Effect of Molecular Structure on Mesomorphism. 18.¹ Twin Dimers Having Methylene, Ethylene Oxide and Siloxane Spacers

David Creed, University of Southern Mississippi
John R.D. Gross, University of Southern Mississippi
Sarah L. Sullivan, University of Southern Mississippi
Anselm C. Griffin, University of Southern Mississippi
Charles E. Hoyle, University of Southern Mississippi

Abstract

Six Twin dimeric compounds having two rigid cores connected by a central spacer group are described. Two types of rigid units, 4-pentyloxyphenyl cinnamates and 4-cyano-4-oxybiphenyl, were employed. The spacer groups were pentamethylene (PM), diethylene oxide (EO) and disiloxane (DS). For each rigid core the nematic-isotropic temperature followed the order PM > EO > DS. Investigation of the ΔH and ΔS parameters for the nematic-isotropic (clearing) transition revealed that for these compounds the clearing transition was driven by ΔS. The EO mesogens have larger ΔS values than for the PM mesogens, which result in lowered clearing temperatures due to relatively constant ΔH values. The conformational preference for gauche isomers in the spacer of the EO compounds is seen as conducive to proper orientational alignment of the rigid cores in the nematic phase, better so than for the PM and DS spacers.