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Synthesis of boltorn 1,2,3-triazole dendrimers by click chemistry

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dc.contributor.author Sakhuja, Rajeev
dc.date.accessioned 2021-11-11T11:02:21Z
dc.date.available 2021-11-11T11:02:21Z
dc.date.issued 2009
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/pola.23427
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3393
dc.description.abstract Second-, third-, and fourth-generation hyperbranched aliphatic polyols namely Boltorn® H20, Boltorn H30, and Boltorn H40 were endcapped with azido and activated acetylenic groups in good to excellent yields (75–95%) following an acid catalyzed procedure. The resultant terminally functionalized dendritic azido and acetylenic groups undergo 1,3-dipolar cycloaddition using methyl (or ethyl) propiolate and benzyl azide, respectively, under catalytic or noncatalytic conditions below 40 °C to yield 1,2,3-triazole dendrimeric polymers in 82–95% yield, under extremely mild conditions that could be applied for compounds sensitive to acid, base, or heat. The dendritic azido and activated acetylenic derivatives may act as novel scaffolds to tune the mechanical properties of different polymers. en_US
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Chemistry en_US
dc.subject Synthesis en_US
dc.subject Boltorn 1,2,3-triazole en_US
dc.subject Click chemistry en_US
dc.title Synthesis of boltorn 1,2,3-triazole dendrimers by click chemistry en_US
dc.type Article en_US


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