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Detalle de: Single‐Electron Self‐Exchange between Cage Hydrocarbons and Their Radical Cations in the Gas Phase

Title Single‐Electron Self‐Exchange between Cage Hydrocarbons and Their Radical Cations in the Gas Phase
Abstract

We show that the radical cations of adamantane (C 10 H 16 .+ , 1 H .+ ) and perdeuteroadamantane (C 10 D 16 .+ , 1 D .+ ) are stable species in the gas phase. The radical cation of adamantylideneadamantane (C 20 H 28 .+ , 2 H .+ ) is also stable (as in solution). By using the natural 13 C abundances of the ions, we determine the rate constants for the reversible isergonic single‐electron transfer (SET) processes involving the dyads 1 H .+ / 1 H, 1 D .+ / 1 D and 2 H .+ / 2 H. Rate constants for the reaction 1 H .+ + 1 D⇄ 1 H+ 1 D .+ are also determined and Marcus’ cross‐term equation is shown to hold in this case. The rate constants for the isergonic processes are extremely high, practically collision‐controlled. Ab initio computations of the electronic coupling ( H DA ) and the reorganization energy ( λ ) allow rationalization of the mechanism of the process and give insights into the possible role of intermediate complexes in the reaction mechanism.

Apa Reference Guerrero, A., Herrero, R., Quintanilla, E., Dávalos, J.Z., Abboud, J.M., Coto, P.B. & Lenoir, D. (2010). Single‐Electron Self‐Exchange between Cage Hydrocarbons and Their Radical Cations in the Gas Phase. ChemPhysChem, 11(3), 713-721. 10.1002/cphc.200900824
Doi 10.1002/cphc.200900824
Publication Date 15 Feb 2010
Publication Type Article
Researcher Pedro Braña Coto
Ontology Structure-function relationship
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