期刊
JOURNAL OF MATERIALS CHEMISTRY
卷 20, 期 37, 页码 8099-8106出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c0jm01180k
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资金
- DST, New Delhi
- NanoScience and Technology Initiative of DST
- CSIR, New Delhi
A new organosilane precursor has been designed via Vilsmeier-Haack formylation of phloroglucinol followed by its Schiff base condensation with 3-aminopropyl-triethoxysilane (APTES). A novel organic-inorganic hybrid periodic mesoporous organosilica (PMO) LHMS-3 containing the highly coordinating bis(propyliminomethyl)-phloroglucinol moiety inside the pore wall has been synthesized by using this precursor organosilane molecule. Phenolic-OH and imine-N donor sites present in this PMO material have been utilized to anchor Pd(II) species at the surface of the mesopores. Small angle neutron scattering, XRD, HR TEM, SEM, C-13 and Si-29 solid state MAS NMR, UV-vis and FT IR spectroscopic tools are utilized to characterize the 2D-hexagonal mesophase and the presence of the bis(propyliminomethyl)-phloroglucinol moiety inside the pore wall. This Pd-anchored material Pd-LHMS-3 showed excellent catalytic activity and trans-selectivity in Heck C-C bond formation reactions for the synthesis of a series of value-added aromatic and aliphatic olefins.
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