Mussel-Inspired One-Pot Synthesis of a Fluorescent and Water-Soluble Polydopamine-Polyethyleneimine Copolymer
Inspired by the molecular mechanics of mussel adhesive formation, a novel water‐soluble fluorescent macromolecule (polydopamine–polyethyleneimine (PDA–PEI)) is prepared by one‐pot copolymerization of dopamine (DA) and PEI. In this method, DA is polymerized to form PDA, which is then coupled with PEI...
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Published in | Macromolecular rapid communications. Vol. 36; no. 10; pp. 909 - 915 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Blackwell Publishing Ltd
01.05.2015
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Inspired by the molecular mechanics of mussel adhesive formation, a novel water‐soluble fluorescent macromolecule (polydopamine–polyethyleneimine (PDA–PEI)) is prepared by one‐pot copolymerization of dopamine (DA) and PEI. In this method, DA is polymerized to form PDA, which is then coupled with PEI mainly through Michael addition. The fluorescence property of PDA–PEI is mainly attributed to the Michael addition of PEI on the 5,6‐dihydroxyindole (DHI) units of PDA, where PEI can form hydrogen bonds with oxidative products such as DHI and force the DHI units to twist out of plane, resulting in a decrease in the intra‐ and intermolecular coupling of PDA. In addition, the influence of various metal cations on the fluorescence of the PDA–PEI copolymer is investigated. This work may facilitate the development of new strategies for controlling the emission characteristics of PDA.
Mussel‐inspired one‐pot copolymerization of dopamine and polyethyleneimine (PEI) yields a novel fluorescent macromolecule, polydopamine–polyethyleneimine (PDA–PEI). The fluorescence property of PDA–PEI is mainly attributed to the Michael addition of PEI at the 5,6‐dihydroxyindole unit of PDA. This work may facilitate the discovery of new strategies for controlling the emission characteristics of the PDA polymer. |
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Bibliography: | ArticleID:MARC201500021 istex:BAFB2F08B9B7416BA21C509FE577CBC97047141B ark:/67375/WNG-JN81DP9D-7 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1022-1336 1521-3927 1521-3927 |
DOI: | 10.1002/marc.201500021 |