A combined experimental and theoretical study on supramolecular assemblies in octahedral cobalt(III) salicylaldimine complexes having pendant side arms

被引:19
作者
Ghosh, Kousik [1 ]
Banerjee, Abhisek [1 ]
Roy, Sumit [1 ]
Bauza, Antonio [2 ]
Frontera, Antonio [2 ]
Chattopadhyay, Shouvik [1 ]
机构
[1] Jadavpur Univ, Inorgan Sect, Dept Chem, Kolkata 700032, India
[2] Univ Illes Balears, Dept Quim, Crta Valldemossa Km 7-5, Palma De Mallorca 07122, Baleares, Spain
关键词
Cobalt(III); Schiff base; Crystal structure; Meridional; DFT study; TRANSFER RADICAL POLYMERIZATION; DONOR SCHIFF-BASE; NICKEL(II) COMPLEXES; CRYSTAL-STRUCTURES; ELECTROCATALYTIC REDUCTION; BRIDGING ACETATE; METAL-COMPLEXES; WATER; ANTIBACTERIAL; COPPER(II);
D O I
10.1016/j.poly.2016.03.008
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two mononuclear cobalt(III) complexes, [Co(L-1)(N-3)(2)(deen)] (1) and [Co(L-2)(N-3)(2)(DMSO)] (2), where HL1 {2-(2-(diethylamino)ethyliminomethyl)-4-bromophenol} and HL2 {2-(2-(diethylamino)ethyliminomethyl)-6-methoxyphenol} are tridentate and tetradentate Schiff bases, respectively and deen is a bidentate chelating ligand, N,N-diethyl-1,2-diaminoethane, were prepared and characterized by elemental and spectral analysis. X-ray crystal structure determination confirmed their structures. Both complexes are meridional isomers. The solid state structures show the participation of the organic ligands in concurrent conventional and unconventional C-H center dot center dot center dot pi interactions along with hydrogen bonding. The energetic features of these interactions have also been studied by means of DFT calculations. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:86 / 95
页数:10
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