C
Cheng Wang
Researcher at Xiamen University
Publications - 192
Citations - 14114
Cheng Wang is an academic researcher from Xiamen University. The author has contributed to research in topics: Catalysis & Metal-organic framework. The author has an hindex of 45, co-authored 157 publications receiving 11112 citations. Previous affiliations of Cheng Wang include Peking University & University of North Carolina at Chapel Hill.
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Doping Metal–Organic Frameworks for Water Oxidation, Carbon Dioxide Reduction, and Organic Photocatalysis
TL;DR: The inactivity of the parent UiO-67 framework and the reaction supernatants in catalytic water oxidation, CO(2) reduction, and organic transformations indicate both the molecular origin and heterogeneous nature of these catalytic processes.
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Rational synthesis of noncentrosymmetric metal-organic frameworks for second-order nonlinear optics.
Cheng Wang,Teng Zhang,Wenbin Lin +2 more
TL;DR: The term nonlinear optics (NLO) was coined to describe the nonlinear relationship between dielectric polarization P and electric field E in optical media to develop materials with the ability to alter the frequency of light, to amplify light signal, and to modulate light intensity or phase factors.
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Metal-organic frameworks as a tunable platform for designing functional molecular materials.
Cheng Wang,Demin Liu,Wenbin Lin +2 more
TL;DR: Through the combination of molecular synthesis and crystal engineering, MOFs present an unprecedented opportunity for the rational and precise design of functional materials.
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Metal–Organic Frameworks for Light Harvesting and Photocatalysis
TL;DR: In this paper, the authors summarize recent progress on light harvesting and photocatalysis with metal-organic frameworks (MOFs), a new class of crystalline molecular solids built from linking organic ligands with metal or metal-cluster connecting points.
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Isoreticular chiral metal-organic frameworks for asymmetric alkene epoxidation: tuning catalytic activity by controlling framework catenation and varying open channel sizes.
TL;DR: The results suggest that, although the diffusion of bulky alkene and oxidant reagents can be a rate-limiting factor in MOF-catalyzed asymmetric reactions, the catalytic activity of the CMOFs with large open channels is limited by the intrinsic reactivity of the catalytical molecular building blocks.