Access to Highly Efficient Energy Transfer in Metal–Organic Frameworks via Mixed Linkers Approach
Author(s) -
Jiangtao Jia,
Luis GutiérrezArzaluz,
Osama Shekhah,
Norah Alsadun,
Justyna CzabanJóźwiak,
Sheng Zhou,
Osman M. Bakr,
Omar F. Mohammed,
Mohamed Eddaoudi
Publication year - 2020
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.0c02007
Subject(s) - chemistry , benzimidazole , metal organic framework , picosecond , acceptor , energy transfer , ligand (biochemistry) , combinatorial chemistry , spectroscopy , ultrashort pulse , absorption spectroscopy , photochemistry , topology (electrical circuits) , nanotechnology , chemical physics , organic chemistry , optics , laser , biochemistry , physics , receptor , mathematics , materials science , adsorption , quantum mechanics , combinatorics , condensed matter physics
Herein, we report a new light-harvesting mixed-ligand Zr(IV)-based metal-organic framework (MOF),with underlying fcu opology, encompassing the [Zr 6 (μ 3 -O) 4 (μ 3 -OH) 4 (O 2 C-) 12 ] cluster and an equimolar mixture of thiadiazole- and benzimidazole-functionalized ligands. The successful integration of ligands with similar structural features but with notable chemical distinction afforded the attainment of a highly efficient energy transfer (ET). Notably, the very strong spectral overlap between the emission spectrum of benzimidazole (energy donor) and the absorption spectrum of thiadiazole (energy acceptor) provided an ideal platform to achieve very rapid (picosecond time scale) and highly efficient energy transfer (around 90% efficiency), as evidenced by time-resolved spectroscopy. Remarkably, the ultrafast time-resolved experiments quantified for the first time the anticipated close proximity of the two linkers with an average distance of 17 Å. This finding paves the way for the design and synthesis of periodic MOFs affording very efficient and fast ET to mimic natural photosynthetic systems.
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