Expanding the aqueous-based redox-facilitated self-polymerization chemistry of catecholamines to 5,6-dihydroxy-1H-benzimidazole and its 2-substituted derivatives-Reference-Cited by-同舟云学术

Expanding the aqueous-based redox-facilitated self-polymerization chemistry of catecholamines to 5,6-dihydroxy-1H-benzimidazole and its 2-substituted derivatives

Published:2016 Issue:30 Volume:6 Page:25203-25214
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Fan Ka Wai¹²³⁴⁵,Peterson Matthew B.⁶³⁴⁵,Ellersdorfer Peter¹²³⁴⁵,Granville Anthony M.¹²³⁴⁵

Affiliation:

1. Centre for Advanced Macromolecular Design

2. School of Chemical Engineering

3. The University of New South Wales

4. Kensington

5. Australia

6. School of Chemistry

Abstract

Redox-facilitated self-polymerization can be performed with 5,6-dihydroxy-1H-benzimidazole to generate materials analogous to polydopamine, proving the possibility to expand the catecholamine-based chemistry to N-heterocyclic catechol derivatives.

Funder

Australian Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C5RA25590B

Reference65 articles.

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