Hydrogen fluoride orbital energies

The greater stability of the digonal vinyl cation 161 than of the bridged cation 162 would imply that, at least in the gas phase, race-mization is involved as stereochemical course of any reaction with nucleophiles since both lobes of the empty p-orbital of 161 are available for a nucleophilic attack. Efforts to rationalize (Bumelle, 1964) early reports of stereospecific trans addition to acetylene derivatives have recently been complemented by a theoretical calculation of the energy profile for addition of hydrogen fluoride to acetylene in the gas phase (Hopkinson et at., 1971). The results of these calculations suggest that the bridged cation is possibly a transition state and not an intermediate. 

In 1969, Thomas published two papers [11,12] in which a molecular structure theory was developed without invoking the Bom-Oppenheimer approximation. In these publications and two further papers published in 1970 [13,14], Thomas studied methane, ammonia, water and hydrogen fluoride adding the kinetic energy operators of the protons to the electronic hamiltonian and using Slater-type orbitals centered on the heavier nuclei for the protonic wave functions. Over the years, a number of authors [15-23] have attempted the development of a non-Bom-Oppenheimer theory of molecular structure, but problems of accuracy and/or feasibility remain for applications to arbitrary molecular systems. 

Hydrogen fluoride (HF) aqueous, pAa, 139 BDE, 76 geometry of, 32 orbital energies, 26 total energy, 29... 

Figure 1.10. A schematic representation of a few of the molecular orbital energies in hydrogen fluoride (HF). The sigma (o) and pi (ti) bonding relative positions are shown, but only the sigma (o ) antibonding orbital position is provided.

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