Issue 48, 2017

Escape of anions from geminate recombination in THF due to charge delocalization

Abstract

Geminate recombination of 24 radical anions (M˙) with solvated protons (RH2+) was studied in tetrahydrofuran (THF) with pulse radiolysis. The recombination has two steps: (1) diffusion of M˙ and RH2+ together to form intimate (contact and solvent separated) ion pairs, driven by Coulomb attraction; (2) annihilation of anions due to proton transfer (PT) from RH2+ to M˙. The non-exponential time-dependence of the geminate diffusion was determined. For all molecules protonated on O or N atoms the subsequent PT step is too fast (<0.2 ns) to measure, except for the anion of TCNE which did not undergo proton transfer. PT to C atoms was as slow as 70 ns and was always slow enough to be observable. A possible effect of charge delocalization on the PT rates could not be clearly separated from other factors. For 21 of the 24 molecules studied here, a free ion yield (71.6 ± 6.2 nmol J−1) comprising ∼29% of the total, was formed. This yield of “Type I” free ions is independent of the PT rate because it arises entirely by escape from the initial distribution of ion pair distances without forming intimate ion pairs. Three anions of oligo(9,9-dihexyl)fluorenes, Fn˙ (n = 2–4) were able to escape from intimate ion-pairs to form additional yields of “Type II” free ions with escape rate constants near 3 × 106 s−1. These experiments find no evidence for an inverted region for proton transfer.

Graphical abstract: Escape of anions from geminate recombination in THF due to charge delocalization

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
28 авг 2017
Accepted
23 ное 2017
First published
24 ное 2017

Phys. Chem. Chem. Phys., 2017,19, 32272-32285

Escape of anions from geminate recombination in THF due to charge delocalization

H. Chen, A. R. Cook, S. Asaoka, J. S. Boschen, T. L. Windus and J. R. Miller, Phys. Chem. Chem. Phys., 2017, 19, 32272 DOI: 10.1039/C7CP05880B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements