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N-Octadecyl-N′-maleoyl-L-phenylalanine(ODMA-L-Phe)was synthesized through the condensation,deprotection and acid- ylation reaction of BOC-L-phenylalauine,octadecylamine and maleic anhydride,ODMA-L-Phe can self-assemble in some organic solvents and turned them into thermally reversible physical supramolecular organogels.The morphology of ODMA-L-Phe aggregates was characterized by polarized optical microscopy(POM)and field emission scanning electron microscope(FE-SEM). The aggregates of ODMA-L-Phe were needle-like fibrils with diameters of approximately 100-200 nm.The mechanism of ODMA- L-Phe serf-assembly in organic solvents was investigated using ~1H NMR and circular dichroism(CD).The results indicated that hydrogen bonding was one of the main driving forces for the self-assembly of ODMA-L-Phe.
N-Octadecyl-N’-maleoyl-L-phenylalanine (ODMA-L-Phe) was synthesized through the condensation, deprotection and acid-reaction reaction of BOC-L-phenylalauine, octadecylamine and maleic anhydride, -assemble in some organic solvents and turned them into thermally reversible physical supramolecular organisms. The morphology of ODMA-L-Phe aggregates was characterized by polarized optical microscopy (POM) and field emission scanning electron microscope (FE-SEM) -L-Phe were needle-like fibrils with diameters of approximately 100-200 nm. The mechanism of ODMA-L-Phe serf-assembly in organic solvents was investigated using 1H NMR and circular dichroism (CD). The results indicated that hydrogen bonding was one of the main driving forces for the self-assembly of ODMA-L-Phe.