Synthesis of Poly[(3-(6-(9-anthracenylmethoxy)hexyl)thiophene)-co-(3-(6-bromohexyl)thiophene)] Postfunctionalized from Poly(3-(6-bromohexyl)thiophene): A Comparative Study of the Base Polymer with Its Chlorinated Analogous

A synthetic method based on the postfunctionalization of a reactive homopolymer precursor, which allows for the preparation of different copolymers derived from poly(3-alkylthiophene), was studied. Although these groups decrease the solubility of the resultant material, they enable controlling the d...

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Main Authors: F. R. Díaz-Alzamora, M. A. del Valle, C. M. Núñez, P. P. Zamora, J. P. Soto, J. C. Bernède
Format: Article
Language:English
Published: Wiley 2009-01-01
Series:International Journal of Polymer Science
Online Access:http://dx.doi.org/10.1155/2009/974307
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author F. R. Díaz-Alzamora
M. A. del Valle
C. M. Núñez
P. P. Zamora
J. P. Soto
J. C. Bernède
author_facet F. R. Díaz-Alzamora
M. A. del Valle
C. M. Núñez
P. P. Zamora
J. P. Soto
J. C. Bernède
author_sort F. R. Díaz-Alzamora
collection DOAJ
description A synthetic method based on the postfunctionalization of a reactive homopolymer precursor, which allows for the preparation of different copolymers derived from poly(3-alkylthiophene), was studied. Although these groups decrease the solubility of the resultant material, they enable controlling the degree of substitution to obtain a material with improved spectroscopic (absorption and emission) properties making them useful for the fabrication of electronic devices, for example, solar cells and light-emitting diodes. Furthermore, a comparative study of two halogenated (Cl and Br) reactive poly(3-ω-haloalkyl)thiophenes was carried out.
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id doaj-art-3d1c47ca04a643239f6528ec3229fd92
institution Kabale University
issn 1687-9422
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language English
publishDate 2009-01-01
publisher Wiley
record_format Article
series International Journal of Polymer Science
spelling doaj-art-3d1c47ca04a643239f6528ec3229fd922025-02-03T01:26:49ZengWileyInternational Journal of Polymer Science1687-94221687-94302009-01-01200910.1155/2009/974307974307Synthesis of Poly[(3-(6-(9-anthracenylmethoxy)hexyl)thiophene)-co-(3-(6-bromohexyl)thiophene)] Postfunctionalized from Poly(3-(6-bromohexyl)thiophene): A Comparative Study of the Base Polymer with Its Chlorinated AnalogousF. R. Díaz-Alzamora0M. A. del Valle1C. M. Núñez2P. P. Zamora3J. P. Soto4J. C. Bernède5Laboratorio de Polímeros, Facultad de Química, Pontificia Universidad Católica de Chile, Vicuña Mackenna 4860, Macul, Santiago, ChileLaboratorio de Polímeros, Facultad de Química, Pontificia Universidad Católica de Chile, Vicuña Mackenna 4860, Macul, Santiago, ChileLaboratorio de Polímeros, Facultad de Química, Pontificia Universidad Católica de Chile, Vicuña Mackenna 4860, Macul, Santiago, ChileLaboratorio de Polímeros, Facultad de Química, Pontificia Universidad Católica de Chile, Vicuña Mackenna 4860, Macul, Santiago, ChileLaboratorio de Polímeros, Facultad de Química, Pontificia Universidad Católica de Chile, Vicuña Mackenna 4860, Macul, Santiago, ChileFaculté des Sciences et dês Techniques, Universite de Nantes Atlantique, LAMP, EA 3829, 2 rue de la Houssieniere, BP 922098, 44000 Nantes, FranceA synthetic method based on the postfunctionalization of a reactive homopolymer precursor, which allows for the preparation of different copolymers derived from poly(3-alkylthiophene), was studied. Although these groups decrease the solubility of the resultant material, they enable controlling the degree of substitution to obtain a material with improved spectroscopic (absorption and emission) properties making them useful for the fabrication of electronic devices, for example, solar cells and light-emitting diodes. Furthermore, a comparative study of two halogenated (Cl and Br) reactive poly(3-ω-haloalkyl)thiophenes was carried out.http://dx.doi.org/10.1155/2009/974307
spellingShingle F. R. Díaz-Alzamora
M. A. del Valle
C. M. Núñez
P. P. Zamora
J. P. Soto
J. C. Bernède
Synthesis of Poly[(3-(6-(9-anthracenylmethoxy)hexyl)thiophene)-co-(3-(6-bromohexyl)thiophene)] Postfunctionalized from Poly(3-(6-bromohexyl)thiophene): A Comparative Study of the Base Polymer with Its Chlorinated Analogous
International Journal of Polymer Science
title Synthesis of Poly[(3-(6-(9-anthracenylmethoxy)hexyl)thiophene)-co-(3-(6-bromohexyl)thiophene)] Postfunctionalized from Poly(3-(6-bromohexyl)thiophene): A Comparative Study of the Base Polymer with Its Chlorinated Analogous
title_full Synthesis of Poly[(3-(6-(9-anthracenylmethoxy)hexyl)thiophene)-co-(3-(6-bromohexyl)thiophene)] Postfunctionalized from Poly(3-(6-bromohexyl)thiophene): A Comparative Study of the Base Polymer with Its Chlorinated Analogous
title_fullStr Synthesis of Poly[(3-(6-(9-anthracenylmethoxy)hexyl)thiophene)-co-(3-(6-bromohexyl)thiophene)] Postfunctionalized from Poly(3-(6-bromohexyl)thiophene): A Comparative Study of the Base Polymer with Its Chlorinated Analogous
title_full_unstemmed Synthesis of Poly[(3-(6-(9-anthracenylmethoxy)hexyl)thiophene)-co-(3-(6-bromohexyl)thiophene)] Postfunctionalized from Poly(3-(6-bromohexyl)thiophene): A Comparative Study of the Base Polymer with Its Chlorinated Analogous
title_short Synthesis of Poly[(3-(6-(9-anthracenylmethoxy)hexyl)thiophene)-co-(3-(6-bromohexyl)thiophene)] Postfunctionalized from Poly(3-(6-bromohexyl)thiophene): A Comparative Study of the Base Polymer with Its Chlorinated Analogous
title_sort synthesis of poly 3 6 9 anthracenylmethoxy hexyl thiophene co 3 6 bromohexyl thiophene postfunctionalized from poly 3 6 bromohexyl thiophene a comparative study of the base polymer with its chlorinated analogous
url http://dx.doi.org/10.1155/2009/974307
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