Trend in the Electron Affinities of Fluorophenyl Radicals ·C6H5-xFx (1 ≤ x ≤ 4)
Author:
Affiliation:
1. Department of Chemistry, Indiana University, 800 East Kirkwood Avenue, Bloomington, Indiana 47405, United States
Funder
Division of Chemistry
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.3c04327
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5. Temporary Anion States and Dissociative Electron Attachment to Isothiocyanates
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2. Predicting the increase in electron affinity of phenoxy upon fluorination;Journal of Fluorine Chemistry;2024-07
3. Isomer-Dependent Electron Affinities of Fluorophenyl Radicals, •C6H5–xFx (2 ≤ x ≤ 4);Journal of the American Chemical Society;2024-03-05
4. Predicting the Increase in Electron Affinity of Phenoxy Upon Fluorination;2024
5. Anion Photoelectron Imaging Spectroscopy of C6HF5–, C6F6–, and the Absence of C6H2F4–;The Journal of Physical Chemistry A;2023-10-10
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