Dinuclear tereplithalato-bridged nickel(II) complexes. Structural characterization and magnetic properties

被引:29
|
作者
Massoud, Salah S.
Mautner, Franz A.
Vicente, Ramon
Rodrigue, Brett M.
机构
[1] Univ Louisiana Lafayette, Dept Chem, Lafayette, LA USA
[2] Graz Univ Technol, Inst Phys & Theoret Chem, A-8010 Graz, Austria
[3] Univ Barcelona, Dept Quim Inorgan, E-08028 Barcelona, Spain
关键词
nickel(II) complexes; dinuclear complexes; terephthalato bridged; crystal structure; magnetic properties;
D O I
10.1016/j.ica.2006.03.036
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The dinuclear terephthalato-bridged nickel(II) complexes [Ni-2(cyclen)(2)(mu-tP)](ClO4)(2) (1) [Ni-2(trp)(2)(mu-tp)(H2O)(2)](ClO4)(2) (2) and [Ni-2(3,3,3-tet)(2)(mu-tp)(H2O)(2)](ClO4)(2) center dot 2H(2)O (3), where tp = terephthalate dianion, cyclen = 1,4,7,10-tetraazacyclododecane, trpn = tris(3-aminopropyl)amine and 3,3,3-tet = 1,5,9,13-tetraazatridecane, were synthesized and structurally characterized by X-ray crystallography. Their magnetic susceptibilities were also determined at variable temperatures over the range 2-300 K. The structures of these complexes consist of mu-tp bridging two Ni(II) centers in a bis(bidentate) bonding fashion in 1 and in bis(monodentate) bonding fashion in 2 and 3. The coordination geometry around the Ni(II) ions in these compounds has a distorted octahedral geometry with four nitrogen atoms from the amine ligand (cyclen, trpn or 3,3,3-tet) and two coordinated oxygen atoms supplied by the chelated carboxylate group of the bridged terephthalate ligand in 1, and by one tp-carboxylate-oxygen in 2 and 3. The sixth coordination site in the last two complexes 2 and 3 is achieved via an oxygen atom from a coordinated water molecule. The intradimer Ni...Ni distances in these complexes are 10.740, 11.428 and 11.537 angstrom for 1, 2 and 3, respectively. The electronic spectra of the complexes in aqueous solutions are in complete agreement with the assigned X-ray geometry around the Ni(II) centers. Also, the analysis of the infrared spectral data for the (v)(COO-) stretching frequencies of the tp-carboxalato groups reveals the existence of the bis(bidentate) and bis(monodentate) coordination modes for the bridged terephthalate ligand in 1, 2 and 3, respectively. Despite the different coordination modes of the tp bridging ligand in these complexes, they all exhibit very weak antiferromagnetic coupling. The coupling constants J were found to be -2.2, -0.6 and -1.5 cm(3) K mol(-1) for the complexes 1, 2 and 3, respectively. The structural and magnetic results of 1-3 are discussed in relation to the other related published mu-terephthalato dinuclear Ni(II) compounds. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:3321 / 3329
页数:9
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