Morphology dependence of the triplet excited state formation and absorption in polyfluorene

2005 ◽  
Vol 71 (24) ◽  
Author(s):  
Anna Hayer ◽  
Amena L. T. Khan ◽  
Richard H. Friend ◽  
Anna Köhler
2015 ◽  
Vol 17 (43) ◽  
pp. 29090-29096 ◽  
Author(s):  
Dawn M. Marin ◽  
Sonia Payerpaj ◽  
Graham S. Collier ◽  
Angy L. Ortiz ◽  
Gaurav Singh ◽  
...  

Singly halogenated carbomethoxyphenylporphyrins show decreased singlet fluorescence lifetimes and increased rates of triplet excited state formation.


2018 ◽  
Vol 20 (12) ◽  
pp. 8016-8031 ◽  
Author(s):  
Mikhail A. Filatov ◽  
Safakath Karuthedath ◽  
Pavel M. Polestshuk ◽  
Susan Callaghan ◽  
Keith J. Flanagan ◽  
...  

Heavy atom-free BODIPY–anthracene dyads show triplet excited state formation via PeT, controlled by molecular rotation and environmental polarity.


2014 ◽  
Vol 43 (40) ◽  
pp. 14942-14948 ◽  
Author(s):  
Hans Moons ◽  
Andrei Loas ◽  
Sergiu M. Gorun ◽  
Sabine Van Doorslaer

Anaerobic red-light illumination leads to reduction of perfluoroisopropyl-substituted zinc(ii) phthalocyanine in ethanol, while low power UV illumination favours the formation of a triplet excited state.


2021 ◽  
Author(s):  
Javier Ramos-Soriano ◽  
Alfonso Pérez-Sánchez ◽  
Sergio Ramírez-Barroso ◽  
Beatriz M. Illescas ◽  
Khalid Azmani ◽  
...  

Author(s):  
Sergey A. Bagnich ◽  
Alexander Rudnick ◽  
Pamela Schroegel ◽  
Peter Strohriegl ◽  
Anna Köhler

We present a spectroscopic investigation on the effect of changing the position where carbazole is attached to biphenyl in carbazolebiphenyl (CBP) on the triplet state energies and the propensity to excimer formation. For this, two CBP derivatives have been prepared with the carbazole moieties attached at the ( para ) 4- and 4 ′ -positions ( p CBP) and at the ( meta ) 3- and 3 ′ -positions ( m CBP) of the biphenyls. These compounds are compared to analogous m CDBP and p CDBP, i.e. two highly twisted carbazoledimethylbiphenyls, which have a high triplet energy at about 3.0 eV and tend to form triplet excimers in a neat film. This torsion in the structure is associated with localization of the excited state onto the carbazole moieties. We find that in m CBP and p CBP, excimer formation is prevented by localization of the triplet excited state onto the central moiety. As conjugation can continue from the central biphenyls into the nitrogen of the carbazole in the para -connected p CBP, emission involves mainly the benzidine. By contrast, the meta -linkage in m CBP limits conjugation to the central biphenyl. The associated shorter conjugation length is the reason for the higher triplet energy of 2.8 eV in m CBP compared with the 2.65 eV in p CBP.


Author(s):  
Dariane Clerici Jornada ◽  
Rafael de Queiroz Garcia ◽  
Carolina Hahn da Silveira ◽  
Lino Misoguti ◽  
Cleber Renato Mendonça ◽  
...  

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