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Asymmetric polymerization of N-vinylcarbazole with optically active anionic initiators

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Abstract

The anionic polymerization of N-vinylcarbazole (NVC) by using optically active anionic initiators such as the lithium salts of (S)-1-(9H-fluoren-2-yl)-4-isopropyl-4,5-dihydrooxazole ((S)-1-FIDH) and (S)-2-(9H-fluoren-2-yl)-4- isopropyl-4,5-dihydrooxazole ((S)-2-FIDH) and complexes of (-)-Sparteine with n-butylithium (n-BuLi-(-)-Sp) or fluorenyl lithium (FILi-(-)-Sp) was achieved. The yield and specific rotation of poly(N-vinylcarbazole)s (poly(NVC)s) were considerably affected by the molar ratio of (S)-FIDH to NVC. The highest yield and specific rotation were obtained with Li- (S)-1-FIDH as an initiator, with a molar ratio of monomer and initiator [M]/[I] = 10/1. The effects of the chiral initiators, type of solvent and the polymerization temperature were investigated. The obtained optical activity of polymers was attributed to asymmetric induction of the chiral initiators.

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Correspondence to Jing Cao  (曹靖).

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This work was financially supported by the open project program of Key Laboratory of Environmentally Friendly Chemistry and Applications of the Ministry of Education, China (No. 09HJYH04) and Xiangtan University Doctoral Scientific Research Fund.

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Hu, W., Cao, J., Huang, Yl. et al. Asymmetric polymerization of N-vinylcarbazole with optically active anionic initiators. Chin J Polym Sci 33, 1618–1624 (2015). https://doi.org/10.1007/s10118-015-1689-9

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  • DOI: https://doi.org/10.1007/s10118-015-1689-9

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