Abstract

The structures of more than 70 low-lying water clusters ranging in size from (H2O)3 to (H2O)10 have been fully optimized with several different quantum mechanical electronic structure methods, including second-order Møller-Plesset perturbation theory (MP2) in conjunction with correlation consistent triple-ζ basis sets (aug-cc-pVTZ for O and cc-pVTZ for H, abbreviated haTZ). Optimized structures obtained with less demanding computational procedures were compared to the MP2/haTZ ones using both MP2/haTZ single point energies and the root-mean-square (RMS) deviations of unweighted Cartesian coordinates. Based on these criteria, B3LYP/6-31+G(d,2p) substantially outperforms both HF/haTZ and MP2/6-31Gz.ast. B3LYP/6-31+G(d,2p) structures never deviate from the MP2/haTZ geometries by more than 0.44 kcal mol-1 on the MP2/haTZ potential energy surface, whereas the errors associated with the HF/haTZ and MP2/6-31G* structures grow as large as 12.20 and 2.98 kcal mol-1, respectively. The most accurate results, however, were obtained with the two-body:many-body QM:QM fragmentation method for weakly bound clusters, in which all one- and two-body interactions are calculated at the high-level, while a low-level calculation is performed on the entire cluster to capture the cooperative effects (Non additivity). With the haTZ basis set, the MP2:HF two-body:many-body fragmentation method generates structures that deviate from the MP2/haTZ ones by 0.01 kcal mol-1 on average and not by more than 0.03 kcal mol-1. © 2011 American Chemical Society.

Department(s)

Chemistry

International Standard Serial Number (ISSN)

1549-9626; 1549-9618

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 2024 American Chemical Society, All rights reserved.

Publication Date

13 Sep 2011

Download

Additional files available below

Full Text Link

Included in

Chemistry Commons

Share

 
COinS