Nickel(II) complexes with N-(thio)phosphorylthioureas AdNHC(S)NHP(X)(OiPr)2: Versatile coordination of phosphoryl (X = O) and thiophosphoryl (X = S) derivatives
Autor: | Igor A. Litvinov, Dmitriy B. Krivolapov, Łukasz Szyrwiel, Maria G. Babashkina, Felix D. Sokolov, Timur R. Gimadiev, Damir A. Safin, Henryk Kozlowski, F. Ekkehardt Hahn |
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Rok vydání: | 2008 |
Předmět: |
Hydrogen bond
Stereochemistry Thio chemistry.chemical_element Crystal structure Inorganic Chemistry Metal Crystallography chemistry.chemical_compound Nickel Deprotonation Thiourea chemistry visual_art Materials Chemistry visual_art.visual_art_medium Physical and Theoretical Chemistry Cis–trans isomerism |
Zdroj: | Polyhedron. 27:2271-2276 |
ISSN: | 0277-5387 |
Popis: | The reaction of the potassium salts of N-(thio)phosphorylated thioureas of the common formula AdN(H)C(S)N(H)P(X)(OiPr)2 (X = O, HLI; X = S, HLII) with the Ni(II) cation in aqueous EtOH leads to [Ni(LI,II)2] chelate complexes. The molecular structures of the thioureas HLI,II and the complexes [Ni(LI-N,S)2] and [Ni(LII-S,S′)2] were elucidated by single crystal X-ray diffraction analysis, IR, 1H and 31P NMR spectroscopy and microanalysis. In the complex [Ni(LI)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 LI ligands. The ligands are in a trans configuration. The Ni(II) atom in complex [Ni(LII)2], with the deprotonated thiourea LII, is coordinated in a square-planar fashion by the C S and P S sulfur atoms of two anionic ligands. The ligands are in a cis configuration. |
Databáze: | OpenAIRE |
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