Tunable Organogelator from Alkyl-Polypeptide Diblock Prepared by Ring-Opening Polymerization
Keyword(s):
Three alkyl-polypeptide hybrid amphiphiles were synthesized by the ring-opening polymerization (ROP) of γ-(2-methoxyethoxy)esteryl-l-glutamate N-carboxyanhydride (l-EG1Glu NCA) using alkylamine, i.e. C6H13NH2, C14H29NH2, and C16H33NH2, as initiators. As-prepared alkyl-poly-l-EG1Glu hybrids were found to form clear organogels in several organic solvents at low concentration. FTIR and circular dichroism characterizations suggested that poly-l-EG1Glu formed a predominantly β-sheet conformation, which accounted for the gelation. Transmission electron and atomic force microscopy characterizations revealed that these copolymers formed nanoribbon structures in THF.
2021 ◽
pp. 1759-1829
1995 ◽
Vol 262
(1)
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pp. 221-233
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2019 ◽
Vol 561
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pp. 194-200
2018 ◽
pp. 185-211
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