Advances in Solid-State Transformations of Coordination Bonds: From the Ball Mill to the Aging Chamber

被引:117
作者
Mottillo, Cristina [1 ]
Friscic, Tomislav [1 ]
机构
[1] McGill Univ, Dept Chem, 801 Sherbrooke St West, Montreal, PQ H1P 1W1, Canada
来源
MOLECULES | 2017年 / 22卷 / 01期
基金
加拿大自然科学与工程研究理事会;
关键词
mechanochemistry; coordination polymers; metal-organic frameworks; green chemistry; solid-state chemistry; solvent-free synthesis; reaction mechanisms; sustainable synthesis; METAL-ORGANIC FRAMEWORKS; SOLVENT-FREE SYNTHESIS; ZEOLITIC IMIDAZOLATE FRAMEWORKS; QUANTITATIVE MECHANOCHEMICAL PREPARATION; TWIN-SCREW EXTRUSION; X-RAY-DIFFRACTION; IN-SITU; REAL-TIME; STRUCTURAL-CHARACTERIZATION; ORGANOMETALLIC SYNTHESIS;
D O I
10.3390/molecules22010144
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Controlling the formation of coordination bonds is pivotal to the development of a plethora of functional metal-organic materials, ranging from coordination polymers, metal-organic frameworks (MOFs) to metallodrugs. The interest in and commercialization of such materials has created a need for more efficient, environmentally-friendly routes for making coordination bonds. Solid-state coordination chemistry is a versatile greener alternative to conventional synthesis, offering quantitative yields, enhanced stoichiometric and topological selectivity, access to a wider range of precursors, as well as to molecules and materials not readily accessible in solution or solvothermally. With a focus on mechanochemical, thermochemical and accelerated aging approaches to coordination polymers, including pharmaceutically-relevant materials and microporous MOFs, this review highlights the recent advances in solid-state coordination chemistry and techniques for understanding the underlying reaction mechanisms.
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页数:38
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