Abstract
The gas-phase molecular structure of 6,6-dimethyl-1-oxa-spiro[2.5]octane has been investigated by joint analysis of the microwave spectrum and molecular mechanics calculations. Both experimental and theoretical data concur showing the presence of two stable conformational isomers having a chair cyclohexane ring. A set of structural parameters which reproduce the ground state rotational constants has been derived. The influence of 1,4 disubstitution is discussed in terms of deformations of the cyclohexane ring.
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