Приказ основних података о документу

dc.creatorKop, Tatjana
dc.creatorBjelaković, Mira
dc.creatorMilić, Dragana
dc.date.accessioned2019-01-30T17:43:42Z
dc.date.available2019-01-30T17:43:42Z
dc.date.issued2015
dc.identifier.issn0040-4020
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/1631
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.publisherOxford : Pergamon-Elsevier Science Ltd
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.abstractБјелаковић, Мира; Коп, Татјана; Милиц, Драгана;
dc.citation.volume71
dc.citation.issue29
dc.citation.spage4801
dc.citation.epage4809
dc.citation.other71(29): 4801-4809
dc.citation.rankM22
dc.identifier.doi10.1016/j.tet.2015.05.038
dc.identifier.scopus2-s2.0-84937152081
dc.identifier.wos000357348100014
dc.type.versionpublishedVersion


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Приказ основних података о документу