Addition Reaction of Allylic Stannanes to the Triplet Excited State of C60 via Photoinduced Electron Transfer Process Leading to Asymmetric Hybridization Chemistry for Fullerene Terpenoid

Synlett ◽  
2004 ◽  
Vol 1 (01) ◽  
pp. 85-87 ◽  
Author(s):  
Koichi Mikami ◽  
Shoji Matsumoto ◽  
Takayuki Tonoi ◽  
Tomoyoshi Suenobu ◽  
Akito Ishida ◽  
...  
2017 ◽  
Vol 19 (22) ◽  
pp. 14412-14423 ◽  
Author(s):  
Ewelina Krzyszkowska ◽  
Justyna Walkowiak-Kulikowska ◽  
Sven Stienen ◽  
Aleksandra Wojcik

Quenching of the thionine singlet excited state in covalently functionalized graphene oxide with an efficient back electron transfer process.


2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Jinseok Kim ◽  
Juwon Oh ◽  
Seongchul Park ◽  
Jose L. Zafra ◽  
Justin R. DeFrancisco ◽  
...  

Abstract The scientific significance of excited-state aromaticity concerns with the elucidation of processes and properties in the excited states. Here, we focus on TMTQ, an oligomer composed of a central 1,6-methano[10]annulene and 5-dicyanomethyl-thiophene peripheries (acceptor-donor-acceptor system), and investigate a two-electron transfer process dominantly stabilized by an aromatization in the low-energy lying excited state. Our spectroscopic measurements quantitatively observe the shift of two π-electrons between donor and acceptors. It is revealed that this two-electron transfer process accompanies the excited-state aromatization, producing a Baird aromatic 8π core annulene in TMTQ. Biradical character on each terminal dicyanomethylene group of TMTQ allows a pseudo triplet-like configuration on the 8π core annulene with multiexcitonic nature, which stabilizes the energetically unfavorable two-charge separated state by the formation of Baird aromatic core annulene. This finding provides a comprehensive understanding of the role of excited-state aromaticity and insight to designing functional photoactive materials.


2003 ◽  
Vol 90 (1-3) ◽  
pp. 256-263 ◽  
Author(s):  
E.Vélez López ◽  
G.Pina Luis ◽  
J.L. Suárez-Rodrı́guez ◽  
I.A. Rivero ◽  
M.E. Dı́az-Garcı́a

1997 ◽  
Vol 22 (0) ◽  
pp. 83-92
Author(s):  
Marinônio Lopes CORNÉLIO

Photoacoustic spectroscopy provides information about both amplitude and phase of the response of a system to an optical excitation process. This paper presents the studies of the phase in the electron transfer process between octaethylporphyn (OEP) and quinone molecules dispersed in a polymeric matrix. It was observed a tendency in the phase behavior to small values only in the spectral region near to 620 nm, while for shorter wavelength did not show any tendency. These measurements suggested that the electron transfer to acceptor occurred with the participation of octaethylporphyn singlet excited state.


2019 ◽  
Vol 21 (40) ◽  
pp. 22409-22419 ◽  
Author(s):  
Reshma Mathew ◽  
Surajit Kayal ◽  
Adithya Lakshmanna Yapamanu

The photo-initiated proton-coupled electron transfer process in the 4-cyano-4′-hydroxystilbene–tert-butylamine adduct strongly affects the excited-state structural dynamics of CHSB.


2007 ◽  
Vol 13 (6) ◽  
pp. 1709-1714 ◽  
Author(s):  
Yu Chen ◽  
Mohamed E. El-Khouly ◽  
Xiao-Dong Zhuang ◽  
Nan He ◽  
Yasuyuki Araki ◽  
...  

2001 ◽  
Vol 340 (3-4) ◽  
pp. 232-236 ◽  
Author(s):  
Christoph J Brabec ◽  
Gerald Zerza ◽  
Giulio Cerullo ◽  
Sandro De Silvestri ◽  
Silvia Luzzati ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (60) ◽  
pp. 55560-55567 ◽  
Author(s):  
Genbai Chu ◽  
Feng Lu ◽  
Jianting Xin ◽  
Tao Xi ◽  
Min Shui ◽  
...  

Insights into the excited-state dynamics and electron transfer processes of nitro explosives offer an efficient tool for unravelling ultrafast and complex detonation physics.


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