Perfluoroalkylfullerenes

dc.bibliographicCitation.firstPage1051eng
dc.bibliographicCitation.issue2eng
dc.bibliographicCitation.lastPage1105eng
dc.bibliographicCitation.volume115eng
dc.contributor.authorBoltalina, Olga V.
dc.contributor.authorPopov, Alexey A.
dc.contributor.authorKuvychko, Igor V.
dc.contributor.authorShustova, Natalia B.
dc.contributor.authorStrauss, Steven H.
dc.date.accessioned2022-06-30T06:09:52Z
dc.date.available2022-06-30T06:09:52Z
dc.date.issued2015
dc.description.abstractNew chemical derivatives that possess the greatest variety of addition patterns than any other class of fullerene derivatives represent an important addition to the existing classes of perfluorocarbons, that is, compounds that are composed only of the two types of atoms, carbon and fluorine. These include aromatic and aliphatic perfluorocarbons such as perfluorodecalin, perfluorononane, hexafluorobenzene, etc., which are important as fluorous solvents used in medicine. The propensity of perfluoroalkylfullerenes (PFAFs) to readily crystallize from organic solutions upon slow evaporation in open air provided a straightforward access to their molecular structures via X-ray crystallography. Another crucial aspect that ensures future success in the characterization of numerous PFAFs of higher fullerenes and endohedral metallofullerenes is the possibility to apply HPLC methodologies to the separation of product mixtures. PFAFs, especially those of C60 and C70, are unique fullerene derivatives in terms of the number of structurally characterized derivatives with different number of RF groups and different addition patterns.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/9315
dc.identifier.urihttps://doi.org/10.34657/8353
dc.language.isoengeng
dc.publisherWashington, DC : ACS Publ.eng
dc.relation.doihttps://doi.org/10.1021/cr5002595
dc.relation.essn1520-6890
dc.relation.ispartofseriesChemical reviews : CR 115 (2015), Nr. 2eng
dc.rights.licenseACS AuthorChoiceeng
dc.rights.urihttps://pubs.acs.org/page/policy/authorchoice_termsofuse.htmleng
dc.subjectChemical compoundseng
dc.subjectCrystallographyeng
dc.subjectDerivativeseng
dc.subjectFullereneseng
dc.subjectEndohedral metallofullereneseng
dc.subjectFluorous solventseng
dc.subjectFullerene derivativeeng
dc.subjectHexafluorobenzeneeng
dc.subjectHigher fullereneseng
dc.subjectOrganic solutionseng
dc.subjectPerfluoroalkylfullereneseng
dc.subjectPerfluorodecalineng
dc.subjectX ray crystallographyeng
dc.subjectfullerene derivativeeng
dc.subjectalkylationeng
dc.subjectchemistryeng
dc.subjectconformationeng
dc.subjecthalogenationeng
dc.subjectisolation and purificationeng
dc.subjectnuclear magnetic resonance spectroscopyeng
dc.subjectquantum theoryeng
dc.subjectspectrofluorometryeng
dc.subjectX ray crystallographyeng
dc.subjectAlkylationeng
dc.subjectCrystallography, X-Rayeng
dc.subjectFullereneseng
dc.subjectHalogenationeng
dc.subjectMagnetic Resonance Spectroscopyeng
dc.subjectMolecular Conformationeng
dc.subjectQuantum Theoryeng
dc.subjectSpectrometry, Fluorescenceeng
dc.subject.ddc540eng
dc.titlePerfluoroalkylfullereneseng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleChemical reviews : CReng
tib.accessRightsopenAccesseng
wgl.contributorIFWDeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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