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Synthesis and Properties of Azadipyrromethene‐Based Complexes with Nitrile Substitution
Author(s) -
Wang Chunlai,
Daddario Cassie,
Pejić Sandra,
Sauvé Geneviève
Publication year - 2020
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201901736
Subject(s) - nitrile , chemistry , substituent , electron acceptor , electron affinity (data page) , electron donor , fluorine , substitution (logic) , cyclic voltammetry , photochemistry , medicinal chemistry , stereochemistry , electrochemistry , organic chemistry , molecule , catalysis , electrode , computer science , programming language
Azadipyrromethene (ADP)‐based complexes have gained interest due to their strong absorption in the visible to near‐IR region and high electron affinity. Attempts to increase their electron accepting properties by electron withdrawing group substitutions have been limited. We previously found that substitution with fluorine at the p ‐distal phenyls or at the p ‐pyrrolic‐phenylethynyls of ADP do not shift reduction potentials and thus have no effect on electron affinity. This could be because fluorine also acts as pi‐donor, thus, a pi‐acceptor substituent may have a greater impact on the energy levels. To test this hypothesis, we synthesized three new ADP‐based complexes with nitrile substitutions. Cyclic voltammetry shows that the nitrile substitutions indeed anodically shifts the reduction potentials, leading to increased electron affinity. The shift was ≈ 0.3 V for the p ‐distal phenyl substitution and 0.16V for the p ‐phenylethynyl substitution. Nitrile substitution was also found to improve electron accepting ability and electron mobility in diodes, as compared to the un‐substituted analogues.