Syntheses and structures of photochromic molybdenum(II) and rhodium(II) complexes with 1,2-dicyano-1,2-bis(2,4,5-trimethyl-3-thienyl)ethene
作者:Jing Han、Hisashi Konaka、Takayoshi Kuroda-Sowa、Masahiko Maekawa、Yusaku Suenaga、Hiromichi Isihara、Megumu Munakata
DOI:10.1016/j.ica.2005.08.023
日期:2006.1
[Rh2(O2CCF3)4(closed-dbe)](p-xylene) (4). The structures of four metal complexes were revealed by X-ray crystallographic analyses and the correlation between the crystal structures and the photochromic performance was discussed. In all complexes, two cyano groups of the ligand bridged two dimetal carboxylates to give a 1-D zigzag infinite chain structure. Upon irradiation with 405 nm light, complex
四个新颖的Mo(II)和Rh(II)与顺式-1,2-二氰基-1,2-双(2,4,5-三甲基-3-噻吩基)乙烯(顺式-dbe)或闭式-dbe的配合物是合成和表征。将[M(O 2 CCF 3)4 ](M = Mo,Rh)与顺式-dbe或密闭-dbe一起使用可得到络合物[Mo 2(O 2 CCF 3)4(顺式-dbe)](苯)(1) ,[Rh 2(O 2 CCF 3)4(顺式-dbe)](苯)(2),[Mo 2(O 2CCF 3)4 } 2(闭-dbe)](3)和[Rh 2(O 2 CCF 3)4(闭-dbe)](对二甲苯)(4)。通过X射线晶体学分析揭示了四种金属配合物的结构,并讨论了晶体结构与光致变色性能之间的相关性。在所有络合物中,配体的两个氰基桥接两个双金属羧酸盐,从而形成一维之字形无限链结构。在405 nm的光照射下,配合物1从黄色变成红紫色,并且在暴露于563 nm光线后,颜色