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Broadly Applicable Synthesis of Arylated Dithieno[3,2‐ b :2′,3′‐ d ]pyrroles as Building Blocks for Organic Electronic Materials
Author(s) -
Vogt Astrid,
Schwer Fabian,
Förtsch Sebastian,
Lorenz Christoph,
MenaOsteritz Elena,
Aubele Anna,
Kraus Teresa,
Bäuerle Peter
Publication year - 2021
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202101478
Subject(s) - cruciform , pyrrole , acceptor , organic solar cell , redox , chemistry , combinatorial chemistry , materials science , quantum chemical , organic chemistry , molecule , polymer , physics , composite material , condensed matter physics
A novel and versatile method for the N‐arylation of dithieno[3,2‐ b :2′,3′‐ d ]pyrrole (DTP) is presented. By Pd‐ or Cu‐catalyzed coupling a variety of arenes and acenes were directly attached at the DTP−nitrogen yielding a variety of functionalized DTPs. Investigations on optical and redox properties led to valuable structure‐property relationships, which were corroborated by quantum chemical calculations. Further functionalization and elongation of the conjugation of an acceptor‐substituted DTP was elaborated to result in complex cruciform‐type donor−acceptor oligomers, which were investigated and implemented in single material organic solar cells.