THE CONFORMATIONS OF THE DIASTEREOMERIC 2,5-DIMETHYL-2,5-DIMETHOXY-3,4-DIPHENYLHEXANES
- 1 July 1959
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 37 (7) , 1132-1145
- https://doi.org/10.1139/v59-168
Abstract
The electric dipole moments of six possible rotamers comprising the two diastereomeric forms of 2,5-dimethyl-2,5-dimethoxy-3,4-diphenylhexane have been calculated vectorially. Comparison of these values with the experimental determination of polarization in benzene and carbon tetrachloride shows that only two of the rotamers of the dd,ll form and only one of the meso form are present in significant amount. The moment of the dd,ll diastereomer decreases with increasing temperature but that of the meso form is almost invariant. It is probable that all six central linkages in these diastereomers are hindered from free rotation.Keywords
This publication has 6 references indexed in Scilit:
- THE ELECTRICAL POLARIZATIONS OF BIS-MERCURIALSCanadian Journal of Chemistry, 1958
- SOME ANOMALOUS ELECTRICAL POLARIZATIONSCanadian Journal of Chemistry, 1958
- Interpretation of Abnormalities in Atom Polarization in Terms of Electric MomentJournal of the American Chemical Society, 1957
- ROTAMERISM DURING DEMETHYLATION OF THE 2,5-DIMETHOXY-2,5-DIMETHYL-3,4-DIPHENYLHEXANESCanadian Journal of Chemistry, 1954
- REACTIONS OF THE STILBENE-DISODIUM AND -DILITHIUM ADDUCTSThe Journal of Organic Chemistry, 1953
- THE METHOXYMERCURATION OF 2-METHYL-1-PHENYLPROPENE-1Canadian Journal of Chemistry, 1952