Synthesis and crystal structure of oxalato-bridged dicopper(II) complex with hydrogen bonds [Cu-2(mu-C2O4) (bpy)(2)(H2O)(2)(NO3)(2)]

Citation
Jk. Tang et al., Synthesis and crystal structure of oxalato-bridged dicopper(II) complex with hydrogen bonds [Cu-2(mu-C2O4) (bpy)(2)(H2O)(2)(NO3)(2)], J MOL STRUC, 525, 2000, pp. 271-275
Citations number
13
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF MOLECULAR STRUCTURE
ISSN journal
00222860 → ACNP
Volume
525
Year of publication
2000
Pages
271 - 275
Database
ISI
SICI code
0022-2860(20000712)525:<271:SACSOO>2.0.ZU;2-K
Abstract
A new dicopper(II) complex [Cu-2(mu-C2O4)(bpy)(2)(H2O)(2)(NO3)(2)] (1) has been synthesized and its structure determined (bpy = 2,2'-bipyridine). The structure consists of centrosymmetric [Cu-2(mu-C2O4)(bpy)(2)(H2O)(2)(NO3)(2 )] molecules with each Cu(ll) ion in a distorted octahedral environment: tw o nitrogen atoms from bpy, two oxygen atoms from the oxalate ion in the bas al piano and two oxygen atoms from H2O and the nitrate group in the two axi al positions. The unusual ligand arrangement in (1) and the packing of mole cules are attributed to intermolecular and intramolecular hydrogen bonding. The intermolecular and intramolecular hydrogen bonding formed a hydrogen b ond plane and the intermolecular hydrogen bonding gave rise to a zigzag cha in structure. The e.p.r, study of the polycrystalline powder at 110 K gives g(perpendicular to) = 2.04 and g(parallel to) = 2.20, typical of axially e longated copper(II) systems, and the appearance of the half-field signals s uggests a magnetic interaction between the two Cu(II) ions. (C) 2000 Elsevi er Science B.V. All rights reserved.