Conformational properties

  • István Hargittai
Part of the Lecture Notes in Chemistry book series (LNC, volume 6)

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.

Keywords

Benzene Phenyl Benzyl Diamine Isothiocyanate 

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Copyright information

© Springer-Verlag Berlin Heidelberg 1978

Authors and Affiliations

  • István Hargittai
    • 1
  1. 1.Central Research Institute of ChemistryHungarian Academy of SciencesBudapestHungary

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