4.7 Article

Bipyridine Periodic Mesoporous Organosilica: A Solid Ligand for the Iridium- Catalyzed Borylation of C-H Bonds

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ADVANCED SYNTHESIS & CATALYSIS
卷 356, 期 4, 页码 673-679

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201400125

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CH activation; heterogenous catalysis; iridium; organic-inorganic hybrid materials; periodic mesoporous organosilicas; surface chemistry

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With the goal to obtain a molecularly defined iridium(I) heterogeneous CH functionalization catalyst, a periodic mesoporous organosilica (PMO) containing bipyridylene moieties in a matrix of biphenylene units as ligand platform was designed and fully characterized. The material exhibits a high surface area with small mesopores in a vermicular arrangement, and the pore walls show a highly crystal-like character. After surface passivation with chlorotrimethylsilane and functionalization with chloro(1,5-cyclooctadiene)iridium(I) dimer [{IrCl(COD)}(2)] a molecularly defined Ir(I) surface complex was obtained according to EXAFS and UV-Vis spectroscopy. This functionalized material catalyzes the direct CH borylation of arenes to yield the corresponding boronic esters and can be reused without significant loss of activity.

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