Why vertically π-expanded imidazo[1,2-a]pyridines are weak fluorescence emitters: experimental and computational studies

Photophysics of π-expanded analogs of imidazo[1,2-a]pyridine, a well-known heterocyclic compound, has been experimentally and theoretically studied. Two regioisomeric systems differing only in the arrangement of the benzene ring have shown different optical properties (electronic transition energies...

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Veröffentlicht in:Physical chemistry chemical physics : PCCP 2015-04, Vol.17 (14), p.8945-8950
Hauptverfasser: Banasiewicz, Marzena, Deperasińska, Irena, Makarewicz, Artur, Firmansyah, Dikhi, Gryko, Daniel T, Kozankiewicz, Bolesław
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container_issue 14
container_start_page 8945
container_title Physical chemistry chemical physics : PCCP
container_volume 17
creator Banasiewicz, Marzena
Deperasińska, Irena
Makarewicz, Artur
Firmansyah, Dikhi
Gryko, Daniel T
Kozankiewicz, Bolesław
description Photophysics of π-expanded analogs of imidazo[1,2-a]pyridine, a well-known heterocyclic compound, has been experimentally and theoretically studied. Two regioisomeric systems differing only in the arrangement of the benzene ring have shown different optical properties (electronic transition energies, fluorescence quantum yields and decay times). DFT calculations have been in agreement with experimental results. Low fluorescence quantum yields have been attributed to the S1→ T2 intersystem crossing channel. Additional computations predict architectures which should possess higher fluorescence quantum yields.
doi_str_mv 10.1039/c5cp00216h
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Channels
Computation
Decay
Electronics
Fluorescence
Heterocyclic compounds
Mathematical analysis
Optical properties
title Why vertically π-expanded imidazo[1,2-a]pyridines are weak fluorescence emitters: experimental and computational studies
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