Conformational properties

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


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.


Conformational Property Benzyl Chloride Phenyl Isocyanate Electron Diffraction Data Experimental Electron Diffraction 
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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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