| Literature DB >> 26617393 |
Sonia Castellanos1, Alexis Goulet-Hanssens2, Fangli Zhao2, Alla Dikhtiarenko3, Alexey Pustovarenko3, Stefan Hecht2, Jorge Gascon3, Freek Kapteijn3, David Bléger4.
Abstract
The ability to control the interplay of materials with low-energy photons is important as visible light offers several appealing features compared to ultraviolet radiation (less damaging, more selective, predominant in the solar spectrum, possibility to increase the penetration depth). Two different metal-organic frameworks (MOFs) were synthesized from the same linker bearing all-visible ortho-fluoroazobenzene photoswitches as pendant groups. The MOFs exhibit different architectures that strongly influence the ability of the azobenzenes to isomerize inside the voids. The framework built with Al-based nodes has congested 1D channels that preclude efficient isomerization. As a result, local light-heat conversion can be used to alter the CO2 adsorption capacity of the material on exposure to green light. The second framework, built with Zr nodes, provides enough room for the photoswitches to isomerize, which leads to a unique bistable photochromic MOF that readily responds to blue and green light. The superiority of green over UV irradiation was additionally demonstrated by reflectance spectroscopy and analysis of digested samples. This material offers promising perspectives for liquid-phase applications such as light-controlled catalysis and adsorptive separation.Entities:
Keywords: azo compounds; carboxylate ligands; metal-organic frameworks; photochromism; photoswitches
Year: 2015 PMID: 26617393 DOI: 10.1002/chem.201503503
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236