Issue 18, 2015

Polypyridyl Ru(ii)-derivatized polypropylacrylate polymer with a terminal water oxidation catalyst. Application of reversible addition–fragmentation chain transfer polymerization

Abstract

A Ru(II) polypyridyl-derivatized polypropylacrylate end-capped with a water-oxidation-catalyst (WOC) has been synthesized by using reversible addition–fragmentation chain transfer polymerization (RAFT) followed by click reaction and end-group functionalization. In cyclic voltammograms in propylene carbonate, chromophore oxidation occurs at 1.27 V vs. NHE and the RuIII/II wave for the catalyst at 0.84 V vs. NHE. Upon excitation of the Ru(II) chromophore, excited-state energy migration occurs by site-to-site, –RuII*– → –RuII–, energy transfer hopping along the polymer chain, in part, reaching the terminal catalyst site where –RuII*– → –RuII–OH22+ energy transfer is favored by ΔGen = −2100 cm−1. Added MV2+ as an electron transfer acceptor oxidizes the –RuII*– excited state on the polymer to Ru(III), –RuII*– + MV2+ → –RuIII– + MV+, and ultimately, the catalyst, by site-to-site electron transfer hopping and oxidation, Image ID:c5dt00287g-t1.gif. Oxidation is followed by relatively slow, diffusional back electron transfer from MV˙+ to Ru(III) sites on the polymer chain. The mixed chromophore-catalyst polymer is a water oxidation catalyst with potential for enhanced light harvesting and water oxidation.

Graphical abstract: Polypyridyl Ru(ii)-derivatized polypropylacrylate polymer with a terminal water oxidation catalyst. Application of reversible addition–fragmentation chain transfer polymerization

Supplementary files

Article information

Article type
Paper
Submitted
20 Jan 2015
Accepted
25 Mar 2015
First published
25 Mar 2015
This article is Open Access
Creative Commons BY license

Dalton Trans., 2015,44, 8640-8648

Author version available

Polypyridyl Ru(II)-derivatized polypropylacrylate polymer with a terminal water oxidation catalyst. Application of reversible addition–fragmentation chain transfer polymerization

Z. Fang, A. Ito, H. Luo, D. L. Ashford, J. J. Concepcion, L. Alibabaei and T. J. Meyer, Dalton Trans., 2015, 44, 8640 DOI: 10.1039/C5DT00287G

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