4.7 Article

A general diversity oriented synthesis of asymmetric double-decker shaped silsesquioxanes

Journal

CHEMICAL COMMUNICATIONS
Volume 55, Issue 59, Pages 8623-8626

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc03972d

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Funding

  1. Office of Naval Research [N00014-16-2109]

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A strategically novel synthesis of nano-sized, asymmetrically functionalized double-decker shaped silsesquioxanes (DDSQ) is reported. Selective protection with a boronic acid affords the crucial mono-protected intermediate en route to the asymmetric products. Generation of symmetric by-products is minimized by judicious choice of base, and high recovery of recyclable starting DDSQ tetraol is achieved.

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