Regioselective Bond Cleavage in the Dissociative Electron Transfer to Benzyl Thiocyanates:  The Role of Radical/Ion Pair Formation

2006 ◽  
Vol 128 (20) ◽  
pp. 6595-6604 ◽  
Author(s):  
Emad M. Hamed ◽  
Hanh Doai ◽  
Christopher K. McLaughlin ◽  
Abdelaziz Houmam

2017 ◽  
Vol 875 ◽  
pp. 082002
Author(s):  
M. Kelley ◽  
S. Buathong ◽  
F. B. Dunning


2008 ◽  
Vol 47 (16) ◽  
pp. 7121-7132 ◽  
Author(s):  
Svetlana Begel ◽  
Peter Illner ◽  
Simon Kern ◽  
Ralph Puchta ◽  
Rudi van Eldik


2020 ◽  
Vol 32 (6) ◽  
pp. 1379-1383
Author(s):  
L. Devaraj Stephen ◽  
S.G. Gunasekaran ◽  
M. Soundarrajan

Reduction of CoIII centre in CoIII(pn)2(Cl)(L)2+ with reference to solvent medium and structure of the complex via ion pair charge transfer (IPCT) paves way for the novel reaction mechanism route. In this work, we prepared, characterized and photoinduced the complexes CoIII(pn)2(Cl)(L)2+ (where L = RC6H4NH2, R = m-OMe, p-F and H) in the presence of iodide ion. Quantum yield for 254 nm excitation of CoIII(pn)2(Cl)(L)2+(where L = RC6H4NH2, R = m-OMe, p-F and H) in water-1,4-dioxane mixtures (Diox = 0, 5, 10, 15, 20, 25, and 30% (v/v)) were also derived for all the complexes in presence of added iodide ion, in which CoIII was reduced via [CoIII(pn)2(Cl)(L)2+….. I-] ion-pair formation. The photoinduced state is ion-pair charge transfer transition state and the quantum efficiency is solvent reliant and they are non-reactive. That is, change in ΦCo(II) is dependable with observed increase in xDiox of the mixed solvent medium. Correlation analysis using empirical parameters εr, Y, ET N and DNN provides a model to understand the solvent medium participation and interaction. This work gains an insight into the role of aqueous-organic solvent medium in CoIII(pn)2(Cl)(L)2+ photoreduction, which may be of great significance in developing novel approaches in the field of high performance catalysis



1996 ◽  
Vol 51 (9) ◽  
pp. 1222-1228 ◽  
Author(s):  
Hans Bock ◽  
Markus Kleine

UV/VIS and ESR spectra of electron transfer reaction products in aprotic (cH⊕ < 0,1 ppm) solution can be measured in an especially designed and sealed glass apparatus and provide information on unknown facets of the microscopic pathway through the network of interdependent equilibria. For tetraphenyl-p-benzoquinone in tetrahydrofuran, single-electron reduction by a sodium metal mirror produces a red solution and, unexpectedly, after addition of 2.2.2. cryptand, contact with a potassium metal mirror generates a green (!) one. For both, ESR/ENDOR spectra prove the presence of tetraphenyl-p-benzoquinone radical anion. UV/VIS measurements provide the clue: In the equilibrium revealed by repetetive spectra recording, M·⊖solv + Me⊕solv ⇄ [M·⊖···Me⊖]solv, the radical anion is green (vm = 16900 cm-1) and the contact ion pair red (vm=18900 cm-1 ). On ion pair formation, therefore, the excitation energy of the radical anion increases by 0.25 eV.



2020 ◽  
Vol 56 (45) ◽  
pp. 6058-6061 ◽  
Author(s):  
Dili R. Subedi ◽  
Habtom B. Gobeze ◽  
Yuri E. Kandrashkin ◽  
Prashanth K. Poddutoori ◽  
Art van der Est ◽  
...  

Radical ion-pair energy as high as 1.48 eV with lifetime as much as ∼1 μs, exclusively from the triplet excited state of a photosensitizer, is established in a novel donor–acceptor conjugate.



2017 ◽  
Vol 146 (18) ◽  
pp. 184307 ◽  
Author(s):  
M. Kelley ◽  
S. Buathong ◽  
F. B. Dunning


2019 ◽  
Vol 7 ◽  
Author(s):  
Mónica Mendes ◽  
Beatriz Pamplona ◽  
Sarvesh Kumar ◽  
Filipe Ferreira da Silva ◽  
Antonio Aguilar ◽  
...  


2013 ◽  
Vol 139 (4) ◽  
pp. 044311 ◽  
Author(s):  
S. Marggi Poullain ◽  
K. Veyrinas ◽  
P. Billaud ◽  
M. Lebech ◽  
Y. J. Picard ◽  
...  


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