dc.creator Higgins, Kelly J. en_US dc.creator Klemperer, William en_US dc.date.accessioned 2006-06-15T19:55:47Z dc.date.available 2006-06-15T19:55:47Z dc.date.issued 2000 en_US dc.identifier 2000-MF-09 en_US dc.identifier.uri http://hdl.handle.net/1811/19668 dc.description Author Institution: Department of Chemistry and Chemical Biology, Harvard University en_US dc.description.abstract The dependence of the ArHF intermolecular potential upon $v_{HF}$ is now known through experiment for $v_{HF}=0 - 4$. For the ground state hydrogen-bonded structure Ar-HF it can be characterized by an increasing red shift and increasing rotational constant as the HF is stretched from v=0 to v = 4. This indicates that The intermolecular bond is getting stronger and the heavy atom distance (Ar-F) is shrinking. Less well known is the explicit $r_{HF}$ dependence of the potential and at what point will the Ar-H repulsion become evident? In addition, does this same behavior extend to other, non-hydrogen bonded systems? In order to answer these and other questions, CCSD(T) ab initio calculations have been performed on ArHF and ArCIF to generate full three-dimensional $(R, \theta,r)$ potential energy surfaces for a wide range $r_{XF}$ values. In addition, three-dimensional quantum calculations of the bound states for the two systems have been performed to provide comparison with experiment and predictions for future experiments. The result for ArHF are in excellent agreement with experiment in terms of red shift and change in rotational constant. They predict that the increase in the red shift will slow at $v_{HF} = 7$ and turn around at $v_{HF} = 9$. While this is well beyond current experimental accessibility, the results also predict that the rotational constant should be smaller for ArHF $v_{HF}= 5$ than for $v_{HF} = 4$, thus showing the first signs of Ar-H repulsion. ArHF $v_{HF} = 4$ experimental results have recently been obtained by Chuang and Klemperer, and ArHF $v_{HF} = 5$ should be accessible with their current set-up. The intermolecular potential of ArCIF shows a dramatic increase in depth for wells at both ends of CIF upon stretching of the CIF bond. Accompanying this is a decrease in Ar-CI and Ar-F distance until $r_{CIF} = 2.0 {\AA}$, at which point the well depths begin to decrease and the atom-atom distances begin to increase Bound state calculations show a steady increase in red shift and a steady decrease in Ar-CI distance from $v_{ClF} = 0$ to at least $v_{ClF} = 11$ for the ground state Ar-CIF configuration. It appears the increase in binding energy and the decrease in intermolecular distance upon stretching of the HF bond observed in ArHF is a general phenomena in atom-diatomic molecule systems. en_US dc.format.extent 208512 bytes dc.format.mimetype image/jpeg dc.language.iso English en_US dc.publisher Ohio State University en_US dc.title AN AB INITIO STUDY ON THE EXPLICIT $r_{XF}$ DEPENDENCE OF THE INTERMOLECULAR POTENTIALS OF ArHF AND ArCIF: WHEN DOES Ar-X REPULSION BEGIN TO SHOW? en_US dc.type article en_US
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