@phdthesis{Akdemir2009, author = {Akdemir, {\"O}zg{\"u}r}, title = {Synthesis of novel non-viral gene carriers via atom transfer radical polymerization and click chemistry}, address = {Potsdam}, pages = {X, 121 S. : Ill., graph. Darst.}, year = {2009}, language = {en} } @phdthesis{AlNakeeb2019, author = {Al Nakeeb, Noah}, title = {Self-assembly and crosslinking approaches of double hydrophilic linear-brush block copolymers}, pages = {133}, year = {2019}, language = {en} } @phdthesis{Alahverdjieva2007, author = {Alahverdjieva, Veneta}, title = {Experimental study of mixed protein/surfactant systems at the aqueous solution/air interface}, address = {Potsdam}, pages = {XIV, 146 S., X : graph. Darst.}, year = {2007}, language = {en} } @phdthesis{Ali2005, author = {Ali, Abu Md. Imroz}, title = {Morphology control in nanoscopic composite polymer particles}, address = {Potsdam}, pages = {97, XXXV S. : Ill., graph. Darst.}, year = {2005}, language = {en} } @phdthesis{Ambrogi2015, author = {Ambrogi, Martina}, title = {Application of Poly(Ionic Liquid)s for the synthesis of functional carbons}, school = {Universit{\"a}t Potsdam}, pages = {125}, year = {2015}, language = {en} } @phdthesis{Antipov2003, author = {Antipov, Alexei}, title = {Polyelectrolyte multilayer capsules as controlled permeability vehicles and catalyst carriers}, pages = {100 S.}, year = {2003}, language = {en} } @phdthesis{Asfaw2005, author = {Asfaw, Mesfin}, title = {Adhesion of multi-component membbranes and strings}, address = {Potsdam}, pages = {102 S. : graph. Darst.}, year = {2005}, language = {en} } @phdthesis{Ast2013, author = {Ast, Cindy}, title = {Design and photophysical characterization of single fluorophore-based ammonium sensors}, address = {Potsdam}, pages = {90 S.}, year = {2013}, language = {en} } @phdthesis{Ast2012, author = {Ast, Sandra}, title = {Integration of the 1,2,3-Triazole "Click" motif as a potent signalling element into metal ion responsive fluorescent probes for physiological cations}, address = {Potsdam}, pages = {137 S.}, year = {2012}, language = {en} } @phdthesis{Award2009, author = {Award, Duhan Jawad}, title = {Mixed 1,2-D{\"u}mine-1,2-Dithiolate Ligand Complexes : Structure, Proberties and EPR Spectroscopy}, address = {Potsdam}, pages = {130 S.}, year = {2009}, language = {en} } @phdthesis{BahrkeEinarssonGislasonetal.2003, author = {Bahrke, Sven and Einarsson, Jon M. and Gislason, Johannes and Haebel, Sophie and Peter-Katalinic, Jasna and Peter, Martin G.}, title = {Characterization of chitooligosaccharides by mass spectrometry}, isbn = {82-47-15901-5}, year = {2003}, language = {en} } @phdthesis{Bai2010, author = {Bai, Shuo}, title = {Active hydrogels with nanocomposites}, address = {Potsdam}, pages = {VI, 109 Bl. : Ill., graph. Darst.}, year = {2010}, language = {en} } @phdthesis{Baryzewska2023, author = {Baryzewska, Agata W.}, title = {Reconfigurable Janus emulsions as signal transducers for biosensing applications}, school = {Universit{\"a}t Potsdam}, pages = {133}, year = {2023}, language = {en} } @phdthesis{Bellin2006, author = {Bellin, Ingo}, title = {Thermosensitive Polymer Networks with Two Different Shapes in Memory}, address = {Potsdam}, pages = {117 S. : graph. Darst.}, year = {2006}, language = {en} } @phdthesis{Belova2010, author = {Belova, Valentina}, title = {Composite fabrication and surface modification via high intensity ultrasound}, address = {Potsdam}, pages = {113, XII S. : zahlr. Ill. und graph. Darst.}, year = {2010}, language = {en} } @phdthesis{Berg2011, author = {Berg, John K.}, title = {Size-dependent wetting behavior of organic molecules on solid surfaces}, address = {Potsdam}, pages = {99 S.}, year = {2011}, language = {en} } @phdthesis{Bettenbuehl2012, author = {Bettenb{\"u}hl, Mario}, title = {Microsaccades: symbols in fixational eye movements}, address = {Potsdam}, pages = {117 S.}, year = {2012}, language = {en} } @phdthesis{Bhaskar2020, author = {Bhaskar, Thanga Bhuvanesh Vijaya}, title = {Biomimetic layers of extracellular matrix glycoproteins as designed biointerfaces}, school = {Universit{\"a}t Potsdam}, year = {2020}, abstract = {The goal of regenerative medicine is to guide biological systems towards natural healing outcomes using a combination of niche-specific cells, bioactive molecules and biomaterials. In this regard, mimicking the extracellular matrix (ECM) surrounding cells and tissues in vivo is an effective strategy to modulate cell behaviors. Cellular function and phenotype is directed by the biochemical and biophysical signals present in the complex 3D network of ECMs composed mainly of glycoproteins and hydrophilic proteoglycans. While cellular modulation in response to biophysical cues emulating ECM features has been investigated widely, the influence of biochemical display of ECM glycoproteins mimicking their presentation in vivo is not well characterized. It remains a significant challenge to build artificial biointerfaces using ECM glycoproteins that precisely match their presentation in nature in terms of morphology, orientation and conformation. This challenge becomes clear, when one understands how ECM glycoproteins self-assemble in the body. Glycoproteins produced inside the cell are secreted in the extra-cellular space, where they are bound to the cell membrane or other glycoproteins by specific interactions. This leads to elevated local concentration and 2Dspatial confinement, resulting in self-assembly by the reciprocal interactions arising from the molecular complementarity encoded in the glycoprotein domains. In this thesis, air-water (A-W) interface is presented as a suitable platform, where self-assembly parameters of ECM glycoproteins such as pH, temperature and ionic strength can be controlled to simulate in vivo conditions (Langmuir technique), resulting in the formation of glycoprotein layers with defined characteristics. The layer can be further compressed with surface barriers to enhance glycoprotein-glycoprotein contacts and defined layers of glycoproteins can be immobilized on substrates by horizontal lift and touch method, called Langmuir-Sch{\"a}fer (LS) method. Here, the benefit of Langmuir and LS methods in achieving ECM glycoprotein biointerfaces with controlled network morphology and ligand density on substrates is highlighted and contrasted with the commonly used (glyco)protein solution deposition (SO) method on substrates. In general, the (glyco)protein layer formation by SO is rather uncontrolled, influenced strongly by (glyco)protein-substrate interactions and it results in multilayers and aggregations on substrates, while the LS method results in (glyco)proteins layers with a more homogenous presentation. To achieve the goal of realizing defined ECM layers on substrates, ECM glycoproteins having the ability to self-assemble were selected: Collagen-IV (Col-IV) and fibronectin (FN). Highly packed FN layer with uniform presentation of ligands was deposited on polydimethysiloxane VIII (PDMS) by LS method, while a heterogeneous layer was formed on PDMS by SO with prominent aggregations visible. Mesenchymal stem cells (MSC) on PDMS equipped with FN by LS exhibited more homogeneous and elevated vinculin expression and weaker stress fiber formation than on PDMS equipped with FN by SO and these divergent responses could be attributed to the differences in glycoprotein presentation at the interface. Col-IV are scaffolding components of specialized ECM called basement membranes (BM), and have the propensity to form 2D networks by self-polymerization associated with cells. Col- IV behaves as a thin-disordered network at the A-W interface. As the Col-IV layer was compressed at the A-W interface using trough barriers, there was negligible change in thickness (layer thickness ~ 50 nm) or orientation of molecules. The pre-formed organization of Col-IV was transferred by LS method in a controlled fashion onto substrates meeting the wettability criterion (CA ≤ 80°). MSC adhesion (24h) on PET substrates deposited with Col-IV LS films at 10, 15 and 20 mN·m-1 surface pressures was (12269.0 ± 5856.4) cells for LS10, (16744.2 ± 1280.1) cells for LS15 and (19688.3 ± 1934.0) cells for LS20 respectively. Remarkably, by selecting the surface areal density of Col-IV on the Langmuir trough on PET, there is a linear increase between the number of adherent MSCs and the Col-IV ligand density. Further, FN has the ability to self-stabilize and form 2D networks (even without compression) while preserving native β-sheet structure at the A-W interface on a defined subphase (pH = 2). This provides the possibility to form such layers on any vessel (even on standard six-well culture plates) and the cohesive FN layers can be deposited by LS transfer, without the need for expensive LB instrumentation. Multilayers of FN can be immobilized on substrates by this approach, as easily as Layer-by-Layer method, even without the need for secondary adlayer or activated bare substrate. Thus, this facile glycoprotein coating strategy approach is accessible to many researchers to realize defined FN films on substrates for cell culture. In conclusion, Langmuir and LS methods can create biomimetic glycoprotein biointerfaces on substrates controlling aspects of presentation such as network morphology and ligand density. These methods will be utilized to produce artificial BM mimics and interstitial ECM mimics composed of more than one ECM glycoprotein layer on substrates, serving as artificial niches instructing stem cells for cell-replacement therapies in the future.}, language = {en} } @phdthesis{Cao2020, author = {Cao, Qian}, title = {Graphitic carbon nitride and polymer hybrid materials}, school = {Universit{\"a}t Potsdam}, pages = {132}, year = {2020}, abstract = {Advanced hybrid materials are recognized as one of the most significant enablers for new technologies, which holds true especially on the quest for sustainable energy sources and energy production schemes (e.g., semiconductor based photocatalytic materials). Usually, a single component is far from meeting all the demands needed for these advanced applications. Hybrid materials are composed of at least two components commonly an inorganic and an organic material on the molecular level, which feature novel properties exceeding the sum of the individual parts and might be the milestones of next-generation applications. This dissertation aims to provide novel combinations of the metal-free semiconductor graphitic carbon nitride (g-C3N4) with polymers to obtain materials with advanced properties and applications. Visible light constitutes the core of the present work as it is the only energy source utilized either in synthesis or in the application process. In the area of applications by combination of g-C3N4 and polymers, two different hybrids were thoroughly elucidated, i.e.. their design and construction as well as potential application in photocatalysis. Novel soft 3D liquid objects were formed via charge-interaction driven interfacial jamming between polyelectrolytes in aqueous environment and colloidal dispersions of g-C3N4 in edible sunflower oil. As such, stable liquid objects could be molded into specific shapes and utilized for photodegradation of organic dyes in water. Furthermore, the grafting of polymers onto g-C3N4 was investigated. Allyl-end functionalized polymers were grafted onto g-C3N4 by a photoinitiated process to yield g-C3N4 with versatile and improved properties, e.g. advanced dispersibility enabling processing via spin coating. As g-C3N4 produces radicals under visible light irradiation, which is of significant interest for polymer science, g-C3N4 containing polymer latex and macrogel beads (MGB) were synthesized by emulsion photopolymerization and inverse suspension photopolymerization, respectively. A well-controlled emulsion photopolymerization process via g-C3N4 initiation was designed, which features synthesis of well-defined and cross-linked polymer particles. Furthermore, the polymerization process was investigated thoroughly, indicating an ad-layer polymerization in early stages of the process. The utilization of functionalized g-C3N4 allowed the polymerization of various monomer types. Moreover, g-C3N4 was utilized as photoinitiator in hydrogel MGB formation. The formed MGB properties could be tailored via process design, e.g. stirring rate, cross-linker content and g-C3N4 content. Finally, MGBs were introduced as photocatalyst for waste water remediation, i.e. the degradation of Rhodamine B in aqueous solution was studied. The present thesis therefore builds a bridge between g-C3N4 and polymers and provides strategies for hybrid material formation. Furthermore, several potential applications are revealed with significant implications for photocatalysis, polymerization processes and polymer materials.}, language = {en} } @phdthesis{Cataldo2020, author = {Cataldo, Vincenzo Alessandro}, title = {Design and synthesis of alkylating ionic liquids and their application in synthesis, materials and proteomics}, school = {Universit{\"a}t Potsdam}, pages = {153}, year = {2020}, language = {en} } @phdthesis{CerdaDonate2020, author = {Cerd{\´a} Do{\~n}ate, Elisa}, title = {Microfluidics for the study of magnetotactic bacteria towards single-cell analysis}, school = {Universit{\"a}t Potsdam}, pages = {X, 92}, year = {2020}, abstract = {Magnetotactic bacteria comprise a heterogeneous group of Gram negative bacteria which share the ability to synthesise intracellular magnetic nanoparticles surrounded by a lipid bilayer, known as magnetosomes, which are arranged in linear chains. The bacteria exert a unique level of control onto the biomineralization of these nanoparticles, which is seen in the controlled size and shape they have. These characteristics have attracted great attention on understanding the process by which the bacteria synthesise the magnetosomes. Moreover, the magnetosome chain impart the bacteria with a net magnetic dipole which makes them susceptible to interact with magnetic fields and thus orient with the Earth's magnetic field. This feature has attracted as well much interest to understand how the swimming motility of these microorganisms is affected by the presence of magnetic fields. Most of the studies performed in these bacteria so far have been conducted in the traditional manner using large populations of cells. Such studies have the disadvantage of averaging many different individuals with heterogeneous behaviours and fail to consider individual variations. In addition, in large populations each bacterium will be subjected to a different microenvironment that will influence the bacterial behaviour, but which cannot be defined using these traditional methods. In this thesis, different microfluidic platforms are proposed to overcome these limitations and to offer the possibility to study magnetotactic bacteria in defined environments and down to a single-cell resolution. First, a sediment-like microfluidic platform is presented with the purpose of mimicking the porous environment they bacteria naturally dwell in. The platform allows to observe via transmitted light microscopy that bacterial navigation in crowded environments is enhanced by the Earth's magnetic field strengths (B = 50 μT) rather than by null (B = 0 μT) or higher magnetic fields (B = 500 μT). Second, a microfluidic system to confine single-bacterial cells in physically defined environments is presented. The system allows to study via transmitted light microscopy the interplay between wall curvature, magnetic fields and bacterial speed affect the motion of a confined bacterium, and shows how bacterial trajectories depend on those three parameters. Third, a microfluidic platform to conduct semi in vivo magnetosome nucleation with a single-cell resolution via X-ray fluorescence is fabricated. It is shown that signal arising from magnetosome full chains can be observed individually in each bacterium. Finally, the iron uptake kinetics of a single bacterium are studied via a fluorescent reporter through confocal microscopy. Two different approaches are used for this: one of the previously mentioned platforms, as well as giant lipid vesicles. It is observed how iron uptake rates vary between cells, as well as how these rates are consistent with magnetosome formation taking place within some hours. The present thesis shows therefore how microfluidic technologies can be implemented for the study of magnetotactic bacteria at different degrees, and the level of resolution that can be attained by going into the single- cell scale.
}, language = {en} } @phdthesis{Chanana2010, author = {Chanana, Munish}, title = {Synthesis of stimuli-responsive and switchable inorganic nanoparticles for biomedical applications}, address = {Potsdam}, pages = {128, E-1 S. : Ill., graph. Darst.}, year = {2010}, language = {en} } @phdthesis{Chen2018, author = {Chen, Guoxiang}, title = {Nanoparticles at solid interfaces}, school = {Universit{\"a}t Potsdam}, pages = {112}, year = {2018}, abstract = {Nanoparticles (NPs) are particles between 1 and 100 nanometers in size. They have attracted enormous research interests owing to their remarkable physicochemical properties and potential applications in the optics, catalysis, sensing, electronics, or optical devices. The thesis investigates systems of NPs attached to planar substrates. In the first part of the results section of the thesis a new method is presented to immobilize NPs. In many NP applications a strong, persistent adhesion to substrates is a key requirement. Up to now this has been achieved with various methods, which are not always the optimum regarding adhesion strength or applicability. We propose a new method which uses capillarity to enhance the binding agents in the contact area between NP and substrate. The adhesion strength resulting from the new approach is investigated in detail and it is shown that the new approach is superior to older methods in several ways. The following section presents the optical visualization of nano-sized objects through a combination of thin film surface distortion and interference enhanced optical reflection microscopy. It is a new, fast and non-destructive technique. It not only reveals the location of NPs as small as 20nm attached to planar surfaces and embedded in a molecularly thin liquid film. It also allows the measurement of the geometry of the surface distortion of the liquid film. Even for small NPs the meniscus reaches out for micrometers, which is the reason why the NPs produce such a pronounced optical footprint. The nucleation and growth of individual bubbles is presented in chapter 5. Nucleation is a ubiquitous natural phenomenon and of great importance in numerous industrial processes. Typically it occurs on very small scales (nanometers) and it is of a random nature (thermodynamics of small systems). Up to now most experimental nucleation studies deal with a large number of individual nucleation processes to cope with its inherently statistical, spatio-temporal character. In contrast, in this thesis the individual O2-bubble formation from single localized platinum NP active site is studied experimentally. The bubble formation is initiated by the catalytic reaction of H2O2 on the Pt surface. It is studied how the bubble nucleation and growth depends on the NP size, the H2O2 concentration and the substrate surface properties. It is observed that in some cases the bubbles move laterally over the substrate surface, driven by the O2-production and the film ablation.}, language = {en} } @phdthesis{Chen2015, author = {Chen, Zupeng}, title = {Novel strategies to improve (photo)catalytic performance of carbon nitride-based composites}, pages = {ii, 137}, year = {2015}, language = {en} } @phdthesis{CruzLemus2020, author = {Cruz Lemus, Saul Daniel}, title = {Enhancing Efficiency of Inverted Perovskite Solar Cells}, school = {Universit{\"a}t Potsdam}, pages = {117}, year = {2020}, abstract = {Carbon nitride and poly(ionic liquid)s (PILs) have been successfully applied in various fields of materials science owing to their outstanding properties. This thesis aims at the successful application of these polymers as innovative materials in the interfaces of hybrid organic-inorganic perovskite solar cells. A critical problem in harnessing the full thermodynamic potential of halide perovskites in solar cells is the design and modification of interfaces to reduce carrier recombination. Therefore, the interface must be properly studied and improved. This work investigated the effect of applying carbon nitride and PILs on a perovskite surface on the device performance. The facile synthetic method for modifying carbon nitride with vinyl thiazole and barbituric acid (CMB-vTA) yields 2.3 nm layers when solution processing is performed using isopropanol. The nanosheets were applied as a metal-free electron transport layer in inverted perovskite solar cells. The application of carbon nitride layers (CMB-vTA) resulted in negligible current-voltage hysteresis with a high open circuit voltage (Voc) of 1.1 V and a short-circuit current (Jsc) of 20.28 mA cm-2, which afforded efficiencies of up to 17\%. Thus, the successful implementation of a carbon nitride-based structure enabled good charge extraction with minimized interface recombination between the perovskite and PCBM. Similarly, PILs represent a new strategy of interfacial modification using an ionic polymer in an n-i-p perovskite architecture.. The application of PILs as an interfacial modifier resulted in solar cell devices with an extraordinarily high efficiency of 21.8\% and a Voc of 1.17 V. The implementation reduced non-radiative recombination at the perovskite surface through defect passivation. Finally, our work proposes a novel method to efficiently suppress non-radiative charge recombination using the unexplored properties of carbon nitride and PILs in the solar cell field. Additionally, the method for interfacial modification has general applicability because of the simplicity of the post-treatment approach, and therefore has potential applicability in other solar cells. Thus, this work opens the door to a new class of materials to be implemented.}, language = {en} } @phdthesis{Cui2010, author = {Cui, Jing}, title = {Preparation of medical grade, amorphous polymer systems with adjustable stiffness and development of self- surfficiently moving model scaffolds based on shape-memory polymer composites}, address = {Potsdam}, year = {2010}, language = {en} } @phdthesis{Coelfen2000, author = {C{\"o}lfen, Helmut}, title = {Biomimetric mineralisation using hydrophilic copolymers : synthesis of hybrid colloids with complex from and pathways towards their analysis in solution}, pages = {155 S.}, year = {2000}, language = {en} } @phdthesis{Dechtrirat2013, author = {Dechtrirat, Decha}, title = {Combination of self-assembled monolayers (SAMs) and molecularly imprinted polymers (MIPs) in biomimetic sensors}, address = {Potsdam}, pages = {107 S.}, year = {2013}, language = {en} } @phdthesis{DemirCakan2009, author = {Demir-Cakan, Rezan}, title = {Synthesis, characterization and applications of nanostructured materials using hydrothermal carbonization}, address = {Potsdam}, pages = {IV, 126 Bl. : Ill., graph. Darst.}, year = {2009}, language = {en} } @phdthesis{DereseYenesewMidiwoetal.2003, author = {Derese, Solomon and Yenesew, Abiy and Midiwo, Jacob O. and Heydenreich, Matthias and Peter, Martin G.}, title = {A new isoflavone from stem bark of Millettia dura}, issn = {1011-3924}, year = {2003}, language = {en} } @phdthesis{Diehl2009, author = {Diehl, Christina}, title = {Functional microspheres through crystallization of thermoresponsive poly(2-oxazoline)s}, address = {Potsdam}, pages = {125 S. : Ill., graph. Darst.}, year = {2009}, language = {en} } @phdthesis{Dittrich2011, author = {Dittrich, Matthias}, title = {Physical-chemical characterisation of new lipids designed for non-viral gene transfection}, address = {Potsdam}, pages = {111 S.}, year = {2011}, language = {en} } @phdthesis{Dominguez2013, author = {Dom{\´i}nguez, Pablo Haro}, title = {Nanostructured poly(benzimidazole)s by chemical modification}, address = {Potsdam}, pages = {95, XXVIII S.}, year = {2013}, language = {en} } @phdthesis{Dong2004, author = {Dong, Wen-Fei}, title = {Polyelectrolyte Multilayer Capsules: structure, encapsulation, and optical properties}, address = {Potsdam}, pages = {130 S. : Ill., graph. Darst.}, year = {2004}, language = {en} } @phdthesis{Draffehn2016, author = {Draffehn, S{\"o}ren}, title = {Optical Spectroscopy-Based Characterization of Micellar and Liposomal Systems with Possible Applications in Drug Delivery}, school = {Universit{\"a}t Potsdam}, pages = {VII, 106, XII}, year = {2016}, language = {en} } @phdthesis{Duan2005, author = {Duan, Hongwei}, title = {Functional Nanoparticles as Self-Assembling Building Block and Synthetic Templates}, address = {Potsdam}, pages = {III, 107 S. : Ill., graph. Darst.}, year = {2005}, language = {en} } @phdthesis{ElamparuthiLinkerKellingetal.2009, author = {Elamparuthi, Elangovan and Linker, Torsten and Kelling, Alexandra and Schilde, Uwe}, title = {Crystal structure of methyl 3,4,6-tri-O-benzyl-2-deoxy-2-C-nitromethyl-beta-D-galactopyranoside, C29H33NO7}, issn = {1433-7266}, doi = {10.1524/ncrs.2009.0054}, year = {2009}, language = {en} } @phdthesis{Elangovan2009, author = {Elangovan, Elamparuthi}, title = {Radical additions to glycals : synthesis and transformations of 2-functionalized carbohydrates}, address = {Potsdam}, pages = {VI, 11 Bl. : graph. Darst.}, year = {2009}, language = {en} } @phdthesis{EntrialgoCastano2007, author = {Entrialgo Castano, Maria}, title = {Hydrolytic degradation of aliphatic polyester: molecular modeling and quantum mechanical investigations}, address = {Potsdam}, pages = {141 S. : graph. Darst.}, year = {2007}, language = {en} } @phdthesis{Firkala2017, author = {Firkala, Tam{\´a}s}, title = {Investigation of nanoparticle-molecule interactions and pharmaceutical model formulations by means of surface enhanced raman spectroscopy}, school = {Universit{\"a}t Potsdam}, pages = {118}, year = {2017}, language = {en} } @phdthesis{Flehr2012, author = {Flehr, Roman}, title = {Design and development of novel three color-FRET systems in synthetic peptides and oligonucleotides}, address = {Potsdam}, pages = {VII, 149 S.}, year = {2012}, language = {en} } @phdthesis{Frank2023, author = {Frank, Bradley D.}, title = {Complex and adaptive soft colloids}, school = {Universit{\"a}t Potsdam}, pages = {XIV, 154}, year = {2023}, language = {en} } @phdthesis{Frankovitch2007, author = {Frankovitch, Christine Marie}, title = {Optical methods for monitoring biological parameters of phototropic microorganisms during cultivation}, address = {Potsdam}, pages = {iii, 95 S. : graph. Darst.}, year = {2007}, language = {en} } @phdthesis{Frede, author = {Frede, Katja}, title = {Light-modulated biosynthesis of carotenoids in Brassica rapa ssp. chinensis and the activation of Nrf2 by lutein in human retinal pigment epithelial cells}, pages = {98}, language = {en} } @phdthesis{Friese2016, author = {Friese, Viviane A.}, title = {Solvato-, vapo, mechanochromic and luminescent behavior of Rhodium, Platinum and Gold complexes and their coordination polymers}, school = {Universit{\"a}t Potsdam}, pages = {100 S.}, year = {2016}, language = {en} } @phdthesis{Friess2016, author = {Frieß, Fabian}, title = {Shape-memory polymer micronetworks}, school = {Universit{\"a}t Potsdam}, pages = {xiv, 111 S.}, year = {2016}, language = {en} } @phdthesis{Frueh2011, author = {Fr{\"u}h, Johannes}, title = {Structural change of polyelectrolyte multilayers under mechanical stress}, address = {Potsdam}, pages = {194 S.}, year = {2011}, language = {en} } @phdthesis{Giusto2020, author = {Giusto, Paolo}, title = {Chemical vapor deposition of carbon-based thin films}, school = {Universit{\"a}t Potsdam}, pages = {165}, year = {2020}, language = {en} } @phdthesis{Glatzel2012, author = {Glatzel, Stefan}, title = {Cellulose based transition metal nano-composites : structuring and development}, address = {Potsdam}, pages = {102, XXIII S.}, year = {2012}, language = {en} } @phdthesis{Guenther, author = {G{\"u}nther, Erika}, title = {Intracellular processes in magnetotactic bacteria studied by optical tools}, school = {Universit{\"a}t Potsdam}, pages = {113}, language = {en} }