Poly(Pyridinium Phenylene)s: Water-Soluble N-Type Polymers

Poly(pyridinium phenylene) conjugated polymers are synthesized by a cross-coupling and cyclization sequence. These polyelectrolytes are freely soluble in water and display high degrees of electroactivity. When reduced (n-doped) these materials display in situ conductivities as high as 160 S/cm. The...

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Main Authors: Swager, Timothy Manning, Izuhara, Daisuke
Other Authors: Massachusetts Institute of Technology. Department of Chemistry
Format: Article
Language:en_US
Published: American Chemical Society (ACS) 2012
Online Access:http://hdl.handle.net/1721.1/74232
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author Swager, Timothy Manning
Izuhara, Daisuke
author2 Massachusetts Institute of Technology. Department of Chemistry
author_facet Massachusetts Institute of Technology. Department of Chemistry
Swager, Timothy Manning
Izuhara, Daisuke
author_sort Swager, Timothy Manning
collection MIT
description Poly(pyridinium phenylene) conjugated polymers are synthesized by a cross-coupling and cyclization sequence. These polyelectrolytes are freely soluble in water and display high degrees of electroactivity. When reduced (n-doped) these materials display in situ conductivities as high as 160 S/cm. The high conductivity is attributed to the planar structure that is enforced by the cyclic structures of the polymer. The electron affinities are compared to PCBM, a C[subscript 60] based n-type material. We find that these polymers undergo excited state electron transfer reactions with other donor conjugated polymers and hence may find utility in photovoltaic devices.
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spelling mit-1721.1/742322022-09-27T20:25:06Z Poly(Pyridinium Phenylene)s: Water-Soluble N-Type Polymers Swager, Timothy Manning Izuhara, Daisuke Massachusetts Institute of Technology. Department of Chemistry Swager, Timothy Manning Swager, Timothy Manning Izuhara, Daisuke Poly(pyridinium phenylene) conjugated polymers are synthesized by a cross-coupling and cyclization sequence. These polyelectrolytes are freely soluble in water and display high degrees of electroactivity. When reduced (n-doped) these materials display in situ conductivities as high as 160 S/cm. The high conductivity is attributed to the planar structure that is enforced by the cyclic structures of the polymer. The electron affinities are compared to PCBM, a C[subscript 60] based n-type material. We find that these polymers undergo excited state electron transfer reactions with other donor conjugated polymers and hence may find utility in photovoltaic devices. National Science Foundation (U.S.) (DMR-0706408) Toray Industries, Inc. 2012-10-24T18:10:01Z 2012-10-24T18:10:01Z 2009-11 2009-08 Article http://purl.org/eprint/type/JournalArticle 0002-7863 1520-5126 http://hdl.handle.net/1721.1/74232 Izuhara, Daisuke, and Timothy M. Swager. “Poly(Pyridinium Phenylene)s: Water-Soluble N-Type Polymers.” Journal of the American Chemical Society 131.49 (2009): 17724–17725. en_US http://dx.doi.org/ 10.1021/ja906513u Journal of the American Chemical Society Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. application/pdf American Chemical Society (ACS) Prof. Swager via Erja Kajosalo
spellingShingle Swager, Timothy Manning
Izuhara, Daisuke
Poly(Pyridinium Phenylene)s: Water-Soluble N-Type Polymers
title Poly(Pyridinium Phenylene)s: Water-Soluble N-Type Polymers
title_full Poly(Pyridinium Phenylene)s: Water-Soluble N-Type Polymers
title_fullStr Poly(Pyridinium Phenylene)s: Water-Soluble N-Type Polymers
title_full_unstemmed Poly(Pyridinium Phenylene)s: Water-Soluble N-Type Polymers
title_short Poly(Pyridinium Phenylene)s: Water-Soluble N-Type Polymers
title_sort poly pyridinium phenylene s water soluble n type polymers
url http://hdl.handle.net/1721.1/74232
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