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Lester Andrews

Bio: Lester Andrews is an academic researcher from University of Virginia. The author has contributed to research in topics: Infrared spectroscopy & Molecule. The author has an hindex of 68, co-authored 888 publications receiving 24613 citations. Previous affiliations of Lester Andrews include Ames Research Center & Environmental Molecular Sciences Laboratory.


Papers
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Journal ArticleDOI
TL;DR: In this paper, it was shown that the species M + O 3 − and M + NO 2 − have been produced in matrix samples of alkali atoms, N 2 O and O 2 or NO by mercury arc photolysis.

4 citations

Journal ArticleDOI
TL;DR: Investigations with OCS emphasized differences in the CS and CO bond insertion products, which produced SMCO, OMCS, and the simple M(eta2-CO)S adduct.
Abstract: Laser-ablated titanium, zirconium, and hafnium atoms were reacted with CS2 and OCS molecules during condensation in excess argon. With CS2, the SMCS and S−M(η2-CS) products were formed on sample de...

4 citations

01 Jan 1976
TL;DR: In this article, the authors investigated the mechanism for trapping new chemical species by condensing the products of a microwave discharge with inert matrices and found that the major product species, HCl2 radical or anion, was formed under conditions where neither ions nor atomic species produced in the discharge were condensed in the matrix.
Abstract: The mechanism for trapping new chemical species by condensing the products of a microwave discharge with inert matrices has been investigated. Variation of geometrical, electrical, and chemical parameters of the Ar, HCl, Cl2 system indicated that the major product species—HCl2 radical or anion—was formed under conditions where neither ions nor atomic species produced in the discharge were condensed in the matrix. The mechanism for forming the product species is vacuum ultraviolet photolysis of the sample during deposition with radiation from the microwave discharge, since a coaxial orifice discharge tube provided photolysis and produced the product species, while studies with an off‐axis orifice discharge tube, which could not serve as a photolysis source, did not produce the product. The H atom–Cl2 reaction gave HCl using both discharge tubes, but the HClx2 species was produced only with the coaxial tube. Hence, this species requires vacuum ultraviolet light in addition to H and Cl atoms for its producti...

4 citations

Journal ArticleDOI
TL;DR: Reactions of laser-ablated scandium, yttrium, lanthanum, and several lanthanide metal atoms with dimethyl ether have been studied using matrix isolation infrared spectroscopy and density functional calculations reveal that the M(CH( 3)OCH(3)) complexes possess C(2v) symmetry with metal atoms bound to the oxygen side ofDimethyl ether.
Abstract: Reactions of laser-ablated scandium, yttrium, lanthanum, and several lanthanide metal atoms with dimethyl ether have been studied using matrix isolation infrared spectroscopy. Identifications of the major products, M(CH3OCH3) and CH3OMCH3 (M = Sc, Y, La, Ce, Gd, Tb, Yb, and Lu), are supported by experiments with deuterium substitution as well as theoretical calculations. It is found that most ground-state metal atoms react with dimethyl ether to give the M(CH3OCH3) complexes spontaneously on annealing, which isomerize to the CH3OMCH3 insertion products with visible irradiation. Density functional calculations reveal that the M(CH3OCH3) complexes possess C2v symmetry with metal atoms bound to the oxygen side of dimethyl ether, and bent geometries are found for the inserted CH3OMCH3 molecules with direct M–O and C–O bonds. All of these products have the same ground states as their corresponding metal atoms except for Tb. Although the Lu(CH3OCH3) complex is predicted to be a stable molecule, it is not observ...

4 citations


Cited by
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Book
01 Sep 2001
TL;DR: A Chemist's Guide to Density Functional Theory should be an invaluable source of insight and knowledge for many chemists using DFT approaches to solve chemical problems.
Abstract: "Chemists familiar with conventional quantum mechanics will applaud and benefit greatly from this particularly instructive, thorough and clearly written exposition of density functional theory: its basis, concepts, terms, implementation, and performance in diverse applications. Users of DFT for structure, energy, and molecular property computations, as well as reaction mechanism studies, are guided to the optimum choices of the most effective methods. Well done!" Paul von RaguE Schleyer "A conspicuous hole in the computational chemist's library is nicely filled by this book, which provides a wide-ranging and pragmatic view of the subject.[...It] should justifiably become the favorite text on the subject for practioneers who aim to use DFT to solve chemical problems." J. F. Stanton, J. Am. Chem. Soc. "The authors' aim is to guide the chemist through basic theoretical and related technical aspects of DFT at an easy-to-understand theoretical level. They succeed admirably." P. C. H. Mitchell, Appl. Organomet. Chem. "The authors have done an excellent service to the chemical community. [...] A Chemist's Guide to Density Functional Theory is exactly what the title suggests. It should be an invaluable source of insight and knowledge for many chemists using DFT approaches to solve chemical problems." M. Kaupp, Angew. Chem.

3,550 citations

Journal ArticleDOI
TL;DR: In this paper, the authors survey the local density functional formalism and some of its applications and discuss the reasons for the successes and failures of the local-density approximation and some modifications.
Abstract: A scheme that reduces the calculations of ground-state properties of systems of interacting particles exactly to the solution of single-particle Hartree-type equations has obvious advantages. It is not surprising, then, that the density functional formalism, which provides a way of doing this, has received much attention in the past two decades. The quality of the energy surfaces calculated using a simple local-density approximation for exchange and correlation exceeds by far the original expectations. In this work, the authors survey the formalism and some of its applications (in particular to atoms and small molecules) and discuss the reasons for the successes and failures of the local-density approximation and some of its modifications.

3,285 citations

Journal ArticleDOI
TL;DR: The specific advantages brought up by a design based on the use of the halogen bond will be demonstrated in quite different fields spanning from material sciences to biomolecular recognition and drug design.
Abstract: The halogen bond occurs when there is evidence of a net attractive interaction between an electrophilic region associated with a halogen atom in a molecular entity and a nucleophilic region in another, or the same, molecular entity. In this fairly extensive review, after a brief history of the interaction, we will provide the reader with a snapshot of where the research on the halogen bond is now, and, perhaps, where it is going. The specific advantages brought up by a design based on the use of the halogen bond will be demonstrated in quite different fields spanning from material sciences to biomolecular recognition and drug design.

2,582 citations

Journal ArticleDOI
TL;DR: The detection methods and generation mechanisms of the intrinsic reactive oxygen species (ROS) in photocatalysis were surveyed comprehensively and the major photocatalyst used in heterogeneous photocatalytic systems was found to be TiO2.
Abstract: The detection methods and generation mechanisms of the intrinsic reactive oxygen species (ROS), i.e., superoxide anion radical (•O2–), hydrogen peroxide (H2O2), singlet oxygen (1O2), and hydroxyl radical (•OH) in photocatalysis, were surveyed comprehensively. Consequently, the major photocatalyst used in heterogeneous photocatalytic systems was found to be TiO2. However, besides TiO2 some representative photocatalysts were also involved in the discussion. Among the various issues we focused on the detection methods and generation reactions of ROS in the aqueous suspensions of photocatalysts. On the careful account of the experimental results presented so far, we proposed the following apprehension: adsorbed •OH could be regarded as trapped holes, which are involved in a rapid adsorption–desorption equilibrium at the TiO2–solution interface. Because the equilibrium shifts to the adsorption side, trapped holes must be actually the dominant oxidation species whereas •OH in solution would exert the reactivity...

2,249 citations

01 Feb 1995
TL;DR: In this paper, the unpolarized absorption and circular dichroism spectra of the fundamental vibrational transitions of the chiral molecule, 4-methyl-2-oxetanone, are calculated ab initio using DFT, MP2, and SCF methodologies and a 5S4P2D/3S2P (TZ2P) basis set.
Abstract: : The unpolarized absorption and circular dichroism spectra of the fundamental vibrational transitions of the chiral molecule, 4-methyl-2-oxetanone, are calculated ab initio. Harmonic force fields are obtained using Density Functional Theory (DFT), MP2, and SCF methodologies and a 5S4P2D/3S2P (TZ2P) basis set. DFT calculations use the Local Spin Density Approximation (LSDA), BLYP, and Becke3LYP (B3LYP) density functionals. Mid-IR spectra predicted using LSDA, BLYP, and B3LYP force fields are of significantly different quality, the B3LYP force field yielding spectra in clearly superior, and overall excellent, agreement with experiment. The MP2 force field yields spectra in slightly worse agreement with experiment than the B3LYP force field. The SCF force field yields spectra in poor agreement with experiment.The basis set dependence of B3LYP force fields is also explored: the 6-31G* and TZ2P basis sets give very similar results while the 3-21G basis set yields spectra in substantially worse agreements with experiment. jg

1,652 citations