Asymmetric μ2-1,1-azido bridged copper(II) complex:: Synthesis, X-ray structure, magnetic study and DFT calculations

被引:68
作者
Zbiri, M
Saha, S
Adhikary, C
Chaudhuri, S
Daul, C
Koner, S
机构
[1] Jadavpur Univ, Dept Chem, Kolkata 700032, W Bengal, India
[2] Univ Fribourg, Dept Chim, CH-1700 Fribourg, Switzerland
[3] Bose Inst, SAIF, Kolkata 700009, W Bengal, India
关键词
Copper(II)-azido complex; dimer; DFT; magnetic properties; X-ray crystal structure;
D O I
10.1016/j.ica.2005.09.005
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A new rare variety asymmetric mu(2)-1,1-azido bridged copper(II) complex has been synthesized and characterized structurally and magnetically. The complex [Cu2L2(mu(2)-1,1-N-3)(2)]center dot H2O center dot CH3OH (L = 1-(N-ortho-hydroxyacetophenimine)-2-aminoethane) (1), crystallizes in monoclinic space group, P2(1)/n, with a = 9.469(4) angstrom, b = 12.526(8) angstrom, c = 12.899(10) angstrom, beta = 105.79(6)degrees, V = 1472.2(16) angstrom(3). X-ray study reveals that he Cu-N(azide)-Cu angles in this complex is 90.4 degrees. This is unusually low in comparison to that of the same angle in other end-on azido-bridged binuclear complexes. Though a strong ferromagnetic interaction between the metal centers is expected in the complex, the coupling has actually been found to be anti ferromagnetic (J = -4.2 cm(-1)), instead. To rationalize this paradoxical magnetic behavior, DFT calculation of this and other four complexes with very similar structure have been performed within broken symmetry framework. The calculated magnetic coupling constants (J) are in excellent agreement, both in sign and in the magnitude of the exchange interaction, with the experimental data, and the spin density map is correctly reproduced. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1193 / 1199
页数:7
相关论文
共 78 条
[1]   On the calculation and modeling of magnetic exchange interactions in weakly bonded systems:: The case of the ferromagnetic copper(II) μ2-azido bridged complexes [J].
Adamo, C ;
Barone, V ;
Bencini, A ;
Totti, F ;
Ciofini, I .
INORGANIC CHEMISTRY, 1999, 38 (09) :1996-2004
[2]   SYNTHESIS, STRUCTURE, AND SPECTROSCOPIC PROPERTIES OF COPPER(II) COMPOUNDS CONTAINING NITROGEN SULFUR DONOR LIGANDS - THE CRYSTAL AND MOLECULAR-STRUCTURE OF AQUA[1,7-BIS(N-METHYLBENZIMIDAZOL-2'-YL)-2,6-DITHIAHEPTANE]COPPER(II) PERCHLORATE [J].
ADDISON, AW ;
RAO, TN ;
REEDIJK, J ;
VANRIJN, J ;
VERSCHOOR, GC .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1984, (07) :1349-1356
[3]   Spin density maps in the triplet ground state of [Cu2(t-Bupy)4(N3)2](ClO4)2 (t-bupy = p-tert-butylpyridine):: A polarized neutron diffraction study [J].
Aebersold, MA ;
Gillon, B ;
Plantevin, O ;
Pardi, L ;
Kahn, O ;
Bergerat, P ;
von Seggern, I ;
Tuczek, F ;
Öhrström, L ;
Grand, A ;
Lelièvre-Berna, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (21) :5238-5245
[4]   DICOPPER(II) CHLORO AND AZIDO INCLUSION COMPLEXES OF THE [24-ANE-N2S4] BINUCLEATING MACROCYCLE - SYNTHESIS, CRYSTAL AND MOLECULAR-STRUCTURES, AND SPECTRAL, MAGNETIC, AND ELECTROCHEMICAL PROPERTIES [J].
AGNUS, Y ;
LOUIS, R ;
GISSELBRECHT, JP ;
WEISS, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (01) :93-102
[5]  
ALTMORE A, 1994, APPL CRYST, V27, P435
[6]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[7]   DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR [J].
BECKE, AD .
PHYSICAL REVIEW A, 1988, 38 (06) :3098-3100
[8]   DFT description of the magnetic structure of polynuclear transition-metal clusters [J].
Bencini, A ;
Totti, F .
INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2005, 101 (06) :819-825
[9]   Crystal and molecular structure and magnetic exchange properties of bis(di-μ-ethoxo-bis(3,5-di-tert-butylsemiquinonato)dicopper(II)) complex.: A synergy between DFT and experimental magnetochemistry [J].
Bencini, A ;
Dei, A ;
Sangregorio, C ;
Totti, F ;
Vaz, MGF .
INORGANIC CHEMISTRY, 2003, 42 (24) :8065-8071
[10]  
Beurskens P. T., 1994, DIRDIF 94 DIRDIF 94