This website uses cookies to give you the best user experience. If you continue without changing your settings we'll assume you are happy to receive all RSC cookies. You can change your cookie settings by navigating to our Privacy and Cookies page and following the instructions. These instructions are also obtainable from the privacy link at the bottom of any RSC page.
Lite Version|Standard version
Home > Polymer Chemistry >
To gain access to this content please
Log in via your home Institution.
Log in with your member or subscriber username and password.
Download


Buy PDF Add PDF to Basket (£42.50*)
*Exclusive of taxes
This article contains 7 page(s)
Abstract | Cited by

Poly(thienylene phenylene) with bromoaryl groups on its side chains (P1) was directly synthesized without protection via the Migita–Kosugi–Stille coupling polycondensation. ortho-Substituted electron-withdrawing imide-carbonyl groups play an important role in the chemoselective intramolecular catalyst transfer system. In addition, the post-modification reaction of P1 successfully produced thienyl-side-chain-functionalized P1.

Graphical abstract: Direct synthesis of π-conjugated polymers with bromoaryl groups in side chains via a chemoselective intramolecular catalyst transfer system

Page: ^ Top


Enter Keywords, author, title,reference, or DOI
Log in | Register