The effect of coordinated solvent molecules on metal coordination environments in single-crystal-to-single-crystal transformations

被引:24
|
作者
Li, Quan-Quan [1 ,2 ]
Liu, Hua [1 ]
Zheng, Ting-Ting [1 ]
Liu, Ping [1 ]
Song, Jin-Xi [2 ]
Wang, Yao-Yu [1 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol, Shaanxi Key Lab Phys Inorgan Chem,Minist Educ, Xian 710127, Peoples R China
[2] Northwest Univ, Coll Urban & Environm Sci, Shaanxi Key Lab Earth Surface Syst & Environm Car, Xian 710127, Peoples R China
来源
CRYSTENGCOMM | 2020年 / 22卷 / 41期
关键词
REVERSIBLE SCSC TRANSFORMATION; SOLID-STATE REACTIVITY; STRUCTURAL TRANSFORMATIONS; ORGANIC FRAMEWORK; SUPRAMOLECULAR ISOMERISM; POLYMERS; EXCHANGE; MAGNET; SORPTION; CO2;
D O I
10.1039/d0ce01024c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Single-crystal-to-single-crystal (SCSC) transformation has been demonstrated to provide an ideal platform to explore the formation process of chemical bonds, which is conducive to making function-oriented crystal synthesis a reality. A solvent as a ligand or a structure-directing agent plays a significant role in the structural formation of coordination polymers (CPs), and its removal/adsorption or exchange can affect the change in metal coordination environments. In this article, we provide a brief overview of recent progress in the effect of coordinated solvent molecules on metal coordination environments of CPs in SCSC transformations. We highlight three different categories based on their stimuli conditions, heat treatment, immersion in solvent or mother liquid, and exposure to vapor. We try to discuss the criteria for CPs in which the metal coordination spheres can be affected by the coordinated solvents, which may provide new insights into the rational design and construction of CPs with the desired structures and properties.
引用
收藏
页码:6750 / 6775
页数:26
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