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dc.contributor.authorAndrikopoulos, B
dc.contributor.authorSidhu, PK
dc.contributor.authorTaggert, B
dc.contributor.authorNathanael, JG
dc.contributor.authorO'Hair, RAJ
dc.contributor.authorWille, U
dc.date.accessioned2020-12-03T23:51:03Z
dc.date.available2020-12-03T23:51:03Z
dc.date.issued2020-01-01
dc.identifier.citationAndrikopoulos, B., Sidhu, P. K., Taggert, B., Nathanael, J. G., O'Hair, R. A. J. & Wille, U. (2020). Reaction of Distonic Aryl and Alkyl Radical Cations with Amines: The Role of Charge and Spin Revealed by Mass Spectrometry, Kinetic Studies, and DFT Calculations. ChemPlusChem, 85 (1), pp.195-206. https://doi.org/10.1002/cplu.201900706.
dc.identifier.issn2192-6506
dc.identifier.urihttp://hdl.handle.net/11343/252773
dc.description.abstractGas‐phase reaction of the aromatic distonic radical cations 4‐Pyr+. and 3‐Pyr+. with amines led to formation of the corresponding amino pyridinium ions 4‐Pyr+NR2 and 3‐Pyr+NR2 through amine addition at the site of the radical, followed by homolytic β‐fragmentation. The reaction efficiencies range from 66–100 % for 4‐Pyr+. and 57–86 % for 3‐Pyr+., respectively, indicating practically collision‐controlled processes in some cases. Computational studies revealed that the combination of positive charge and spin makes nucleophilic attack by the amine at the site of the radical barrierless and strongly exothermic by about 175±15 kJ mol−1, thereby rendering ‘conventional’ radical pathways through hydrogen abstraction or addition onto π systems less important. Exemplary studies with 4‐Pyr+. showed that this reaction can be reproduced in solution. A similar addition/radical fragmentation sequence occurs also in the gas‐phase reaction of amines with the aliphatic distonic radical cation Oxo+C., showing that the observed charge‐spin synergism is not limited to aromatic systems.
dc.languageEnglish
dc.publisherWiley
dc.titleReaction of Distonic Aryl and Alkyl Radical Cations with Amines: The Role of Charge and Spin Revealed by Mass Spectrometry, Kinetic Studies, and DFT Calculations
dc.typeJournal Article
dc.identifier.doi10.1002/cplu.201900706
melbourne.affiliation.departmentSchool of Chemistry
melbourne.source.titleChemPlusChem
melbourne.source.volume85
melbourne.source.issue1
melbourne.source.pages195-206
melbourne.elementsid1430173
melbourne.internal.embargodate2021-01-01
melbourne.contributor.authorWille, Uta
melbourne.contributor.authorO'Hair, Richard
melbourne.contributor.authorNathanael, Joses
melbourne.contributor.authorTaggert, Bethany
dc.identifier.eissn2192-6506
melbourne.accessrightsOpen Access


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