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Nuclear Quadrupole Resonance and Stereochemistry II. Vicinal cis- and trans-dichloro derivatives of carbocyclic systems

✍ Scribed by Ziba Ardalan; Edwin A. C. Lucken; S. Masson


Book ID
102251436
Publisher
John Wiley and Sons
Year
1973
Tongue
German
Weight
313 KB
Volume
56
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The ^35^Cl quadrupole resonance frequencies of sets of isomeric vicinal dichloro derivatives of carbocyclic molecules are presented. In all cases except one – cis‐ and trans‐1, 2‐dichloro‐acenaphthene – the configuration has only a small effect on the resonance frequency. This implies that the frequency‐differences in cyclic α‐chloroethers reported in Part I of this series [1] are indeed due to a specific interaction with the oxygen atom. The difference between the acenaphthenes may be due to hyperconjugation between the CCl bond and the aromatic system.