TY  - JOUR
A1  - Hentrich, Doreen
A1  - Junginger, Mathias
A1  - Bruns, Michael
A1  - Börner, Hans Gerhard
A1  - Brandt, Jessica
A1  - Brezesinski, Gerald
A1  - Taubert, Andreas
T1  - Interface-controlled calcium phosphate mineralization
BT  - effect of oligo(aspartic acid)-rich interfaces
JF  - CrystEngComm
N2  - 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.
Y1  - 2015
U6  - https://doi.org/10.1039/C4CE02274B
SN  - 1466-8033
IS  - 17
SP  - 6901
EP  - 6913
PB  - Royal Society of Chemistry
CY  - London
ER  - 
TY  - JOUR
A1  - Kirchhecker, Sarah
A1  - Tröger-Müller, Steffen
A1  - Bake, Sebastian
A1  - Antonietti, Markus
A1  - Taubert, Andreas
A1  - Esposito, Davido
T1  - Renewable pyridinium ionic liquids from the continuous hydrothermal decarboxylation of furfural-amino acid derived pyridinium zwitterions
JF  - Green chemistry
N2  - 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.
Y1  - 2015
U6  - https://doi.org/10.1039/c5gc00913h
SN  - 1463-9262
SN  - 1463-9270
VL  - 8
IS  - 17
SP  - 4151
EP  - 4156
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - INPR
A1  - Vioux, Andre
A1  - Taubert, Andreas
T1  - Ionic liquids 2014 and selected papers from ILMAT 2013: highlighting the ever-growing potential of ionic liquids
T2  - International journal of molecular sciences
Y1  - 2014
U6  - https://doi.org/10.3390/ijms151222815
SN  - 1422-0067
VL  - 15
IS  - 12
SP  - 22815
EP  - 22818
PB  - Molecular Diversity Preservation International
CY  - Basel
ER  - 
TY  - JOUR
A1  - Abouserie, Ahed
A1  - Schilde, Uwe
A1  - Taubert, Andreas
T1  - The crystal structure of N-butylpyridinium bis(μ2-dichlorido)-tetrachloridodicopper(II), C₁₈H₂₈N₂Cu₂Cl₆
JF  - Zeitschrift für Kristallographie - New Crystal Structures
N2  - C₉H₁₄Cl₃CuN, monoclinic, P2₁/n (no. 14), a = 9.6625(6) Å, b = 9.3486(3) Å, c = 14.1168(8) Å, β = 102.288(5)°, V = 1245.97(11) ų, Z = 4, Rgₜ(F) = 0.0182, wRᵣₑf(F²) = 0.0499, T = 210(2) K.
KW  - Ionic Liquid Precursor
KW  - Thermochromism
KW  - Salts
KW  - Nanostructures
KW  - Catalysis
KW  - Solvents
KW  - Complex
KW  - Gas
Y1  - 2018
U6  - https://doi.org/10.1515/NCRS-2018-0099
SN  - 2194-4946
SN  - 2196-7105
VL  - 233
IS  - 4
SP  - 743
EP  - 746
PB  - de Gruyter
CY  - Berlin und München
ER  - 
TY  - JOUR
A1  - Hentrich, Doreen
A1  - Tauer, Klaus
A1  - Espanol, Montserrat
A1  - Ginebra, Maria-Pau
A1  - Taubert, Andreas
T1  - EDTA and NTA effectively tune the mineralization of calcium phosphate from bulk aqueous solution
JF  - Biomimetics
N2  - This study describes the effects of nitrilotriacetic acid (NTA) and ethylenediaminotetraacetic acid (EDTA) on themineralization of calciumphosphate from bulk aqueous solution. Mineralization was performed between pH 6 and 9 and with NTA or EDTA concentrations of 0, 5, 10, and 15 mM. X-ray diffraction and infrared spectroscopy show that at low pH, mainly brushite precipitates and at higher pH, mostly hydroxyapatite forms. Both additives alter the morphology of the precipitates. Without additive, brushite precipitates as large plates. With NTA, the morphology changes to an unusual rod-like shape. With EDTA, the edges of the particles are rounded and disk-like particles form. Conductivity and pH measurements suggest that the final products form through several intermediate steps.
KW  - biomineralization
KW  - biomimetic mineralization
KW  - calcium phosphate
KW  - NTA
KW  - EDTA
KW  - precipitation
KW  - brushite
KW  - hydroxyapatite
Y1  - 2017
U6  - https://doi.org/10.3390/biomimetics2040024
SN  - 2313-7673
VL  - 2
IS  - 4
PB  - MDPI
CY  - Basel
ER  - 
TY  - JOUR
A1  - Taubert, Andreas
A1  - Leroux, Fabrice
A1  - Rabu, Pierre
A1  - de Zea Bermudez, Veronica
T1  - Advanced hybrid nanomaterials
JF  - Beilstein journal of nanotechnology
KW  - colloidal chemistry
KW  - environmental remediation
KW  - hybrid nanomaterials
KW  - nanocomposite
KW  - nanofillers
KW  - nanomedicine
KW  - nanostructures
KW  - polymer fillers
KW  - pore templating
KW  - smart materials
Y1  - 2019
U6  - https://doi.org/10.3762/bjnano.10.247
SN  - 2190-4286
VL  - 10
SP  - 2563
EP  - 2567
PB  - Beilstein-Institut zur Förderung der Chemischen Wissenschaften
CY  - Frankfurt am Main
ER  - 
TY  - JOUR
A1  - Mai, Tobias
A1  - Boye, Susanne
A1  - Yuan, Jiayin
A1  - Völkel, Antje
A1  - Gräwert, Marlies
A1  - Günter, Christina
A1  - Lederer, Albena
A1  - Taubert, Andreas
T1  - Poly(ethylene oxide)-based block copolymers with very high molecular weights for biomimetic calcium phosphate mineralization
JF  - RSC Advances : an international journal to further the chemical sciences
N2  - The present article is among the first reports on the effects of poly(ampholyte)s and poly(betaine)s on the biomimetic formation of calcium phosphate. We have synthesized a series of di- and triblock copolymers based on a non-ionic poly(ethylene oxide) block and several charged methacrylate monomers, 2-(trimethylammonium)ethyl methacrylate chloride, 2-((3-cyanopropyl)-dimethylammonium)ethyl methacrylate chloride, 3-sulfopropyl methacrylate potassium salt, and [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide. The resulting copolymers are either positively charged, ampholytic, or betaine block copolymers. All the polymers have very high molecular weights of over 106 g mol−1. All polymers are water-soluble and show a strong effect on the precipitation and dissolution of calcium phosphate. The strongest effects are observed with triblock copolymers based on a large poly(ethylene oxide) middle block (nominal Mn = 100 000 g mol−1). Surprisingly, the data show that there is a need for positive charges in the polymers to exert tight control over mineralization and dissolution, but that the exact position of the charge in the polymer is of minor importance for both calcium phosphate precipitation and dissolution.
Y1  - 2015
U6  - https://doi.org/10.1039/c5ra20035k
SN  - 2046-2069
IS  - 5
SP  - 103494
EP  - 103505
PB  - RSC Publishing
CY  - London
ER  - 
TY  - GEN
A1  - Zehbe, Kerstin
A1  - Kollosche, Matthias
A1  - Lardong, Sebastian
A1  - Kelling, Alexandra
A1  - Schilde, Uwe
A1  - Taubert, Andreas
T1  - Ionogels based on poly(methyl methacrylate) and metal-containing ionic liquids
BT  - correlation between structure and mechanical and electrical properties
N2  - Ionogels (IGs) based on poly(methyl methacrylate) (PMMA) and the metal-containing ionic liquids (ILs) bis-1-butyl-3-methlimidazolium tetrachloridocuprate(II), tetrachloride cobaltate(II), and tetrachlorido manganate(II) have been synthesized and their mechanical and electrical properties have been correlated with their microstructure. Unlike many previous examples, the current IGs show a decreasing stability in stress-strain experiments on increasing IL fractions. The conductivities of the current IGs are lower than those observed in similar examples in the literature. Both effects are caused by a two-phase structure with micrometer-sized IL-rich domains homogeneously dispersed an IL-deficient continuous PMMA phase. This study demonstrates that the IL-polymer miscibility and the morphology of the IGs are key parameters to control the (macroscopic) properties of IGs.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 361 
KW  - microstructure
KW  - ionogels
KW  - ionic liquids
KW  - phase separation
KW  - mechanical properties
KW  - ionic conductivity
Y1  - 2017
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-400607
ER  - 
TY  - GEN
A1  - Abouserie, Ahed
A1  - Schilde, Uwe
A1  - Taubert, Andreas
T1  - The crystal structure of N-butylpyridinium bis(μ2-dichlorido)-tetrachloridodicopper(II), C₁₈H₂₈N₂Cu₂Cl₆
T2  - Zeitschrift für Kristallographie - New Crystal Structures
N2  - C₉H₁₄Cl₃CuN, monoclinic, P2₁/n (no. 14), a = 9.6625(6) Å, b = 9.3486(3) Å, c = 14.1168(8) Å, β = 102.288(5)°, V = 1245.97(11) ų, Z = 4, Rgₜ(F) = 0.0182, wRᵣₑf(F²) = 0.0499, T = 210(2) K.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 465 
KW  - Ionic Liquid Precursor
KW  - Thermochromism
KW  - Salts
KW  - Nanostructures
KW  - Catalysis
KW  - Solvents
KW  - Complex
KW  - Gas
Y1  - 2018
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-417310
ER  - 
TY  - GEN
A1  - Winter, Alette
A1  - Thiel, Kerstin
A1  - Zabel, André
A1  - Klamroth, Tillmann
A1  - Pöppl, Andreas
A1  - Kelling, Alexandra
A1  - Schilde, Uwe
A1  - Taubert, Andreas
A1  - Strauch, Peter
T1  - Tetrahalidocuprates(II) – structure and EPR spectroscopy
BT  - Part 2: tetrachloridocuprates(II)
N2  - We present and discuss the results of crystallographic and electron paramagnetic resonance (EPR) spectroscopic analyses of five tetrachloridocuprate(II) complexes to supply a useful tool for the structural characterisation of the [CuCl4]2− moiety in the liquid state, for example in ionic liquids, or in solution. Bis(benzyltriethylammonium)-, bis(trimethylphenylammonium)-, bis(ethyltriphenylphosphonium)-, bis(benzyltriphenylphosphonium)-, and bis(tetraphenylarsonium)tetrachloridocuprate(II) were synthesised and characterised by elemental, IR, EPR and X-ray analyses. The results of the crystallographic analyses show distorted tetrahedral coordination geometry of all [CuCl4]2− anions in the five complexes and prove that all investigated complexes are stabilised by hydrogen bonds of different intensities. Despite the use of sterically demanding ammonium, phosphonium and arsonium cations to obtain the separation of the paramagnetic Cu(II) centres for EPR spectroscopy no hyperfine structure was observed in the EPR spectra but the principal values of the electron Zeeman tensor, g∥ and g⊥, could be determined. With these EPR data and the crystallographic parameters we were able to carry out a correlation study to anticipate the structural situation of tetrachloridocuprates in different physical states. This correlation is in good agreement with DFT calculations.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 240 
KW  - electron-spin resonance
KW  - liquid-crystal precursors
KW  - copper(II) halide salts
KW  - ionic liquid
KW  - square planar
KW  - tetrachlorocuprate(II) salts
KW  - molecular-structure
KW  - magnetic-properties
KW  - paramagnetic-resonance
KW  - temperature phase
Y1  - 2013
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-95012
SP  - 1019
EP  - 1030
ER  -