Chemical reactivity under nanoconfinement

被引:587
作者
Grommet, Angela B. [1 ]
Feller, Moran [1 ]
Klajn, Rafal [1 ]
机构
[1] Weizmann Inst Sci, Dept Organ Chem, Rehovot, Israel
基金
欧洲研究理事会;
关键词
METAL-ORGANIC FRAMEWORKS; TUNABLE ELECTRICAL-CONDUCTIVITY; AZA-COPE REARRANGEMENT; HOST-GUEST COMPLEXES; DIELS-ALDER REACTION; SUPRAMOLECULAR CATALYSIS; COORDINATION CAGE; ZEOLITE CHEMISTRY; DIRECT CONVERSION; CONFINED SPACES;
D O I
10.1038/s41565-020-0652-2
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
This Review surveys strategies to control chemical reactivity of species under different types of nanoconfinement. Confining molecules can fundamentally change their chemical and physical properties. Confinement effects are considered instrumental at various stages of the origins of life, and life continues to rely on layers of compartmentalization to maintain an out-of-equilibrium state and efficiently synthesize complex biomolecules under mild conditions. As interest in synthetic confined systems grows, we are realizing that the principles governing reactivity under confinement are the same in abiological systems as they are in nature. In this Review, we categorize the ways in which nanoconfinement effects impact chemical reactivity in synthetic systems. Under nanoconfinement, chemical properties can be modulated to increase reaction rates, enhance selectivity and stabilize reactive species. Confinement effects also lead to changes in physical properties. The fluorescence of light emitters, the colours of dyes and electronic communication between electroactive species can all be tuned under confinement. Within each of these categories, we elucidate design principles and strategies that are widely applicable across a range of confined systems, specifically highlighting examples of different nanocompartments that influence reactivity in similar ways.
引用
收藏
页码:256 / 271
页数:16
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