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dc.creatorKop, Tatjana
dc.creatorBjelaković, Mira
dc.creatorDordevic, Jelena
dc.creatorZekic, Andrijana
dc.creatorMilić, Dragana
dc.date.accessioned2019-01-30T17:47:50Z
dc.date.available2019-01-30T17:47:50Z
dc.date.issued2015
dc.identifier.issn2046-2069
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/1829
dc.description.abstractTwo different alpha,omega-diglicynes linked by linear polyoxaalkyl chains in the presence of formaldehyde underwent Prato reaction to the fullerene C-60. The shorter linker templated formation of only cis-bisadducts, while the longer one afforded a mixture of four bisadducts (all cis and the equatorial) and difullerene dumbbell compound. Their structures were confirmed by the extensive analysis of the spectral data and molecular symmetry, as well. All compounds expressed an ability to arrange into hierarchically ordered supramolecular aggregates, the form of which depended both on the addition pattern and the spacer structure. The attenuated electron-accepting affinity, examined by cyclic voltammetry was in agreement with diminished delocalization of the pi-electronic system. In addition, all compounds exerted a notable radical scavenging activity.en
dc.publisherRoyal Soc Chemistry, Cambridge
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172002/RS//
dc.rightsopenAccess
dc.sourceRSC Advances
dc.titleFulleropyrrolidines derived from dioxa- and trioxaalkyl-tethered diglycinesen
dc.typearticle
dc.rights.licenseBY-NC
dcterms.abstractЗекиц, Aндријана; Коп, Татјана; Милиц, Драгана; Бјелаковић, Мира; Дордевиц, Јелена;
dc.citation.volume5
dc.citation.issue115
dc.citation.spage94599
dc.citation.epage94606
dc.citation.other5(115): 94599-94606
dc.citation.rankM21
dc.identifier.doi10.1039/c5ra17392b
dc.identifier.rcubConv_3444
dc.identifier.fulltexthttp://cer.ihtm.bg.ac.rs//bitstream/id/8270/1827.pdf
dc.identifier.scopus2-s2.0-84946945297
dc.identifier.wos000364906600010
dc.type.versionpublishedVersion


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