钴-紫罗碱配位化合物中的价态互变异构现象。
Valence tautomerism in a cobalt-verdazyl coordination compound.
机构信息
Department of Chemistry, San Jose State University, One Washington Square, San Jose, CA 95126, USA.
Department of Physics, University of South Florida, Tampa, Florida 33620, USA.
出版信息
Chem Commun (Camb). 2020 Apr 21;56(32):4400-4403. doi: 10.1039/d0cc01770a.
Abstract
Coordination of 1-isopropyl-3,5-dipyridyl-6-oxoverdazyl to cobalt results in a dication best described in the solid state as a high spin cobalt(ii) ion coordinated to two radical ligands with an S = 3/2 ground state. On dissolution in acetonitrile, the cobalt(ii) form equilibrates with a cobalt(iii) valence tautomer with an S = 1/2 ground state.
摘要
1-异丙基-3,5-二吡啶基-6-氧代-1,2,4,5-四嗪与钴配位，在固态下最好描述为高自旋钴（II）离子与两个自由基配体配位，基态为 S = 3/2。在乙腈中溶解时，钴（II）形式与 S = 1/2 基态的钴（III）价态互变异构体达到平衡。
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