Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator
Poly(3-hexyl thiophene)-b-poly(styrene-co-chloromethylstyrene) copolymers, to be used as a prepolymer for preparing donor-acceptor block copolymers for organic solar cells, have been synthesised by reacting P3HT macroinitiators with styrene and chloromethylstyrene via three types of atom transfer ra...
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2015-01-01
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Series: | Advances in Materials Science and Engineering |
Online Access: | http://dx.doi.org/10.1155/2015/973632 |
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author | Nattawoot Rattanathamwat Jatuphorn Wootthikanokkhan Nonsee Nimitsiriwat Chanchana Thanachayanont Udom Asawapirom |
author_facet | Nattawoot Rattanathamwat Jatuphorn Wootthikanokkhan Nonsee Nimitsiriwat Chanchana Thanachayanont Udom Asawapirom |
author_sort | Nattawoot Rattanathamwat |
collection | DOAJ |
description | Poly(3-hexyl thiophene)-b-poly(styrene-co-chloromethylstyrene) copolymers, to be used as a prepolymer for preparing donor-acceptor block copolymers for organic solar cells, have been synthesised by reacting P3HT macroinitiators with styrene and chloromethylstyrene via three types of atom transfer radical polymerisation (ATRP) systems, which are (1) a normal ATRP, (2) activators generated by electron transfer (AGET), and (3) a simultaneous reverse and normal initiation (SR&NI). The kinetics of these ATRP systems were studied as a function of monomers to the macroinitiator molar ratio. It was found that all of the three types of ATRP systems led to first order kinetics with respect to monomers. The highest rate constant (k) of 3.4 × 10−3 s−1 was obtained from the SR&NI ATRP system. The molecular weights of the product determined by the GPC were lower than were the theoretical values. The result was discussed in light of the chain transfer reaction to the poly(chloromethylstyrene) repeating units. Morphology of the synthesized block copolymers, examined by an atomic force microscopy (AFM), were also compared and discussed. |
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institution | Kabale University |
issn | 1687-8434 1687-8442 |
language | English |
publishDate | 2015-01-01 |
publisher | Wiley |
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series | Advances in Materials Science and Engineering |
spelling | doaj-art-7639b8d7467b4513ad9c558bede0876b2025-02-03T06:13:52ZengWileyAdvances in Materials Science and Engineering1687-84341687-84422015-01-01201510.1155/2015/973632973632Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) MacroinitiatorNattawoot Rattanathamwat0Jatuphorn Wootthikanokkhan1Nonsee Nimitsiriwat2Chanchana Thanachayanont3Udom Asawapirom4Division of Materials Technology, School of Energy, Environment and Materials, King Mongkut’s University of Technology Thonburi (KMUTT), Bangkok 10140, ThailandDivision of Materials Technology, School of Energy, Environment and Materials, King Mongkut’s University of Technology Thonburi (KMUTT), Bangkok 10140, ThailandNanotec-KMUTT Center of Excellence on Hybrid Nanomaterials for Alternative Energy (HyNAE), Bangkok 10140, ThailandNational Metal and Materials Technology Center (MTEC), Pathumthani 12120, ThailandNational Nanotechnology Center (NANOTEC), Pathumthani 12120, ThailandPoly(3-hexyl thiophene)-b-poly(styrene-co-chloromethylstyrene) copolymers, to be used as a prepolymer for preparing donor-acceptor block copolymers for organic solar cells, have been synthesised by reacting P3HT macroinitiators with styrene and chloromethylstyrene via three types of atom transfer radical polymerisation (ATRP) systems, which are (1) a normal ATRP, (2) activators generated by electron transfer (AGET), and (3) a simultaneous reverse and normal initiation (SR&NI). The kinetics of these ATRP systems were studied as a function of monomers to the macroinitiator molar ratio. It was found that all of the three types of ATRP systems led to first order kinetics with respect to monomers. The highest rate constant (k) of 3.4 × 10−3 s−1 was obtained from the SR&NI ATRP system. The molecular weights of the product determined by the GPC were lower than were the theoretical values. The result was discussed in light of the chain transfer reaction to the poly(chloromethylstyrene) repeating units. Morphology of the synthesized block copolymers, examined by an atomic force microscopy (AFM), were also compared and discussed.http://dx.doi.org/10.1155/2015/973632 |
spellingShingle | Nattawoot Rattanathamwat Jatuphorn Wootthikanokkhan Nonsee Nimitsiriwat Chanchana Thanachayanont Udom Asawapirom Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator Advances in Materials Science and Engineering |
title | Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator |
title_full | Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator |
title_fullStr | Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator |
title_full_unstemmed | Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator |
title_short | Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator |
title_sort | kinetic studies of atom transfer radical polymerisations of styrene and chloromethylstyrene with poly 3 hexyl thiophene macroinitiator |
url | http://dx.doi.org/10.1155/2015/973632 |
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