个人简介

B.Sc., University of Waterloo, Canada, 1972 Ph.D., Queen抯 University, Canada, 1975 Postdoctoral Fellow, 1976, Princeton University and 1977, Carnegie-Mellon University Industrial, 1978-80, Merck, Sharp and Dohme

研究领域

Development and application of methods for exploring potential energy surfaces for chemical reactions using molecular orbital calculations

With theoretical calculations it is possible to investigate details of chemical reactions and molecular properties that are often difficult to study experimentally. Molecular orbital computations can be used to explore potential energy surfaces for reactions, determine equilibrium geometries, locate transition states, follow reaction paths and choose between different proposed reaction mechanisms. Heats of formation, NMR spectra, vibrational spectra and a variety of molecular properties can also be calculated reliably by ab initio molecular orbital methods. These calculations are particularly useful for highly reactive molecules and unstable intermediates that are problematic to observe experimentally. Our lab is involved in both the development and the application of new methods in ab initio molecular orbital (MO) theory. The development efforts are centered around analytical energy derivatives and the use of these derivatives to explore potential energy surfaces. Over the past 30 years, our group and others have developed efficient computer programs to calculate energy derivatives for a variety of levels of ab initio MO theory. Our current efforts include the development of new algorithms using derivatives for geometry optimization, searching for transition states and following reaction paths. We have devised efficient code to compute classical trajectories for molecular dynamics directly from the MO calculations. To aid in the study of radicals, we have developed spin projection methods to obtain more accurate energetics for open shell systems. The remarkable advances in quantum chemical software and the rapid increase in the speed of computers have opened new realms of chemistry for investigation by ab initio molecular orbital methods. Many of our applications of quantum chemical calculations are in direct collaboration with experimental groups in order to maximize the benefits of our studies. In the area of bio-organic chemistry, we have been looking at oxidative damage to DNA with Cynthia Borrows (U. of Utah), specifically processes involving guanine oxidation. In the area of materials and inorganic chemistry, we have a long standing association with the Winter group investigating precursors for chemical vapor deposition (CVD) and atomic layer deposition (ALD). We are working closely with the Verani and Endicott groups on solar energy conversion and water splitting catalysts. Within physical chemistry, we are studying reaction path branching by ab initio molecular dynamics (AIMD) methods. In collaboration with Wen Li, we are using AIMD to investigate the behavior of molecules in intense laser fields.

近期论文

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Schlegel, H. B.; Geometry Optimization, WIREs Comput. Mol. Sci. 2011,1, 790-806 (10.1002/wcms.34). Psciuk, B. T.; Lord, R. L.; Munk, B. H.; Schlegel, H. B.; Theoretical Determination of One-Electron Oxidation Potentials for Nucleic Acid Bases. J. Chem. Theory Comput. 2012, 8, 5107?5123 (10.1021/ct300550x). Psciuk, B. T.; Lord, R. L.; Winter, C. H.; Schlegel, H. B.; Can Metallapyrimidines Be Aromatic? A Computational Study into a New Class of Metallacycles? J. Chem. Theory Comput. 2012, 8, 4950?4959 (10.1021/ct3006979). Allard, M. M.; Sonk, J. A.; Heeg, M. J.; McGarvey, B. R.; Schlegel, H. B.; Verani, C. N. Bioinspired Five-Coordinate Iron(III) Complexes for Stabilization of Phenoxyl Radicals. Angew. Chem., Int. Ed. 2012, 51, 3178-3182 (10.1002/anie.201103233) Sonk, J. A.; Schlegel, H. B.; TD-CI Simulation of the Electronic Optical Response of Molecules in Intense Fields: Comparison of DFT Functionals and EOM-CCSD. J. Phys. Chem. A 2011, 115, 11832-11840 (10.1021/jp206437s) Lee, S. K.; Suits, A. G.; Schlegel, H. B.; Li, W.; A Reaction Accelerator: Mid-Infrared Strong Field Dissociation Yields Mode Selective Chemistry, J. Phys. Chem. Lett. 2012, 3, 2541-2547 (10.1021/jz301038b)