Dehydrogenation of icosahedral carborane anions via gas-phase collisional activation

2016 ◽  
Vol 30 (10) ◽  
pp. 1223-1227
Author(s):  
Omar M. Hamdy ◽  
Huong T. Pham ◽  
Scott G. McArthur ◽  
Vincent Lavallo ◽  
Ryan R. Julian
Keyword(s):  
Gas Phase ◽  
Collisional Activation ◽  
Carborane Anions

Collisional activation of captured intermediates in the gas-phase SN2 reaction chloride + bromomethane .fwdarw. bromide + chloromethane

1991 ◽  
Vol 113 (25) ◽  
pp. 9697-9699 ◽  
Author(s):  
Donna M. Cyr ◽  
Lynmarie A. Posey ◽  
Gregory A. Bishea ◽  
Chau Chung Han ◽  
Mark A. Johnson
Keyword(s):  
Gas Phase ◽  
Collisional Activation ◽  
Sn2 Reaction

Efficient isomerization of Si(C2H5)H2+ to Si(CH3)2H+ by collisional activation in the gas phase

1993 ◽  
Vol 12 (3) ◽  
pp. 621-623 ◽  
Author(s):  
R. Bakhtiar ◽  
C. M. Holznagel ◽  
D. B. Jacobson
Keyword(s):  
Gas Phase ◽  
Collisional Activation

Ionized ethylidene ketene and its homologue methylene ketene

1983 ◽  
Vol 61 (8) ◽  
pp. 1722-1724 ◽  
Author(s):  
Johan K. Terlouw ◽  
John L. Holmes ◽  
F. P. Lossing
Keyword(s):  
Mass Spectrum ◽  
Gas Phase ◽  
Collisional Activation ◽  
Heats Of Formation ◽  
Ionization Energies ◽  
Molecular Ion

The gas phase pyrolyses of crotonic and acrylic-trifluoroacetic anhydrides were shown to yield ethylidene ketene [CH3CH=C=C=O] and methylene ketene [CH2=C=C=O], respectively. The former was identified via the collisional activation mass spectrum of its molecular ion. The ionization energies of the two ketenes, 8.68 and 9.12 ± 0.05 eV respectively, measured using energy selected electrons, lead to 215 and 233 kcal mol−1 for their ionic heats of formation.

scholarly journals Experimental Determination of Activation Energies for Covalent Bond Formation via Ion/Ion Reactions and Competing Processes

2021 ◽  
Author(s):  
Melanie Cheung See Kit ◽  
Samantha O. Shepherd ◽  
James Prell ◽  
Ian Webb
Keyword(s):  
Gas Phase ◽  
Collisional Activation ◽  
Collision Cross Section ◽  
Bond Formation ◽  
Protein Structures ◽  
Covalent Bond ◽  
Activation Energies ◽  
Supporting Evidence ◽  
Simple Modification ◽  
Covalent Bond Formation

The combination of ion/ion chemistry with commercially available ion mobility/mass spectrometry systems has allowed rich structural information to be obtained for gaseous protein ions. Recently, the simple modification of such an instrument with an electrospray reagent source has allowed three-dimensional gas-phase interrogation of protein structures through covalent and non-covalent interactions coupled with collision cross section measurements. However, the energetics of these processes have not yet been studied quantitatively. In this work, previously developed Monte Carlo simulations of ion temperatures inside traveling wave ion guides are used to characterize the energetics of the transition state of activated ubiquitin cation/reagent anion long-lived complexes formed via ion/ion reactions. The ΔH<sup>‡</sup> and ΔS<sup>‡</sup> of major processes observed from collisional activation of long-lived gas phase ion/ion complexes, namely collision induced unfolding (CIU), covalent bond formation, or neutral loss of the anionic reagent via intramolecular proton transfer, were determined. Covalent bond formation via ion/ion complexes was found to be significantly lower energy compared to unfolding and bond cleavage. ΔG<sup>‡</sup> of activation of all three processes lie between 55 and 75 kJ/mol, easily accessible with moderate collisional activation. Bond formation is favored over reagent loss at lower activation energies, whereas reagent loss becomes competitive at higher collision energies. Though ΔG<sup>‡</sup> are between CIU of a precursor ion and covalent bond formation of its ion/ion product complex are comparable, our data suggest covalent bond formation does not require extensive isomerization, supporting evidence from previous structural studies that these ion/ion reactions measure compact gas phase structures.

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