Organic Triplet Sensitizer Library Derived from a Single Chromophore (BODIPY) with Long-Lived Triplet Excited State for Triplet–Triplet Annihilation Based Upconversion

2011 ◽  
Vol 76 (17) ◽  
pp. 7056-7064 ◽  
Author(s):  
Wanhua Wu ◽  
Huimin Guo ◽  
Wenting Wu ◽  
Shaomin Ji ◽  
Jianzhang Zhao
Keyword(s):  
Excited State ◽  
Triplet Excited State ◽  
Triplet Triplet Annihilation

Triplet excited state of diiodoBOPHY derivatives: preparation, study of photophysical properties and application in triplet–triplet annihilation upconversion

2016 ◽  
Vol 4 (8) ◽  
pp. 1623-1632 ◽  
Author(s):  
Caishun Zhang ◽  
Jianzhang Zhao
Keyword(s):  
Excited State ◽  
Absorption Spectroscopy ◽  
Transient Absorption ◽  
Photophysical Properties ◽  
Transient Absorption Spectroscopy ◽  
Triplet Excited State ◽  
Triplet Triplet Annihilation

A pyrrole-BF2-based chromophore (BOPHY) was used for the preparation of triplet photosensitizers and the photophysical properties were studied using transient absorption spectroscopy.

Triplet Excited State of BODIPY Accessed by Charge Recombination and Its Application in Triplet–Triplet Annihilation Upconversion

2017 ◽  
Vol 121 (40) ◽  
pp. 7550-7564 ◽  
Author(s):  
Kepeng Chen ◽  
Wenbo Yang ◽  
Zhijia Wang ◽  
Alessandro Iagatti ◽  
Laura Bussotti ◽  
...  
Keyword(s):  
Excited State ◽  
Charge Recombination ◽  
Triplet Excited State ◽  
Triplet Triplet Annihilation

scholarly journals Ultra long‐lived triplet excited state in water at room temperature: Insights on the molecular design of tridecafullerenes

2021 ◽  
Author(s):  
Javier Ramos-Soriano ◽  
Alfonso Pérez-Sánchez ◽  
Sergio Ramírez-Barroso ◽  
Beatriz M. Illescas ◽  
Khalid Azmani ◽  
...  
Keyword(s):  
Excited State ◽  
Room Temperature ◽  
Molecular Design ◽  
Triplet Excited State

scholarly journals Triplet energies and excimer formation in meta - and para -linked carbazolebiphenyl matrix materials

2015 ◽  
Vol 373 (2044) ◽  
pp. 20140446 ◽  
Author(s):  
Sergey A. Bagnich ◽  
Alexander Rudnick ◽  
Pamela Schroegel ◽  
Peter Strohriegl ◽  
Anna Köhler
Keyword(s):  
Excited State ◽  
Triplet State ◽  
Spectroscopic Investigation ◽  
Triplet Excited State ◽  
Conjugation Length ◽  
Triplet Energy ◽  
Excimer Formation

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.

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