| Literature DB >> 27966866 |
Carl-Hugo Pélisson1, Takahiro Nakanishi1, Yang Zhu1, Kei Morisato2, Toshiyuki Kamei3, Ayaka Maeno4, Hironori Kaji4, Shunki Muroyama5, Masamoto Tafu5, Kazuyoshi Kanamori1, Toyoshi Shimada3, Kazuki Nakanishi1.
Abstract
Polymethylhydrosiloxane has been grafted on the surface of a hierarchically porous silica monolith using a facile catalytic reaction between Si-H and silanol to anchor the polymer. This easy methodology leads to the functionalization of the surface of a silica monolith, where a large amount of free Si-H bonds remain available for reducing metal ions in solution. Palladium nanoparticles of 15 nm have been synthesized homogeneously inside the mesopores of the monolith without any stabilizers, using a flow of a solution containing Pd2+. This monolith was used as column-type fixed bed catalyst for continuous flow hydrogenation of styrene and selective hydrogenation of 3-hexyn-1-ol, in each case without a significant decrease of the catalytic activity after several hours or days. Conversion, selectivity, and stereoselectivity of the alkyne hydrogenation can be tuned by flow rates of hydrogen and the substrate solution, leading to high productivity (1.57 mol g(Pd)-1 h-1) of the corresponding cis-alkene.Entities:
Keywords: catalysis; hydrosilylation; mesoporous materials; palladium nanoparticle; polymer; selective hydrogenation; silica monolith
Year: 2016 PMID: 27966866 DOI: 10.1021/acsami.6b12653
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229