4.7 Article

Intramolecular hydrogen bond controlled coordination of N-thiophosphorylated thiourea 2,6-Me2C6H3NHC(S)NHP(S)(OiPr)2 with Ni(II)

期刊

INORGANIC CHEMISTRY COMMUNICATIONS
卷 12, 期 7, 页码 678-681

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.inoche.2009.05.030

关键词

Coordination mode; Crystal structure; Nickel; N-Thiophosphoryl thiourea; NMR spectroscopy

资金

  1. Russian Science Support Foundation
  2. DAAD

向作者/读者索取更多资源

Reaction of O,O'-diisopropylthiophosphoric acid isothiocyanate (iPrO)(2)P(S)NCS with 2,6-dimethylaniline 2,6-Me2C6H3NH2 leads to the new N-thiophosphorylated thiourea 2,6-Me(2)C(6)H(3)NHQS)NHP(S)(OiPr)(2) (HL). Reaction of the potassium salt of HL with Ni(II) in aqueous EtOH leads to the complex of formula (Ni(L-N,S)(2)]. The molecular structures of the thiourea HL and the complex [Ni(L-N,S)(2)] were elucidated by single crystal X-ray diffraction analysis, H-1 and P-31 NMR spectroscopy and microanalysis. In the complex [Ni(L-N,S)(2)], the metal center is found to be in a square-planar N2S2 environment formed by the C=S sulfur atoms and the P-N nitrogen atoms of two deprotonated L ligands. The ligands are in a trans-configuration. (C) 2009 Elsevier B.V. All rights reserved.

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