光致变色
化学
溴化物
电子顺磁共振
光化学
配体(生物化学)
离子
水溶液中的金属离子
金属
激进的
高分子化学
结晶学
无机化学
有机化学
生物化学
物理
受体
核磁共振
作者
Fengyi Yang,Jiali Chen,Jinjian Liu
出处
期刊:Polyhedron
[Elsevier]
日期:2023-09-01
卷期号:241: 116457-116457
被引量:5
标识
DOI:10.1016/j.poly.2023.116457
摘要
Non-photochromic and photochromic complexes [Ni1.5(CBbpy)(H2O)7]·(BTC)·5·.5H2O (1), {[Co(CBbpy)2(H2O)2]·(HBTC)·8H2O}n (2), {[MnNa(CBbpy)(BTC)(H2O)3]·H2O}n (3), {[Zn3(CBbpy)2(BTC)2(H2O)]·H2O}n (4), {[Cd(CBbpy)(HBTC)(H2O)]·H2O}n (5) based on the bipyridinium-based ligand 1-(2-carboxyethyl)-4,4′-bipyridinium bromide (HCBbpyBr) and 1,3,5-benzenetricarboxylic acid (H3BTC) have been successfully obtained by tuning different metal ions. Although five complexes contain the same bipyridinium ligand, only 3–5 possess reversible photochromic behavior. Unfortunately, 1 and 2 exhibit non-photochromic action when exposed to UV light for approximately 2 h. EPR spectra verify that photochromic course of 3–5 is derived from the formation of CBbpy radicals by photo-induced electron transfer after irradiation. The effect of diverse metal ions on the structure and photochromic action of the five complexes has been discussed.
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