Corrado Di Nicola, Effendy, Fabio Marchetti, Claudio Pettinari, Brian W. Skelton, Allan H. White
Twenty-one adducts of the form AgNO3:ER3:L (1:1:1) (E = P, As, Sb; R = Ph, cy, o-tolyl, mes; L = 2,2′-bipyridyl ('bpy')-based ligand), together with AgNO3:Pcy3:tpy (2:2:1) and AgNO3:PPh3:tpy (1:2:1) ('tpy' ≡ (2,2′:6,2″-terpyridine)), have been synthesized and characterized by analytical, spectroscopic (IR, far-IR, 1H and 31P NMR) and single crystal X-ray diffraction studies. The resulting complexes are predominantly of the form [(R3 E) AgL]+ NO3-, with trigonal EAgN2 coordination environments, the planarity of which is perturbed by the approach of the nitrate anion. The nitrate ion shows uni- or (semi-)bidentate coordination, excepting the complex AgNO3:P(o-tol)3:dpca (1:1:1) (dpca = bis(2-picolyl)amine) where the anion is uncoordinated, the donor dpca being a pincer-tridentate. The complex AgNO3:Pcy3:tpy (2:2:1), also reported, is dinuclear with a bridging unidentate nitrate and a terpyridine, the latter bridging through its central ring, with the peripheral rings forming chelates to either side, whereas the complex AgNO3:PPh3:tpy (1:2:1) is ionic with a five-coordinate silver, bonded to tridentate tpy and two phosphines. © 2006 Elsevier B.V. All rights reserved.
Dipartimento di Scienze Chimiche, Università degli Studi di Camerino, 62032 Camerino, MC, Via S. Agostino 1, Italy; Chemistry M313, School of Biomedical, Biomolecular and Chemical Sciences, The University of Western Australia, Crawley, WA 6009, Australia; Jurusan Pendidikan Kimia, FMIPA Universitas Negeri Malang, Malang, 65145, Jalan Surabaya 6, Indonesia
