The role of solvent on selective hydrogenation of conjugated and isolated C=C of Citral (3,7-dimethyl 2,6-octadienal) - a self-consistent reaction field study

被引:14
作者
Chatterjee, A
Chatterjee, M
Ikushima, Y
Mizukami, F
机构
[1] AIST, Lab Membrane Chem, Miyagino Ku, Sendai, Miyagi 9838551, Japan
[2] AIST, Supercrit Fluid Res Ctr, Miyagino Ku, Sendai, Miyagi 9838551, Japan
关键词
D O I
10.1016/j.cplett.2004.07.068
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
Self-consistent reaction field study was performed to rationalize the selective formation of 3,7-dimethyloctanal by hydrogenation of citral (3,7-dimethyl 2,6-octadienal) exclusively in supercritical carbon dioxide medium. We have used density functional theory (DFT) to calculate and compare the reactivity of the atoms present in the reactant molecule for a range of solvent with variable dielectric constant. Solvent with low dielectric constant was found to be reducing the electrophilicity of the sites present and hence enhances the selectivity of an isolated and conjugated C=C bond-breaking phenomenon. In contrast to that, solvents with high dielectric constant prefer to hydrogenate the conjugated C=C. The geometric and electronic aspects were compared to propose a plausible explanation for the unprecedented selectivity observed in supercritical carbon dioxide medium. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 149
页数:7
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