Metal-oxygen versus metal-sulfur bonding of the ambident monothiophosphinato ligand in some triphenylmeta(IV) derivatives, Ph3M[OSPR2] (M = Ge, Sn, Pb). Crystal structures of Ph3Ge[O(S)PPh2] and [Ph2Sn{O(S)PPh2} (μ-OH)]2-Reference-Cited by-同舟云学术

Metal-oxygen versus metal-sulfur bonding of the ambident monothiophosphinato ligand in some triphenylmeta(IV) derivatives, Ph3M[OSPR2] (M = Ge, Sn, Pb). Crystal structures of Ph3Ge[O(S)PPh2] and [Ph2Sn{O(S)PPh2} (μ-OH)]2

Published:1997-01 Issue:6 Volume:16 Page:949-961
ISSN:0277-5387
Container-title:Polyhedron
language:en
Short-container-title:Polyhedron

Author:

Silvestru Anca,Silvestru Cristian,Haiduc Ionel,Drake John E.,Yang Jincai,Caruso Francesco

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry

Reference40 articles.

1. Stereochemical aspects of phosphor-1,1-dithiolato metal complexes (dithiophosphates, dithiophosphinates): Coordination patterns, molecular structures and supramolecular associations—I

2. Dialkyldithiophosphate derivatives of non-transition elements

3. Zur Struktur von Thiophosphins�uren Die Kristall- und Molek�lstruktur der Dimethylthiophosphins�ure, (CH3)2PSOH, und der Dicyclohexylthiophosphins�ure, (C6H11)2PSOH, bei 140 K

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