scholarly journals Guest and solvent modulated photo-driven charge separation and triplet generation in a perylene bisimide cyclophane

2016 ◽  
Vol 7 (8) ◽  
pp. 5428-5434 ◽  
Author(s):  
Peter Spenst ◽  
Ryan M. Young ◽  
Michael R. Wasielewski ◽  
Frank Würthner

The modulation of the excited state dynamics in a perylene bisimide cyclophane was achieved by solvent and guest variation.

2009 ◽  
Vol 113 (42) ◽  
pp. 18358-18368 ◽  
Author(s):  
Nguyen Vân Anh ◽  
Felix Schlosser ◽  
Michiel M. Groeneveld ◽  
Ivo H. M. van Stokkum ◽  
Frank Würthner ◽  
...  

2009 ◽  
Vol 113 (29) ◽  
pp. 8202-8212 ◽  
Author(s):  
Natalie Banerji ◽  
Guillaume Duvanel ◽  
Alejandro Perez-Velasco ◽  
Santanu Maity ◽  
Naomi Sakai ◽  
...  

1997 ◽  
Vol 101 (51) ◽  
pp. 9828-9836 ◽  
Author(s):  
Robert W. J. Zijlstra ◽  
Piet Th. van Duijnen ◽  
Ben L. Feringa ◽  
Thomas Steffen ◽  
Koos Duppen ◽  
...  

2018 ◽  
Vol 20 (48) ◽  
pp. 30219-30230 ◽  
Author(s):  
Romain Letrun ◽  
Bernhard Lang ◽  
Oleksandr Yushchenko ◽  
Roland Wilcken ◽  
Denis Svechkarev ◽  
...  

Intramolecular charge separation and enhanced spin orbit coupling explain the weak fluorescence of a T-shaped dyad comprising two strong fluorophores.


ChemPhysChem ◽  
2015 ◽  
Vol 16 (8) ◽  
pp. 1757-1767 ◽  
Author(s):  
Minjung Son ◽  
Benjamin Fimmel ◽  
Volker Dehm ◽  
Frank Würthner ◽  
Dongho Kim

2017 ◽  
Vol 21 (02) ◽  
pp. 152-157 ◽  
Author(s):  
Won-Young Cha ◽  
Juwon Oh ◽  
Masaaki Kitano ◽  
Atsuhiro Osuka ◽  
Dongho Kim

Excited state dynamics of meso-arylethynyl-substituted subporphyrins can be tuned by 4-substituent at the arylethynyl group and solvent polarity. In polar acetonitrile, phenylethynyl subporphyrin 1 exhibited enhanced fluorescence, while (4-dimethylaminophenyl)ethynyl subporphyrin 2 showed red-shifted fluorescence from its charge-separated state and (4-nitrophenyl)ethynyl subporphyrin 3 displayed efficient fluorescence quenching due to charge separation.


2019 ◽  
Author(s):  
Matthew M. Brister ◽  
Carlos Crespo-Hernández

<p></p><p> Damage to RNA from ultraviolet radiation induce chemical modifications to the nucleobases. Unraveling the excited states involved in these reactions is essential, but investigations aimed at understanding the electronic-energy relaxation pathways of the RNA nucleotide uridine 5’-monophosphate (UMP) have not received enough attention. In this Letter, the excited-state dynamics of UMP is investigated in aqueous solution. Excitation at 267 nm results in a trifurcation event that leads to the simultaneous population of the vibrationally-excited ground state, a longlived <sup>1</sup>n<sub>O</sub>π* state, and a receiver triplet state within 200 fs. The receiver state internally convert to the long-lived <sup>3</sup>ππ* state in an ultrafast time scale. The results elucidate the electronic relaxation pathways and clarify earlier transient absorption experiments performed for uracil derivatives in solution. This mechanistic information is important because long-lived nπ* and ππ* excited states of both singlet and triplet multiplicities are thought to lead to the formation of harmful photoproducts.</p><p></p>


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