旋转交叉
化学
结晶学
自旋跃迁
多稳态
八面体
双稳态
多态性(计算机科学)
掺杂剂
晶体结构
自旋态
无机化学
凝聚态物理
物理
兴奋剂
生物化学
非线性系统
量子力学
基因型
基因
作者
Yingying Wu,Shuang Peng,Ziyi Zhang,Yue Gao,Guangyan Xu,Jingwei Dai,Zhao‐yang Li,Masahiro Yamashita
标识
DOI:10.1002/cjoc.202300679
摘要
Comprehensive Summary Regulating spin crossover (SCO) behavior, especially controlling the spin transition steps, is an important scientific issue, mainly because people aim to control spin bistability and multistability. Presently, SCO bistability can be regulated by changing the ligand‐modifying species, non‐coordinated anions, guest molecules, and metal‐ion dopant. However, the control of multistability is extremely challenging, especially in Fe(III) SCO compounds. Here, we report that [Fe III (H‐5‐Br‐thsa)(5‐Br‐thsa)]·H 2 O (5‐Br‐thsa = (5‐bromo‐2‐hydroxybenzylidene)hydrazinecarbothioamide), a compound we have reported before, exists in two polymorphic forms: polymorph 1 exhibits three‐step SCO, and polymorph 2 shows five‐step SCO, with multi‐step SCO behavior effectively regulated by polymorphism. According to single‐crystal and powder X‐ray diffractometry, polymorphs 1 and 2 crystallize in different space groups during their spin transitions, with two‐step symmetry breaking observed ( Pbcn → Pnc 2 → Pbcn for polymorph 1 ; P 2 1 / n → Pn → P 2 1 / n for polymorph 2 ). We realized that the behavior of these two polymorphs depends significantly on the structure, including (i) the average Fe—N bond distance, (ii) deformation of octahedral Fe III atoms, and (iii) distinct crystal packing, which account for the large differences observed in magnetic properties.
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