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Synthesis, Characterization and Photophysical Studies of D‐π‐A Based Conjugated Triphenylamine Derivatives

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Abstract We synthesized a new series of intramolecular charge transfer (ICT) molecules by attaching very strong electron‐withdrawing groups to a triphenylamine backbone. ICT interactions can be found for all the triphenylamine (TPA) derivatives due to the electron withdrawing properties of the cyanide on the end terminal triphenylamine moiety. When introducing the electron withdrawing group on the TPA moiety giving rise to efficient emission tuning from blue to green in polar solvents, due to the increase in ICT interactions which results in the bathochromically shifted ICT band observed. Further, from these results, we found that all the compounds exhibit intensive ICT interactions leading to substantial extension of their absorption spectral response.
Title: Synthesis, Characterization and Photophysical Studies of D‐π‐A Based Conjugated Triphenylamine Derivatives
Description:
Abstract We synthesized a new series of intramolecular charge transfer (ICT) molecules by attaching very strong electron‐withdrawing groups to a triphenylamine backbone.
ICT interactions can be found for all the triphenylamine (TPA) derivatives due to the electron withdrawing properties of the cyanide on the end terminal triphenylamine moiety.
When introducing the electron withdrawing group on the TPA moiety giving rise to efficient emission tuning from blue to green in polar solvents, due to the increase in ICT interactions which results in the bathochromically shifted ICT band observed.
Further, from these results, we found that all the compounds exhibit intensive ICT interactions leading to substantial extension of their absorption spectral response.

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