S
Stanislav Groysman
Researcher at Wayne State University
Publications - 71
Citations - 1979
Stanislav Groysman is an academic researcher from Wayne State University. The author has contributed to research in topics: Ligand & Reactivity (chemistry). The author has an hindex of 26, co-authored 62 publications receiving 1769 citations. Previous affiliations of Stanislav Groysman include Tel Aviv University & University of Waterloo.
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Pentabenzyltantalum: Straightforward synthesis, X-ray structure, and application in the synthesis of [O2N]TaBn3-Type and [O3N]TaBn2-Type complexes
TL;DR: In this article, the X-ray structure of pentabenzyltantalum reveals a square-pyramidal geometry and was found to be an efficient starting material for the preparation of amine-phenolate complexes via toluene elimination reactions.
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A biomimetic approach to oxidized sites in the xanthine oxidoreductase family: synthesis and stereochemistry of tungsten(VI) analogue complexes.
TL;DR: Computational and experimental structures indicate that protein sites adopt intrinsic coordination geometries rather than those dictated by protein structure and environment.
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Salophan complexes of group IV metals
TL;DR: In this article, the coordination chemistry of tetradentate Salophan ligands with titanium and zirconium alkoxides is described for the first time, and three new SALophan precursors featuring different phenolate substituents (ortho-Me, ortho,para-di-Cl, Ortho,Para-Di-tBu) were synthesized in addition to the known prototypical salophan precursor, by a sequence of condensation and reduction.
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Reductive coupling of azides mediated by an iron(II) bis(alkoxide) complex.
TL;DR: The iron(III) hexazene complex (RO)2Fe(μ-κ(2):κ( 2)-AdN6Ad)Fe(OR)2 (3) was synthesized via reductive coupling of 1-azidoadamantane at the iron(II) bis(alkoxide) complex Fe( OR)2(THF) 2 (2).
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Group IV complexes of a tetradentate amine mono(phenolate) ligand: a second side-arm donor stabilizes cationic species.
TL;DR: An amine mono(phenolate) ligand bearing two side-arm donors led to octahedral trialkoxo and trialkyl group IV metal complexes, in which one of the donors was unbound, and to exceptionally stable cationic complexes in which the two side ofarm donors were tightly bound.