Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5275
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dc.contributor.authorALURI, RAJENDRAen_US
dc.contributor.authorJAYAKANNAN, MANICKAMen_US
dc.date.accessioned2020-10-26T06:38:20Z-
dc.date.available2020-10-26T06:38:20Z-
dc.date.issued2015en_US
dc.identifier.citationPolymer Chemistry, 6(25), 4641-4649.en_US
dc.identifier.issn-en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5275-
dc.identifier.urihttps://doi.org/10.1039/c5py00602cen_US
dc.description.abstractWe report a novel one-pot ABB' synthetic route for linear polyester and hyperbranched poly(ester-urethane) s based on multi-functional L-amino acid monomers via a temperature selective melt polycondensation approach. L-Serine, D-serine and L-threonine amino acids were converted into multi-functional ABB' monomers (A = hydroxyl, B = carboxylic ester and B' = urethane). At 120 degrees C, the ABB' monomer underwent thermo-selective transesterification polycondensation (A reacted with B) to produce linear polyesters with B' functionality as the pendent functionality in each repeating units. At 150 degrees C, the ABB' monomer underwent dual ester-urethane self-polycondensation to produce new classes of hyperbranched poly(ester-urethane) s (A reacted with B and B'). Interestingly, the secondary hydroxyl group in the L-threonine monomer did not react at 120 degrees C; however, it became active at 150 degrees C to yield exclusively linear polyesters. The temperature selective polycondensation process was confirmed by appropriate model reactions and H-1 and C-13 NMR spectroscopic analysis. The role of the macrocyclic formation in the polycondensation process was also investigated by MALDI-TOF MS. The amino acid based new polymers were found to exhibit diverse molecular self-assembly. The linear polyesters adopted a beta-sheet conformation which produced a helical nano-fibrous morphology. The hyperbranched polymers underwent a globular coil-like conformation for spherical nano-particular assemblies. Both the secondary structure formation as well as their morphological features were confirmed by circular dichroism spectroscopy and electron and atomic microscopy analyses. The new one-pot synthetic pathway is versatile in making diverse linear and branched polymers based on natural L-amino acids with a nano-fibrous or a spherical morphology for future applications in biomedical and thermoplastic industries.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectCouple-Monomer Approachen_US
dc.subjectMechanistic Aspectsen_US
dc.subjectStep Synthesisen_US
dc.subjectL-Lysineen_US
dc.subjectPolyurethanesen_US
dc.subjectPolyetheren_US
dc.subjectTransetherificationen_US
dc.subjectPolymerizationen_US
dc.subjectArchitecturesen_US
dc.subject2015en_US
dc.titleOne-pot two polymers: ABB' melt polycondensation for linear polyesters and hyperbranched poly(ester-urethane)s based on natural L-amino acidsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitlePolymer Chemistryen_US
dc.publication.originofpublisherForeignen_US
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