@article{KoerzdoerferParrishSearsetal.2012, author = {K{\"o}rzd{\"o}rfer, Thomas and Parrish, Robert M. and Sears, John S. and Sherrill, C. David and Bredas, Jean-Luc}, title = {On the relationship between bond-length alternation and many-electron self-interaction error}, series = {The journal of chemical physics : bridges a gap between journals of physics and journals of chemistr}, volume = {137}, journal = {The journal of chemical physics : bridges a gap between journals of physics and journals of chemistr}, number = {12}, publisher = {American Institute of Physics}, address = {Melville}, issn = {0021-9606}, doi = {10.1063/1.4752431}, pages = {8}, year = {2012}, abstract = {Predicting accurate bond-length alternations (BLAs) in long conjugated molecular chains has been a major challenge for electronic-structure theory for many decades. While Hartree-Fock (HF) overestimates BLA significantly, second-order perturbation theory and commonly used density functional theory (DFT) approaches typically underestimate it. Here, we discuss how this failure is related to the many-electron self-interaction error (MSIE), which is inherent to both HF and DFT approaches. We use tuned long-range corrected hybrids to minimize the MSIE for a series of polyenes. The key result is that the minimization of the MSIE alone does not yield accurate BLAs. On the other hand, if the range-separation parameter is tuned to yield accurate BLAs, we obtain a significant MSIE that grows with chain length. Our findings demonstrate that reducing the MSIE is one but not the only important aspect necessary to obtain accurate BLAs from density functional theory.}, language = {en} } @phdthesis{Grothe2012, author = {Grothe, Dorian C.}, title = {Entwicklung und Synthese von Materialien f{\"u}r Polyelektrolytmembranen mit ionischen Fl{\"u}ssigkeiten zum Einsatz in Lithium-Ionen-Batterien}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-63690}, school = {Universit{\"a}t Potsdam}, year = {2012}, abstract = {F{\"u}r den Einsatz in Autobatterien gibt es besondere Anforderungen an den Elektrolyten im Bereich der Energie- und Leistungsdichten, um beispielsweise thermische Verluste gering zu halten. Hochleitf{\"a}hige Elektrolyte mit Leitf{\"a}higkeiten im Millisiemensbereich sind hier ebenso notwendig wie auch sichere, d.h. m{\"o}glichst nicht brennbare und einen niedrigen Dampfdruck besitzende Materialien. Um diese Vorgaben zu erreichen, ist es notwendig, einen polymeren Separator zu entwickeln, welcher auf brennbare organische L{\"o}sungsmittel verzichtet und damit eine drastische Steigerung der Sicherheit gew{\"a}hrleistet. Gleichzeitig m{\"u}ssen hierbei die Leistungsvorgaben bez{\"u}glich der Leitf{\"a}higkeit erf{\"u}llt werden. Zu diesem Zweck wurde ein Konzept basierend auf der Kombination von einer polymeren sauerstoffreichen Matrix und einer ionischen Fl{\"u}ssigkeit entwickelt und verifiziert. Dabei wurden folgende Erkenntnisse gewonnen: 1. Es wurden neuartige diacrylierte sauerstoffreiche Matrixkomponenten mit vielen Carbonylfunktionen, f{\"u}r eine gute Lithiumleitf{\"a}higkeit, synthetisiert. 2. Es wurden mehrere neue ionische Fl{\"u}ssigkeiten sowohl auf Imidazolbasis als auch auf Ammoniumbasis synthetisiert und charakterisiert. 3. Die Einfl{\"u}sse der Kationenstruktur und der Einfluss der Gegenionen im Bezug auf Schmelzpunkte und Leitf{\"a}higkeiten wurden untersucht. 4. Aus den entwickelten Materialien wurden Blendsysteme hergestellt und mittels Impedanzspektrometrie untersucht: Leitf{\"a}higkeiten von 10-4S/cm bei Raumtemperatur sind realisierbar. 5. Die Blendsysteme wurden auf ihre thermische Stabilit{\"a}t hin untersucht: Stabilit{\"a}ten bis 250°C sind erreichbar. Dabei wird keine kristalline Struktur beobachtet.}, language = {de} } @article{DzhigaevShabalinStankevicetal.2016, author = {Dzhigaev, D. and Shabalin, A. and Stankevic, T. and Lorenz, Ulf and Kurta, R. P. and Seiboth, F. and Wallentin, J. and Singer, A. and Lazarev, S. and Yefanov, O. M. and Borgstrom, M. and Strikhanov, M. N. and Samuelson, L. and Falkenberg, G. and Schroer, C. G. and Mikkelsen, A. and Vartanyants, I. A.}, title = {Bragg coherent x-ray diffractive imaging of a single indium phosphide nanowire}, series = {Journal of optics}, volume = {18}, journal = {Journal of optics}, publisher = {IOP Publ. Ltd.}, address = {Bristol}, issn = {2040-8978}, doi = {10.1088/2040-8978/18/6/064007}, pages = {10}, year = {2016}, abstract = {Three-dimensional (3D) Bragg coherent x-ray diffractive imaging (CXDI) with a nanofocused beam was applied to quantitatively map the internal strain field of a single indium phosphide nanowire. The quantitative values of the strain were obtained by pre-characterization of the beam profile with transmission ptychography on a test sample. Our measurements revealed the 3D strain distribution in a region of 150 nm below the catalyst Au particle. We observed a slight gradient of the strain in the range of +/- 0.6\% along the [111] growth direction of the nanowire. We also determined the spatial resolution in our measurements to be about 10 nm in the direction perpendicular to the facets of the nanowire. The CXDI measurements were compared with the finite element method simulations and show a good agreement with our experimental results. The proposed approach can become an effective tool for in operando studies of the nanowires.}, language = {en} } @article{BrauneGrossWalteretal.2016, author = {Braune, Steffen and Gross, M. and Walter, M. and Zhou, Shengqiang and Dietze, Siegfried and Rutschow, S. and Lendlein, Andreas and Tschoepe, C. and Jung, Friedrich}, title = {Adhesion and activation of platelets from subjects with coronary artery disease and apparently healthy individuals on biomaterials}, series = {Journal of biomedical materials research : an official journal of the Society for Biomaterials, the Japanese Society for Biomaterials; the Australian Society for Biomaterials}, volume = {104}, journal = {Journal of biomedical materials research : an official journal of the Society for Biomaterials, the Japanese Society for Biomaterials; the Australian Society for Biomaterials}, publisher = {Wiley-Blackwell}, address = {Hoboken}, issn = {1552-4973}, doi = {10.1002/jbm.b.33366}, pages = {210 -- 217}, year = {2016}, abstract = {On the basis of the clinical studies in patients with coronary artery disease (CAD) presenting an increased percentage of activated platelets, we hypothesized that hemocompatibility testing utilizing platelets from healthy individuals may result in an underestimation of the materials' thrombogenicity. Therefore, we investigated the interaction of polymer-based biomaterials with platelets from CAD patients in comparison to platelets from apparently healthy individuals. In vitro static thrombogenicity tests revealed that adherent platelet densities and total platelet covered areas were significantly increased for the low (polydimethylsiloxane, PDMS) and medium (Collagen) thrombogenic surfaces in the CAD group compared to the healthy subjects group. The area per single platelet—indicating the spreading and activation of the platelets—was markedly increased on PDMS treated with PRP from CAD subjects. This could not be observed for collagen or polytetrafluoroethylene (PTFE). For the latter material, platelet adhesion and surface coverage did not differ between the two groups. Irrespective of the substrate, the variability of these parameters was increased for CAD patients compared to healthy subjects. This indicates a higher reactivity of platelets from CAD patients compared to the healthy individuals. Our results revealed, for the first time, that utilizing platelets from apparently healthy donors bears the risk of underestimating the thrombogenicity of polymer-based biomaterials.}, language = {en} } @article{BahrkeEinarssonGislasonetal.2002, author = {Bahrke, Sven and Einarsson, Jon M. and Gislason, Johannes and Haebel, Sophie and Letzel, Matthias C. and Peter-Katalinic, Jasna and Peter, Martin G.}, title = {Sequence analysis of chitooligosaccharides by matrix-assisted laser desorption ionization postsource decay mass spectrometry}, year = {2002}, abstract = {Oligosaccharides composed of 2-acetamido-2-deoxy-D-glucopyranose (GlcNAc) and/or 2-amino-2-deoxy-D- glucopyranose (GlcN) were prepd. by chem. degrdn. of chitin or chitosan and sepd. by gel permeation chromatog. Oligosaccharides obtained after enzymic hydrolysis of chitosan [FA 0.19] with a fungal chitinase were derivatized by reductive amination with 2-aminoacridone and sequenced by matrix-assisted laser desorption ionization time-of-flight postsource decay (PSD) mass spectrometry (MS). The sequence of a trimer, D1A2, was established as D-A-A. The compn. of a hexamer D3A3 was .apprx.65\% D-A-D-D-A-A and 35\% D-D-A-D-A-A. The PSD MS of a nonamer D5A4-amac revealed four isobaric species D-X-Y-D-X-Y-D-A-A, where A is GlcNAc, D is GlcN, and X and Y (X ¹ Y) are mutually either D or A. This structure motif was also obsd. in a dodecamer D7A5 which was composed of eight isobaric sequences of the general formula (D-X-Y)3- D-A-A.}, language = {en} } @article{LetzelPeterKatalinicPeter2001, author = {Letzel, Matthias C. and Peter-Katalinic, Jasna and Peter, Martin G.}, title = {Mass spectrometry of chitin and chitosan oligosaccharides}, year = {2001}, language = {en} } @article{Illenseer2001, author = {Illenseer, C.}, title = {Investigation of ion-molecule collisions with laser-based ion mobility spectrometry}, year = {2001}, language = {en} } @article{StrehmelHenbestSarkeretal.2001, author = {Strehmel, Bernd and Henbest, K. B. and Sarker, A. M. and Malpert, J. H. and Chen, D. Y. and Rodgers, M. A. J. and Neckers, D. C.}, title = {Ion induced man ipulation of photochemical pathways in crown ether compounends based on fluorinated oligophenylenevinylenes}, publisher = {Journal of nanoscience and nanotechnology. - 1 (2001), 1, S. 107 - 124}, year = {2001}, language = {en} } @article{JansenBuschmannWegoetal.2001, author = {Jansen, K. and Buschmann, Hans-J{\"u}rgen and Wego, A. and Dopp, D. and Mayer, C. and Holdt, Hans-Joachim and Schollmeyer, E.}, title = {Curcubit[5]uril, decamethylcururbit[5]uril and curcurbit[6]uril : synthesis, solubility and amin complex formation}, year = {2001}, abstract = {A simple way to prepare cucurbit[5]uril is described. The macrocycles of the cucurbituril type are nearly insoluble in water. The solubilities of cucurbit[5]uril, decamethylcucurbit[5]uril and cucurbit[6]uril in hydrochloric acid, formic acid and acetic acid of different concentrations have been investigated. Due to the formation of complexes between cucurbit[n]urils and protons the solubility increases in aqueous acids. The macrocyclic ligands are able to form complexes with several organic compounds. Thus, the complex formation of the cucurbituril macrocycles with different amines has beenstudied by means of calorimetric titrations. The reaction enthalpy gives noevidence of the formation of inclusion or exclusion complexes. 1H-NMR measurements show that in the case of cucurbit[5]uril and cucurbit[6]uril the organic guest compound is included within the hydrophobic cavity. Decamethylcucurbit[5]uril forms only exclusion complexes with organicamines. This was confirmed by the crystal structure of the decamethylcucurbit[5]uril-1,6- diaminohexane complex. complex formation - cucurbit[5]uril - cucurbit[6]uril - decamethylcucurbit[5]uril - solubility - synthesis}, language = {en} } @article{KumkeSpechtFrimmel2000, author = {Kumke, Michael Uwe and Specht, C. H. and Frimmel, Fritz Hartmann}, title = {Characterization of NOM adsorption to clay minerals by sizs exclusion chromatography}, year = {2000}, language = {en} } @article{LetzelSynstadEijsinketal.1999, author = {Letzel, Matthias C. and Synstad, Bjoenar and Eijsink, Vincent G. H. and Peter-Katalinic, Jasna and Peter, Martin G.}, title = {Libraries of chito-oligosaccharides of mixed acetylation patterns and their interactions with chitinases}, isbn = {3-9806494-5-8}, year = {1999}, language = {en} } @article{SchwarzAndraeArnoldetal.1999, author = {Schwarz, W. H. Eugen and Andrae, Dirk and Arnold, S. R. and Heidberg, Joachim and Hellmann jr., H. and Hinze, J. and Karachalios, A. and Kovner, M. A. and Schmidt, P. C. and Z{\"u}licke, Lutz}, title = {Hans G. Hellmann (1903 - 1938) : ein deutscher Pionier der Quantenchemie in Moskau}, year = {1999}, language = {de} } @article{SchwarzAndraeArnoldetal.1999, author = {Schwarz, W. H. Eugen and Andrae, Dirk and Arnold, S. R. and Heidberg, Joachim and Hellmann jr., H. and Hinze, J. and Karachalios, A. and Kovner, M. A. and Schmidt, P. C. and Z{\"u}licke, Lutz}, title = {Hans G. Hellmann (1903 - 1938) : ein Pionier der Quantenchemie}, year = {1999}, language = {de} } @article{TeixeiraBlanzatKoetzetal.2006, author = {Teixeira, C. V. and Blanzat, Muriel and Koetz, Joachim and Rico-Lattes, I. and Brezesinski, Gerald}, title = {In-plane miscibility and mixed bilayer microstructure in mixtures of catanionic glycolipids and zwitterionic phospholipids}, series = {Biochimica et biophysica acta : Biomembranes}, volume = {1758}, journal = {Biochimica et biophysica acta : Biomembranes}, publisher = {Elsevier}, address = {Amsterdam}, issn = {0005-2736}, doi = {10.1016/j.bbamem.2006.05.025}, pages = {1797 -- 1808}, year = {2006}, abstract = {SAXS/WAXS studies were performed in combination with freeze fracture electron microscopy using mixtures of a new Gemini catanionic surfactant (Gem 16-12, formed by two sugar groups bound by a hydrocarbon spacer with 12 carbons and two 16-carbon chains) and the zwitterionic phospholipid 1,2-dipalmitoyl-sn-glycero-3-phosphocholine(DPPC) to establish the phase diagram. Gem 16-12 in water forms bilayers with the same amount of hydration water as DPPC. A frozen interdigitated phase with a low hydration number is observed below room temperature. The kinetics of the formation of this crystalline phase is very slow. Above the chain melting temperature, multilayered vesicles are formed. Mixing with DPPC produces mixed bilayers above the corresponding chain melting temperature. At room temperature, partially lamellar aggregates with local nematic order are observed. Splitting of infinite lamellae into discs is linked to immiscibility in frozen state. The ordering process is always accompanied by dehydration of the system. As a consequence, an unusual order-disorder phase transition upon cooling is observed.}, language = {en} } @article{BouaklineAlthorpeLarregarayetal.2010, author = {Bouakline, Foudhil and Althorpe, Stuart C. and Larregaray, Pascal and Bonnet, Laurent}, title = {Strong geometric-phase effects in the hydrogen-exchange reaction at high collision energies : II. quasiclassical trajectory analysis}, issn = {0026-8976}, doi = {10.1080/00268971003610218}, year = {2010}, abstract = {Recent calculations on the hydrogen-exchange reaction [Bouakline et al., J. Chem. Phys. 128, 124322 (2008)], have found strong geometric phase (GP) effects in the state-to-state differential cross-sections (DCS), at energies above the energetic minimum of the conical intersection (CI) seam, which cancel out in the integral cross-sections (ICS). In this article, we explain the origin of this cancellation and make other predictions about the nature of the reaction mechanisms at these high energies by carrying out quasiclassical trajectory (QCT) calculations. Detailed comparisons are made with the quantum results by splitting the quantum and the QCT cross-sections into contributions from reaction paths that wind in different senses around the CI and that scatter the products in the nearside and farside directions. Reaction paths that traverse one transition state (1-TS) scatter their products in just the nearside direction, whereas paths that traverse two transition states (2-TS) scatter in both the nearside and farside directions. However, the nearside 2-TS products scatter into a different region of angular phase-space than the 1-TS products, which explains why the GP effects cancel out in the ICS. Analysis of the QCT results also suggests that two separate reaction mechanisms may be responsible for the 2-TS scattering at high energies.}, language = {en} } @article{JankunasZareBouaklineetal.2012, author = {Jankunas, Justin and Zare, Richard N. and Bouakline, Foudhil and Althorpe, Stuart C. and Herraez-Aguilar, Diego and Aoiz, F. Javier}, title = {Seemingly anomalous angular distributions in H+D-2 reactive scattering}, series = {Science}, volume = {336}, journal = {Science}, number = {6089}, publisher = {American Assoc. for the Advancement of Science}, address = {Washington}, issn = {0036-8075}, doi = {10.1126/science.1221329}, pages = {1687 -- 1690}, year = {2012}, abstract = {When a hydrogen (H) atom approaches a deuterium (D-2) molecule, the minimum-energy path is for the three nuclei to line up. Consequently, nearly collinear collisions cause HD reaction products to be backscattered with low rotational excitation, whereas more glancing collisions yield sideways-scattered HD products with higher rotational excitation. Here we report that measured cross sections for the H + D-2 -> HD(v' = 4, j') + D reaction at a collision energy of 1.97 electron volts contradict this behavior. The anomalous angular distributions match closely fully quantum mechanical calculations, and for the most part quasiclassical trajectory calculations. As the energy available in product recoil is reduced, a rotational barrier to reaction cuts off contributions from glancing collisions, causing high-j' HD products to become backward scattered.}, language = {en} } @article{KathreinBaiCurrivanIncorviaetal.2015, author = {Kathrein, Christine C. and Bai, Wubin and Currivan-Incorvia, Jean Anne and Liontos, George and Ntetsikas, Konstantinos and Avgeropoulos, Apostolos and B{\"o}ker, Alexander and Tsarkova, Larisa and Ross, Caroline A.}, title = {Combining Graphoepitaxy and Electric Fields toward Uniaxial Alignment of Solvent-Annealed Polystyrene-b-Poly(dimethylsiloxane) Block Copolymers}, series = {Chemistry of materials : a publication of the American Chemical Society}, volume = {27}, journal = {Chemistry of materials : a publication of the American Chemical Society}, number = {19}, publisher = {American Chemical Society}, address = {Washington}, issn = {0897-4756}, doi = {10.1021/acs.chemmater.5b03354}, pages = {6890 -- 6898}, year = {2015}, abstract = {We report a combined directing effect of the simultaneously applied graphoepitaxy and electric field on the self-assembly of cylinder forming polystyrene-b-poly(dimethylsiloxane) block copolymer in thin films. A correlation length of up to 20 mu m of uniaxial ordered striped patterns is an order of magnitude greater than that produced by either graphoepitaxy or electric field alignment alone and is achieved at reduced annealing times. The angle between the electric field direction and the topographic guides as well as the dimensions of the trenches affected both the quality of the ordering and the direction of the orientation of cylindrical domains: parallel or perpendicular to the topographic features. We quantified the interplay between the electric field and the geometry of the topographic structures by constructing the phase diagram of microdomain orientation. This combined approach allows the fabrication of highly ordered block copolymer structures using macroscopically prepatterned photolithographic substrates.}, language = {en} } @article{KathreinBaiNunnsetal.2016, author = {Kathrein, Christine C. and Bai, Wubin and Nunns, Adam and Gwyther, Jessica and Manners, Ian and B{\"o}ker, Alexander and Tsarkova, Larisa and Ross, Caroline A.}, title = {Electric field manipulated nanopatterns in thin films of metalorganic 3-miktoarm star terpolymers}, series = {Soft matter}, volume = {12}, journal = {Soft matter}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1744-683X}, doi = {10.1039/c6sm00451b}, pages = {4866 -- 4874}, year = {2016}, abstract = {We report the effect of electric field on the morphological transitions and ordering behavior of polyferrocenylethylmethylsilane block (PFEMS)-containing copolymers. By analyzing structures in solvent-annealed films of metalorganic sphere-and cylinder-forming diblock copolymers, as well as of 3-miktoarm polyisoprene-arm-polystyrene-arm-PFEMS (3 mu-ISF) terpolymers, we decouple two types of responses to the electric field: morphological transformations as a result of an increase in the volume fraction of the PFEMS block by oxidation of the ferrocenyl groups, and the orientation of the dielectric interfaces of microdomains parallel to the electric field vector. In the case of 3m-ISF, the former effect dominates at high electric field strengths which results in an unexpected cylinder-to-sphere transition, leading to a well-ordered hexagonal dot pattern. Our results demonstrate multiple tunability of ordered microdomain morphologies, suggesting future applications in nanofabrication and surface patterning.}, language = {en} } @article{KathreinPesterRuppeletal.2016, author = {Kathrein, Christine C. and Pester, Christian and Ruppel, Markus and Jung, Maike and Zimmermann, Marc and B{\"o}ker, Alexander}, title = {Reorientation mechanisms of block copolymer/CdSe quantum dot composites under application of an electric field}, series = {Soft matter}, volume = {12}, journal = {Soft matter}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1744-683X}, doi = {10.1039/c6sm01073c}, pages = {8417 -- 8424}, year = {2016}, abstract = {Time- and temperature-resolved in situ birefringence measurements were applied to analyze the effect of nanoparticles on the electric field-induced alignment of a microphase separated solution of poly(styrene)-block-poly(isoprene) in toluene. Through the incorporation of isoprene-confined CdSe quantum dots the reorientation behavior is altered. Particle loading lowers the order-disorder transition temperature, and increases the defect density, favoring nucleation and growth as an alignment mechanism over rotation of grains. The temperature dependent alteration in the reorientation mechanism is analyzed via a combination of birefringence and synchrotron SAXS. The detailed understanding of the effect of nanoparticles on the reorientation mechanism is an important prerequisite for optimization of electricfield-induced alignment of block copolymer/nanoparticle composites where the block copolymer guides the nanoparticle self-assembly into anisotropic structures.}, language = {en} } @article{PereiraZehbeGuenteretal.2018, author = {Pereira, Rui F. P. and Zehbe, Kerstin and G{\"u}nter, Christina and dos Santos, Tiago and Nunes, Silvia C. and Almeida Paz, Filipe A. and Silva, Maria M. and Granja, Pedro L. and Taubert, Andreas and de Zea Bermudez, Ver{\´o}nica}, title = {Ionic liquid-assisted synthesis of mesoporous silk fibroin/silica hybrids for biomedical applications}, series = {ACS Omega}, volume = {3}, journal = {ACS Omega}, number = {9}, publisher = {American Chemical Society}, address = {Washington}, issn = {2470-1343}, doi = {10.1021/acsomega.8b02051}, pages = {10811 -- 10822}, year = {2018}, abstract = {New mesoporous silk fibroin (SF)/silica hybrids were processed via a one-pot soft and energy-efficient sol-gel chemistry and self-assembly from a silica precursor, an acidic or basic catalyst, and the ionic liquid 1-butyl-3-methylimidazolium chloride, acting as both solvent and mesoporosity-inducer. The as-prepared materials were obtained as slightly transparent-opaque, amorphous monoliths, easily transformed into powders, and stable up to ca. 300 degrees C. Structural data suggest the formation of a hexagonal mesostructure with low range order and apparent surface areas, pore volumes, and pore radii of 205-263 m(2) g(-1), 0.16-0.19 cm(3) g(-1), and 1.2-1.6 nm, respectively. In all samples, the dominating conformation of the SF chains is the beta-sheet. Cytotoxicity/bioactivity resazurin assays and fluorescence microscopy demonstrate the high viability of MC3T3 pre-osteoblasts to indirect (>= 99 +/- 9\%) and direct (78 +/- 2 to 99 +/- 13\%) contact with the SF/silica materials. Considering their properties and further improvements, these systems are promising candidates to be explored in bone tissue engineering. They also offer excellent prospects as electrolytes for solid-state electrochemical devices, in particular for fuel cells.}, language = {en} }