Ultrafast Time-Resolved Emission and Absorption Spectra of meso-Pyridyl Porphyrins upon Soret Band Excitation Studied by Fluorescence Up-Conversion and Transient Absorption Spectroscopy

2016 ◽  
Vol 120 (35) ◽  
pp. 9410-9421 ◽  
Author(s):  
Yeduru Venkatesh ◽  
M. Venkatesan ◽  
B. Ramakrishna ◽  
Prakriti Ranjan Bangal
2006 ◽  
Vol 110 (25) ◽  
pp. 12766-12781 ◽  
Author(s):  
Michel Negrerie ◽  
Simona Cianetti ◽  
Marten H. Vos ◽  
Jean-Louis Martin ◽  
Sergei G. Kruglik

2021 ◽  
Author(s):  
Sergei V. Lepeshkevich ◽  
Igor V. Sazanovich ◽  
Marina V. Parkhats ◽  
Syargey N. Gilevich ◽  
Boris M. Dzhagarov

Picosecond to millisecond laser time-resolved transient absorption spectroscopy was used to study molecular oxygen (O2) rebinding and conformational relaxation following O2 photodissociation in the α and β subunits within human...


2016 ◽  
Vol 18 (21) ◽  
pp. 14644-14653 ◽  
Author(s):  
Adam S. Chatterley ◽  
Florian Lackner ◽  
Daniel M. Neumark ◽  
Stephen R. Leone ◽  
Oliver Gessner

Using femtosecond time-resolved extreme ultraviolet absorption spectroscopy, the dissociation dynamics of the haloalkane 1,2-dibromoethane (DBE) have been explored following strong field ionization by femtosecond near infrared pulses at intensities between 7.5 × 1013 and 2.2 × 1014 W cm−2.


2017 ◽  
Vol 21 (10) ◽  
pp. 646-657 ◽  
Author(s):  
B. Shivaprasad Achary ◽  
A. R. Ramya ◽  
Rajiv Trivedi ◽  
P. R. Bangal ◽  
L. Giribabu

We report here the design and synthesis of corrole-metallocene dyads consisting of a metallocene (either ferrocene (Dyad 1) or mixed sandwich [Formula: see text]-[C[Formula: see text]H[Formula: see text](COOH)]Co([Formula: see text]-C[Formula: see text]Ph[Formula: see text] (Dyad 2)) connected via an ester linkage at meso phenyl position. Both the dyads were characterized by [Formula: see text]H NMR, MALDI-TOF, UV-visible, fluorescence spectroscopies (steady-state, picosecond time-resolved), femtosecond transient absorption spectroscopy (fs-TA) and electrochemical methods. The absorption spectra of these dyads showed slight broadening and splitting of the Soret band that indicates a weak ground state interaction between the corrole macrocycle and metallocene part of the present donor–acceptor (D–A) system. However, in both the dyad systems, fluorescence emission of the corrole was quenched in polar solvents as compared to its parent compound 10-(4-hydroxyphenyl)-5,15-bis-(pentafluorophenyl ) corrole (Ph-Corr). The quenching was more pronounced in ferrocene derivatives than in cobaltocenyl derivatives. Transient absorption studies confirm the absence of photoinduced electron transfer from metallocene to correl for these dyad systems and the quenching of singlet state of corrole is found to enhance intersystem crossing due to heavy atom effect.


2006 ◽  
Vol 110 (45) ◽  
pp. 22872-22885 ◽  
Author(s):  
Dariusz M. Niedzwiedzki ◽  
James O. Sullivan ◽  
Tomáš Polívka ◽  
Robert R. Birge ◽  
Harry A. Frank

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