Investigating polaron dynamics in PM6:Y6 films for use in organic photovoltaics using time-resolved infrared spectroscopy

Author(s):  
John R. Swartzfager ◽  
Guoyan Zhang ◽  
Stephen Wong ◽  
Enrique D. Gomez ◽  
John B. Asbury
2020 ◽  
Vol 22 (45) ◽  
pp. 26459-26467
Author(s):  
Jessica L. Klocke ◽  
Tilman Kottke

Flavin photoreduction in H2O is elucidated by developing a quantum cascade laser setup for time-resolved infrared spectroscopy on irreversible reactions.


2019 ◽  
Vol 33 (1) ◽  
pp. 1029-1033 ◽  
Author(s):  
Daniel Hallinan ◽  
Maria Grazia De Angelis ◽  
Marco Giacinti Baschetti ◽  
Giulio Sarti ◽  
Yossef A. Elabd

2021 ◽  
Vol 120 (3) ◽  
pp. 8a-9a
Author(s):  
Brennan Ashwood ◽  
Paul J. Sanstead ◽  
Qing Dai ◽  
Chuan He ◽  
Andrei Tokmakoff

1999 ◽  
Vol 274 (9) ◽  
pp. 5508-5513 ◽  
Author(s):  
Frithjof von Germar ◽  
Asier Galán ◽  
Oscar Llorca ◽  
Jose L. Carrascosa ◽  
Jose M. Valpuesta ◽  
...  

1995 ◽  
Vol 117 (41) ◽  
pp. 10311-10316 ◽  
Author(s):  
Andreas Barth ◽  
Karin Hauser ◽  
Werner Maentele ◽  
John E. T. Corrie ◽  
David R. Trentham

2008 ◽  
Vol 22 (2-3) ◽  
pp. 63-82 ◽  
Author(s):  
Andreas Barth

This review discusses the contribution of time-resolved infrared spectroscopy to the understanding of the Ca2+pump in the sarcoplasmic reticulum membrane of skeletal muscle cells (SERCA1a). The focus is on interactions of the substrate ATP with the ATPase and on the bond parameters of the phosphoenzyme phosphate group. Functional groups throughout the ATP molecule are important for stabilising the closed conformation of the ATP–ATPase complex and for fast phosphorylation of the ATPase. Dissociation of the reaction product ADP after phosphorylation leads to a more open average conformation of the enzyme and does not trigger the transition from the first phosphoenzyme Ca2E1P to the second E2P. The P–O bond between phosphate and aspartyl moieties is weaker in Ca2E1P and E2P than in acetyl phosphate in aqueous solution, which explains the high reactivity of the phosphoenzymes. This ground state property of the phosphoenzymes prepares for a phosphate transfer reaction with dissociative character.


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