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Using molecular mechanics, we calculated the total electrostatic contribution to the binding energy and found that it was less than 10% at distances less than 3.8 Å, indicating that repulsion (A, B) parameters account for most of the energy at the HF/aug-cc-pvDz level at these distances.
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Calculations of noble gas dimer dispersion (ref 19) using augmented Dunning basis sets at the MP2, MP4, and CCSD(T) levels of theory showed increasingly close agreement with experimental well depths, and the agreement at all levels of theory was better when complete basis set estimations were used. Recent work on small molecules representative of the functional groups of organic materials (ref 20) suggested that the use of a large number of diffuse functions (augmented sets) leads to an overpolarization of the molecular liquids and violation of Pauli exclusion in the condensed phase, both of which lead to an overestimation of the dielectric constants and heats of vaporization. Our own investigations of PEO and small alkane molecules at the MP2 level have shown that augmented double-ζ calculations underestimate dispersion but that the complete basis set expansion can in many instances overestimate it.
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