Probing the excited state dynamics of a new family of Cu(i)-complexes with an enhanced light absorption capacity: excitation-wavelength dependent population of states through branching

2013 ◽  
Vol 15 (31) ◽  
pp. 13128 ◽  
Author(s):  
Panagiotis A. Papanikolaou ◽  
Nikolai V. Tkachenko
ChemPhysChem ◽  
2004 ◽  
Vol 5 (8) ◽  
pp. 1171-1177 ◽  
Author(s):  
Benjamin Dietzek ◽  
Raman Maksimenka ◽  
Gudrun Hermann ◽  
Wolfgang Kiefer ◽  
Jürgen Popp ◽  
...  

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

2014 ◽  
Vol 50 (87) ◽  
pp. 13304-13306 ◽  
Author(s):  
Darren Achey ◽  
Erinn C. Brigham ◽  
Brian N. DiMarco ◽  
Gerald J. Meyer

The Co(i) form of vitamin B12 was found to undergo excitation wavelength-dependent excited state electron transfer to TiO2.


1995 ◽  
Vol 69 (5) ◽  
pp. 2044-2055 ◽  
Author(s):  
G. Hastings ◽  
L.J. Reed ◽  
S. Lin ◽  
R.E. Blankenship

2020 ◽  
Author(s):  
Tomislav Rovis ◽  
Benjamin D. Ravetz ◽  
Nicholas E. S. Tay ◽  
Candice Joe ◽  
Melda Sezen-Edmonds ◽  
...  

We describe a new family of catalysts that undergo direct ground state singlet to excited state triplet excitation with IR light, leading to photoredox catalysis without the energy waste associated with intersystem crossing. The finding allows a mole scale reaction in batch using infrared irradiation.


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>


2019 ◽  
Author(s):  
Gergely Samu ◽  
R.A. Scheidt ◽  
A. Balog ◽  
C. Janáky ◽  
P.V. Kamat

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