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Ion/molecule reactions of naphthalene and 1-chloronaphthalene radical cations

โœ Scribed by Wan Yong Feng; Chava Lifshitz


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
533 KB
Volume
152
Category
Article
ISSN
0168-1176

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๐Ÿ“œ SIMILAR VOLUMES


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Radical cations were produced by y-irradiation of solutes in zeolites at 77 K. The radical cation of tetramethylethylene (TME) was examined by EPR in a variety of zeolites at different temperatures and loading. The TME monomer radical cation, the TME dimer radical cation and the neutral radical form

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Hexamethylethane (HME) and trimethylbutane (TMB) radical cations produced in ZSM-5 zeolite by y radiolysis undergo an elimination process followed by an ion-molecule reaction. The tetramethylethylene radical cation intermediate formed by CH, elimination from TMB+' is observed directly in the tempera

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Isomeric C 5 H 5 N โ…ฯฉ and C 6 H 7 N โ…ฯฉ radical cations were allowed to interact with various neutral reagents in the quadrupole collision chamber of a six sector magnetic deflection type tandem mass spectrometer. Using CH 3 SSCH 3 , CH 3 OH, or H 2 O, iso-C 3 H 7 I, and tert-C 4 H 9 NC as substrates

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The ESR spectrum of the radical cation of 1,4-bis(methylthio)naphthalene is reported together with the efficiency of its formation in sulfuric acid. The concentration of radical species, obtained from the ESR measurements is used to determine the extinction coefficients of the electronic spectrum in