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- W2023793286 abstract "Abstract Selectively O-alkylated inositols of myo-, scyllo- and chiro-configuration allow detailed studies of the relationship between the substitution pattern in the cyclohexane ring and the liquid crystalline properties observed to be made for these mainly novel cyclic compounds containing hydroxyl functions. The types of thermotropic mesophase formed and containing hydrogen bonds are strongly influenced by the number and the stereochemical arrangement of both the hydroxyl groups and the alkyloxy chains, as well as by their positions on the cyclohexane ring. The mesophases of the various new inositol ethers have been studied by polarizing optical microscopy and differential scanning calorimetry, and are discussed here in comparison with known systems, as a function of the above mentioned structural factors." @default.
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- W2023793286 title "Substitution pattern and stereochemistry versus liquid crystalline behaviour [1]" @default.
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- W2023793286 doi "https://doi.org/10.1080/02678299308027826" @default.
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