structure could be a cause of many diseases. Biological membranes are complex systems, therefore simplified models may be introduced in order to understand processes occurring in nature. The lipid monolayers at the air/water interface are suitable model systems to mimic biological membranes since many parameters can be easily controlled. In the present work the lipid monolayers were used as a model membrane and their interactions with two different peptides B18 and Amyloid beta (1-40) peptide were investigated. B18 is a synthetic peptide that binds to lipid membranes that leads to the membrane fusion. It was demonstrated that it adopts different structures in the aqueous solutions and in the membrane interior. It is unstructured in solutions and forms alpha-helix at the air/water interface or in the membrane bound state. The peptide has affinity to the negatively charged lipids and even can fold into beta-sheet structure in the vicinity of charged membranes at high peptide to lipid ratio. It was elucidated that in the absence of electrostatic interactions B18 does not influence on the lipid structure, whereas it provides partial liquidization of the negatively charged lipids. The understanding of mechanism of the peptide action in model system may help to develop the new type of antimicrobial peptides as well as it can shed light on the general mechanisms of peptide/membrane binding. The other studied peptide - Amyloid beta (1-40) peptide, which is the major component of amyloid plaques found in the brain of patients with Alzheimer's disease. Normally the peptide is soluble and is not toxic. During aging or as a result of the disease it aggregates and shows a pronounced neurotoxicity. The peptide aggregation involves the conformational transition from a random coil or alpha-helix to beta-sheets. Recently it was demonstrated that the membrane can play a crucial role for the peptide aggregation and even more the peptide can cause the change in the cell membranes that leads to a neuron death. In the present studies the structure of the membrane bound Amyloid beta peptide was elucidated. It was found that the peptide adopts the beta-sheet structure at the air/water interface or being adsorbed on lipid monolayers, while it can form alpha-helical structure in the presence of the negatively charged vesicles. The difference between the monolayer system and the bulk system with vesicles is the peptide to lipid ratio. The peptide adopts the helical structure at low peptide to lipid ratio and folds into beta-sheet at high ratio. Apparently, Abeta peptide accumulation in the brain is concentration driven. Increasing concentration leads to a change in the lipid to peptide ratio that induces the beta-sheet formation. The negatively charged lipids can act as seeds in the plaque formation, the peptide accumulates on the membrane and when the peptide to lipid ratio increases it the peptide forms toxic beta-sheet containing aggregates.},
  subject      = {Lipide},
  language  = {en}
}
@misc{SchmaelzlinDongenKlimantetal.2005,
  author    = {Schm{\"a}lzlin, Elmar and Dongen, Joost T. van and Klimant, Ingo and Marmod{\´e}e, Bettina and Steup, Martin and Fishahn, Joachim and Geigenberger, Peter and L{\"o}hmannsr{\"o}ben, Hans-Gerd},
  title     = {An optical multifrequency phase-modulation method using microbeads for measuring intracellular oxygen concentrations in plants},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-12232},
  year      = {2005},
  abstract  = {A technique has been developed to measure absolute intracellular oxygen concentrations in green plants. Oxygen-sensitive phosphorescent microbeads were injected into the cells and an optical multifrequency phase-modulation technique was used to discriminate the sensor signal from the strong autofluorescence of the plant tissue. The method was established using photosynthesis-competent cells of the giant algae Chara corallina L., and was validated by application to various cell types of other plant species.},
  language  = {en}
}
@misc{LoehmannsroebenKantorKumkeetal.2005,
  author    = {L{\"o}hmannsr{\"o}ben, Hans-Gerd and Kantor, Zoltan and Kumke, Michael Uwe and Schm{\"a}lzlin, Elmar and Reich, Oliver},
  title     = {OPQS - optische Prozess- und Qualit{\"a}ts-Sensorik},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-13205},
  year      = {2005},
  abstract  = {Im vorliegenden Beitrag wird an Hand dreier Beispiele der Einsatz von optischer Sensorik zur Produktcharakterisierung dargestellt, n{\"a}mlich Untersuchungen zum O2-Gehalt in Fruchts{\"a}ften, zur Isotopiesignatur von CO2 in Mineralw{\"a}ssern und zu Lichtstreueigenschaften eines Sonnenschutzmittels. Inhalt: Bestimmung von O2 mit Lumineszenzsonden Isotopenselektive Bestimmung von CO2 mit TDLAS Optische Charakterisierung stark streuender Materialien mit Photonendichtewellen},
  language  = {de}
}
@misc{DoscheKumkeLoehmannsroebenetal.2004,
  author    = {Dosche, Carsten and Kumke, Michael Uwe and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Ariese, F. and Bader, Arjen N. and Gooijer, C. and Miljanic, O. S. and Iwamoto, M. and Vollhardt, K. Peter C. and Puchta, R. ; van Eikema Hommes, N. J. R.},
  title     = {Deuteration effects on the vibronic structure of the fluorescence spectra and the internal conversion rates of triangular [4]Phenylene},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-11881},
  year      = {2004},
  abstract  = {Deuteration effects on the vibronic structure of the emission and excitation spectra of triangular [4]phenylene (D3h[4]phenylene) were studied using laser-excited Shpolskii spectroscopy (LESS) in an octane matrix at 4.2 K. For correct assignment of the vibrational modes, the experimental results were compared with calculated frequencies (B3LYP/6-31G*). CH vibrations were identified by their characteristic isotopic shifts in the spectra of deuterated triangular [4]phenylenes. Two CC stretching modes, at 100 cm-1 and 1176 cm-1, suitable as probes for bond strength changes in the excited state, were identified. The isotope effect on the internal conversion rates of triangular [4]phenylene was evaluated from measurements of temperature dependent lifetime. Isotope dependency and the magnitude of the internal conversion rates indicate that internal conversion in triangular [4]phenylene is most likely induced by CH vibrations. The results obtained by LESS and lifetime measurements were compared with PM3 PECI calculations of the excited state structure. The theoretical results and the relation between ground and excited state vibration energies of the 1176 cm-1 probe vibration indicate a reduction of bond alternation of the central cyclohexatriene ring in the excited state.},
  language  = {de}
}
@misc{LoehmannsroebenBeitzLuadienetal.2004,
  author    = {L{\"o}hmannsr{\"o}ben, Hans-Gerd and Beitz, Toralf and Luadien, Robert and Schultze, Rainer},
  title     = {Laser-based ion mobility spectrometry for sensing of aromatic compounds},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-11892},
  year      = {2004},
  abstract  = {The drift time spectra of polycyclic aromatic hydrocarbons (PAH), alkylbenzenes and alkylphenylethers were recorded with a laser-based ion mobility (IM) spectrometer. The ion mobilities of all compounds were determined in helium as drift gas. This allows the calculation of the diffusion cross sections (Omegacalc) on the basis of the exact hard sphere scattering model (EHSSM) and their comparison with the experimentally determined diffusion cross sections (Omegaexp). These Omegaexp/Omegacalc-correlations are presented for molecules with a rigid structure like PAH and prove the reliability of the theoretical model and experimental method. The increase of the selectivity of IM spectrometry is demonstrated using resonance enhanced multiphoton ionisation (REMPI) at atmospheric pressure, realized by tuneable lasers. The REMPI spectra of nine alkylbenzenes and alkylphenylethers are investigated. On the basis of these spectra, the complete qualitative distinction of eight compounds in a mixture is shown. These experiments are extended to alkylbenzene isomer mixtures.},
  language  = {en}
}
@misc{HoernerLauLoehmannsroeben2004,
  author    = {H{\"o}rner, Gerald and Lau, Steffen and L{\"o}hmannsr{\"o}ben, Hans-Gerd},
  title     = {NIR-diode laser spectroscopy for isotope-selective sensing of soil-respired carbon dioxide},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-10148},
  year      = {2004},
  abstract  = {The performance of a home-built tunable diode laser (TDL) spectrometer has been optimized regarding multi-line detection of carbon dioxide in natural gases. In the regime of the (30<SUP>0</SUP>1)<SUB>III</SUB> ← (000) band of <SUP>12</SUP>CO<SUB>2</SUB> around 1.6 μm, the dominating isotope species <SUP>12</SUP>CO<SUB>2</SUB>, <SUP>13</SUP>CO<SUB>2</SUB>, and <SUP>12</SUP>C<SUP>18</SUP>O<SUP>16</SUP>O were detected simultaneously. In contrast to most established techniques, selective measurements are performed without any sample preparation. This is possible since the CO<SUB>2</SUB> detection is free of interference from water, ubiquitous in natural gases. Detection limits in the range of a few ppmv were obtained for each species utilizing wavelength modulation (WM) spectroscopy with balanced detection in a long-path absorption cell set-up. Linear calibration plots cover a dynamic range of four orders of magnitude, allowing for quantitative CO<SUB>2</SUB> detection in various samples, like soil and breath gas. High isotopic resolution enables the excellent selectivity, sensitivity, and stability of the chosen analytical concept. The obtained isotopic resolution of typically ± 1.0  per mille and ± 1.5  per mille (for 3 vol. \% and 0.7 vol. \% of CO<SUB>2</SUB>, respectively) offers a promising analytical tool for isotope-ratio determination of carbon dioxide in soil gas. Preliminary experiments on soil respiration for the first time combine the on-line quantification of the overall carbon dioxide content with an optode sensor and isotopic determination (TDL system) of natural gas species.},
  subject      = {Kohlendioxid},
  language  = {en}
}
@misc{HoernerLauKantoretal.2004,
  author    = {H{\"o}rner, Gerald and Lau, Steffen and Kantor, Zoltan and L{\"o}hmannsr{\"o}ben, Hans-Gerd},
  title     = {Isotope selective analysis of CO2 with tunable diode laser (TDL) spectroscopy in the NIR},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-10167},
  year      = {2004},
  abstract  = {The performance of a home-built tunable diode laser (TDL) spectrometer, aimed at multi-line detection of carbon dioxide, has been evaluated and optimized. In the regime of the (30<SUP>0</SUP>1)<SUB>III</SUB> / (000) band of <SUP>12</SUP>CO<SUB>2</SUB> around 1.6 μm, the dominating isotope species <SUP>12</SUP>CO<SUB>2</SUB>, <SUP>13</SUP>CO<SUB>2</SUB>, and <SUP>12</SUP>C<SUP>18</SUP>O<SUP>16</SUP>O were detected simultaneously without interference by water vapor. Detection limits in the range of few ppmv were obtained for each species utilizing wavelength modulation (WM) spectroscopy with balanced detection in a long-path absorption cell set-up. High sensitivity in conjunction with high precision —typically ±1 per mille and ±6 per mille for 3\% and 0.7\% of CO<SUB>2</SUB>, respectively— renders this experimental approach a promising analytical concept for isotope-ratio determination of carbon dioxide in soil and breath gas. For a moderate <SUP>12</SUP>CO<SUB>2</SUB> line, the pressure dependence of the line profile was characterized in detail, to account for pressure effects on sensitive measurements.},
  subject      = {Isotopenverh{\"a}ltnis},
  language  = {en}
}
@misc{DoscheKumkeArieseetal.2003,
  author    = {Dosche, Carsten and Kumke, Michael Uwe and Ariese, F. and Bader, Arjen N. and Gooijer, C. and Dosa, P. I. and Han, S. and Miljanic, O. S. and Vollhardt, K. Peter C. and Puchta, R. and Eikema Hommes, N. J. R. van},
  title     = {Shpol'skii spectroscopy and vibrational analysis of [N]phenylenes},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-13075},
  year      = {2003},
  abstract  = {Vibrationally resolved fluorescence spectra of four angular [N]phenylenes were recorded with laser excited Shpol'skii spectroscopy (LESS) in an n-octane matrix at 10 K. In general, the same vibrational frequencies were observed in the fluorescence excitation and emission spectra, indicating that the geometries of ground and electronically excited state are very similar. Because of intensity borrowing from the S2 state, vibrations of two different symmetries were observed in the fluorescence excitation spectra of angular [3]phenylene and zig-zag[5]phenylene. This finding allowed the location of the S2 state for these compounds. DFT calculations(RB3LYP/6-31G*) of the ground state vibrational frequencies were made. The calculated vibrational modes were in reasonably good agreement with the experimental data. A new very low-frequency vibration of approximately 100 cm-1 was predicted and experimentally confirmed for all [N]phenylenes investigated. This vibration seems to be unique for [N]phenylenes and is attributed to an in-plane movement of the carbon backbone.},
  language  = {de}
}
@misc{BillardAnsoborloAppersonetal.2003,
  author    = {Billard, Isabelle and Ansoborlo, Eric and Apperson, Kathleen and Arpigny, Sylvie and Azenha, M. Emilia and Birch, David and Bros, Pascal and Burrows, Hugh D. and Choppin, Gregory and Kumke, Michael Uwe},
  title     = {Aqueous solutions of Uranium(VI) as studied by time-resolved emission spectroscopy : a Round-Robin Test},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-12318},
  year      = {2003},
  abstract  = {Results of an inter-laboratory round-robin study of the application of time-resolved emission spectroscopy (TRES) to the speciation of uranium(VI) in aqueous media are presented. The round-robin study involved 13 independent laboratories, using various instrumentation and data analysis methods. Samples were prepared based on appropriate speciation diagrams and, in general, were found to be chemically stable for at least six months. Four different types of aqueous uranyl solutions were studied: (1) acidic medium where UO22+aq is the single emitting species, (2) uranyl in the presence of fluoride ions, (3) uranyl in the presence of sulfate ions, and (4) uranyl in aqueous solutions at different pH, promoting the formation of hydrolyzed species. Results between the laboratories are compared in terms of the number of decay components, luminescence lifetimes, and spectral band positions. The successes and limitations of TRES in uranyl analysis and speciation in aqueous solutions are discussed.},
  language  = {en}
}
@misc{ReichLoehmannsroebenSchael2003,
  author    = {Reich, Oliver and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Schael, Frank},
  title     = {Optical sensing with photon density waves: investigation of model media},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-13147},
  year      = {2003},
  abstract  = {Investigations with frequency domain photon density waves allow elucidation of absorption and scattering properties of turbid media. The temporal and spatial propagation of intensity modulated light with frequencies up to more than 1 GHz can be described by the P1 approximation to the Boltzmann transport equation. In this study, we establish requirements for the appropriate choice of turbid model media and characterize mixtures of isosulfan blue as absorber and polystyrene beads as scatterer. For these model media, the independent determination of absorption and reduced scattering coefficients over large absorber and scatterer concentration ranges is demonstrated with a frequency domain photon density wave spectrometer employing intensity and phase measurements at various modulation frequencies.},
  language  = {en}
}
@misc{KumkeFrimmel2002,
  author    = {Kumke, Michael Uwe and Frimmel, Fritz Hartmann},
  title     = {Stationary and time-resolved fluorescence for humic substances characterization},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-12353},
  year      = {2002},
  abstract  = {Steady-state and time-resolved fluorescence methods were applied to investigate the fluorescence properties of humic substances of different origins. Using standard 2D emission and total luminescence spectra, fluorescence maxima, the width of the fluorescence band and a relative fluorescence quantum efficiency were determined. Different trends for fulvic acids and humic acids were observed indicating differences in the heterogeneity of the sample fractions. The complexity of the fluorescence decay of humic substances is discussed and compared to simple model compounds. The effect of oxidation of humic substances on their fluorescence properties is discussed as well.},
  language  = {en}
}
@misc{DoscheLoehmannsroebenBieseretal.2002,
  author    = {Dosche, Carsten and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Bieser, A. and Dosa, P. I. and Han, S. and Iwamoto, M. and Schleifenbaum, A. and Vollhardt, K. Peter C.},
  title     = {Photophysical properties of [N]phenylenes},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-11936},
  year      = {2002},
  abstract  = {In the present study, photophysical properties of [N]phenylenes were studied by means of stationary and time-resolved absorption and fluorescence spectroscopy (in THF at room temperature). For biphenylene (1) and linear [3]phenylene (2a), internal conversion (IC) with quantum yields ΦIC > 0.99 is by far the dominant mechanism of S1 state deactivation. Angular [3]phenylene (3a), the zig-zag [4]- and [5]phenylenes (3b), (3c), and the triangular [4]phenylene (4) show fluorescence emission with fluorescence quantum yieds and lifetimes between ΦF = 0.07 for (3a) and 0.21 for (3c) and τF = 20 ns for (3a) and 81 ns for (4). Also, compounds (3) and (4) exhibit triplet formation upon photoexcitation with quantum yields as high as ΦISC = 0.45 for (3c). The strong differences in the fluorescence properties and in the triplet fromation efficiencies between (1) and (2a) on one hand and (3) and (4) on the other are related to the remarkable variation of the internal conversion (IC) rate constants kIC. A tentative classification of (1) and (2a) as "fast IC compounds", with kIC > 109 s-1, and of (3) and (4) as "slow IC compounds", with kIC ≈ 107 s-1, is suggested. This classification cannot simply be related to H{\"u}ckel's rule-type concepts of aromaticity, because the group of "fast IC compounds" consists of "antiaromatic" (1) and "aromatic" (2a), and the group of "slow IC compounds" consists of "antiaromatic" (3b), (4) and "aromatic" (3a), (3c). The IC in the [N]phenylenes is discussed within the framework of the so-called energy gap law established for non-radiative processes in benzenoid hydrocarbons.},
  language  = {en}
}
@misc{KaafaraniWexStrehmeletal.2002,
  author    = {Kaafarani, Bilal R. and Wex, Brigitte and Strehmel, Bernd and Neckers, Douglas C.},
  title     = {Structural concept for fluorinated Y-enynes with solvatochromic properties},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-13168},
  year      = {2002},
  abstract  = {An approach to the development of fluorescent probes to follow polymerizations in situ using fluorinated cross-conjugated enediynes (Y-enynes) is reported. Different substitution patterns in the Y-enynes result in distinct solvatochromic behavior. β,β-Bis(phenylethynyl)pentafluorostyrene 7, which bears no donor substituents and only fluorine at the styrene moiety, shows no solvatochromism. Donor substituted β,β-bis(3,4,5-trimethoxyphenylethynyl) pentafluorostyrene 8 and β,β-bis(4-butyl-2,3,5,6-tetrafluorophenylethynyl)-3,4,5-trimethoxystyrene 9 exhibit solvatochromism upon change of solvent polarity. Y-enyne 8 showed the largest solvatochromic shift (94 nm bathochromic shift) upon changing solvent from cyclohexane to acetonitrile. A smaller solvatochromic response (44 nm bathochromic shift) was observed for 9. Lippert-Mataga treatment of 8 and 9 yields slopes of -10,800 and -6,400 cm -1, respectively. This corresponds to a change in dipole moment of 9.6 and 6.9 D, respectively. The solvatochromic behavior in 8 and 9 supports the formation of an intramolecular charge transfer (ICT) state. The low fluorescence quantum yields are caused by competitive double bond rotation. The fluorescence decay time of 9 decreases in methyltetrahydrofuran from 2.1 ns at 77 K to 0.11 ns at 200 K. Efficient single bond rotation in 9 was frozen at -50 °C in a configuration in which the trimethoxyphenyl ring is perpendicular to the fluorinated rings. 7-9 are photostable compounds. The X-ray structure of 7 shows it is not planar and that its conjugation is distorted. Y-enyne 7 stacks in the solid state showing coulombic, actetylene-arene, and fluorine-π interactions.},
  language  = {en}
}
@misc{FrimmelKumke1998,
  author    = {Frimmel, Fritz Hartmann and Kumke, Michael Uwe},
  title     = {Optische Parameter zur Stoffcharakterisierung vom Trinkwasser bis zum Abwasser},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-13088},
  year      = {1998},
  abstract  = {Die Anwendung von optischen Parametern zur Stoffcharakterisierung wird diskutiert. Dabei ist der Schwerpunkt der Diskussion auf absorptions- und fluoreszenzspektroskopische Methoden gesetzt. Beide Methoden k{\"o}nnen schnell und zuverl{\"a}ssig - auch im on-line Betrieb - eingesetzt werden. Der Beitrag soll einen {\"U}berblick {\"u}ber die grundlegenden M{\"o}glichkeiten der Anwendung beider Methoden geben.},
  language  = {de}
}
@misc{AntonLaschewskyWard1995,
  author    = {Anton, Peter and Laschewsky, Andr{\´e} and Ward, M. D.},
  title     = {Solubilization control by redox-switching of polysoaps},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17336},
  year      = {1995},
  abstract  = {Reversible changes in the self-organization of polysoaps may be induced by controlling their charge numbers via covalently bound redox moieties. This is illustrated with two viologen polysoaps, which in response to an electrochemical stimulus, change their solubility and aggregation in water, leading from homogeneously dissolved and aggregated molecules to collapsed ones and vice verse. Using the electrochemical quartz crystal microbalance (EQCM), it could be shown that the reversibility of this process is better than 95\% in 16 cycles.},
  language  = {en}
}
@misc{CochinHendlingerLaschewsky1995,
  author    = {Cochin, Didier and Hendlinger, P. and Laschewsky, Andr{\´e}},
  title     = {Polysoaps with fluorocarbon hydrophobic chains},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17347},
  year      = {1995},
  abstract  = {A series of amphiphilic copolymers is prepared by copolymerization of choline methacrylate with 1,1,2,2-tetrahydroperfluorooctyl methacrylate in varying amounts. The copolymers bearing fluorocarbon chains are studied concerning their effects on viscosity, solubilization and surface activity in aqueous solution, exhibiting a general behavior characteristic for polysoaps. The results are compared with the ones obtained for an analogous series of amphiphilic copolymers bearing hydrocarbon chains.},
  language  = {en}
}
@misc{Laschewsky1995,
  author    = {Laschewsky, Andr{\´e}},
  title     = {Molecular concepts, self-organisation and properties of polysoaps},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-26895},
  year      = {1995},
  abstract  = {The article reviews water-soluble polymers characterized by surfactant side chains, and related amphiphilic polymers. Various synthetic approaches are presented, and rules for useful molecular architectures are given. Models for the self-organization of such polymers in water are presented comparing them with the micellization of low molecular weight surfactants. Highlighting key properties of aqueous polysoap solutions such as viscosity, surface tension and solubilization power, some structure-property relationships are established. Further, the formation of mesophases and of superstructures in bulk is addressed. Finally, the functionalization of polysoaps, and potential applications are discussed.},
  language  = {en}
}
@misc{RozanskiKremerKoeberleetal.1995,
  author    = {Rozanski, Stanislaw A. and Kremer, Friedrich and K{\"o}berle, Peter and Laschewsky, Andr{\´e}},
  title     = {Relaxation and charge transport in mixtures of zwitterionic polymers and inorganic salts},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17438},
  year      = {1995},
  abstract  = {Dielectric spectroscopy is employed to analyze the molecular dynamics and the charge transport in mixtures of zwitterionic polymers of the type poly{3 [N(-methacryloyloxyalkyl)] N, [N-dimethylammonio propanesulfonate] with sodium iodide in the frequency range of 10²Hz-10(up)7 Hz and in the temperature range of 110 K-400 K. The amount of inorganic salt added varies from 0-200 mol-\% relative to the number of zwitterionic groups present in the polymer, contributing strongly to the conductivity. One relaxation process is observed whose relaxation rate depends strongly on the length of the aliphatic spacer between the polymethacrylate main chain and the zwitterionic group. Exhibiting an Arrhenius-like temperature depence with activation energy EA = 47 KJ/mol, this relaxation process is assigned to fluctuation of the quaternary ammonium groups in the side chains. At higher temperatures, the dielectric properties and the conductivity are primarily dominated by the mobile inorganic ions: conductivity strongly depends on the salt concentration, showing a pronounced electrode polarization effect. The frequency and salt concentration, dependences of the conductivity can be quantitatively described as hopping of charge carriers being subject to spatially randomly varying energy barriers. For the low-frequency regime and for the critical frequency marking the onset of the conductivity's dispersion, the Barton-Nakajima-Namikawa (BNN) relationship is fulfilled.},
  language  = {en}
}
@misc{KoeberleLaschewsky1994,
  author    = {K{\"o}berle, Peter and Laschewsky, Andr{\´e}},
  title     = {Hybrid materials from organic polymers and inorganic salts},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-26884},
  year      = {1994},
  abstract  = {The prepaparation of amorphous, homogeneous blends of zwitterionic polymers and transition metal salts was investigated. Homogeneous miscibility was achieved in many cases up to equimolar amounts of salt, depending on the anion and cation chosen. Various analytical techniques point to a solid state solution of the inorganic ions in the polymer matrix.},
  language  = {en}
}
@misc{AntonLaschewsky1994,
  author    = {Anton, Peter and Laschewsky, Andr{\´e}},
  title     = {Solubilization by polysoaps},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17327},
  year      = {1994},
  abstract  = {The aqueous solubilization power of several series of micellar homopolymers and copolymers (polysoaps) is investigated. Using five insoluble or poorly water-soluble dyes, comparisons of the capacities are made with respect ot the influence of structural variables such as the polymer backbone, the polymer geometry, the comonomer content, and the charge of the hydrophilic group. Some guidelines for polysoap structures suited for efficient solubilization are established. Noteworthy is that the solubilization capacities of the polysoaps are neither linked to the ability to reduce the surface tension of water, nor to the polarity of the solubilization sites deduced from spectroscopic probes.},
  language  = {en}
}
@misc{AntonLaschewsky1993,
  author    = {Anton, Peter and Laschewsky, Andr{\´e}},
  title     = {Zwitterionic polysoaps with reduced density of surfactant side groups},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17301},
  year      = {1993},
  abstract  = {Several zwitterionic polymers were prepared by radical homopolymerization of surfactant monomers which bear diallyl, diene or vinylcyclopropane moieties. These polymer systems were complemented by alternating copolymers of appropriate zwitterionic vinyl compounds. Thus, polymers with reduced (as compared with simple vinylic homopolymers, or statistical copolymers) and well defined density of surfactant side groups are obtained. The solubilities found for these polymers are dominated by polymer geometry rather than by the balance of hydrophilic and hydrophobic fragments, thus corroborating a main-chain spacer model proposed recently. All water-soluble polymers exhibit characteristic features of classical polysoaps, as shown by surface tension measurements and by solubilization of hydrophobic dyes. In contrast, the water-insoluble copolymers are capable to form stable monolayers at the air-water interface.},
  language  = {en}
}
@misc{AntonKoeberleLaschewsky1993,
  author    = {Anton, Peter and K{\"o}berle, Peter and Laschewsky, Andr{\´e}},
  title     = {Recent developments in the field of micellar polymers},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17263},
  year      = {1993},
  abstract  = {This article describes recent achievements in the field of micellar polymers, or polysoaps. Taking advantage of zwitterionic model polymers, systematic variations of the molecular architecture have provided an improved understanding of the relationship between the molecular structure of the polymers and their key properties such as surface activity and solubilization capacity. Useful rules are established, which take into account much of the previous data in the literature.},
  language  = {en}
}
@misc{LaschewskySchulzHanke1993,
  author    = {Laschewsky, Andr{\´e} and Schulz-Hanke, Wolfgang},
  title     = {Ring-opening metathesis polymerization of amphiphilic norbornenes functionalized with non-linear optical (NLO) chromophores},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-26917},
  year      = {1993},
  abstract  = {Contents: Potential of amphiphilic NLO polymers Ring-opening metathesis polymerization (ROMP) Properties of the polymers Monolayer properties Experimental part - Methods - Materials - Analytical data - General polymerization procedure Conclusions},
  language  = {en}
}
@misc{KoeberleLaschewskyTsukruk1992,
  author    = {K{\"o}berle, Peter and Laschewsky, Andr{\´e} and Tsukruk, Vladimir},
  title     = {The structural order of some novel ionic polymers : 1. X-ray scattering studies},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17247},
  year      = {1992},
  abstract  = {A set of novel zwitterionic side-chain polyacrylates and polymethacrylates is studied by X-ray scattering. The structural order both in the short-range and long-range scale is investigated. The influence of the polymer backbone, of different locations of the ionic groups in isomeric polymers, of bound water and of added inorganic salts on the bulk structures is studied, and the observed rearrangements are analysed.},
  language  = {en}
}