Issue 71, 2018
From the journal:

Chemical Communications

Styrylsilane coupling reagents for immobilization of organic functional groups on silica and glass surfaces†

Soo-Bin Kim,‡a   Chang-Hee Lee‡a  and  Chul-Ho Jun ORCID logo *a  

* Corresponding authors

a Department of Chemistry, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Republic of Korea
E-mail: junch@yonsei.ac.kr

Abstract

Styrylsilanes serve as new coupling reagents for introducing organic functional groups on silica and glass surfaces. Functionalized styrylsilanes, which are readily prepared via catalytic hydrosilylation of the corresponding phenylacetylenes with silanes, are immobilized on silica through acid catalyzed processes under mild conditions.

Graphical abstract: Styrylsilane coupling reagents for immobilization of organic functional groups on silica and glass surfaces

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C8CC04863K
Article type
Communication
Submitted
18 Jun 2018
Accepted
09 Aug 2018
First published
09 Aug 2018

Chem. Commun., 2018,54, 9961-9964

Permissions

Request permissions

Styrylsilane coupling reagents for immobilization of organic functional groups on silica and glass surfaces

S. Kim, C. Lee and C. Jun, Chem. Commun., 2018, 54, 9961 DOI: 10.1039/C8CC04863K

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