Revised 7/15/13 curriculum vitae

III. BOOKS – AUTHOR

1. I. Shavitt and R.J. Bartlett, Many-Body Methods in Chemistry and Physics: MBPT and Coupled-Cluster Theory, Cambridge Press, 2009.

IV. Journal Publications (1^st of each year in blue)

(1970’s)

R. J. Bartlett and E. J. Brändas, “Geometric sumrule and the reduced partitioning procedure,” Int. J. Quantum Chem. Symp. 5, 151-159 (1971).

E. J. Brändas and R. J. Bartlett, “Reduced partitioning technique for configuration interaction calculations using Padé approximants and inner-projections,” Chem. Phys. Lett. 8, 153-156 (1971).

R. J. Bartlett and E. J. Brändas, “Reduced partitioning procedure in configuration interaction studies. I. Ground states,” J. Chem. Phys. 56, 5467-5477 (1972).

R. J. Bartlett and E. J. Brändas, “Reduced partitioning procedure in configuration interaction studies. II. Excited states,” J. Chem. Phys. 59, 2032-2042 (1973).

R. J. Bartlett, J. C. Bellum and E. J. Brändas, “The treatment of correlation effects in second-order properties,” Int. J. Quantum Chem. Symp. 7, 449-462 (1973).

R. J. Bartlett and D. M. Silver, “Correlation energy in LiH, BH, and HF with many-body perturbation theory using Slater-type atomic orbitals,” Int. J. Quantum Chem. Symp.8, 271-276 (1974).

R. J. Bartlett and D. M. Silver, “Pair-correlation energies in sodium hydride with many-body perturbation theory,” Phys. Rev. A 10, 1927-1931 (1974). Erratum: Phys. Rev. A 13 (2), 912 (1976).

R. J. Bartlett and D. M. Silver, “Many-body perturbation theory applied to hydrogen fluoride,” Chem. Phys. Lett. 29, 199-203 (1974).

R. J. Bartlett and H. Weinstein, “Theoretical treatment of multiple site reactivity in large molecules,” Chem. Phys. Lett. 30, 441-447 (1975).

R. J. Bartlett and D. M. Silver, “Many-body perturbation theory applied to electron pair correlation energies. I. Closed-shell first-row diatomic hydrides,” J. Chem. Phys. 62, 3258-3268 (1975). Erratum: J. Chem. Phys. 64 (3) 1260 (1976).

R. J. Bartlett and D. M. Silver, “Some aspects of diagrammatic perturbation theory,” Int. J. Quantum Chem. Symp. 9, 183-198 (1975).

D. M. Silver and R. J. Bartlett, “Modified potentials in many-body perturbation theory,” Phys. Rev. A 13, 1-12 (1976).

T.-S. Nee, R. G. Parr and R. J. Bartlett, “Direct determination of the rotational barrier in ethane using perturbation theory,” J. Chem. Phys. 64, 2216-2225 (1976).

G. Blyholder, D. Shihabi, W. V. Wyatt and R. J. Bartlett, “Adsorption and interaction of C₂H₄, H_2,CO and organic acids on Fe, Co, and Ni,” J. Catalysis 43, 122-130 (1976).

R. J. Bartlett and D. M. Silver, “Many-body perturbation theory applied to electron pair correlation energies. II. Closed-shell second row-diatomic hydrides,” J. Chem. Phys. 64, 4578-4586 (1976).

D. D. Koelling, D. E. Ellis and R. J. Bartlett, “Relativistic energy levels and bonding in actinide hexafluorides,” J. Chem. Phys. 65, 3331-3340 (1976).

D. M. Silver, S. Wilson and R. J. Bartlett, “Modified potentials in many-body perturbation theory: three-body and four-body contributions,” Phys. Rev. A 16, 477-483 (1977).

R. J. Bartlett and I. Shavitt, “Comparison of high-order many-body perturbation theory and configuration interaction for H₂O,” Chem. Phys. Lett. 50, 190-198 (1977).

R. J. Bartlett and R. G. Parr, “Polyatomic force constants from charge densities and field gradients,” J. Chem. Phys. 67, 5828-5837 (1977).

R. J. Bartlett and I. Shavitt, “Determination of the size-consistency error in the single and double excitation configuration interaction model,” Int. J. Quantum Chem. Symp. 11, 165-173 (1977).

S. Wilson, D. M. Silver and R. J. Bartlett, “Many-body effects in the X¹⁺ states of the hydrogen fluoride, lithium fluoride and boron fluoride molecules,” Mol. Phys. 33, 1177-1193 (1977).

R. J. Bartlett, S. Wilson and D. M. Silver, “Third-order many-body perturbation theory for the ground state of the carbon monoxide molecule,” Int. J. Quantum Chem. 12, 737-757 (1977).

G.D. Purvis and R. J. Bartlett, “The potential energy curve for the X state of Mg₂ calculated with many-body perturbation theory,” J. Chem. Phys. 68, 2114-2124 (1978).

J. W. Kenney III, J. Simons, G. D. Purvis and R. J. Bartlett, “Low-lying electronic states of unsaturated carbenes. Comparison with methylene,” J. Am. Chem. Soc. 100, 6930-6936 (1978).

R. J. Bartlett and G. D. Purvis, “Many-body perturbation theory, coupled-pair many-electron theory and the importance of quadruple excitations for the correlation problem,” Proceedings of the American Theoretical Chemistry Conference, Boulder, Colorado, Int. J. Quantum Chem. 14, 561-581 (1978).

L. T. Redmon, G. D. Purvis and R. J. Bartlett, “The unimolecular isomerization of methyl isocyanide to methyl cyanide (Acetonitrile),” J. Chem. Phys. 69, 5386-5392 (1978).

R. J. Bartlett, I. Shavitt and G. D. Purvis III, “The quartic force field of H₂O determined by many-body methods that include quadruple excitation effects,” J. Chem. Phys. 71, 281-291 (1979).

L. T. Redmon, G. D. Purvis III and R. J. Bartlett, “Accurate binding energies of diborane, borane carbonyl and borazane determined by many-body perturbation theory,” J. Am. Chem. Soc. 101, 2856-2862 (1979).

R. J. Bartlett and G. D. Purvis III, “Molecular hyperpolarizabilities I: Theoretical calculations including correlation,” Phys. Rev. A 20, 1313-1322 (1979).

G. D. Purvis III and R. J. Bartlett, “The potential energy curve for the X state of Mg₂ calculated with coupled pair many electron theory,” J. Chem. Phys. 71, 548-550 (1979).

G. F. Adams, G. D. Bent, G. D. Purvis and R. J. Bartlett, “The electronic structure of the formyl radical HCO,” J. Chem. Phys. 71, 3697-3702 (1979).