Theoretical Study of Substituent Effects on the Lewis Acid−Base Property of Aminoboranes
- 23 June 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry A
- Vol. 104 (28) , 6649-6655
- https://doi.org/10.1021/jp0007742
Abstract
No abstract availableThis publication has 45 references indexed in Scilit:
- Theoretical Study of the Effects of Structure and Substituents on Reactivity in AllylborationThe Journal of Organic Chemistry, 1998
- Quantum Mechanical Methods and the Interpretation and Prediction of Pericyclic Reaction MechanismsThe Journal of Physical Chemistry A, 1997
- Reactions of (CF 3 ) 2 BNMe 2 with ω‐Halonitriles — Crystal and Molecular Structure of [ cyclo ‐C 3 H 4 (CN)](CF 3 ) 2 B·NHMe 2European Journal of Inorganic Chemistry, 1996
- Theoretical studies of boranamine and its conjugate base. Comparison of the boron-nitrogen and boron-phosphorus .pi. bond energiesInorganic Chemistry, 1993
- Intermolecular interactions from a natural bond orbital, donor-acceptor viewpointChemical Reviews, 1988
- The methyl/trifluoromethyl substitution effect in boranes. A gas-phase electron diffraction and vibrational study of bis(dimethylamino)-(trifluoromethyl)borane and dimethylaminobis(trifluoromethyl)boraneJ. Chem. Soc., Dalton Trans., 1987
- An aspect of substituents and peripheral structures in chemical reactivities of moleculesThe Journal of Physical Chemistry, 1986
- Coupled fragment molecular orbital method for interacting systemsJournal of the American Chemical Society, 1981
- Solvent effects on internal rotation about the B-N bond in aminoboranes as studied by proton magnetic resonance spectroscopyMagnetic Resonance in Chemistry, 1971
- Electronic structure of aminoborane: a comparison between non-empirical and semiempirical theoretical methodsJ. Chem. Soc. A, 1969