二聚体有机-无机杂化锆取代反单钨酸盐的光致变色反应

IF 4.3 2区化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR

Inorganic Chemistry Pub Date : 2025-04-20 DOI:10.1021/acs.inorgchem.4c05173

Miao Zhang, Lihua Liu, Yizhen Song, Mengmeng Hou, Lin Sun, Pengtao Ma

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引用次数: 0

摘要

光致变色材料因其在智能设备中的潜在应用而越来越受到人们的关注。本文合成了一种新型的含锆多金属氧酸盐[H2N(CH3)2]10H8[Zr(DL-tart)2(SbW17ZrO58)2]·36H2O （DL-tartH4 = dl-酒石酸）(1)。二聚体聚阴离子1含有两个类似于道森的{SbW17ZrO58}7 -亚基，由一个{Zr(DL-tart)2}4 -连接连接。有趣的是，化合物1表现出快速的光致变色反应，半衰期（t1/2）为6.62 s，可逆性好，在空气环境中容易褪色。值得注意的是，化合物1在暴露于可见光照射下也保持其光致变色行为。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Dimeric Organic–Inorganic Hybrid Zr-Substituted Antimonotungstate-Featured Photochromic Responses

查看原文本刊更多论文

Dimeric Organic–Inorganic Hybrid Zr-Substituted Antimonotungstate-Featured Photochromic Responses

Photochromic materials are increasingly attracting attention for their potential applications in smart devices. Here, a novel organic–inorganic hybrid Zr-containing polyoxometalate [H₂N(CH₃)₂]₁₀H₈[Zr(DL-tart)₂(SbW₁₇ZrO₅₈)₂]·36H₂O (DL-tartH₄ = dl-Tartaric Acid) (1) was synthesized. The dimeric polyanion of 1 contains two Dawson-like {SbW₁₇ZrO₅₈}^7– subunits bridged by one {Zr(DL-tart)₂}^4– connector. Interestingly, compound 1 exhibits a rapid photochromic response with a half-life (t_1/2) of 6.62 s, good reversibility, and an easy fading process in an air environment. Notably, compound 1 also retains its photochromic behavior upon exposure to visible light irradiation.

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来源期刊

Inorganic Chemistry 化学-无机化学与核化学

CiteScore

7.60

自引率

13.00%

发文量

1960

审稿时长

1.9 months

期刊介绍： Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.