Bis-o-semiquinonato complexes of transition metals with 5,7-di-tert-butyl-2-(pyridine-2-yl)benzoxazole

被引:16
作者
Protasenko, Natalia A. [1 ]
Poddel'sky, Andrey I. [1 ]
Bogomyakov, Artem S. [2 ]
Somov, Nikolay V. [3 ]
Abakumov, Gleb A. [1 ]
Cherkasov, Vladimir K. [1 ]
机构
[1] Russian Acad Sci, GA Razuvaev Inst Organometall Chem, Nizhnii Novgorod 603950, Russia
[2] Russian Acad Sci, Int Tomog Ctr, Siberian Branch, Novosibirsk 630090, Russia
[3] Nizhniy Novgorod State Univ, Fac Phys, Nizhnii Novgorod 603950, Russia
关键词
Transition metals; o-Semiquinone; O-donor ligand; N-donor ligand; Magnetochemistry; X-ray analysis; VALENCE TAUTOMERISM; QUINONE COMPLEXES; COBALT COMPLEXES; REDOX ISOMERISM; X-RAY; CATECHOLATE; ANTICANCER; ESR;
D O I
10.1016/j.poly.2012.10.016
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
New cobalt(II) (I), iron(II) (2) and manganese(II) (3) complexes of M(3,6-SQ)(2)L type containing 3,6-di-tert-butyl-o-benzosemiquinonato ligands (3,6-SQ) and 5,7-di-tert-butyl-2-(pyridine-2-yl)benzoxazole (L) were synthesized and characterized in details. Magnetic susceptibility measurements and spectroscopic studies have shown that all complexes include metal(II) in the high-spin state and two radical-anionic o-semiquinonato ligands. The antiferromagnetic ligand-ligand coupling in cobalt(II) and iron(II) complexes takes place, while manganese(II) complex demonstrates metal-ligand antiferromagnetic interactions. Molecular structure of Co(3,6-SQ)(2)L was determined by X-ray analysis. Cobalt(II) atom has a distorted trigonal prismatic environment. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:239 / 243
页数:5
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