Preparation and characterization of semiconducting polymeric blends. Photochemical synthesis of poly(3-alkylthiophenes) using host microporous matrices of poly(vinylidene fluoride)

Literature Information

Publication Date 2012-03-26
DOI 10.1039/C2PY00003B
Impact Factor 5.582
Authors

Maria Beny Pinto Zakia, José Godoy Filho, João Sinezio de Carvalho Campos


View Original

Abstract

Chemical and electrochemical synthesis techniques have been the principal methods of obtaining polymers in industry and scientific research laboratories. However, during the last two decades, photochemical synthesis, although poorly studied, has been reported to present several advantages, in that it is a fast and cheap technique, and it is not aggressive to the environment. The technique has been applied to the production of some conducting polymers. In this study, semiconducting polymeric blends composed of PT3AA-K–PVDF and PT3MA–PVDF were respectively obtained by photochemical polymerization in aqueous solutions of 3-thiophene acetic acid and 3-thiophene methyl acetate monomers using PVDF microporous matrices and potassium dichromate as catalyst. The percentage of products and by-products incorporated in the host matrix was obtained by gravimetric analysis. The chemical structures of the polymers synthesized were analyzed by FTIR, UV-vis and 1H NMR. GPC analysis indicated the formation of oligomers composed of 5–6 mers. The morphology of the matrices and polymeric blends was observed by SEM-EDS and their electric behavior evaluated by measures of electric conductivity. The SEM images show the presence of polythiophene in the pores of the PVDF microporous membrane. The thermal properties of the polymers and their blends were evaluated by DSC and TGA. Thermal analysis by DSC demonstrated an increase in melting temperature of the blends, attributed to the confinement of PVDF crystalline phases for the polymer photosynthesized. The results of volumetric conductivity measurements of polymeric blends show an increase in conductivity in the matrices from 10−15 to 10−11 S cm−1.

Related Literature

Dendrimer–doxorubicin conjugate as enzyme-sensitive and polymeric nanoscale drug delivery vehicle for ovarian cancer therapy

Chengyuan Zhang, Dayi Pan, Kui Luo, Ning Li, Chunhua Guo, Xiuli Zheng, Zhongwei Gu

2014-05-20 Paper

DOI: 10.1039/C4PY00601A

Hyperbranched PEG-based multi-NHS polymer and bioconjugation with BSA

Sigen A, Qian Xu, Dezhong Zhou, Yongsheng Gao, Jeddah Marie Vasquez, Udo Greiser, Wenguang Liu

2017-01-04 Communication

DOI: 10.1039/C6PY01719C

Camptothecin prodrug block copolymer micelles with high drug loading and target specificity

Sue Watson, Anna M. Grabowska

2014-05-15 Paper

DOI: 10.1039/C4PY00369A

Naphthobisthiazole diimide-based n-type polymer semiconductors: synthesis, π-stacking, field-effect charge transport, and all-polymer solar cells

Selvam Subramaniyan, Taeshik Earmme, Nishit M. Murari, Samson A. Jenekhe

2014-07-02 Paper

DOI: 10.1039/C4PY00566J

6-Oxoverdazyl radical polymers with tunable electrochemical properties

2014-07-04 Communication

DOI: 10.1039/C4PY00829D

Contents list

Front/Back Matter

DOI: 10.1039/C7PY90035J

Tumor-targeted aggregation of pH-sensitive nanocarriers for enhanced retention and rapid intracellular drug release

Wei Wu, Qiujing Zhang, Jiantao Wang, Miao Chen, Shuai Li, Zaifu Lin, Jianshu Li

2014-05-30 Paper

DOI: 10.1039/C4PY00575A

Heterogeneous organocatalysts composed of microporous polymer networks assembled by Tröger's base formation

Mariolino Carta, Matthew Croad, Keith Bugler, Kadhum J. Msayib, Neil B. McKeown

2014-06-20 Paper

DOI: 10.1039/C4PY00608A

Synthesis of nanoscaled poly(styrene-co-n-butyl acrylate)/silica particles with dumbbell- and snowman-like morphologies by emulsion polymerization

Lucie Malosse, Etienne Duguet, Muriel Lansalot, Elodie Bourgeat-Lami, Serge Ravaine

2014-06-05 Paper

DOI: 10.1039/C4PY00370E

You might also like

Compound Q&A

Are there alternatives to 1-(4-Chlorophenyl)-N-hydroxymethanimine (CAS: 3848-36-0) in synthesis?

When considering alternatives to 1-(4-Chlorophenyl)-N-hydroxymethanimine (CAS: 3...

3848-36-01-(4-Chlorophenyl)-N...
Compound Q&A

How is 3-(4-Bromophenyl)-5-(2-fluorophenyl)-1,2,4-oxadiazole (CAS: 419553-16-5) typically synthesized?

3-(4-Bromophenyl)-5-(2-fluorophenyl)-1,2,4-oxadiazole is synthesized through a m...

419553-16-53-(4-Bromophenyl)-5-...
Compound Q&A

How is 5-Chloro-2-(4-chlorophenyl)-4-methyl-6-[3-(1-piperidinyl)propoxy]pyrimidine (CAS: 1639220-19-1) typically synthesized?

5-Chloro-2-(4-chlorophenyl)-4-methyl-6-[3-(1-piperidinyl)propoxy]pyrimidine (CAS...

1639220-19-15-Chloro-2-(4-chloro...
Compound Q&A

What industries use 2-Chloro-4-(difluoromethoxy)pyridine (CAS: 1206978-15-5)?

2-Chloro-4-(difluoromethoxy)pyridine is used in the pharmaceutical industry for ...

1206978-15-52-Chloro-4-(difluoro...
Compound Q&A

What regulatory guidelines apply to 3-Chloro-6-methylpyridazine (CAS: 1121-79-5)?

3-Chloro-6-methylpyridazine (CAS: 1121-79-5) is classified under the Globally Ha...

1121-79-53-Chloro-6-methylpyr...
Compound Q&A

Are there alternatives to Methyl 4,5-dimethyl-2-nitrobenzoate in synthesis?

Several alternatives can be used in the synthesis of Methyl 4,5-dimethyl-2-nitro...

90922-74-0Methyl 4,5-dimethyl-...
Compound Q&A

Are there alternatives to (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylaldehyde in synthesis?

Alternatives to (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylaldehyde include other acry...

63405-68-5(2E,2'E)-3,3'-(1,4-P...
Compound Q&A

What is 3-Amino-5-chloropyridin-2-ol hydrochloride (CAS: 1261906-29-9)?

3-Amino-5-chloropyridin-2-ol hydrochloride is an organic compound with the CAS n...

1261906-29-93-Amino-5-chloropyri...
Compound Q&A

What precautions should be taken when handling 6,7-Difluoro-2,3-dihydro-4H-chromen-4-one (CAS: 1092349-93-3)?

When handling 6,7-Difluoro-2,3-dihydro-4H-chromen-4-one, it is essential to wear...

1092349-93-36,7-Difluoro-2,3-dih...

Source Journal

Polymer Chemistry

Polymer Chemistry
CiteScore: 8.6
Self-citation Rate: 7.3%
Articles per Year: 457

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.