scholarly journals Influence of Viscous Media on Charge Transfer Reactions

1986 ◽  
Vol 5 (6) ◽  
pp. 351-366 ◽  
Author(s):  
T. H. Tran-Thi ◽  
A. M. Koulkes-Pujo ◽  
J. C. Mialocq ◽  
G. Folcher

The influence of viscous H2O-Dextran media on two charge transfer reactions has been investigated using laser photolysis coupled with pico and nanosecond time resolved absorption spectroscopy.In the first case, a charge-transfer reaction from a solute (potassium ferrocyanide) to the solvent was studied and the electron solvation dynamics was followed. A solvation time delay, depending on the polymer concentration, is observed which indicates that electrons remain quasi-free for longer periods in these media.In the second case, the quenching process of the triplet state of an excited metallo porphyrin(ZnP4+) by an electron acceptor, methylviologen chloride (MV2+, 2 Cl–) is studied. The measured triplet quenching rate constant values decrease with increasing dextran concentration, but remain higher than those calculated, taking into account a simple viscosity effect. This result is explained in terms of a competition between a decay of the diffusion rate constants of (ZnP4+)* and MV2+ due to a viscosity effect and an enhanced cage effect around the ions (ZnP4+*, MV2+). Once formed, this last effect favours the charge transfer reaction.

1991 ◽  
Vol 69 (5) ◽  
pp. 581-583
Author(s):  
Stephen L. Howard ◽  
Jaiming Wang ◽  
Alan L. Rockwood

The crossed-beam method was used to investigate the charge-transfer reaction of CO+ (X2Σ+, ν = 0) with CO (X1Σ+, ν = 0). Scattering of CO+ demonstrates that several vibrational states are populated. At a collisional energy of 1.1 eV, transfer of translational energy to vibrational energy is shown to occur by changes of an even number of vibrational quanta.


2019 ◽  
Vol 205 ◽  
pp. 09008
Author(s):  
Changmin Lee ◽  
Taecheon Lyu ◽  
Cheol Ho Choi ◽  
Taiha Joo

Symmetry-breaking charge transfer reaction of 9,9’-bianthracene is driven exclusively by the rotational fluctuation of solvents, not including the inertial component in the solvation dynamics. Torsional motion and bond shortening during the reaction were observed.


1975 ◽  
Vol 53 (5) ◽  
pp. 680-687 ◽  
Author(s):  
Guy J. Collin ◽  
Pierre Ausloos

The [Formula: see text] ions formed in the photoionization of cyclohexane (resonance lines of argon: 11.6–11.8 eV) react with cyclic (C3 and C4) and unsaturated hydrocarbons by H2 transfer. This reaction is quantitative with propene, 1-butene, 1-pentene, 1,3-butadiene, and isobutene. This transfer is efficient only if there is a terminal double bond. There is ring opening with the C3 and C4 hydrocarbons. H atom transfer reactions are also observed between [Formula: see text] ions and several compounds and the structure of the radical formed in such a reaction is determined by chemical analysis. With cis-2-butene, there is only charge transfer reaction.


2014 ◽  
Vol 16 (26) ◽  
pp. 13008-13026 ◽  
Author(s):  
Yutaka Nagasawa ◽  
Hiroshi Miyasaka

In this perspective, we review the recent studies concerning the liquid structure and solvation dynamics of ionic liquids, and their influence upon electron transfer and charge transfer reactions.


1988 ◽  
Vol 89 (2) ◽  
pp. 859-865 ◽  
Author(s):  
J.‐K. Hwang ◽  
S. Creighton ◽  
G. King ◽  
D. Whitney ◽  
A. Warshel

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