Syntheses and structures of some adducts of silver(I) oxyanion salts with some 2-N,O-donor-substituted pyridine bases

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Graham A. Bowmaker, Effendy, Maksum Nitiatmodjo, Brian W. Skelton, Allan H. White

2005 Inorganica Chimica Acta Vol. 358 Issue 14 Article Cited by 31

Abstract

Syntheses and room-temperature single crystal X-ray structural characterizations are recorded for a variety of silver(I) oxyanion (perchlorate, nitrate and trifluoroacetate ('tfa') (increasing basicity)) adducts, AgX, with a number of pyridine ('py') bases, L, functionalized in the 2-position with N- or O-donor groups, namely 2-amino-, 2-amino-6-methyl-, 2-aminomethyl-, 2-hydroxy-, 2-methoxy- and 2-acetyl- pyridines, '2np', 'nmp', 'amp', 'ohp', 'mop', and 'acp'. A variety of stoichiometries and associated structural types are defined: [Ag(chelate)2]X, L/X = amp,acp/ClO4, [XAg(chelate)2], L/X = acp/tfa, of 1:2 AgX:L stoichiometry; for 1:1 stoichiometry, although a discrete mononuclear complex [(chelate)Ag(O 2NO)] is defined for AgNO3: acp (1:1), all others are polymers, successive silver atoms being linked by N,N′-bridging ligands singly (L/X = 2np/ClO4 (⋯HAgHTAgTHAgH⋯), amp/ClO 4, NO3 (⋯HTAgHTAg⋯) ('H' ≡ head, 'T' = tail)) or pairwise, ⋯L2AgX2AgL 2Ag⋯ (L/X = 2np/tfa, nmp/NO3). More complex polymeric arrays are found with L/X = ohp/NO3, tfa, where interaction with the metal takes place via the O-donor only, the py functionality being protonated, and in adducts of more complex stoichiometry AgNO3:mop (2:3) and AgNO3:2np (3:4). © 2005 Elsevier B.V. All rights reserved.

Affiliations

Department of Chemistry, University of Auckland, Auckland, Private Bag 92019, New Zealand; Chemistry M313, University of Western Australia, Crawley, WA 6009, Australia; Jurusan Kimia, FMIPA Universitas Negeri Malang, Malang 65145, Jalan Surabaya 6, Indonesia