Synthesis and crystal structure of some (2,2 '-dipyridylamine)(carboxylato)(phenoxo)copper(II) complexes with rather unusual phenoxo ligands

Citation
A. Facchinetti et al., Synthesis and crystal structure of some (2,2 '-dipyridylamine)(carboxylato)(phenoxo)copper(II) complexes with rather unusual phenoxo ligands, INORG CHIM, 324(1-2), 2001, pp. 162-172
Citations number
38
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
INORGANICA CHIMICA ACTA
ISSN journal
00201693 → ACNP
Volume
324
Issue
1-2
Year of publication
2001
Pages
162 - 172
Database
ISI
SICI code
0020-1693(20011112)324:1-2<162:SACSOS>2.0.ZU;2-8
Abstract
Some ternary Cu(dipyam)(OOCR)(OR) complexes (dipyam = 2,2'-dipyridylamine; RCOO- = acetate, benzoate, cmb (2-chloro-5-methylthio-benzoate), mta (methy lthioacetate), min (2-methylthio-nicotinate); OR- = pnp (p-nitrophenolate), dcp (2,6-dichlorophenolate), tcp (2,4,6-trichlorophenolate)) have been syn thesized. Their IR spectra are included and the X-ray diffraction structure is given for the crystals of [Cu(dipyam)(OOCCH3)(dcp)] (I), [Cu(dipyam)(mt a)(dcp)] (II). [Cu(dipyam)(mtn)(dcp)] (III) and [Cu(dipyam)(cmb)(tcp)] (IV) . The copper coordination is square pyramidal in 1, with a rather rare axia l position of the phenolate ligand, while in II and III is distorted octahe dral with equatorial phenolate and weak apical bonds (II Cl, S; III Cl, O). The copper coordination in IV can be better described as square planar, bu t with distortion toward a flattened tetrahedral geometry and with a rather long apical Cu-O distance, involving an oxygen of the carboxylate ion. The entrance of the phenolate in an axial or equatorial position is due to the geometry imposed to the complex by the auxiliary ligand. (C) 2001 Elsevier Science B.V. All rights reserved.