Thionine–graphene oxide covalent hybrid and its interaction with light

2017 ◽  
Vol 19 (22) ◽  
pp. 14412-14423 ◽  
Author(s):  
Ewelina Krzyszkowska ◽  
Justyna Walkowiak-Kulikowska ◽  
Sven Stienen ◽  
Aleksandra Wojcik
Keyword(s):  
Electron Transfer ◽  
Graphene Oxide ◽  
Excited State ◽  
Transfer Process ◽  
Singlet Excited State ◽  
Functionalized Graphene ◽  
Electron Transfer Process ◽  
Functionalized Graphene Oxide ◽  
Back Electron Transfer

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

scholarly journals Electron transfer by singlet excited state of porphyn and electron acceptor affinity in rigid medium: photoacoustic phase angle analysis

1997 ◽  
Vol 22 (0) ◽  
pp. 83-92
Author(s):  
Marinônio Lopes CORNÉLIO
Keyword(s):  
Electron Transfer ◽  
Excited State ◽  
Phase Behavior ◽  
Electron Acceptor ◽  
Transfer Process ◽  
Spectral Region ◽  
Optical Excitation ◽  
Singlet Excited State ◽  
Electron Transfer Process ◽  
Excitation Process

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.

scholarly journals Two-electron transfer stabilized by excited-state aromatization

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Jinseok Kim ◽  
Juwon Oh ◽  
Seongchul Park ◽  
Jose L. Zafra ◽  
Justin R. DeFrancisco ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Excited State ◽  
Excited States ◽  
Transfer Process ◽  
Comprehensive Understanding ◽  
Electron Transfer Process ◽  
Photoactive Materials ◽  
Donor Acceptor ◽  
Scientific Significance

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.

scholarly journals Excited state structural dynamics of 4-cyano-4′-hydroxystilbene: deciphering the signatures of proton-coupled electron transfer using ultrafast Raman loss spectroscopy

2019 ◽  
Vol 21 (40) ◽  
pp. 22409-22419 ◽  
Author(s):  
Reshma Mathew ◽  
Surajit Kayal ◽  
Adithya Lakshmanna Yapamanu
Keyword(s):  
Electron Transfer ◽  
Excited State ◽  
Structural Dynamics ◽  
Transfer Process ◽  
Electron Transfer Process ◽  
Proton Coupled Electron Transfer

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.

Excited-state dynamics and electron transfer process of 1,3,5-triamino-2,4,6-trinitrobenzene

RSC Advances ◽  
2016 ◽  
Vol 6 (60) ◽  
pp. 55560-55567 ◽  
Author(s):  
Genbai Chu ◽  
Feng Lu ◽  
Jianting Xin ◽  
Tao Xi ◽  
Min Shui ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Excited State ◽  
Transfer Process ◽  
Efficient Tool ◽  
Electron Transfer Process ◽  
Excited State Dynamics ◽  
Transfer Processes ◽  
Nitro Explosives ◽  
Electron Transfer Processes

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

Surface photochemistry: Semiconductor mediated reactions of some saturated strained hydrocarbons

1988 ◽  
Vol 66 (7) ◽  
pp. 1579-1588 ◽  
Author(s):  
N. Colin Baird ◽  
Anthony M. Draper ◽  
Paul de Mayo
Keyword(s):  
Electron Transfer ◽  
Quantum Yield ◽  
Transfer Process ◽  
Radical Cations ◽  
Thermal Reaction ◽  
Electron Transfer Process ◽  
Electron Transfer Mechanism ◽  
Valence Isomerization ◽  
Back Electron Transfer

Quadricyclane (1) and 1,8-bishoniocubane (2) have been found to undergo valence isomerization to norborndiene and tricyclo[4.2.2.02,5]deca-3,7-diene, respectively, on illuminated CdS and ZnO. An electron transfer mechanism is proposed. Quantum yield, solvent effects, the role of oxygen, and the quenching of the reaction were investigated, and were consistent with this interpretation. The thermal reaction of 1 on CdS was also suggested to be an electron transfer process involving, in this case, defects or trapped holes on the surface of the semiconductor. An examination of a series of strained hydrocarbons structurally related to 1 (tetracyclo[3.3.0.02,8.04,6]octane 3, pentacyclo[4.3.0.02,4.03.805,7]nonane 4 and pentacyclo[4.4.0.02,4.03,8.05,7]decane 5) resulted, largely, in a demonstration of the resistance of their respective radical cations to rearrangement prior to back electron transfer. Calculations by MNDO, in combination with a modified version of MM2, were used to explore the differences in the reactivity of the radical cations of 1, 3, 4, 5, and an interpretation is presented.

scholarly journals Ultrafast Excited-State Dynamics of Diketopyrrolopyrrole (DPP)-Based Materials: Static versus Diffusion-Controlled Electron Transfer Process

2015 ◽  
Vol 119 (28) ◽  
pp. 15919-15925 ◽  
Author(s):  
Qana A. Alsulami ◽  
Shawkat M. Aly ◽  
Subhadip Goswami ◽  
Erkki Alarousu ◽  
Anwar Usman ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Excited State ◽  
Transfer Process ◽  
Electron Transfer Process ◽  
Excited State Dynamics ◽  
Diffusion Controlled

scholarly journals Ion Selective Electrode Mediated by Transfer Layer of Graphene Oxide for Detection of Ca2+ with Highly Sensitivity and Selectivity

2022 ◽  
Author(s):  
Yuandong Liu ◽  
Liming Zhang ◽  
Jingwen Mo ◽  
Yi Zhou ◽  
Yang Tian
Keyword(s):  
Electron Transfer ◽  
Graphene Oxide ◽  
Detection Limit ◽  
Carbon Fiber ◽  
Transfer Process ◽  
Selective Electrode ◽  
Transfer Layer ◽  
Electron Transfer Process ◽  
Enhanced Sensitivity ◽  
Sensitivity And Selectivity

Abstract A Ca2+ selective microelectrode was proposed through electrodepositing graphene oxide (GO) on carbon fiber as an efficient ion-electron transfer layer. The gold leaves were further synthesized at GO surface to increase the specific surface area and provide a substrate for assembly of the specific ligands for Ca2+. GO with negative charges greatly facilitated the electron transfer process from the recognition center to electrode surface, resulting in the apparently enhanced sensitivity towards Ca2+. Moreover, the developed ion-selective microelectrode exhibited good selectivity to Ca2+, and a good linear range from 10 μM to 10 mM with a detection limit of 5.91±0.46 μM.

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