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B. Mossety-Leszczak, P. Wojciechowski, H. Galina, J. Ulański

The synthesis of epoxy monomers with mesogenie groups - RAPID COMMUNICATION

Polimery 2001, No 5, 374



Summary

A two-step synthesis was developed to prepare new types of diepoxy and diolefinic liquid crystalline (LC) monomers. The synthesis involved (i) esterification of 4-hydroxyphenyl-4-hydroxybenzoate or 4',4' -biphenol (I) with 4-pentenoic acid (II); (ii) epoxidation of the resulting diolefins with m-chloroperoxybenzoic acid. The structure of the resulting products was confirmed in terms of FTIR and 1H NMR spectra. A hot-stage polarizing microscope showed mesophases to occur in the monomers 2b, 3a and 3b (cf. scheme of reaction 1), but not in the produet of esterification of 1 with II. Differential scanning calorimetry and thermooptical analysis were used to determine (crystal to mesomorphic (LC), and LC to isotropic) phase transition temperatures (Table 1, Fig. 1).
Keywords: mesogenic groups, liquid crystalline epoxy monomers, esterification, epoxidation
B. Mossety-Leszczak, P. Wojciechowski, H. Galina, J. Ulański (151.8 KB)
The synthesis of epoxy monomers with mesogenie groups - RAPID COMMUNICATION