ChemInform Abstract: MECHANISMS OF IONIC REACTIONS IN THE GAS PHASE. DISPLACEMENT REACTIONS AT CARBONYL CARBON

1978 ◽  
Vol 9 (37) ◽  
Author(s):  
J. K. PAU ◽  
J. K. KIM ◽  
M. C. CASERIO
Keyword(s):  
Gas Phase ◽  
Carbonyl Carbon ◽  
Phase Displacement ◽  
Displacement Reactions ◽  
Ionic Reactions

scholarly journals THE RELATIVE ACCEPTOR POWER OF BORON TRIHALIDES AND BORANE TOWARD TRIMETHYLAMINE

1963 ◽  
Vol 41 (11) ◽  
pp. 2898-2902 ◽  
Author(s):  
J. M. Miller ◽  
M. Onyszchuk
Keyword(s):  
Dipole Moment ◽  
Gas Phase ◽  
Theoretical Calculations ◽  
Phase Displacement ◽  
Infrared Measurements ◽  
Displacement Reactions

Gas phase displacement reactions of boron trihalides from their trimethylamine adducts show that the order of acceptor power is: BBr3 > BCl3 > BF3 > 1/2(B2H6). This order agrees with recent theoretical calculations and dipole moment, calorimetric, and infrared measurements on boron trihalide complexes with other reference bases.

The gas phase reactivity of the dimethylchloronium ion with alkylbenzenes

1981 ◽  
Vol 59 (15) ◽  
pp. 2412-2416 ◽  
Author(s):  
John A. Stone ◽  
Margaret S. Lin ◽  
Jeffrey Varah
Keyword(s):  
High Pressure ◽  
Gas Phase ◽  
Mass Spectrometer ◽  
Aromatic Hydrocarbons ◽  
Relative Rate ◽  
Ion Source ◽  
Nucleophilic Displacement ◽  
Rate Of Reaction ◽  
Displacement Reactions ◽  
Bonded Complexes

The reactivity of the dimethylchloronium ion with a series of aromatic hydrocarbons has been studied in a high pressure mass spectrometer ion source using the technique of reactant ion monitoring. Benzene is unreactive but all others, from toluene to mesitylene, react by CH3+ transfer to yield σ-bonded complexes. The relative rate of reaction increases with increasing exothermicity in line with current theories of nucleophilic displacement reactions.

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