Tripodal polyphosphine ligands in silver (I) coordination chemistry: Mononuclear cf. polynuclear complex dependence vis-a-vis counterion and ligand to metal ratio

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Effendy, Claudio Pettinari, Riccardo Pettinari, Massimo Ricciutelli, Brian W. Skelton, Allan H. White

2005 Inorganica Chimica Acta Vol. 358 Issue 13 Article Cited by 10

Abstract

1:2, 1:1, 3:2 and 6:2 AgX:L adducts (where L is a tridentate phosphine, in detail: 1,1,1-tris(diphenylphosphinomethyl)ethane (Me-triphos) and bis(2-diphenylphosphinoethyl)phenylphosphine (Ph-triphos), X = O 3SCF3, O3SCH3, BF4 or O2CCF3) have been synthesized and characterized by IR, NMR (1H, 31P and 19F) and ESI MS spectroscopy. The stoichiometry of the complexes is strongly dependent on the ligand to metal ratio employed and also on the nature of the counterion. 31P NMR (solution) data also show the complexes existing in solution, in some cases, however, disproportionating to adducts of different nuclearity. Oligonuclear species have been detected through ESI MS spectroscopy that has been demonstrated as a powerful tool for the identification of the solution species. AgBF4:Me-triphos (1:2) has been structurally characterized as [Ag(P,P′-Me-triphos)2](BF4) • H2O • 7/2 MeOH, while Ag(O3SCF3): Ph-triphos: H 2O (6:2:4) is a spectacular two-dimensional polymer. © 2005 Elsevier B.V. All rights reserved.

Affiliations

Dipartimento di Scienze Chimiche, Università degli Studi di Camerino, 62032 Camerino MC, via S. Agostino 1, Italy; Jurusan Kimia, FMIPA Universitas Negeri Malang, Malang 65145, Jalan Surabaya 6, Indonesia; Chemistry M313, School of Biomolecular, Biomedical and Chemical Sciences, University of Western Australia, Crawley, WA 6009, Australia