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A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange.
Chemical Communications ( IF 4.9 ) Pub Date : 2020-04-02 , DOI: 10.1039/d0cc00548g
Xiaozhou Ma 1 , Elizaveta A Suturina , Mathieu Rouzières , Fabrice Wilhelm , Andrei Rogalev , Rodolphe Clérac , Pierre Dechambenoit
Affiliation  

Successive chemical reductions of the heteroleptic complex [(tpy)CrIII(tphz)]3+ (tpy = terpyridine; tphz = tetrapyridophenazine) give rise to the mono- and di-radical redox isomers, [(tpy)CrIII(tphz˙-)]2+ and [(tpy˙-)CrIII(tphz˙-)]+, respectively. As designed, the optimized overlap of the involved magnetic orbitals leads to extremely strong magnetic interactions between the S = 3/2 metal ion and S = 1/2 radical spins, affording well isolated ST = 1 and ST = 1/2 ground states at room temperature.

中文翻译:

具有扩展的自旋离域和大分子内磁交换的杂多双自由基Cr(iii)配合物。

连续化学还原杂配体[[(tpy)CrIII(tphz)] 3+(tpy =叔吡啶; tphz =四吡啶吩嗪)会产生单和双自由基氧化还原异构体,[(tpy)CrIII(tphz˙-)分别为] 2+和[(tpy˙-)CrIII(tphz˙-)] +。根据设计,所涉及的磁轨道的最佳重叠会导致S = 3/2金属离子与S = 1/2自由基自旋之间极强的磁相互作用,从而在以下位置提供良好隔离的ST = 1和ST = 1/2基态室内温度。
更新日期:2020-03-24
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