NMR Studies of Hindered Rotation. The Diels-Alder Adduct of Phencyclone with Maleic Anhydride: Restricted Motion of Bridgehead Phenyls |
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Authors: | Ronnie Benshafrut Ronald Callahan Robert Rothchild |
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Affiliation: | 1. Hunter College, Chemistry Department , 695 Park Avenue, New York, NY, 10021;2. The City University of New York, John Jay College of Criminal Justice, Toxicology Research and Training Center, Science Department , 445 West 59th Street, New York, NY, 10019-1199;3. Doctoral Faculty , The Graduate School and University Center, City University of New York |
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Abstract: | 1H NMR studies at 300 MHz have been performed for the Diels-Alder adduct of phencyclone and maleic anhydride in CDCl3 at ambient temperatures. The 1D spectrum shows four equal (2H) intensity doublets in the aryl region (in addition to other absorptions) which is fully consistent with a slow exchange limit (SEL) spectrum of a system in which the unsubstituted bridgehead phenyls exhibit hindered rotation around the C(sp2)-C (sp3) bond on the NMR timescale. These protons are assigned to H-1,8 and H-4,5 of the phenanthrene moiety and to H-2′ and H-6′ of the phenvls based on the two-dimensional (2D) homonuclear chemical shift correlation spectrum (COSY) together with arguments regarding carbonyl and aromatic ring anisotropy. Full proton assignments are given. |
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Keywords: | Dynamic NMR 1H NMR One- and two-dimensional NMR COSY Restricted rotation Anisotropy |
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