Abstract
Series of ether-ester-substituted 1,4:3,6-dianhydrohexitols were synthesized and studied as chiral dopants to nematics as compositions with 4′-pentyl-4-cyanobiphenyl. The most helical twisting power was found for bis-esters. Lesser values were found for mixed ether-esters with certain configuration. Other ethers and ether-esters revealed noticeably smaller values. Supramolecular peculiarities of such systems and their role in helical twisting are discussed.
Acknowledgments
We thank the National Academy of Science of Ukraine for the financial support, grant no. 0110U000623.