Lattice-Modulated Phase Transition Coupled with Redox-Isomeric Interconversion of o-Semiquinone-Catecholato into Bis(o-semiquinonato) Cobalt Complexes

被引:23
作者
Bubnov, Michael P. [1 ,2 ]
Skorodumova, Nina A. [1 ]
Arapova, Alla V. [1 ]
Smirnova, Natalia N. [2 ]
Samsonov, Maxim A. [1 ]
Fukin, Georgy K. [1 ,2 ]
Cherkasov, Vladimir K. [1 ,2 ]
Abakumov, Gleb A. [1 ,2 ]
机构
[1] RAS, GA Razuvaev Inst Organometall Chem, Nizhnii Novgorod 603950, Russia
[2] Lobachevsky State Univ Nizhny Novgorod, Nizhnii Novgorod 603950, Russia
基金
俄罗斯基础研究基金会;
关键词
INDUCED SPIN TRANSITION; METAL DILUTION; THERMODYNAMIC PROPERTIES; ELECTRON-TRANSFER; VALENCE TAUTOMERISM; MAGNETIC-PROPERTIES; BISTABILITY;
D O I
10.1021/acs.inorgchem.5b00716
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two redox-isomeric (valence tautomeric) complexes (2,2'-bpy)-Co(3,6-DBSQ), (1) and (1,10-phen)Co(3,6-DBSQ)(2) (2) (where 2,2'-bpy = 2,2'dipyridine; 1,10-phen = 1,10-phenanthroline; 3,6-DBSQ = 3,6-di-tert-butylbenzosemiquinone-1,2) reveal phase transitions that accompany redox-isomeric interconversions of semiquinone catecholato isomer into a bis-(semiquinonato) one. Phase transitions differ one from another by thermodynamic parameters (transition temperature and interval, enthalpy, and entropy). Complexes 1 and 2 have the same crystal system and space group, and they form solid solutions with any molar ratio. The number of solid solutions with the molar ratios of 2:1, 1:1, 1:2, 1:4, 1:8, and 1:16 of 1 per 2, respectively, were obtained. Product with 1:1 ratio was studied by precise calorimetry, by variable-temperature magnetic susceptibility, and by X-ray structural analysis. All solid solutions were investigated by means of differential scanning calorirnetry. Each solid solution possesses phase transition whose parameters depend on its composition. Transition temperature and enthalpy gradually grow with increasing of molar fraction of 1. The diagram "enthalpy composition" is linear, whereas phase diagram "transition temperature composition" is the bent-up arc.
引用
收藏
页码:7767 / 7773
页数:7
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