Correlation Function Formalism for Triplet Excited State Decay: Combined Spin–Orbit and Nonadiabatic Couplings

2013 ◽  
Vol 9 (2) ◽  
pp. 1132-1143 ◽  
Author(s):  
Qian Peng ◽  
Yingli Niu ◽  
Qinghua Shi ◽  
Xing Gao ◽  
Zhigang Shuai
RSC Advances ◽  
2020 ◽  
Vol 10 (23) ◽  
pp. 13442-13450
Author(s):  
Aimin Duan ◽  
Suosuo An ◽  
Jiadan Xue ◽  
Xuming Zheng ◽  
Yanying Zhao

The excited state decay process of N-heterocyclic compounds is attracting increasing attention due to their fundamental applications in pharmaceutical and biological sciences.


2018 ◽  
Vol 54 (87) ◽  
pp. 12329-12332 ◽  
Author(s):  
Yingjie Zhao ◽  
Ruomeng Duan ◽  
Jianzhang Zhao ◽  
Chen Li

Efficient triplet excited state production (57%) was observed for perylenemonoimide–phenothiazine compact electron donor–acceptor dyads based on spin–orbit charge transfer ISC.


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 ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document