TY - JOUR A1 - Kraus, Werner A1 - Stephan, H. A1 - Reck, Günter T1 - Käfigstrukturen für den Einschluss von Pertechnetat und Perrhenat PY - 2004 SN - 0930-486X VL - 21 SP - 70 PB - Oldenbourg CY - München AN - OPUS4-3489 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meißner, T. A1 - Richter, W. A1 - Stephan, H. A1 - Zänker, H. A1 - Kraus, Werner T1 - Darstellung und Charakterisierung von Nanopartikeln auf der Basis von [Ti2W10PO40]7- und Chitosan KW - Polyoxometallate KW - Nanopartikel KW - Clusterverbindung PY - 2005 U6 - https://doi.org/10.1002/cite.200590281 SN - 0009-286X SN - 1522-2640 VL - 77 IS - 8 SP - 1227 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-11080 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meißner, T. A1 - Bergmann, R. A1 - Oswald, J. A1 - Rode, K. A1 - Stephan, H. A1 - Richter, W. A1 - Zänker, H. A1 - Kraus, Werner A1 - Emmerling, Franziska A1 - Reck, Günter T1 - Chitosan-encapsulated Keggin anion [Ti2W10PO40]7-.Synthesis, characterization and cellular uptake studies N2 - The Keggin type polyoxotungstate [Ti2W10PO40]7- forms stable associates with the biopolymer chitosan in the nanometer size range. The cluster compound crystallizes from aqueous solution as K4H3[Ti2W10PO40] · 15H2O having a tetragonal structure. Both, the cluster compound and the chitosan/[Ti2W10PO40] associates show a high hydrolytic stability at pH 7.4. The associates formed between the cluster anion [Ti2W10PO40]7- with the polyaminosaccharide chitosan have been characterized by photon correlation spectroscopy, scanning electron microscopy, filtration, centrifugation and zeta potential measurements. The size of the associates formed is in the range of ca. 5×101 to 5×102 nm. These particles have a defined stoichiometry with 5–6 cluster anions bound per molecule chitosan. The isoelectric point determined by zeta potential measurements was found for a cluster anion to chitosan molar ratio of 5.5, indicating the charge neutralization between protonated chitosan and [Ti2W10PO40]7- anions. Cellular uptake studies with [Ti2W10PO40]7- using tumor cell lines FaDu (human squamous carcinoma) and HT-29 (human adenocarcinoma) showed that the tungsten amount inside the cells is remarkably enhanced in the presence of chitosan. KW - Cluster compound KW - Keggin structure KW - Bipolymer KW - Chitosan PY - 2006 U6 - https://doi.org/10.1007/s11243-006-0035-z SN - 0340-4285 SN - 1572-901X VL - 31 IS - 5 SP - 603 EP - 610 PB - Springer CY - Dordrecht AN - OPUS4-12568 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kraus, Werner A1 - Stephan, H. A1 - Röllich, A. A1 - Matejka, Z. A1 - Reck, Günter T1 - K6H2[TiW11CoO40].13H2O, with a monotitanoundecatungstocobaltate(II) anion N2 - Hexapotassium dihydrogen monotitanoundeca­tungsto­cobalt­ate(II) trideca­hydrate, K6H2[TiW11CoO40]·13H2O, crystallizes from aqueous solution in the cubic space group P 3m. The structure was refined as an inversion twin. The [TiW11CoO40]8- anion has a Keggin structure with one W-atom site occupied by titanium and a central tetra­hedral CoO4 group. PY - 2005 U6 - https://doi.org/10.1107/S1600536805005180 SN - 1600-5368 VL - 61 IS - 3 SP - i35 EP - i37 PB - Munksgaard CY - Copenhagen AN - OPUS4-7043 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mironov, Y.V. A1 - Shestopalov, M.A. A1 - Brylev, K.A. A1 - Yarovoi, S. S. A1 - Romanenko, G.V. A1 - Fedorov, V.E. A1 - Spies, H. A1 - Pietzsch, H.-J. A1 - Stephan, H. A1 - Geipel, G. A1 - Bernhard, G. A1 - Kraus, Werner T1 - [Re6Q7O(3,5-Me2PzH)6]Br2.3,5-Me2PzH (Q = S, Se) - New Octahedral Rhenium Cluster Complexes with Organic Ligands: Original Synthetic Approach and Unexpected Ligand Exchange in the Cluster Core KW - Rhenium KW - Cluster compounds KW - Ligand exchange KW - Organic ligands KW - Structure elucidation KW - Laser fluorescence spectroscopy PY - 2005 SN - 1434-1948 SN - 1099-0682 SP - 657 EP - 661 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-7039 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Comba, P. A1 - Emmerling, Franziska A1 - Jakob, M. A1 - Kraus, Werner A1 - Kubeil, M. A1 - Morgen, M. A1 - Pietzsch, J. A1 - Stephan, H. T1 - Copper(II) chemistry of the functionalized macrocycle cyclam tetrapropionic acid N2 - The CuII complex of H4TETP (H4TETP = 1,4,8,11-tetraazatetradecane-1,4,8,11-tetrapropionic acid) is five-coordinate with a distorted square-pyramidal structure (τ = 0.45; i.e. the geometry is nearly half-way between square-pyramidal and trigonal-bipyramidal) and a relatively long Cu–N and a short Cu–O bond; the comparison between powder and solution electronic spectroscopy, the frozen solution EPR spectrum and ligand-field-based calculations (angular overlap model, AOM) indicate that the solution and solid state structures are very similar, i.e. the complex has a relatively low 'in-plane' and a significant axial ligand field with a dx²-y² ground state. The ligand-enforced structure is therefore shown to lead to a partially quenched Jahn–Teller distortion and to a relatively low complex stability, lower than with the corresponding acetate-derived ligand H4TETA. This is confirmed by potentiometric titration and by the biodistribution with 64Cu-labeled ligands which show that the uptake in the liver is significantly increased with the H4TETP-based system. KW - Copper(II) KW - Chemistry PY - 2013 U6 - https://doi.org/10.1039/c2dt32356g SN - 1477-9226 SN - 1477-9234 SN - 1364-5447 VL - 42 IS - 17 SP - 6142 EP - 6148 PB - RSC CY - Cambridge AN - OPUS4-28075 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mironov, Y.V. A1 - Brylev, K.A. A1 - Shestopalov, M.A. A1 - Yarovoi, S. S. A1 - Fedorov, V.E. A1 - Spies, H. A1 - Pietzsch, H.-J. A1 - Stephan, H. A1 - Geipel, G. A1 - Bernhard, G. A1 - Kraus, Werner T1 - Octahedral rhenium cluster complexes with organic ligands: Synthesis, structure and properties of [Re6Q8(3,5-Me2PzH)6]Br2 . 2(3,5-Me2PzH) (Q = S, Se) N2 - Two new octahedral cluster complexes – [Re6S8(3,5-Me2PzH)6]Br2 · 2(3,5-Me2PzH) (1) and [Re6Se8(3,5-Me2PzH)6]Br2 · 2(3,5-Me2PzH) (2), where 3,5-Me2PzH is 3,5-dimethylpyrazole, have been synthesized using reaction of rhenium chalcobromide complexes Cs4[Re6S8Br6] · 2H2O and Cs3[Re6Se8Br6] · H2O, respectively, with molten 3,5-dimethylpyrazole. Both compounds synthesized were characterized by X-ray single-crystal diffraction and chemical analysis, IR and luminescent spectra. KW - Synthesis KW - Crystal structure KW - Rhenium complexes KW - Octahedral clusters KW - Organic ligands PY - 2006 U6 - https://doi.org/10.1016/j.ica.2005.08.012 SN - 0020-1693 SN - 1873-3255 VL - 359 IS - 4 SP - 1129 EP - 1134 PB - Elsevier Sequoia CY - Lausanne AN - OPUS4-14489 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gniazdowska, E. A1 - Kraus, Werner A1 - Emmerling, Franziska A1 - Spies, H. A1 - Stephan, H. T1 - Tetrabutylammonium bis(2-amidobenzenethiolato-kappa2S,N)oxorhenate(V) N2 - The structure of the title compound, (C16H36N)[Re(C6H5NS)2O], is isomorphous with the corresponding oxotechnetate(V) complex. KW - Coordination chemistry KW - Rhenium KW - Organometallic PY - 2006 U6 - https://doi.org/10.1107/S160053680601511X SN - 1600-5368 VL - 62 IS - 6 SP - m1197 EP - m1199 PB - Munksgaard CY - Copenhagen AN - OPUS4-12345 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Juran, S. A1 - Walther, M. A1 - Stephan, H. A1 - Bergmann, R. A1 - Steinbach, J. A1 - Kraus, Werner A1 - Emmerling, Franziska A1 - Comba, P. T1 - Hexadentate Bispidine derivatives as versatile bifunctional chelate agents for Copper(II) radioisotopes PY - 2009 U6 - https://doi.org/10.1021/bc800461e SN - 1043-1802 SN - 1520-4812 VL - 20 IS - 2 SP - 347 EP - 359 CY - Washington, DC AN - OPUS4-19068 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Walther, M. A1 - Matterna, M. A1 - Juran, S. A1 - Fähnemann, S. A1 - Stephan, H. A1 - Kraus, Werner A1 - Emmerling, Franziska T1 - Imidazole-containing bispidine ligands: synthesis, structure and Cu(II) complexation N2 - The preparation and characterization of tris-pyridyl bispidine (3,7-diazabicyclo[3.3.1]nonane) derivatives with benzimidazole and imidazole donor groups at the N-3 position of the bispidine Skeleton and their copper(II) complexes are reported. The impact of the hetaryl substituents on the configurational isomerism of piperidones and their corresponding bispidones has been studied by NMR spectroscopy, revealing the exclusive appearance in the enol form for the piperidones in solution and the trans-configuration regarding the two pyridyl substituents, as well as the sole formation of the unsymmetric exo-endo isomers for the corresponding bispidones. Thus, the bispidones are preorganized ligands for building pentacoordinated complexes, confirmed by the preparation and characterization of the corresponding Cu(II) complexes. Of the di-pyridyl piperidones with benzimidazole and imidazole substituents, and of the Cu(II) complex of the benzimidazole-containing bispidone, Crystals have become available for the analysis by X-ray diffraction, showing that the piperidones form the enol tautomers also in the solid state. KW - Piperidone KW - Bispidine KW - Copper(II) KW - Configuration isomerism PY - 2011 SN - 0932-0776 SN - 0340-5087 SN - 0044-3174 VL - 66b SP - 721 EP - 728 PB - Verl. d. Zeitschrift für Naturforschung CY - Tübingen AN - OPUS4-24091 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -