Author: C. H. Watson
Publisher:
ISBN:
Category :
Languages : en
Pages : 28
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Collision induced dissociation and infrared multiphoton dissociation of ions formed in di- and triethylamine, di- and tri-n-propylamine, and diisopropylamine were investigated by Fourier transform ion cyclotron resonance mass spectrometry. Molecular ions of all amines except di-n-propylamine produced similar fragment ions when subjected to either dissociation technique. The initial fragmentation involved C(alpha)-C(beta) bond cleavage, loss of an alkyl radical, and formation of an immonium ion. Subsequent fragmentations of the immonium ions produced by both dissociation mechanisms involved McLafferty type rearrangements and loss of alkenes. The molecular ion of di-n-propylamine fragmented by a different mechanism when subjected to infrared irradiation. Protonated molecules of di- and tri-n-propylamine yielded C3H6 and an ammonium ion upon infrared multiphoton dissociation, while protonated molecules of the other amines did not dissociate using this technique. Collision induced dissociation, on the other hand, produced fragmentation for all protonated molecules. Explanation of the different fragmentations observed for the two dissociation techniques is given in terms of a mechanism involving a tight transition state for protonated di- and tri-n-propylamine dissociation. Keywords: Infrared Multiphoton Dissociation; Collision Induced Dissociation; Alkylamines; Fourier Transform Ion Cyclotron Resonance Mass Spectrometry.
Author:
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ISBN:
Category : Aeronautics
Languages : en
Pages :
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Author: Clifford Hunter Watson
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ISBN:
Category : Ion cyclotron resonance spectrometry
Languages : en
Pages : 304
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Author:
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ISBN:
Category : Science
Languages : en
Pages : 1278
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Author:
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ISBN:
Category : Government reports announcements & index
Languages : en
Pages : 900
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Author: Cindy Linea Berrie
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ISBN:
Category :
Languages : en
Pages : 210
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Author: Alexander Baldwin Young
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ISBN:
Category : Water
Languages : en
Pages : 226
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Author: Stephen Gee Anderson
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ISBN:
Category : Collision spectroscopy
Languages : en
Pages : 636
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Author: Alex Andrew Nickel
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ISBN:
Category : Electronic books
Languages : en
Pages : 398
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Energy-resolved competitive threshold collision-induced dissociation (TCID) measurements for radical species relevant to combustion were made using a guided ion beam tandem mass spectrometer. These ion thermochemistry methods can be used to obtain thermochemical properties of these neutral radicals through the use of thermochemical cycles. The high reactivity of radical species often makes them challenging to directly measure. Study of the peroxyformate anion (HC(O)OO−) revealed a singlet-triplet crossing in the oxygen-oxygen bond dissociation channel. Analysis of the thresholds gives the first experimentally determined enthalpies of formation for both peroxyformic acid and the peroxyformyl radical. We have also studied the TCID of linear and branched hexanol (C6H13OH) complexed with fluoride and acetylide to determine their gas-phase acidities. The role of conformation on the gas-phase acidities of 1-hexanol and 3, 3-dimethyl-1-butanol was explored using modified microcanonical statistical rate theory (RRKM) models with internal rotations treated as one-dimensional hindered rotors. These six-carbon primary alcohols have the same “intrinsic” gas-phase acidity, defined as deprotonation without conformational relaxation, but differ in observed acidity due to conformational stabilization of the anion.
Author: American Chemical Society, Committee on Professional Training Staff
Publisher:
ISBN: 9780841214187
Category : Science
Languages : en
Pages : 1390
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