偏心因子
旋转交叉
结晶学
单斜晶系
铁电性
化学
吡啶
晶体结构
氢键
Crystal(编程语言)
材料科学
分子
电介质
有机化学
程序设计语言
光电子学
计算机科学
作者
Verónica Jornet‐Mollá,Yan Duan,Carlos Giménez‐Saiz,Yuan‐Yuan Tang,Peng‐Fei Li,Francisco M. Romero,Ren‐Gen Xiong
标识
DOI:10.1002/anie.201707401
摘要
Abstract A dual‐function material in which ferroelectricity and spin crossover coexist in the same temperature range has been obtained. Our synthetic strategy allows the construction of acentric crystal structures in a predictable way and is based on the high directionality of hydrogen bonds. The well‐known iron(II) spin crossover complex [Fe(bpp) 2 ] 2+ (bpp=2,6‐bis(pyrazol‐3‐yl)pyridine), a four‐fold noncentrosymmetric H‐bond donor, was combined with a disymmetric H‐bond acceptor such as the isonicotinate (isonic) anion to afford [Fe(bpp) 2 ](isonic) 2 ⋅2 H 2 O. This low‐spin iron(II) compound crystallizes in the acentric nonpolar I space group and shows piezoelectricity and SHG properties. Upon dehydration, it undergoes a single‐crystal to single‐crystal structural rearrangement to a monoclinic polar Pc phase that is ferroelectric and exhibits spin crossover.
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