化学
旋转交叉
双稳态
分子间力
氢键
分子
配体(生物化学)
化学物理
自旋跃迁
限制
结晶学
材料科学
机械工程
生物化学
受体
光电子学
有机化学
工程类
作者
Yingying Wu,Zhao‐Yang Li,Shuang Peng,Ziyi Zhang,Hao‐Min Cheng,Hang Su,Wenqi Hou,Feng‐Lei Yang,Shu‐Qi Wu,Osamu Sato,Jing‐Wei Dai,Wei Li,Xian‐He Bu
摘要
Spin-crossover (SCO) materials exhibit remarkable potential as bistable switches in molecular devices. However, the spin transition temperatures (Tc) of known compounds are unable to cover the entire ambient temperature spectrum, largely limiting their practical utility. This study reports an exemplary two-dimensional SCO solid solution system, [FeIII(H0.5LCl)2–2x(H0.5LF)2x]·H2O (H0.5LX = 5-X-2-hydroxybenzylidene-hydrazinecarbothioamide, X = F or Cl, x = 0 to 1), in which the adjacent layers are adhered via hydrogen bonding. Notably, the Tc of this system can be fine-tuned across 90 K (227–316 K) in a linear manner by modulating the fraction x of the LF ligand. Elevating x results in strengthened hydrogen bonding between adjacent layers, which leads to enhanced intermolecular interactions between adjacent SCO molecules. Single-crystal diffraction analysis and periodic density functional theory calculations revealed that such a special kind of alteration in interlayer interactions strengthens the FeIIIN2O2S2 ligand field and corresponding SCO energy barrier, consequently resulting in increased Tc. This work provides a new pathway for tuning the Tc of SCO materials through delicate manipulation of molecular interactions, which could expand the application of bistable molecular solids to a much wider temperature regime.
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