三吡啶
钴
结晶学
自旋态
八面体
化学
自旋跃迁
取代基
旋转交叉
分子间力
烷氧基
晶体结构
立体化学
无机化学
分子
烷基
金属
有机化学
作者
Manabu Nakaya,Ryo Ohtani,Jong Won Shin,Masaaki Nakamura,Leonard F. Lindoy,Shinya Hayami
出处
期刊:Dalton Transactions
[Royal Society of Chemistry]
日期:2018-01-01
卷期号:47 (39): 13809-13814
被引量:25
摘要
The cobalt(ii) complex incorporating π-conjugated substituent, [Co(Naph-C2-terpy)2](BF4)2 (1; Naph-C2-terpy = 4'-(2-naphthoxy(ethoxy))-2,2':6',2''-terpyridine), exhibits an abrupt spin transition (ST) behavior (cooperative factor C = 0.91) while its solvated product, 1·2MeOH, shows gradual spin crossover (SCO) behavior (C = 0.49). Single crystal X-ray structural analyses demonstrated that the octahedral coordination core [CoN6] in 1 shows larger distortion in both high-spin and low-spin states than solvated 1·2MeOH or another two derivatives, [Co(R-terpy)2](BF4)2 (R = 2-naphthyl (2), 9-anthracenyl (3)). The respective distortion parameters (Σ) are compared with those for previously reported SCO cobalt(ii) compounds. The highly-distorted [CoN6] core in 1 (Σ = 126 in the HS state and 101.6 in the LS state) was stabilized by strong intermolecular interactions and observed an abrupt ST behaviour.
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