Abstract
Figure 30 presents a summary of our findings concerning the prevailing or characteristic rotational isomers in the vapour phase of sulphone molecules. Looking for a characteristic pattern, the following observation may he made. Staggered forms prevail while eclipsed forms appear to he predominant when two double bonds (one of them S=0) may take a syn orientation. This is a very rough qualitative statement only, however, and there remain many important questions unanswered. It may be of interest to list some of them.
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© 1978 Springer-Verlag Berlin Heidelberg
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Hargittai, I. (1978). Conformational properties. In: Sulphone Molecular Structures. Lecture Notes in Chemistry, vol 6. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-93078-2_3
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DOI: https://doi.org/10.1007/978-3-642-93078-2_3
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