A Ni(salen)‐Based Metal–Organic Framework: Synthesis, Structure, and Catalytic Performance for CO2 Cycloaddition with Epoxides
A three‐dimensional (3D) chiral metal–organic framework [Cd2{Ni(salen)}(DMF)3]·4DMF·7H2O (1) based on a new enantiopure tetracarboxyl‐functionalized metallosalen Ni(H4salen) {where H6salen is (R,R)‐N,N′‐bis[3‐tert‐butyl‐5‐(3,5‐dicarboxybenzyl)salicylidene]‐1,2‐diphenylethylenediame} was synthesized...
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Published in | European journal of inorganic chemistry Vol. 2017; no. 43; pp. 4982 - 4989 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
WEINHEIM
Wiley
24.11.2017
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | A three‐dimensional (3D) chiral metal–organic framework [Cd2{Ni(salen)}(DMF)3]·4DMF·7H2O (1) based on a new enantiopure tetracarboxyl‐functionalized metallosalen Ni(H4salen) {where H6salen is (R,R)‐N,N′‐bis[3‐tert‐butyl‐5‐(3,5‐dicarboxybenzyl)salicylidene]‐1,2‐diphenylethylenediame} was synthesized and characterized by infrared spectroscopy, thermogravimetric analysis, nitrogen and carbon dioxide adsorption, and powder and single‐crystal X‐ray diffractions. In 1, the dinuclear Cd2 cluster [Cd2(COO)4(DMF)3] as a node is cross‐linked by four isophthalate groups on the salen ligands, forming a 2D lamellar structure, which are further linked by Ni(salen) into the 3D network with a 1D open channel (ca. 7.0 × 8.0 Å2) along the a axis. On account of its porosity, Lewis acid sites, and moderate uptake for CO2, 1 can be used as an efficient heterogeneous catalyst for the CO2 cycloaddition with epoxides under relatively mild conditions. Moreover, the bulky epoxide shows a decrease in activity with an increase in the alkyl chain length of the substrate as a result of the confinement effect of 1, showing size‐dependent selectivity.
A three‐dimensional chiral metal–organic framework based on a new enantiopure tetracarboxyl‐functionalized metallosalen Ni(H4salen) exhibits high activity and size‐dependent selectivity for CO2 cycloaddition with epoxides under relatively mild conditions. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
ISSN: | 1434-1948 1099-0682 |
DOI: | 10.1002/ejic.201700871 |