Perfluoroalkylfullerenes

dc.bibliographicCitation.firstPage1051eng
dc.bibliographicCitation.issue2eng
dc.bibliographicCitation.journalTitleChemical reviews : CReng
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.rights.licenseACS AuthorChoiceeng
dc.rights.urihttps://pubs.acs.org/page/policy/authorchoice_termsofuse.htmleng
dc.subject.ddc540eng
dc.subject.otherChemical compoundseng
dc.subject.otherCrystallographyeng
dc.subject.otherDerivativeseng
dc.subject.otherFullereneseng
dc.subject.otherEndohedral metallofullereneseng
dc.subject.otherFluorous solventseng
dc.subject.otherFullerene derivativeeng
dc.subject.otherHexafluorobenzeneeng
dc.subject.otherHigher fullereneseng
dc.subject.otherOrganic solutionseng
dc.subject.otherPerfluoroalkylfullereneseng
dc.subject.otherPerfluorodecalineng
dc.subject.otherX ray crystallographyeng
dc.subject.otherfullerene derivativeeng
dc.subject.otheralkylationeng
dc.subject.otherchemistryeng
dc.subject.otherconformationeng
dc.subject.otherhalogenationeng
dc.subject.otherisolation and purificationeng
dc.subject.othernuclear magnetic resonance spectroscopyeng
dc.subject.otherquantum theoryeng
dc.subject.otherspectrofluorometryeng
dc.subject.otherX ray crystallographyeng
dc.subject.otherAlkylationeng
dc.subject.otherCrystallography, X-Rayeng
dc.subject.otherFullereneseng
dc.subject.otherHalogenationeng
dc.subject.otherMagnetic Resonance Spectroscopyeng
dc.subject.otherMolecular Conformationeng
dc.subject.otherQuantum Theoryeng
dc.subject.otherSpectrometry, Fluorescenceeng
dc.titlePerfluoroalkylfullereneseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIFWDeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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