Mizugaki Tomoo, Togo Keito, Maeno Zen, Mitsudome Takato, Jitsukawa Koichiro, Kaneda Kiyotomi
Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama, Toyonaka, Osaka, 560-8531, Japan.
Research Center for Solar Energy Chemistry, Osaka University, 1-3 Machikaneyama, Toyonaka, Osaka, 560-8531, Japan.
Sci Rep. 2017 Oct 25;7(1):14007. doi: 10.1038/s41598-017-14373-1.
Highly selective hydrogenative carbon-carbon bond scission of biomass-derived platform oxygenates was achieved with a cerium oxide-supported ruthenium nanoparticle catalyst in water. The present catalyst enabled the selective cleavage of carbon-carbon σ bonds adjacent to carboxyl, ester, and hydroxymethyl groups, opening new eight synthetic routes to valuable chemicals from biomass derivatives. The high selectivity for such carbon-carbon bond scission over carbon-oxygen bonds was attributed to the multiple catalytic roles of the Ru nanoparticles assisted by the in situ formed Ce(OH).
在水中,使用氧化铈负载的钌纳米颗粒催化剂实现了生物质衍生平台含氧化合物的高选择性氢化碳-碳键断裂。本催化剂能够选择性断裂与羧基、酯基和羟甲基相邻的碳-碳σ键,开辟了从生物质衍生物合成有价值化学品的八条新路线。相对于碳-氧键而言,对这种碳-碳键断裂的高选择性归因于原位形成的Ce(OH)辅助的Ru纳米颗粒的多重催化作用。