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J. Bruckmann

Bio: J. Bruckmann is an academic researcher from Max Planck Society. The author has contributed to research in topics: Trigonal bipyramidal molecular geometry & Crystal structure. The author has an hindex of 2, co-authored 2 publications receiving 97 citations.

Papers
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Journal ArticleDOI
TL;DR: In this article, three complexes of the formula [Zn(2,2′-biny)(CCl3CO2)2(H2O)]n have been synthesized and characterized by elemental analysis, IR spectra, thermal analysis and single-crystal X-ray diffraction for 1 and 2.

78 citations

Journal ArticleDOI
TL;DR: A heptacoordinated Cd(II) complex bis(1,10-phenanthroline)bis(trifluoroacetato)cadmium (II) has been synthesized; its structure is distorted pentagonal bipyramidal as discussed by the authors.

21 citations


Cited by
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Journal ArticleDOI
TL;DR: The role of 4,4'-bipyridine in discovering various coordination polymers with novel topologies that range from one-dimensional to three dimensional are described.

459 citations

Journal ArticleDOI
TL;DR: In this paper, the trinuclear unit is held together by bridging deprotonated phenolic oxygen atoms from the Schiff base and acetate groups, and the structures of the three synthesised complexes have been determined by single-crystal X-ray diffraction.

338 citations

Journal ArticleDOI
TL;DR: In this paper, three dinuclear Zn(II) complexes [Zn(L)(μ1, 1-N3)Zn (L)(N3)]· 1.5H2O (1),[Zn[L]-(OCH3)(OH)C6H3CHN(CH2)2 N(CH3)2], which is the condensation product of o-vanillin and 2-dimethylaminoethylamine have been synthesized from a potentially tetradentate N2O2-donor Schiff base

149 citations

Journal ArticleDOI
TL;DR: The neutral mononuclear zinc complexes with the quinolone antibacterial drug oxolinic acid in the absence or presence of a nitrogen donor heterocyclic ligand 2,2'-bipyridine or 1,10-phenanthroline have been synthesized and characterized.

126 citations

Journal ArticleDOI
TL;DR: The degradation mechanism of polysulfone based anion exchange membranes, carrying pyridine ion exchange groups, under vanadium flow battery (VFB) medium was investigated in detail and it is found that sp(2) hybrid orbital interactions between pyridinic-nitrogen in 4,4'-bipyridine and benzylic carbon disrupt the charge state balance of pristine chloromethylated polys sulfurone.
Abstract: The stability of hydrocarbon ion exchange membranes is one of the critical issues for a flow battery. However, the degradation mechanism of ion exchange membranes has been rarely investigated especially for anion exchange membranes. Here, the degradation mechanism of polysulfone based anion exchange membranes, carrying pyridine ion exchange groups, under vanadium flow battery (VFB) medium was investigated in detail. We find that sp(2) hybrid orbital interactions between pyridinic-nitrogen in 4,4'-bipyridine and benzylic carbon disrupt the charge state balance of pristine chloromethylated polysulfone. This difference in electronegativity inversely induces an electrophilic carbon center in the benzene ring, which can be attacked by the lone pair electron on the vanadium(V) oxygen species, further leading to the degradation of polymer backbone, while leaving the 4,4'-bipyridine ion exchange groups stable. This work represents a step toward design and construction of alternative type of chemically stable hydrocarbon ion exchange membranes for VFB.

110 citations