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Lester

Chuang C, Andrews P M and Lester M I 1995 Intermolecular vibrations and spin-orbit predissooiation dynamios of NeOH J. Chem. Phys. 103 3418-29... [Pg.1262]

Cooks R G, Beynon J H, Capriolo R M and Lester G R 1973 Metastable Ions (Amsterdam Elsevier)... [Pg.1358]

Flammond B L, Lester W A and Reynolds P J 1994 Monte Cario Methods in Ab initio Quantum Chemistry (Singapore World Scientific)... [Pg.2233]

Berry M T, Loomis R A, Gianoarlo L C and Lester M I 1991 Stimulated emission pumping of intermoleoular vibrations... [Pg.2453]

Anderson D T, Schwartz R L and Todd M W and Lester M I 1998 Infrared spectroscopy and time-resolved dynamics of the ortho-Hj-OH entrance channel complex J. Chem. Phys. 109 3461-73... [Pg.2454]

Wheeler M D, Anderson D T, Todd M W, Lester M I, Krause O J and Clary D C 1999 Mode-selective decay dynamics of the ortho-Hj-OH complex experiment and theory Mol. Phys. 97 151-8... [Pg.2454]

Loomis R A and Lester M I 1997 OH-H2 entrance channel complexes Ann. Rev. Phys. Chem. 48 643-73... [Pg.2455]

B. L. Hammond, W. A. Lester, Jr., P. J. Reynolds, Monte Carlo Methods in Ah Initio Quantum ChemistryScientific, Singapore (1994). [Pg.28]

Quantum Monte Carlo (QMC) methods are computations that use a statistical integration to calculate integrals which could not be evaluated analytically. These calculations can be extremely accurate, but often at the expense of enormous CPU times. There are a number of methods for obtaining excited-state energies from QMC calculations. These methods will only be mentioned here and are explained more fully in the text by Hammond, Lester, and Reynolds. [Pg.219]

Chris Kneupper Lester Saathoff The Dow Chemical Company... [Pg.36]

G. R. Lester, "Catalytic Destmction of Ha2ardous Halogenated Organic Chemicals," presented at the 82nd Annual AWMAMeeting oA Exhibition, Anaheim, Calif., June 25—30, 1992. [Pg.516]

G. R. Lester, andJ. C. Summers "Poison-Resistant Catalyst for Purification of Web Offset Press Exhaust," presented at Air Pollution Control... [Pg.516]

Submitted by Lester Friedman and Edward Kosower. Checked by Reynold C. Fuson and Elliott N. Marvell. [Pg.42]

Coenzyme Q4 (Ubiquinone-4, 2,3-dimethoxy-5-methyl-6-[3,7,ll,15-tetrametbyl-hexadeca-2/,6/,10/,14-tetraenyl]-[l,4]benzoquinone [4370-62-l]M 454.7, m 30 , 33-45 , A (275nm) 185. A red oil purified by TLC chromatography on Si02 and eluted with Et20-hexane. Purity can be checked by HPLC (silica column using 7% Et20-hexane). It has A- ax 270 nm (e 14,800) in pet ether. [NMR and MS Naruta J Org Chem 45 4097 1980 cf Morton Biochemical Spectroscopy (Adam Hilger, London, 1975) p 491]. It has also been dissolved in MeOH/EtOH (1 1 v/v) and kept at 5 until crystals appear [Lester and Crane Biochim Biophys Acta 32 497 1958]. [Pg.522]

See other pages where Lester is mentioned: [Pg.2454]    [Pg.2454]    [Pg.474]    [Pg.748]    [Pg.31]    [Pg.178]    [Pg.450]    [Pg.267]    [Pg.85]    [Pg.250]    [Pg.250]    [Pg.246]    [Pg.383]    [Pg.390]    [Pg.423]    [Pg.549]    [Pg.225]    [Pg.554]    [Pg.208]    [Pg.485]    [Pg.181]    [Pg.508]    [Pg.136]    [Pg.388]    [Pg.297]    [Pg.215]    [Pg.29]    [Pg.29]    [Pg.522]    [Pg.522]    [Pg.384]   
See also in sourсe #XX -- [ Pg.52 ]

See also in sourсe #XX -- [ Pg.201 , Pg.202 ]

See also in sourсe #XX -- [ Pg.216 ]



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