Quantum Monte Carlo calculation of the singlet-triplet splitting in methylene

Peter J. Reynolds, Michel Dupuis, William A. Lester

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Abstract

The fixed-node quantum Monte Carlo (QMC) method is used to calculate the total energy of CH2 in the 3B1 and 1A1 states. For both states, the best QMC variationally bounded energies lie more than 15 kcal/mol (0.024 h) below the best previous variational calculations. Subtracting these energies to obtain the singlet-triplet splitting yields Te=9.4±2.2 kcal/mol. Adjusting for zero-point energies and relativistic effects, we obtain T 0=8.9±2.2 kcal/mol. This result is in excellent agreement with the recent direct measurements of McKellar et al. of T0=9. 05±0.06 kcal/mol, and of Leopold et al. of ∼9 kcal/mol, as well as with recent threoretical investigations which indicate an energy gap of 9-11 kcal/mol. We summarize the QMC method, discuss a possible scheme for iteratively correcting the procedure, and note that the present results were obtained using only single determinant functions for both states, in contrast to conventional ab initio approaches which must use at least two configurations to properly describe the singlet state.

Original languageEnglish
Pages (from-to)1983-1990
Number of pages8
JournalJournal of Chemical Physics
Volume82
Issue number4
Publication statusPublished - 1984

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methylene
Monte Carlo methods
Monte Carlo method
Energy gap
zero point energy
relativistic effects
determinants
energy
adjusting
configurations

ASJC Scopus subject areas

  • Atomic and Molecular Physics, and Optics

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Quantum Monte Carlo calculation of the singlet-triplet splitting in methylene. / Reynolds, Peter J.; Dupuis, Michel; Lester, William A.

In: Journal of Chemical Physics, Vol. 82, No. 4, 1984, p. 1983-1990.

Research output: Contribution to journalArticle

Reynolds, Peter J. ; Dupuis, Michel ; Lester, William A. / Quantum Monte Carlo calculation of the singlet-triplet splitting in methylene. In: Journal of Chemical Physics. 1984 ; Vol. 82, No. 4. pp. 1983-1990.
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