Ultrafast fluorescence quenching by electron transfer and fluorescence from the second excited state of a charge transfer complex as studied by femtosecond up-conversion spectroscopy

1998 ◽  
Vol 109 (14) ◽  
pp. 5963-5970 ◽  
Author(s):  
Shinichiro Iwai ◽  
Shigeo Murata ◽  
M. Tachiya

2014 ◽  
Vol 43 (47) ◽  
pp. 17677-17693 ◽  
Author(s):  
Paul A. Scattergood ◽  
Milan Delor ◽  
Igor V. Sazanovich ◽  
Oleg V. Bouganov ◽  
Sergei A. Tikhomirov ◽  
...  




2017 ◽  
Vol 16 (12) ◽  
pp. 1801-1811 ◽  
Author(s):  
Mikhail V. Rusalov ◽  
Valery V. Volchkov ◽  
Vladimir L. Ivanov ◽  
Mikhail Ya. Melnikov ◽  
Ivan V. Shelaev ◽  
...  

The ultrafast photoinduced electron transfer in a supramolecular charge transfer complex was studied.



2019 ◽  
Vol 18 (1) ◽  
pp. 232-241 ◽  
Author(s):  
Valery V. Volchkov ◽  
Mikhail N. Khimich ◽  
Mikhail V. Rusalov ◽  
Fedor E. Gostev ◽  
Ivan V. Shelaev ◽  
...  

The relaxation scheme of the 1·3 singlet state excited by a 25 fs laser pulse was proposed. It includes very fast vibrational relaxation, and direct and back electron transfer resulting in complete fluorescence quenching.



2002 ◽  
Vol 67 (8) ◽  
pp. 1154-1164 ◽  
Author(s):  
Nachiappan Radha ◽  
Meenakshisundaram Swaminathan

The fluorescence quenching of 2-aminodiphenylamine (2ADPA), 4-aminodiphenylamine (4ADPA) and 4,4'-diaminodiphenylamine (DADPA) with tetrachloromethane, chloroform and dichloromethane have been studied in hexane, dioxane, acetonitrile and methanol as solvents. The quenching rate constants for the process have also been obtained by measuring the lifetimes of the fluorophores. The quenching was found to be dynamic in all cases. For 2ADPA and 4ADPA, the quenching rate constants of CCl4 and CHCl3 depend on the viscosity, whereas in the case of CH2Cl2, kq depends on polarity. The quenching rate constants for DADPA with CCl4 are viscosity-dependent but the quenching with CHCl3 and CH2Cl2 depends on the polarity of the solvents. From the results, the quenching mechanism is explained by the formation of a non-emissive complex involving a charge-transfer interaction between the electronically excited fluorophores and ground-state chloromethanes.



2021 ◽  
Author(s):  
Mandeep K. Chahal ◽  
Anuradha Liyanage ◽  
Ajyal Z. Alsaleh ◽  
Paul A. Karr ◽  
Jonathan P. Hill ◽  
...  

A new type of push–pull charge transfer complex, viz., a spiro-locked N-heterocycle-fused zinc porphyrin, ZnP-SQ, is shown to undergo excited state charge separation, which is enhanced by axial F− binding to the Zn center.



2018 ◽  
Vol 149 (24) ◽  
pp. 244107 ◽  
Author(s):  
Tianji Ma ◽  
Matteo Bonfanti ◽  
Pierre Eisenbrandt ◽  
Rocco Martinazzo ◽  
Irene Burghardt


2021 ◽  
Author(s):  
Federico Coppola ◽  
Paola Cimino ◽  
Umberto Raucci ◽  
Maria Gabriella Chiariello ◽  
Alessio Petrone ◽  
...  

We present electronic structure methods to unveil non-radiative pathways of photoinduced charge transfer (CT) reactions that play a main role in photophysics and light harvesting technologies. A prototypical π-stacked molecular...



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