4.7 Article

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

Journal

INORGANIC CHEMISTRY COMMUNICATIONS
Volume 12, Issue 7, Pages 678-681

Publisher

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

Keywords

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

Funding

  1. Russian Science Support Foundation
  2. DAAD

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available