Fluorine and alkyl substituent effects on the gas-phase Lewis acidities of boranes by ion cyclotron resonance spectroscopy

1977 ◽  
Vol 16 (10) ◽  
pp. 2437-2443 ◽  
Author(s):  
M. K. Murphy ◽  
J. L. Beauchamp
Keyword(s):  
Gas Phase ◽  
Cyclotron Resonance ◽  
Substituent Effects ◽  
Alkyl Substituent ◽  
Resonance Spectroscopy ◽  
Ion Cyclotron Resonance ◽  
Ion Cyclotron

ChemInform Abstract: GAS PHASE PROTON AFFINITIES OF CARBONYL COMPOUNDS BY ION CYCLOTRON RESONANCE SPECTROSCOPY

1973 ◽  
Vol 4 (33) ◽  
pp. no-no
Author(s):  
PAULO C. ISOLANI ◽  
JOSE M. RIVEROS ◽  
PETER W. TIEDEMANN
Keyword(s):  
Gas Phase ◽  
Carbonyl Compounds ◽  
Cyclotron Resonance ◽  
Resonance Spectroscopy ◽  
Ion Cyclotron Resonance ◽  
Proton Affinities ◽  
Ion Cyclotron

ChemInform Abstract: ACIDITY, BASICITY, AND ION-MOLECULE REACTIONS OF ARSINE IN THE GAS PHASE BY ION CYCLOTRON RESONANCE SPECTROSCOPY

1974 ◽  
Vol 5 (32) ◽  
pp. no-no
Author(s):  
R. H. WYATT ◽  
D. HOLTZ ◽  
T. B. MCMAHON ◽  
J. L. BEAUCHAMP
Keyword(s):  
Gas Phase ◽  
Cyclotron Resonance ◽  
Resonance Spectroscopy ◽  
Ion Cyclotron Resonance ◽  
Ion Molecule Reactions ◽  
Ion Cyclotron

Nucleophilic reactions of anions with PF3 and OPF3 in the gas phase by ion cyclotron resonance spectroscopy

1978 ◽  
Vol 17 (6) ◽  
pp. 1589-1595 ◽  
Author(s):  
S. A. Sullivan ◽  
J. L. Beauchamp
Keyword(s):  
Gas Phase ◽  
Cyclotron Resonance ◽  
Resonance Spectroscopy ◽  
Ion Cyclotron Resonance ◽  
Nucleophilic Reactions ◽  
Ion Cyclotron

Thermodynamic control in the reactions of gas phase anions. An abinitio and ion cyclotron resonance study of the reactions of anions with diborane

1985 ◽  
Vol 63 (2) ◽  
pp. 281-287 ◽  
Author(s):  
O. Elsenstein ◽  
M. Kayser ◽  
M. Roy ◽  
T. B. McMahon
Keyword(s):  
Gas Phase ◽  
Cyclotron Resonance ◽  
Reaction Pathway ◽  
Basis Set ◽  
Resonance Spectroscopy ◽  
Ion Cyclotron Resonance ◽  
Ion Molecule Reactions ◽  
Ion Cyclotron ◽  
Reaction Channels ◽  
Gas Phase Ion

The gas phase ion molecule reactions of a number of anions, X−, with diborane, B2H6 have been investigated using ion cyclotron resonance spectroscopy. Two distinct reaction channels are observed in addition to simple proton transfer. The first of these is production of BH4− and BH2X while the second is formation of BH3X− and BH3. In order to determine the importance of thermodynamic factors in the course of reaction abinitio calculations have been carried out on the species involved to obtain the relative stabilities of the two possible pairs of products. The 4-31 +G basis set incorporating additional flat s and p functions has been used since this basis set has been demonstrated to give the most accurate description of anions to date. The results obtained indicate that the thermochemical factors are instrumental in determining the reaction pathway.

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