DOI | Resolve DOI: https://doi.org/10.1021/j100267a006 |
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Author | Search for: Ingold, K. U.1; Search for: Nonhebel, D.C.; Search for: Walton, J.C. |
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Affiliation | - National Research Council of Canada
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Format | Text, Article |
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Abstract | The electron paramagnetic resonance (EPR) spectra of CH3CH2C(CH3)2CH2· and CH3CH2C(CD3)2CH2· indicate that at 95 K these radicals exist in a rigid conformation with respect to rotation about the three Cβ-Cγ bonds and that the δ-methyl group (of the ethyl moiety) is gauche to one methyl and to the CH2· group. Analysis of the γ-H hyperfine splittings indicates that in the preferred conformation about the Cα-Cβ bond the SOMO eclipses one of the γ-methyl groups, not the γ-ethyl group. The internal rotation barriers of the CD3 and ethyl groups were estimated to be ca. 4 and 6 kcal/mol from the exchange broadening in the EPR spectra at higher temperatures. © 1985 American Chemical Society. |
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Publication date | 1985 |
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In | |
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Language | English |
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Peer reviewed | Yes |
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NPARC number | 21276623 |
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Export citation | Export as RIS |
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Report a correction | Report a correction (opens in a new tab) |
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Record identifier | 2197dc8b-1d23-4163-9b68-03b2260ea16e |
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Record created | 2015-10-13 |
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Record modified | 2020-03-17 |
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