Direct evidence of hydrogen-atom tunneling dynamics in the excited state hydrogen transfer (ESHT) reaction of phenol–ammonia clusters

2014 ◽  
Vol 16 (8) ◽  
pp. 3757 ◽  
Author(s):  
J. D. Rodríguez ◽  
M. G. González ◽  
L. Rubio-Lago ◽  
L. Bañares
2021 ◽  
Author(s):  
Christophe Jouvet ◽  
Mitsuhiko Miyazaki ◽  
Masaaki Fujii

A general model of excited state hydrogen transfer (ESHT) which unifies ESHT and the excited state proton transfer (ESPT) is presented from experimental and theoretical works on phenol–(NH3)n. The hidden role of ESPT is revealed.


2020 ◽  
Vol 56 (2) ◽  
pp. 201-204 ◽  
Author(s):  
Kinga E. Szkaradek ◽  
Petr Stadlbauer ◽  
Jiří Šponer ◽  
Robert W. Góra ◽  
Rafał Szabla

Formation of an excited-state complex enables ultrafast photorelaxation of dark nπ* states in GC and HC base pairs.


1999 ◽  
Vol 111 (24) ◽  
pp. 10747-10749 ◽  
Author(s):  
G. A. Pino ◽  
C. Dedonder-Lardeux ◽  
G. Grégoire ◽  
C. Jouvet ◽  
S. Martrenchard ◽  
...  

2004 ◽  
Vol 120 (21) ◽  
pp. 10101-10110 ◽  
Author(s):  
O. David ◽  
C. Dedonder-Lardeux ◽  
C. Jouvet ◽  
H. Kang ◽  
S. Martrenchard ◽  
...  

Science ◽  
2019 ◽  
Vol 366 (6463) ◽  
pp. 364-369 ◽  
Author(s):  
Nick Y. Shin ◽  
Jonathan M. Ryss ◽  
Xin Zhang ◽  
Scott J. Miller ◽  
Robert R. Knowles

Deracemization is an attractive strategy for asymmetric synthesis, but intrinsic energetic challenges have limited its development. Here, we report a deracemization method in which amine derivatives undergo spontaneous optical enrichment upon exposure to visible light in the presence of three distinct molecular catalysts. Initiated by an excited-state iridium chromophore, this reaction proceeds through a sequence of favorable electron, proton, and hydrogen-atom transfer steps that serve to break and reform a stereogenic C–H bond. The enantioselectivity in these reactions is jointly determined by two independent stereoselective steps that occur in sequence within the catalytic cycle, giving rise to a composite selectivity that is higher than that of either step individually. These reactions represent a distinct approach to creating out-of-equilibrium product distributions between substrate enantiomers using excited-state redox events.


2020 ◽  
Vol 739 ◽  
pp. 137030
Author(s):  
Yelechakanahalli Lingaraju Ramu ◽  
Kandigowda Jagadeesha ◽  
Tavarekere Shivalingaswamy ◽  
Mariyappa Ramegowda

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