Optimizing stability through conformational locking and ring fusion modulation in organic semiconductors-Reference-Cited by-同舟云学术

Optimizing stability through conformational locking and ring fusion modulation in organic semiconductors

Published:2024 Issue:29 Volume:15 Page:3010-3017
ISSN:1759-9954
Container-title:Polymer Chemistry
language:en
Short-container-title:Polym. Chem.

Author:

Attar Salahuddin S.¹,Bademci Bahattin²,Barłóg Maciej¹,Sredojević Dušan¹³,Al-Thani Hessa¹,Dudley Sandra²^ORCID,Kakosimos Konstantinos¹,Bazzi Hassan S.⁴,Sajjad Muhammad Tariq²^ORCID,Al-Hashimi Mohammed¹^ORCID

Affiliation:

1. Department of Chemical Engineering, Texas A&M University at Qatar, P.O. Box 23874, Doha, Qatar

2. School of Engineering, London South Bank University, 103 Borough Road, London, SE1 0AA, UK

3. Vinča Institute of Nuclear Sciences – National Institute of the Republic of Serbia, University of Belgrade, Centre of Excellence for Photoconversion, P.O. Box 522, 11001 Belgrade, Serbia

4. Division of Arts and Science, Texas A&M University at Qatar, Education City, Doha, P.O. Box 23874, Qatar

Abstract

S,N-Heteroacene-type fused tetrathienophenanthroline monomer was synthesized via intramolecular cyclization, an alternative to the raditional benzodithiophene-4,8-dione units in high-performance photovoltaic materials.

Funder

Qatar National Research Fund

London South Bank University

British Council

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/PY/D4PY00246F

Reference38 articles.

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2. An n -Type All-Fused-Ring Molecule with Narrow Bandgap

3. All-fused-ring small molecule acceptors with near-infrared absorption

4. Design of All-Fused-Ring Electron Acceptors with High Thermal, Chemical, and Photochemical Stability for Organic Photovoltaics

5. S,N-Heteroacenes Up to a Tridecamer