Structural characterization of 1:1 adducts of silver(I) (pseudo-) halides (AgX, X = NCO, Cl, Br, I) with Ph2E(CH2)EPh2 (E = P, As) ('dp(p/a)m') and 4:3 adducts of copper(I) halide (CuX, X = Cl, Br, I), containing trinuclear cations, of the form [X(2)Ag(3)(dppm) (3)]X and [X(2)Cu(3)(dppm)(3)](CuX (2)) and the novel neutral [(OCN)(3)Ag(3)(dpam) (3)]

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Corrado Di Nicola, Effendy, Fauziatul Fazaroh, Claudio Pettinari, Brian W. Skelton, Neil Somers, Allan H. White

2005 Inorganica Chimica Acta Vol. 358 Issue 3 Article Cited by 69

Abstract

The extension of systematic structural definition of arrays of the form MX:EPh3 (1:n) (M = univalent coinage metal, X = (pseudo-)halide, E = P, As, Sb, n = integer (1-4)) into complexes of chelate congeners with ligands of the form 'dpex' (Ph2E(CH2)xEPh 2):MX:dpex (1:n) is commenced. Syntheses, spectroscopic features and single crystal X-ray structural characterizations are reported for 1:1 adducts of bis(diphenylphosphine)methane ('dppm') with silver(I) (pseudo-)halides, AgX (X = Cl, Br, I, NCO), and for their arsenic ('dpam') Cl, NCO counterparts AgX:dpam (1:1), also for an array of 4:3 adducts of copper(I) halides (CuX, X = Cl, Br, I) with dppm. All species recorded here (the novel molecular [(OCN) 3Ag3(dpam)3] excepted) contain trinuclear cations, as [X2A3g(dpem)3]X(·nS) and [X2Cu3(dppm)3](CuX2)(·nS), enabling systematic comparison between a wide diversity of species. © 2004 Elsevier B.V. All rights reserved.

Affiliations

Dipartimento di Scienze Chimiche, Univ. degli Studi di Camerino, Via S. Agostino 1, 62032 Camerino M., Italy; Jurusan Kimia, FMIPA Universitas Negeri Malang, Jalan Surabaya 6, Malang 65145, I., Indonesia; Chemistry M313, The University of Western Australia, Crawley, WA 6009, Australia, Australia