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Synthesis and properties of bis(pyrrolidino)fullerenes bridged by a flexible alkyl-tether

dc.creatorKop, Tatjana
dc.creatorBjelaković, Mira S.
dc.creatorMilić, Dragana
dc.date.accessioned2018-11-22T00:31:47Z
dc.date.available2018-11-22T00:31:47Z
dc.date.issued2015
dc.identifier.issn0040-4020
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/1729
dc.description.abstractThe one-pot bistycloaddition of alkyl-tethered diglycines to C-60 provided five series of bridged bis(pyrrolidino)fullerenes with good regioselectivity, giving mainly cis-2 and cis-3 products. An influence of the bridge length and addition pattern on spectroscopic properties, as well as on the shape of hierarchically organized supramolecular structures was observed. Additional investigation of all synthesized compounds confirmed their strong in vitro antioxidant activity 4-10-fold better than the standard antioxidant vitamin C.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172002/RS//
dc.rightsrestrictedAccess
dc.sourceTetrahedron
dc.subjectFullereneen
dc.subjectBiscycloaddition regioselectivityen
dc.subjectSEMen
dc.subjectFOX methoden
dc.titleSynthesis and properties of bis(pyrrolidino)fullerenes bridged by a flexible alkyl-tetheren
dc.typearticle
dc.rights.licenseARR
dcterms.abstractМилић, Драгана; Бјелаковиц, Мира; Коп, Татјана;
dc.citation.volume71
dc.citation.issue29
dc.citation.spage4801
dc.citation.epage4809
dc.identifier.wos000357348100014
dc.identifier.doi10.1016/j.tet.2015.05.038
dc.citation.other71(29): 4801-4809
dc.citation.rankM22
dc.description.otherSupplementary material: [http://cherry.chem.bg.ac.rs/handle/123456789/3441]
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-84937152081


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