Competitive Coordination of Metals by Phosphorus and Sulfur in Complexes with Polydentate Ligands Containing P(III)-S Bonds
Olga Kataeva, А.Т. Губайдуллин, I.А. Litvinov, Lidiya I. Kursheva, É. S. Batyeva, Оleg G. Sinyashin
Abstract
Olga Kataeva, А.Т. Губайдуллин, I.А. Litvinov, Lidiya I. Kursheva, É. S. Batyeva, Оleg G. Sinyashin
Abstract
A series of complexes of thiophosphites with transition metals has been studied by X-ray single crystal diffraction: CuHalLP(SR)3, CuHalLP(SR)3LNCMe, CuBrLP(SEt)2NEt2, CuSCNLP(SR)3, CpMn(CO)2LP(SR)3, ArCr(CO)2LP(SR)3, with Hal = Cl, Br, I and R = Me, Et, Pr, i-Pr, Bu, Ph. Depending on the metal center, substituents R at sulfur, the conditions of reactions and crystal growth, different coordination modes have been observed: “classical” monodentate binding via phosphorus, unusual bidentate mode with participation of both P and S donor atoms of the ambident P – S system, as well as both monodentate and bidentate modes in one complex.
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A series of complexes of thiophosphites with transition metals has been studied by X-ray single crystal diffraction: CuHalLP(SR)3, CuHalLP(SR)3LNCMe, CuBrLP(SEt)2NEt2, CuSCNLP(SR)3, CpMn(CO)2LP(SR)3, ArCr(CO)2LP(SR)3, with Hal = Cl, Br, I and R = Me, Et, Pr, i-Pr, Bu, Ph. Depending on the metal center, substituents R at sulfur, the conditions of reactions and crystal growth, different coordination modes have been observed: “classical” monodentate binding via phosphorus, unusual bidentate mode with participation of both P and S donor atoms of the ambident P – S system, as well as both monodentate and bidentate modes in one complex.
Key concepts: Denticity, Chemistry, Sulfur, Crystallography, Transition metal, Phosphorus, Metal, Crystal structure