Tuning Cooperativity by Controlling the Linker Length of Silica-Supported Amines in Catalysis and CO2 Capture

被引:167
作者
Brunelli, Nicholas A. [1 ]
Didas, Stephanie A. [1 ]
Venkatasubbaiah, Krishnan [1 ]
Jones, Christopher W. [1 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
关键词
ASYMMETRIC ALDOL REACTIONS; MESOPOROUS SILICA; MICHAEL REACTION; BASE SITES; ACID; ORGANOCATALYSTS; CONDENSATION; KINETICS; DISTANCE;
D O I
10.1021/ja305601g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cooperative interactions between amino-alkylsilanes and silanols on a silica surface can be controlled by varying the length of the alkyl linker attaching the amine to the silica surface from C1 (methyl) to C5 (pentyl). The linker length strongly affects the catalytic cooperativity of amines and silanols in aldol condensations as well as the adsorptive cooperativity for CO2 capture. The catalytic cooperativity increases with the linker length up to propyl (C3), with longer, more flexible linkers (up to CS) providing no additional benefit or hindrance. Short linkers (C1 and C2) limit the beneficial amine-silanol cooperativity in aldol condensations, resulting in lower catalytic rates than with the C3+ linkers. For the same materials, the adsorptive cooperativity exhibits similar trends for CO2 capture efficiency.
引用
收藏
页码:13950 / 13953
页数:4
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