Systematic Tuning of 2,1,3-Benzothiadiazole Acceptor Strength by Monofunctionalization with Alkylamine, Thioalkyl, or Alkoxy Groups in Carbazole Donor–Acceptor Polymers-Reference-Cited by-同舟云学术

Systematic Tuning of 2,1,3-Benzothiadiazole Acceptor Strength by Monofunctionalization with Alkylamine, Thioalkyl, or Alkoxy Groups in Carbazole Donor–Acceptor Polymers

Published:2017-03-23 Issue:7 Volume:50 Page:2736-2746
ISSN:0024-9297
Container-title:Macromolecules
language:en
Short-container-title:Macromolecules

Author:

Creamer Adam¹,Casey Abby¹,Marsh Adam V.¹,Shahid Munazza¹,Gao Mei²,Heeney Martin¹^ORCID

Affiliation:

1. Department of Chemistry and Centre for Plastic Electronics, Imperial College London, London SW7 2AZ, U.K.

2. CSIRO Manufacturing, Private Bag 10, Clayton South, Victoria 3169, Australia

Funder

Engineering and Physical Sciences Research Council

Commonwealth Scientific and Industrial Research Organisation

Publisher

American Chemical Society (ACS)

Subject

Materials Chemistry,Inorganic Chemistry,Polymers and Plastics,Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.macromol.7b00235

Reference47 articles.

1. A Low-Bandgap Diketopyrrolopyrrole-Benzothiadiazole-Based Copolymer for High-Mobility Ambipolar Organic Thin-Film Transistors

2. Highly Emissive Far Red/Near-IR Fluorophores Based on Borylated Fluorene-Benzothiadiazole Donor-Acceptor Materials

3. Thia- and selena-diazole containing polymers for near-infrared light-emitting diodes

4. A Conjugated Polymer for Near Infrared Optoelectronic Applications

5. Efficient organic solar cells processed from hydrocarbon solvents

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