@misc{KitaTokarczykJungingerBelegrinouetal.2011, author = {Kita-Tokarczyk, Katarzyna and Junginger, Mathias and Belegrinou, Serena and Taubert, Andreas}, title = {Amphiphilic polymers at interfaces}, series = {Advances in polymer science}, volume = {242}, journal = {Advances in polymer science}, number = {1}, editor = {Muller, AHE and Borisov, O}, publisher = {Springer}, address = {Berlin}, isbn = {978-3-642-22297-9}, issn = {0065-3195}, doi = {10.1007/12_2010_58}, pages = {151 -- 201}, year = {2011}, abstract = {Self-assembly phenomena in block copolymer systems are attracting considerable interest from the scientific community and industry alike. Particularly interesting is the behavior of amphiphilic copolymers, which can self-organize into nanoscale-sized objects such as micelles, vesicles, or tubes in solution, and which form well-defined assemblies at interfaces such as air-liquid, air-solid, or liquid-solid. Depending on the polymer chemistry and architecture, various types of organization at interfaces can be expected, and further exploited for applications in nanotechnology, electronics, and biomedical sciences. In this article, we discuss the formation and characterization of Langmuir monolayers from various amphiphilic block copolymers, including chargeable and thus pH-responsivematerials. Solid-supported polymer films are reviewed in the context of alteration of surface properties by ultrathin polymer layers and the possibilities for application in tissue engineering, sensors and biomaterials. Finally, we focus on how organic and polymer monolayers influence the growth of inorganic materials. This is a truly biomimetic approach since Nature uses soft interfaces to control the nucleation, growth, and morphology of biominerals such as calcium phosphate, calcium carbonate, and silica.}, language = {en} } @article{ShkilnyyGraefHiebletal.2009, author = {Shkilnyy, Andriy and Gr{\"a}f, Ralph and Hiebl, Bernhard and Neffe, Axel T. and Friedrich, Alwin and Hartmann, Juergen and Taubert, Andreas}, title = {Unprecedented, low cytotoxicity of spongelike calcium phosphate/poly(ethylene imine) hydrogel composites}, issn = {1616-5187}, doi = {10.1002/mabi.200800266}, year = {2009}, abstract = {Covalently crosslinked PEI hydrogels are efficient templates for calcium phosphate mineralization in SBF. In contrast to the PEI hydrogels, non-crosslinked PEI does not lead to calcium phosphate nucleation and growth in SBF. The precipitate is a mixture of brushite and hydroxyapatite. The PEI/calcium phosphate composite material exhibits a sponge like morphology and a chemical composition that is interesting for implants. Cytotoxicity tests using Dictyostelium discoideum amoebae show that both the non-mineralized and mineralized hydrogels have a very low cytotoxicity. This suggests that next generation PEI hydrogels, where also the degradation products are non-toxic, could be interesting for biomedical applications.}, language = {en} } @article{IhlenburgMaiThuenemannetal.2021, author = {Ihlenburg, Ramona and Mai, Tobias and Th{\"u}nemann, Andreas F. and Baerenwald, Ruth and Saalw{\"a}chter, Kay and Koetz, Joachim and Taubert, Andreas}, title = {Sulfobetaine hydrogels with a complex multilength-scale hierarchical structure}, series = {The journal of physical chemistry : B, Condensed matter, materials, surfaces, interfaces \& biophysical chemistry}, volume = {125}, journal = {The journal of physical chemistry : B, Condensed matter, materials, surfaces, interfaces \& biophysical chemistry}, number = {13}, publisher = {American Chemical Society}, address = {Washington}, issn = {1520-6106}, doi = {10.1021/acs.jpcb.0c10601}, pages = {3398 -- 3408}, year = {2021}, abstract = {Hydrogels with a hierarchical structure were prepared from a new highly water-soluble crosslinker N,N,N',N'-tetramethyl-N,N'-bis(2-ethylmethacrylate)-propyl-1,3-diammonium dibromide and from the sulfobetaine monomer 2-(N-3-sulfopropyl-N,N-dimethyl ammonium)ethyl methacrylate. The free radical polymerization of the two compounds is rapid and yields near-transparent hydrogels with sizes up to 5 cm in diameter. Rheology shows a clear correlation between the monomer-to-crosslinker ratio and the storage and loss moduli of the hydrogels. Cryo-scanning electron microscopy, low-field nuclear magnetic resonance (NMR) spectroscopy, and small-angle X-ray scattering show that the gels have a hierarchical structure with features spanning the nanometer to the sub-millimeter scale. The NMR study is challenged by the marked inhomogeneity of the gels and the complex chemical structure of the sulfobetaine monomer. NMR spectroscopy shows how these complications can be addressed via a novel fitting approach that considers the mobility gradient along the side chain of methacrylate-based monomers.}, language = {en} } @article{IhlenburgLehnenKoetzetal.2021, author = {Ihlenburg, Ramona and Lehnen, Anne-Catherine and Koetz, Joachim and Taubert, Andreas}, title = {Sulfobetaine Cryogels for Preferential Adsorption of Methyl Orange from Mixed Dye Solutions}, series = {Polymers / Molecular Diversity Preservation International}, volume = {13}, journal = {Polymers / Molecular Diversity Preservation International}, number = {2}, publisher = {MDPI}, address = {Basel}, issn = {2073-4360}, doi = {10.3390/polym13020208}, pages = {11}, year = {2021}, abstract = {New cryogels for selective dye removal from aqueous solution were prepared by free radical polymerization from the highly water-soluble crosslinker N,N,N',N'-tetramethyl-N,N'-bis(2-ethylmethacrylate)-propyl-1,3-diammonium dibromide and the sulfobetaine monomer 2-(N-3-sulfopropyl-N,N-dimethyl ammonium)ethyl methacrylate. The resulting white and opaque cryogels have micrometer sized pores with a smaller substructure. They adsorb methyl orange (MO) but not methylene blue (MB) from aqueous solution. Mixtures of MO and MB can be separated through selective adsorption of the MO to the cryogels while the MB remains in solution. The resulting cryogels are thus candidates for the removal of hazardous organic substances, as exemplified by MO and MB, from water. Clearly, it is possible that the cryogels are also potentially interesting for removal of other compounds such as pharmaceuticals or pesticides, but this must be investigated further.}, language = {en} } @misc{IhlenburgLehnenKoetzetal.2021, author = {Ihlenburg, Ramona and Lehnen, Anne-Catherine and Koetz, Joachim and Taubert, Andreas}, title = {Sulfobetaine Cryogels for Preferential Adsorption of Methyl Orange from Mixed Dye Solutions}, series = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, journal = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, number = {1093}, issn = {1866-8372}, doi = {10.25932/publishup-48898}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-488987}, pages = {13}, year = {2021}, abstract = {New cryogels for selective dye removal from aqueous solution were prepared by free radical polymerization from the highly water-soluble crosslinker N,N,N',N'-tetramethyl-N,N'-bis(2-ethylmethacrylate)-propyl-1,3-diammonium dibromide and the sulfobetaine monomer 2-(N-3-sulfopropyl-N,N-dimethyl ammonium)ethyl methacrylate. The resulting white and opaque cryogels have micrometer sized pores with a smaller substructure. They adsorb methyl orange (MO) but not methylene blue (MB) from aqueous solution. Mixtures of MO and MB can be separated through selective adsorption of the MO to the cryogels while the MB remains in solution. The resulting cryogels are thus candidates for the removal of hazardous organic substances, as exemplified by MO and MB, from water. Clearly, it is possible that the cryogels are also potentially interesting for removal of other compounds such as pharmaceuticals or pesticides, but this must be investigated further.}, language = {en} } @article{LehmannFranzToebbensetal.2019, author = {Lehmann, Frederike and Franz, Alexandra and Toebbens, Daniel M. and Levcenco, Sergej and Unold, Thomas and Taubert, Andreas and Schorr, Susan}, title = {The phase diagram of a mixed halide (Br, I) hybrid perovskite obtained by synchrotron X-ray diffraction}, series = {RSC Advances}, volume = {9}, journal = {RSC Advances}, number = {20}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {2046-2069}, doi = {10.1039/c8ra09398a}, pages = {11151 -- 11159}, year = {2019}, abstract = {By using synchrotron X-ray powder diffraction, the temperature dependent phase diagram of the hybrid perovskite tri-halide compounds, methyl ammonium lead iodide (MAPbI3, MA+ = CH3NH3+) and methyl ammonium lead bromide (MAPbBr3), as well as of their solid solutions, has been established. The existence of a large miscibility gap between 0.29 ≤ x ≤ 0.92 (±0.02) for the MAPb(I1-xBrx)3 solid solution has been proven. A systematic study of the lattice parameters for the solid solution series at room temperature revealed distinct deviations from Vegard's law. Furthermore, temperature dependent measurements showed that a strong temperature dependency of lattice parameters from the composition is present for iodine rich compositions. In contrast, the bromine rich compositions show an unusually low dependency of the phase transition temperature from the degree of substitution.}, language = {en} } @misc{LehmannBinetFranzetal.2018, author = {Lehmann, Frederike and Binet, Silvia and Franz, Alexandra and Taubert, Andreas and Schorr, Susan}, title = {Cation and anion substitutions in hybrid perovskites}, series = {7th World Conference on Photovoltaic Energy Conversion (WCPEC) (A Joint Conference of 45th IEEE PVSC, 28th PVSEC \& 34th EU PVSEC)}, journal = {7th World Conference on Photovoltaic Energy Conversion (WCPEC) (A Joint Conference of 45th IEEE PVSC, 28th PVSEC \& 34th EU PVSEC)}, publisher = {IEEE}, address = {New York}, isbn = {978-1-5386-8529-7}, issn = {2159-2330}, doi = {10.1109/PVSC.2018.8547645}, pages = {1555 -- 1558}, year = {2018}, abstract = {Organic or inorganic (A) metal (M) halide (X) perovskites (AMX(3)) are semiconductor materials setting the basis for the development of highly efficient, low-cost and multijunction solar energy conversion devices. The best efficiencies nowadays are obtained with mixed compositions containing methylammonium, formamidinium, Cs and Rb as well as iodine, bromine and chlorine as anions. The understanding of fundamental properties such as crystal structure and its effect on the band gap, as well as their phase stability is essential. In this systematic study X-ray diffraction and photoluminescense spectroscopy were applied to evaluate structural and optoelectronic properties of hybrid perovskites with mixed compositions.}, language = {en} } @article{DraudeGallaPelsteretal.2013, author = {Draude, F. and Galla, S. and Pelster, Axel and Tentschert, J. and Jungnickel, H. and Haase, Alfred and Mantion, Alexandre and Thuenemann, Andreas F. and Taubert, Andreas and Luch, A. and Arlinghaus, H. F.}, title = {ToF-SIMS and Laser-SNMS analysis of macrophages after exposure to silver nanoparticles}, series = {Surface and interface analysis : an international journal devoted to the development and application of techniques for the analysis surfaces, interfaces and thin films}, volume = {45}, journal = {Surface and interface analysis : an international journal devoted to the development and application of techniques for the analysis surfaces, interfaces and thin films}, number = {1}, publisher = {Wiley-Blackwell}, address = {Hoboken}, issn = {0142-2421}, doi = {10.1002/sia.4902}, pages = {286 -- 289}, year = {2013}, abstract = {Silver nanoparticles (SNPs) are among the most commercialized nanoparticles because of their antibacterial effects. Besides being employed, e. g. as a coatingmaterial for sterile surfaces in household articles and appliances, the particles are also used in a broad range of medical applications. Their antibacterial properties make SNPs especially useful for wound disinfection or as a coating material for prostheses and surgical instruments. Because of their optical characteristics, the particles are of increasing interest in biodetection as well. Despite the widespread use of SNPs, there is little knowledge of their toxicity. Time-of-flight secondary ion mass spectrometry (ToF-SIMS) and laser post-ionization secondary neutral mass spectrometry (Laser-SNMS) were used to investigate the effects of SNPs on human macrophages derived from THP-1 cells in vitro. For this purpose, macrophages were exposed to SNPs. The SNP concentration ranges were chosen with regard to functional impairments of the macrophages. To optimize the analysis of the macrophages, a special silicon wafer sandwich preparation technique was employed; ToF-SIMS was employed to characterize fragments originating from macrophage cell membranes. With the use of this optimized sample preparation method, the SNP-exposed macrophages were analyzed with ToF-SIMS and with Laser-SNMS. With Laser-SNMS, the three-dimensional distribution of SNPs in cells could be readily detected with very high efficiency, sensitivity, and submicron lateral resolution. We found an accumulation of SNPs directly beneath the cell membrane in a nanoparticular state as well as agglomerations of SNPs inside the cells.}, language = {en} } @article{JungingerKuebelSchacheretal.2013, author = {Junginger, Mathias and K{\"u}bel, Christian and Schacher, Felix H. and M{\"u}ller, Axel H. E. and Taubert, Andreas}, title = {Crystal structure and chemical composition of biomimetric calcium phosphate nanofibers}, doi = {10.1039/c3ra23348k}, year = {2013}, abstract = {Calcium phosphate nanofibers with a diameter of only a few nanometers and a cotton-ball-like aggregate morphology have been reported several times in the literature. Although fiber formation seems reproducible in a variety of conditions, the crystal structure and chemical composition of the fibers have been elusive. Using scanning transmission electron microscopy, low dose electron (nano)diffraction, energy-dispersive X-ray spectroscopy, and energy- filtered transmission electron microscopy, we have assigned crystal structures and chemical compositions to the fibers. Moreover, we demonstrate that the mineralization process yields true polymer/calcium phosphate hybrid materials where the block copolymer template is closely associated with the calcium phosphate.}, language = {en} } @article{KimKimParketal.2022, author = {Kim, Jiyong and Kim, Yohan and Park, Kyoungwon and Boeffel, Christine and Choi, Hyung-Seok and Taubert, Andreas and Wedel, Armin}, title = {Ligand Effect in 1-Octanethiol Passivation of InP/ZnSe/ZnS Quantum Dots-Evidence of Incomplete Surface Passivation during Synthesis}, series = {Small : nano micro}, journal = {Small : nano micro}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1613-6810}, doi = {10.1002/smll.202203093}, pages = {11}, year = {2022}, abstract = {The lack of anionic carboxylate ligands on the surface of InP/ZnSe/ZnS quantum dots (QDs), where zinc carboxylate ligands can be converted to carboxylic acid or carboxylate ligands via proton transfer by 1-octanethiol, is demonstrated. The as-synthesized QDs initially have an under-coordinated vacancy surface, which is passivated by solvent ligands such as ethanol and acetone. Upon exposure of 1-octanethiol to the QD surface, 1-octanethiol effectively induces the surface binding of anionic carboxylate ligands (derived from zinc carboxylate ligands) by proton transfer, which consequently exchanges ethanol and acetone ligands that bind on the incomplete QD surface. These systematic chemical analyses, such as thermogravimetric analysis-mass spectrometry and proton nuclear magnetic resonance spectroscopy, directly show the interplay of surface ligands, and it associates with QD light-emitting diodes (QD-LEDs). It is believed that this better understanding can lead to industrially feasible QD-LEDs.}, language = {en} } @article{HeroldAignerGrilletal.2019, author = {Herold, Heike M. and Aigner, Tamara Bernadette and Grill, Carolin E. and Kr{\"u}ger, Stefanie and Taubert, Andreas and Scheibel, Thomas R.}, title = {SpiderMAEn}, series = {Bioinspired, Biomimetic and Nanobiomaterials}, volume = {8}, journal = {Bioinspired, Biomimetic and Nanobiomaterials}, number = {1}, publisher = {ICE Publishing}, address = {Westminister}, issn = {2045-9858}, doi = {10.1680/jbibn.18.00007}, pages = {99 -- 108}, year = {2019}, abstract = {A growing energy demand requires new and preferably renewable energy sources. The infinite availability of solar radiation makes its conversion into storable and transportable energy forms attractive for research as well as for the industry. One promising example of a transportable fuel is hydrogen (H-2), making research into eco-friendly hydrogen production meaningful. Here, a hybrid system was developed using newly designed recombinant spider silk protein variants as a template for mineralization with inorganic titanium dioxide and gold. These bioinspired organic/inorganic hybrid materials allow for hydrogen production upon light irradiation. To begin with, recombinant spider silk proteins bearing titanium dioxide and gold-binding moieties were created and processed into structured films. These films were modified with gold and titanium dioxide in order to produce a photocatalyst. Subsequent testing revealed hydrogen production as a result of light-induced hydrolysis of water. Therefore, the novel setup presented here provides access to a new principle of generating advanced hybrid materials for sustainable hydrogen production and depicts a promising platform for further studies on photocatalytic production of hydrogen, the most promising future fuel.}, language = {en} } @article{HentrichJungingerBrunsetal.2015, author = {Hentrich, Doreen and Junginger, Mathias and Bruns, Michael and B{\"o}rner, Hans Gerhard and Brandt, Jessica and Brezesinski, Gerald and Taubert, Andreas}, title = {Interface-controlled calcium phosphate mineralization}, series = {CrystEngComm}, journal = {CrystEngComm}, number = {17}, publisher = {Royal Society of Chemistry}, address = {London}, issn = {1466-8033}, doi = {10.1039/C4CE02274B}, pages = {6901 -- 6913}, year = {2015}, abstract = {The phase behavior of an amphiphilic block copolymer based on a poly(aspartic acid) hydrophilic block and a poly(n-butyl acrylate) hydrophobic block was investigated at the air-water and air-buffer interface. The polymer forms stable monomolecular films on both subphases. At low pH, the isotherms exhibit a plateau. Compression-expansion experiments and infrared reflection absorption spectroscopy suggest that the plateau is likely due to the formation of polymer bi- or multilayers. At high pH the films remain intact upon compression and no multilayer formation is observed. Furthermore, the mineralization of calcium phosphate beneath the monolayer was studied at different pH. The pH of the subphase and thus the polymer charge strongly affects the phase behavior of the film and the mineral formation. After 4 h of mineralization at low pH, atomic force microscopy shows smooth mineral films with a low roughness. With increasing pH the mineral films become inhomogeneous and the roughness increases. Transmission electron microscopy confirms this: at low pH a few small but uniform particles form whereas particles grown at higher pH are larger and highly agglomerated. Energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy confirm the formation of calcium phosphate. The levels of mineralization are higher in samples grown at high pH.}, language = {en} } @article{KirchheckerTroegerMuellerBakeetal.2015, author = {Kirchhecker, Sarah and Tr{\"o}ger-M{\"u}ller, Steffen and Bake, Sebastian and Antonietti, Markus and Taubert, Andreas and Esposito, Davido}, title = {Renewable pyridinium ionic liquids from the continuous hydrothermal decarboxylation of furfural-amino acid derived pyridinium zwitterions}, series = {Green chemistry}, volume = {8}, journal = {Green chemistry}, number = {17}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1463-9262}, doi = {10.1039/c5gc00913h}, pages = {4151 -- 4156}, year = {2015}, abstract = {Fully renewable pyridinium ionic liquids were synthesised via the hydrothermal decarboxylation of pyridinium zwitterions derived from furfural and amino acids in flow. The functionality of the resulting ionic liquid (IL) can be tuned by choice of different amino acids as well as different natural carboxylic acids as the counterions. A representative member of this new class of ionic liquids was successfully used for the synthesis of ionogels and as a solvent for the Heck coupling.}, language = {en} } @article{GoebelHesemannWeberetal.2009, author = {Goebel, Ronald and Hesemann, Peter and Weber, Jens and Moeller, El{\´e}onore and Friedrich, Alwin and Beuermann, Sabine and Taubert, Andreas}, title = {Surprisingly high, bulk liquid-like mobility of silica-confined ionic liquids}, issn = {1463-9076}, doi = {10.1039/B821833a}, year = {2009}, abstract = {Mesoporous silica monoliths were prepared by the sol - gel technique and. lled with 1-ethyl-3-methyl imidazolium [Emim]-X (X = dicyanamide [N(CN)(2)], ethyl sulfate [EtSO4], thiocyanate [SCN], and triflate [TfO]) ionic liquids (ILs) using a methanol-IL exchange technique. The structure and behavior of the ILs inside the silica monoliths were studied using X-ray scattering, nitrogen sorption, IR spectroscopy, solid-state NMR, and thermal analysis. DSC finds shifts in both the glass transition temperature and melting points (where applicable) of the ILs. Glass transition and melting occur well below room temperature. There is thus no conflict with the NMR and IR data, which show that the ILs are as mobile at room temperature as the bulk (not confined) ILs. The very narrow line widths of the NMR spectra suggest that the ILs in our materials have the highest mobility reported for confined ILs so far. As a result, our data suggest that it is possible to generate IL/silica hybrid materials (ionogels) with bulk-like properties of the IL. This could be interesting for applications in, e.g., the solar cell or membrane fields.}, language = {en} } @article{KindPlamperGoebeletal.2009, author = {Kind, Lucy and Plamper, Felix A. and Goebel, Ronald and Mantion, Alexandre and Mueller, Axel H. E. and Pieles, Uwe and Taubert, Andreas and Meier, Wolfgang P.}, title = {Silsesquioxane/polyamine nanoparticle-templated formation of star- or raspberry-like silica nanoparticles}, issn = {0743-7463}, doi = {10.1021/La900229n}, year = {2009}, abstract = {Silica is an important mineral in biology and technology, and many protocols have been developed for the synthesis of complex silica architectures. The current report shows that silsesquioxane nanoparticles carrying polymer arms on their surface are efficient templates for the fabrication of silica particles with a star- or raspberry-like morphology. The shape of the resulting particles depends on the chemistry of the polymer arms. With poly(N,N- dimethylaminoethyl methacrylate) (PDMAEMA) arms, spherical particles with a less electron dense core form. With poly {[2- (methacryloyloxy)ethyl] trimethylammonium iodide} (PMETAI), star- or raspberry-like particles form. Electron microscopy, electron tomography, and small-angle X-ray scattering show that the resulting silica particles have a complex structure, where a silsequioxane nanoparticle carrying the polymer arms is in the center. Next is a region that is polymer-rich. The outermost region of the particle is a silica layer, where the outer parts of the polymer arms are embedded. Time- resolved zeta-potential and pH measurements, dynamic light scattering, and electron microscopy reveal that silica formation proceeds differently if PDMAEMA is exchanged for PMETAI.}, language = {en} } @article{GrafMantionFoelskeetal.2009, author = {Graf, Philipp and Mantion, Alexandre and Foelske, Annette and Shkilnyy, Andriy and Ma{\"U}ic, Admir and Thuenemann, Andreas F. and Taubert, Andreas}, title = {Peptide-coated silver nanoparticles : synthesis, surface chemistry, and pH-triggered, reversible assembly into particle assemblies}, issn = {0947-6539}, doi = {10.1002/chem.200802329}, year = {2009}, abstract = {Simple tripeptides are scaffolds for the synthesis and further assembly of peptide/silver nanoparticle composites. Herein, we further explore peptide-con trolled silver nanoparticle assembly processes. Silver nanoparticles with a pH-responsive peptide coating have been synthesized by using a one-step precipitation/coating route. The nature of the peptide/silver interaction and the effect of the peptide oil the formation of the silver particles have been studied via UV/Vis, X-ray photoelectron, and surface-enhanced Raman spectroscopies as well as through electron microscopy, small angle X-ray scattering and powder Xray diffraction with Rietveld refinement. The particles reversibly form aggregates of different sizes in aqueous solution. The state of aggregation call be controlled by the solution pH value. At low pH values, individual particles are present. At neutral pH values, small clusters form and at high pH values, large precipitates are observed.}, language = {en} } @article{NavarroShkilnyyTierschetal.2009, author = {Navarro, Salvador and Shkilnyy, Andriy and Tiersch, Brigitte and Taubert, Andreas and Menzel, Henning}, title = {Preparation, characterization, and thermal gelation of amphiphilic alkyl-poly(ethyleneimine)}, issn = {0743-7463}, doi = {10.1021/La9013569}, year = {2009}, abstract = {Amphiphilic alkyl-poly(ethyleneimine)s (alkyl-PEI) with different degrees of polymerization have been produced by alkaline hydrolysis of alkyl-poly(2-methyl-2-oxazoline). Potentiometric titration of the alkyl-PEI shows the influence of the alkyl chain and the degree of polymerization on the titration curves and hence on the polymer conformation. Karl Fischer titration has been used to determine the water content in the polymers. Subsequent X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and differential scanning calorimetry (DSC) measurements prove the existence of different hydration states of the PEI even under dry storage conditions. Upon cooling from hot aqueous Solutions, hydrogels form. The gelation concentration decreases with increasing degree of polymerization of the PEI segment. Scanning electron microscopy (SEM and cryo-SEM) of the hydrogels reveal an alkyl-PEI fibrous network composed of fan-like units. DSC shows that the percentages of bound and free water in the hydrogels depend on the concentration of polar amino groups.}, language = {en} } @article{SchweizerSchusterJungingeretal.2010, author = {Schweizer, S. and Schuster, T. and Junginger, Matthias and Siekmeyer, Gerd and Taubert, Andreas}, title = {Surface modification of ickel/Titanium Alloy and Titanium Surfaces via a Polyelectrolyte Multilayer/Calcium Phosphate Hybrid Coating}, issn = {1438-7492}, doi = {10.1002/mame.200900347}, year = {2010}, abstract = {The report shows that simple LbL deposition of positively charged chitosan and negatively charged heparin can be used to efficiently modify the native surface of both NiTi and Ti without any previous treatments. Moreover, mineralization of the polymer multilayers with calcium phosphate leads to surfaces with low contact angles around 70 and 20 degrees for NiTi and Ti, respectively. This suggests that a polymer multilayer/calcium phosphate hybrid coating could be useful for making NiTi or Ti implants that are at the same time antibacterial (via the chitosan), suppress blood clot formation (via the heparin), and favor fast endothelialization (via the improved surface hydrophilicity compared to the respective neat material).}, language = {en} } @book{Taubert2007, author = {Taubert, Andreas}, title = {Ionische Fl{\"u}ssigkeiten : chemische Kuriosa oder sind sie doch recht n{\"u}tzlich? ; Antrittsvorlesung 2007-05-24}, publisher = {Univ.-Bibl.}, address = {Potsdam}, year = {2007}, abstract = {Klassischerweise haben Salze, beispielsweise Kochsalz, Schmelzpunkte von einigen hundert Grad Celsius und mehr. Ionische Fl{\"u}ssigkeiten sind dagegen Salze, deren Schmelzpunkt zum Teil weit unter der Raumtemperatur liegt. Sie sind daher bei Raumtemperatur fl{\"u}ssig. Obwohl ionische Fl{\"u}ssigkeiten seit 1914 bekannt sind, hatten sie bis vor 15 Jahren keinerlei Bedeutung. Heute jedoch werden ionische Fl{\"u}ssigkeiten aufgrund ihrer vorteilhaften Eigenschaften, wie hohe Leitf{\"a}higkeit oder hohe Temperaturstabilit{\"a}t, unter anderem zur Papierverarbeitung oder in flexiblen Solarzellen eingesetzt. Die Antrittsvorlesung wird sich insbesondere mit der Herstellung anorganischer Partikel befassen und zeigen, wie ionische Fl{\"u}ssigkeiten zur Herstellung neuer Materialien f{\"u}r verschiedene Anwendungen genutzt werden k{\"o}nnen.}, language = {de} } @misc{BleekTaubert2013, author = {Bleek, Katrin and Taubert, Andreas}, title = {New developments in polymer-controlled, bioinspired calcium phosphate mineralization from aqueous solution}, series = {Acta biomaterialia}, volume = {9}, journal = {Acta biomaterialia}, number = {5}, publisher = {Elsevier}, address = {Oxford}, issn = {1742-7061}, doi = {10.1016/j.actbio.2012.12.027}, pages = {6283 -- 6321}, year = {2013}, abstract = {The polymer-controlled and bioinspired precipitation of inorganic minerals from aqueous solution at near-ambient or physiological conditions avoiding high temperatures or organic solvents is a key research area in materials science. Polymer-controlled mineralization has been studied as a model for biomineralization and for the synthesis of (bioinspired and biocompatible) hybrid materials for a virtually unlimited number of applications. Calcium phosphate mineralization is of particular interest for bone and dental repair. Numerous studies have therefore addressed the mineralization of calcium phosphate using a wide variety of low- and high-molecular-weight additives. In spite of the growing interest and increasing number of experimental and theoretical data, the mechanisms of polymer-controlled calcium phosphate mineralization are not entirely clear to date, although the field has made significant progress in the last years. A set of elegant experiments and calculations has shed light on some details of mineral formation, but it is currently not possible to preprogram a mineralization reaction to yield a desired product for a specific application. The current article therefore summarizes and discusses the influence of (macro)molecular entities such as polymers, peptides, proteins and gels on biomimetic calcium phosphate mineralization from aqueous solution. It focuses on strategies to tune the kinetics, morphologies, final dimensions and crystal phases of calcium phosphate, as well as on mechanistic considerations.}, language = {en} }