Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
55433 | Catalysis Today | 2012 | 6 Pages |
The successful construction of arenetricarbonyl complexes (–C6H4Me(CO)3–; Me = Cr, Mo) was achieved through the direct modification of phenylene (–C6H4–) moieties of phenylene-bridged hybrid mesoporous materials (HMM-ph) by the simple chemical vapor deposition (CVD) of corresponding metal hexacarbonyls. The pore structure as well as high surface area of HMM-ph were retained even after CVD treatment. It was found that HMM-ph incorporating an arenetricarbonyl molybdenum complex (HMM-phMo(CO)3) exhibited higher catalytic performance for the polymerization of phenylacetylene and dehydrochlorination of 2-chloro-2-methylbutane than HMM-phCr(CO)3. Various spectroscopic investigations revealed that the strength of the chemical bond between the phenylene ligand and metal center of the arenetricarbonyl complexes affects the catalytic performance of HMM-phMe(CO)3 (Me = Cr, Mo).
Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (251 K)Download as PowerPoint slideHighlights► Unique inorganic–organic hybrid mesoporous materials incorporating arenetricarbonyl complexes were successfully prepared by a simple CVD treatment of HMM-ph. ► Arenetricarbonyl complexes were stably constructed on HMM-ph by using phenylene moieties as the “framework ligand”. ► These complexes exhibited catalytic performance in polymerization and dehydrochlorination within heterogeneous systems.