Photolytic C-O Bond Cleavage with Quantum Dots

被引:31
|
作者
Enright, Michael J. [1 ]
Gilbert-Bass, Kito [1 ]
Sarsito, Harrison [1 ]
Cossairt, Brandi M. [1 ]
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98195 USA
关键词
VISIBLE-LIGHT PHOTOREDOX; LIGNIN MODEL COMPOUNDS; SEMICONDUCTOR NANOCRYSTALS; HYDROGEN-PRODUCTION; KRAFT LIGNIN; OXIDATION; CATALYSIS; H-2; CDS; DEPOLYMERIZATION;
D O I
10.1021/acs.chemmater.9b00943
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Quantum dots are used as photoredox catalysts to drive bond cleavage in lignin model substrates. Cadmium selenide quantum dots selectively cleave C-O bonds with yields comparable to the best transition-metal-based molecular photocatalysts, thereby emulating depolymerization of the beta-O-4 linkages that account for 45-60% of all linkers in native lignin. Compared to their molecular catalyst counterparts, the quantum dots demonstrate higher turnover frequencies, higher surface tunability for solvent versatility, and lower catalyst loading under mild, ambient temperature reaction conditions. The robust nature and solvent versatility of these quantum dot photoredox catalysts enable a direct, single vessel route to convert benzylic alcohols (a majority of species in native and processed lignin) into high-value guaiacols and acetophenones without any prerequisite filtration, purification, or solvent change.
引用
收藏
页码:2677 / 2682
页数:6
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