THE USE OF THE HELLMANN–FEYNMAN THEOREM TO CALCULATE MOLECULAR ENERGIES

1960 ◽  
Vol 38 (11) ◽  
pp. 2117-2127 ◽  
Author(s):  
Richard F. W. Bader

The Hellmann–Feynman theorem has been employed to calculate the repulsion between two helium atoms and the molecular energies of H2 and H3. The method of molecular orbitals was used to determine the necessary expressions for the electron densities. The screening constants of the atomic orbitals comprising the molecular orbitals were treated as functions of the internuclear separation according to an empirical expression which duplicates very closely the "best" values for these parameters as determined by the variational method. The results of the calculations indicate that the present method is capable of yielding estimates of molecular energies which are comparable to those obtained by the more elaborate and time-consuming variational methods.

1980 ◽  
pp. 150-160
Author(s):  
Rudolf Zahradník ◽  
Rudolf Polák

2013 ◽  
Vol 798-799 ◽  
pp. 75-78
Author(s):  
Cai Xia Xu ◽  
Zhi Ping Huang ◽  
Qi Ping Fan ◽  
Wen Yu Zhang ◽  
Hong Yi Wu ◽  
...  

A molecular orbital is the wave function for the electron, and it extends over the entire molecule. When considering the possible reactions of a molecule, molecular orbitals are required to be known. This paper gives insight into the nature of molecular orbitals and nodal plane, also explain why certain atomic orbitals “missing” in molecular orbitals.


1991 ◽  
Vol 2 (1) ◽  
pp. 81-83
Author(s):  
Joel F. Liebman ◽  
Michelle J. Crockett ◽  
Terrance C. Dymski

2009 ◽  
Vol 898 (1-3) ◽  
pp. 8-16 ◽  
Author(s):  
Maurizio Sironi ◽  
Michela Ghitti ◽  
Alessandro Genoni ◽  
Giorgio Saladino ◽  
Stefano Pieraccini

Photoelectron spectra of chloro-, fluoro- and chlorofluoroethylenes have been measured. Ionization potentials in the range 6 to 21 eV have been determined, and vibrational structure associated with many of the electronic transitions has been interpreted in terms of vibrations of the ion and correlated with those of the parent molecule. The various ionization potentials have been associated with specific orbitals such as the C=C π orbital, and molecular orbitals derived from the p atomic orbitals of halogens. Variations in these ionization potentials have been discussed in relation to inductive and conjugative effects of the halogen substituents. Some observed differences between the spectra of the chloro- and fluoroethylenes have been considered in relation to possible mechanisms of the changes in bond length consequent upon ionization.


2014 ◽  
Vol 70 (6) ◽  
pp. 532-551 ◽  
Author(s):  
Leonardo H. R. Dos Santos ◽  
Alessandro Genoni ◽  
Piero Macchi

The recently developed X-ray constrained extremely localized molecular orbital (XC-ELMO) technique is a potentially useful tool for the determination and analysis of experimental electron densities. Molecular orbitals strictly localized on atoms, bonds or functional groups allow one to combine the quantum-mechanical rigour of the wavefunction-based approaches with the easy chemical interpretability typical of the traditional multipole models. In this paper, using very high quality X-ray diffraction data for the glycylglycine crystal, a detailed assessment of the capabilities and limitations of this new method is given. In particular, the effects of constraining the ELMO wavefunctions to experimental X-ray structure-factor amplitudes and the ability of the method to reproduce benchmark electron distributions have been accurately investigated. Topological analysis of the XC-ELMO electron densities and of the zero-flux surface-integrated charges and dipole moments shows that the new strategy is already reliable, provided that sufficiently flexible basis sets are used. These analyses also raise new questions and call for further improvements of the method.


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