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Desymmetrization of Perylenediimide Bay Regions Using Selective Suzuki–Miyaura Reactions from Dinitro Substituted Derivatives
Author(s) -
Hruzd Mariia,
Rocard Lou,
Goujon Antoine,
Allain Magali,
Cauchy Thomas,
Hudhomme Piétrick
Publication year - 2020
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.202003420
Subject(s) - chemistry , desymmetrization , acceptor , structural isomer , conjugated system , reactivity (psychology) , planarity testing , combinatorial chemistry , catalysis , polymer chemistry , stereochemistry , organic chemistry , polymer , enantioselective synthesis , crystallography , medicine , physics , alternative medicine , pathology , condensed matter physics
Bay decoration of perylenediimide (PDI) is an attractive approach for tuning the optoelectronic properties of the dye as well as breaking backbone planarity, which provides the possibility of preventing the undesired formation of aggregates. This is usually performed through successive bis‐bromination of PDI and pallado‐catalyzed cross‐coupling, which leads to symmetric triads. We now describe an efficient synthetic strategy for desymmetrization of the accepting PDI core by starting from its bis‐nitration. To this end, Suzuki–Miyaura Couplings (SMC) were carried out on a mixture of 1,6‐ and 1,7‐dinitroPDI regioisomers to add triphenylamine donating moieties and obtain donor–acceptor–donor triads. Investigation of the reactivity of dinitro PDI derivatives toward SMC has allowed us to access unprecedented asymmetric π‐conjugated PDI‐centered triads. These 1,6‐ and 1,7‐PDI based triads, prepared as regioisomeric mixtures, were successfully separated and their spectroscopic, crystallographic and optoelectronic differences are reported.