Issue 20, 2024

Organosilanes as synthetic precursors for oligosiloxanes and phenylsilica spheres

Abstract

The study describes the synthesis of disiloxanes, R3SiOSiR3, tetraorganodisiloxanes-1,3-diols, (RR1SiOH)2O, and silanol, t-Bu2Si(H)OH, by AuNP-catalyzed hydrolytic oxidation of Si–H bond(s) in organosilanes. The method relies upon the en-route formation of an oil-in-water microemulsion that is dispersed in the continuous water phase and stabilized by amphiphilic AuNPs. The reaction of (MePhSiOH)2O with (HMe2Si)2NH proceeds via O-silylation of silanol groups to afford an Si–H-terminated chain with the liberation of NH3 as the byproduct. The application of this approach provides a viable synthetic solution to organosilica colloidal structures using primary organosilanes, RSiH3 (R = Ph, n-hexyl) as substrates.

Graphical abstract: Organosilanes as synthetic precursors for oligosiloxanes and phenylsilica spheres

Supplementary files

Article information

Article type
Paper
Submitted
01 Feb 2024
Accepted
18 Apr 2024
First published
19 Apr 2024

New J. Chem., 2024,48, 9224-9230

Organosilanes as synthetic precursors for oligosiloxanes and phenylsilica spheres

R. Jain and R. Shankar, New J. Chem., 2024, 48, 9224 DOI: 10.1039/D4NJ00543K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements