Functionalization of hydroxyl terminated polybutadiene with biologically active fluorescent molecule

dc.contributor.author Sankar, R. Murali
dc.contributor.author Saha, Subhadeep
dc.contributor.author Meera, K. Seeni
dc.contributor.author Jana, Tushar
dc.date.accessioned 2022-03-27T08:58:29Z
dc.date.available 2022-03-27T08:58:29Z
dc.date.issued 2009-11-01
dc.description.abstract A biologically active molecule, 2-chloro-4, 6-bis(dimethylamino)-1, 3, 5-triazine (CBDT), has been covalently attached at the terminal carbon atoms of the hydroxyl terminated polybutadiene (HTPB) backbone. The modification of HTPB backbone by CBDT molecule does not affect the unique physico-chemical properties such as fluidity, hydroxyl value and microstructure of the parent HTPB. The formation of hydrogen bonding between the terminal hydroxyl groups and the nitrogen atoms of triazine moiety is the driving force for the terminal attachment chemistry. The functionalized HTPB (HTPB-CBDT) shows a strong fluorescence emission at 385 nm. © Indian Academy of Sciences. © Indian Academy of Sciences.
dc.identifier.citation Bulletin of Materials Science. v.32(5)
dc.identifier.issn 02504707
dc.identifier.uri 10.1007/s12034-009-0075-z
dc.identifier.uri http://link.springer.com/10.1007/s12034-009-0075-z
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12192
dc.subject Biologically active HTPB
dc.subject Fluorescent active hydroxyl terminated polybutadiene
dc.subject Functionalization of polymers
dc.subject Hydroxyl terminated polybutadiene (HTPB)
dc.subject Intermolecular hydrogen bonding
dc.title Functionalization of hydroxyl terminated polybutadiene with biologically active fluorescent molecule
dc.type Journal. Article
dspace.entity.type
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