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Photoswitching CO2 Capture and Release in a Photochromic Diarylethene Metal-Organic Framework

We demonstrate herein a promising pathway towards low‐energy CO2 capture and release triggered by UV and visible light. A photosensitive diarylethene ligand was used to construct a photochromic diarylethene metal–organic framework (DMOF). A local photochromic reaction originating from the framework...

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Bibliographic Details
Published in:Angewandte Chemie International Edition 2014-08, Vol.53 (35), p.9298-9301
Main Authors: Luo, Feng, Fan, Cong Bin, Luo, Ming Biao, Wu, Xiao Liu, Zhu, Yan, Pu, Shou Zhi, Xu, Wen-Yuan, Guo, Guo-Cong
Format: Article
Language:English
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Summary:We demonstrate herein a promising pathway towards low‐energy CO2 capture and release triggered by UV and visible light. A photosensitive diarylethene ligand was used to construct a photochromic diarylethene metal–organic framework (DMOF). A local photochromic reaction originating from the framework movement induced by the photoswitchable diarylethene unit resulted in record CO2‐desorption capacity of 75 % under static irradiation and 76 % under dynamic irradiation. Low‐energy CO2 capture and release was possible with a metal–organic framework containing a photosensitive diarylethene ligand. The local framework flexibility caused by the photoswitchable diarylethene ligand (see picture) led to a record high CO2‐desorption capacity of 75 % under static irradiation and 76 % under dynamic irradiation.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201311124