Abstract
Vanadium chemistry is of interest due its biological relevance and medical applications. In particular, the interactions of high-valent vanadium ions with sulfur-containing biologically important molecules, such as cysteine and glutathione, might be related to the redox conversion of vanadium in ascidians, the function of amavadin (a vanadium-containing anion) and the antidiabetic behaviour of vanadium compounds. A mechanistic understanding of these aspects is important. In an effort to investigate high-valent vanadium-sulfur chemistry, we have synthesized and characterized the non-oxo divanadium(IV) complex salt tetraphenylphosphonium tri-μ-<!?tlsb=-0.11pt>methanolato-κ6O:O-bis({tris[2-sulfanidyl-3-(trimethylsilyl)phenyl]phosphane-κ4P,S,S',S''}vanadium(IV)) methanol disolvate, (C24H20P)[VIV2(μ-OCH3)3(C27H36PS3)2]·2CH3OH. Two VIV metal centres are bridged by three methanolate ligands, giving a C2-symmetric V2(μ-OMe)3 core structure. Each VIV centre adopts a monocapped trigonal antiprismatic geometry, with the P atom situated in the capping position and the three S atoms and three O atoms forming two triangular faces of the trigonal antiprism. The magnetic data indicate a paramagnetic nature of the salt, with an S = 1 spin state.A non-oxo divanadium(IV) complex with bridging methanolate ligands and tris(2-sulfanidylphenyl)phosphane ligands was synthesized and structurally characterized. The magnetic data indicate a paramagnetic nature with an S = 1 spin state.
| Original language | English |
|---|---|
| Pages (from-to) | 416-420 |
| Number of pages | 5 |
| Journal | Acta Crystallographica Section C: Structural Chemistry |
| Volume | 72 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 2016 May 1 |
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All Science Journal Classification (ASJC) codes
- Condensed Matter Physics
- Physical and Theoretical Chemistry
- Inorganic Chemistry
- Materials Chemistry
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A non-oxo methanolate-bridged divanadium(IV) complex with tris(2-sulfanidylphenyl)phosphane ligands : Synthesis, structural characterization and magnetic investigation. / Wu, Hong Ming; Chang, Ya Ho; Su, Chia Lin; Lee, Gene Hsiang; Hsu, Hua Fen.
In: Acta Crystallographica Section C: Structural Chemistry, Vol. 72, No. 5, 01.05.2016, p. 416-420.Research output: Contribution to journal › Article
TY - JOUR
T1 - A non-oxo methanolate-bridged divanadium(IV) complex with tris(2-sulfanidylphenyl)phosphane ligands
T2 - Synthesis, structural characterization and magnetic investigation
AU - Wu, Hong Ming
AU - Chang, Ya Ho
AU - Su, Chia Lin
AU - Lee, Gene Hsiang
AU - Hsu, Hua Fen
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Vanadium chemistry is of interest due its biological relevance and medical applications. In particular, the interactions of high-valent vanadium ions with sulfur-containing biologically important molecules, such as cysteine and glutathione, might be related to the redox conversion of vanadium in ascidians, the function of amavadin (a vanadium-containing anion) and the antidiabetic behaviour of vanadium compounds. A mechanistic understanding of these aspects is important. In an effort to investigate high-valent vanadium-sulfur chemistry, we have synthesized and characterized the non-oxo divanadium(IV) complex salt tetraphenylphosphonium tri-μ-<!?tlsb=-0.11pt>methanolato-κ6O:O-bis({tris[2-sulfanidyl-3-(trimethylsilyl)phenyl]phosphane-κ4P,S,S',S''}vanadium(IV)) methanol disolvate, (C24H20P)[VIV2(μ-OCH3)3(C27H36PS3)2]·2CH3OH. Two VIV metal centres are bridged by three methanolate ligands, giving a C2-symmetric V2(μ-OMe)3 core structure. Each VIV centre adopts a monocapped trigonal antiprismatic geometry, with the P atom situated in the capping position and the three S atoms and three O atoms forming two triangular faces of the trigonal antiprism. The magnetic data indicate a paramagnetic nature of the salt, with an S = 1 spin state.A non-oxo divanadium(IV) complex with bridging methanolate ligands and tris(2-sulfanidylphenyl)phosphane ligands was synthesized and structurally characterized. The magnetic data indicate a paramagnetic nature with an S = 1 spin state.
AB - Vanadium chemistry is of interest due its biological relevance and medical applications. In particular, the interactions of high-valent vanadium ions with sulfur-containing biologically important molecules, such as cysteine and glutathione, might be related to the redox conversion of vanadium in ascidians, the function of amavadin (a vanadium-containing anion) and the antidiabetic behaviour of vanadium compounds. A mechanistic understanding of these aspects is important. In an effort to investigate high-valent vanadium-sulfur chemistry, we have synthesized and characterized the non-oxo divanadium(IV) complex salt tetraphenylphosphonium tri-μ-<!?tlsb=-0.11pt>methanolato-κ6O:O-bis({tris[2-sulfanidyl-3-(trimethylsilyl)phenyl]phosphane-κ4P,S,S',S''}vanadium(IV)) methanol disolvate, (C24H20P)[VIV2(μ-OCH3)3(C27H36PS3)2]·2CH3OH. Two VIV metal centres are bridged by three methanolate ligands, giving a C2-symmetric V2(μ-OMe)3 core structure. Each VIV centre adopts a monocapped trigonal antiprismatic geometry, with the P atom situated in the capping position and the three S atoms and three O atoms forming two triangular faces of the trigonal antiprism. The magnetic data indicate a paramagnetic nature of the salt, with an S = 1 spin state.A non-oxo divanadium(IV) complex with bridging methanolate ligands and tris(2-sulfanidylphenyl)phosphane ligands was synthesized and structurally characterized. The magnetic data indicate a paramagnetic nature with an S = 1 spin state.
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U2 - 10.1107/S2053229616005222
DO - 10.1107/S2053229616005222
M3 - Article
C2 - 27146571
AN - SCOPUS:84966659368
VL - 72
SP - 416
EP - 420
JO - Acta crystallographica. Section C, Structural chemistry
JF - Acta crystallographica. Section C, Structural chemistry
SN - 2053-2296
IS - 5
ER -