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Author:Bates

47 matching references were found.

Bates, D.R.; Ledsham, K.; Stewart, A.L., Wave functions of the hydrogen molecular ion, Philos. Trans. R. Soc. London A, 1953, 246, 215. [all data]

Bates, D.R., Quenching of O2(5Πg) by N2 and termolecular association of O atoms, Chem. Phys. Lett., 1989, 162, 313-316. [all data]

Bates, D.R.; Carson, T.R., Exact wave functions of HeH2+, Proc. R. Soc. London A, 1956, 234, 207-217. [all data]

Craig, R.S.; Krier, C.A.; Coffer, L.W.; Bates, E.A.; Wallace, W.E., J. Am. Chem. Soc., 1954, 76, 238. [all data]

Feakins, D.; Bates, F.M.; Waghorne, W.E.; Lawrence, K.G., Relative viscosities and quasi-thermodynamics of solutions of tert-butyl alcohol in the methanol-water system: a different view of the alkyl-water interaction, J. Chem. Soc., Faraday Trans., 1993, 89, 3381-8. [all data]

Engstrom, H.; Bates, J.B.; Boatner, L.A., Infrared spectra of hydrogen isotopes in potassium tantalate, J. Chem. Phys., 1980, 73, 1073-1077. [all data]

Bates, J.K.; Dunn, T.M., The electronic (yellow and violet) emission spectra of zirconium nitride, Can. J. Phys., 1976, 54, 1216-1223. [all data]

Bates, J.K.; Ranieri, N.L.; Dunn, T.M., Rotational analysis of the violet electronic emission spectrum of titanium nitride, Can. J. Phys., 1976, 54, 915. [all data]

Bates, J.K.; Gruen, D.M., Absorption spectra of diatomic molybdenum nitride (MoN), molybdenum oxide (MoO), and molybdenum dimer (MO2) molecules isolated in Ar, Ne, and Kr matrices, J. Mol. Spectrosc., 1979, 78, 284-297. [all data]

Bates, J.K.; Gruen, D.M., The electronic and vibrational absorption spectrum of tantalum nitride (TaN) isolated in an argon matrix, J. Chem. Phys., 1979, 70, 4428-4429. [all data]

Carlson, R.C.; Bates, J.K.; Dunn, T.M., Rotational analysis of the red electronic emission spectrum of molybdenum nitride (MoN), J. Mol. Spectrosc., 1985, 110, 215-241. [all data]

Bates, J.K.; Dunn, T.M., Abstract of paper SIGMA8 presented at the 27th Symposium on Molecular Structure and Spectra (reference not verified), Department of Chemistry, University of Michigan, Ann Arbor, Columbus, Ohio, 1972, 1. [all data]

Bates, J.R.; Halford, J.O.; Anderson, L.C., A comparison of some physical properties of hydrogen and deuterium bromides, J. Chem. Phys., 1935, 3, 531. [all data]

Bates, J.R.; Halford, J.O.; Anderson, L.C., J. Chem. Phys., 1935, 3, 415. [all data]

Bates, J.R., Z. Phys. Chem. (Bodenstein-Festband), 1931, 1931, 329-32. [all data]

Ames, J.M.; Defaye, A.B.; Bates, L., The effect of pH on the volatiles formed in an extruded starch-glucose-lysine model system, Food Chem., 1997, 58, 4, 323-327, https://doi.org/10.1016/S0308-8146(96)00171-9 . [all data]

Wylie, P.L.; Bates, M.; Woolfenden, E., Screening for 171 volatiles organic air pollutants using GC/MS with deconvolution reporting software and a new indoor air toxics library, 2006, retrieved from 2005BOO/VAR#3308C. [all data]

Bates, O.K., Thermal Conductivity of Liquid Silicones, Ind. Eng. Chem., 1949, 41, 9, 1966-1968, https://doi.org/10.1021/ie50477a030 . [all data]

Bates, O.K.; Hazzard, G., Thermal Conductivity of Alcohols and Glycols, Ind. Eng. Chem., 1945, 37, 193-195. [all data]

Bates, O.K.; Hazzard, G.; Palmer, G., Ind. Eng. Chem., 1941, 33, 375. [all data]

Bates, O.K.; Hazzard, G.; Palmer, G., Thermal conductivity of Liquids Binary Mixtures of Water-Methyl Alcohol and Water-Ethyl Alcohol, Ind. Eng. Chem., Anal. Ed., 1938, 10, 314-318. [all data]

Bates, O.K., Thermal Conductivity of Liquids Binary Mixtures of Water and Glycerol, Ind. Eng. Chem., 1936, 28, 494-498. [all data]

Bates, R.B.; Cutter, R.S., Acta Crystallogr., Sect. B: Struct. Crystallogr. Cryst. Chem., 1977, 33, 893. [all data]

Jolad, S.D.; Lantz, R.C.; Chen, G.J.; Bates, R.B.; Timmermann, B.N., Commercially processed dry ginger (Zingiber officinale): composition and effects on LPS-stimulated PGE2 production, Phytochemistry, 2005, 66, 13, 1614-1635, https://doi.org/10.1016/j.phytochem.2005.05.007 . [all data]

Paabo, M.; Bates, R.G.; Robinson, R.A., Dissociation of acetic acid-d(4), in deuterium oxide from 5 to 50 c and related isotope effects, J. Phys. Chem., 1966, 70, 2073-7. [all data]

Hetzer, H.B.; Bates, R.G.; Robinson, R.A., J. Phys. Chem., 1966, 70, 2869. [all data]

Woodhead, M.; Paabo, M.; Robinson, R.A.; Bates, R.G., J. Res. Natl. Bur. Stand., Sect. A, 1965, 69, 263. [all data]

Paabo, M.; Robinson, R.A.; Bates, R.G., J. Am. Chem. Soc., 1965, 87, 415. [all data]

Bates, R.G.; Paabo, M.; Robinson, R.A., Interpretation of ph measurements in alcohol-water solvents, J. Phys. Chem., 1963, 67, 1833. [all data]

Hetzer, H.B.; Bates, R.G., Dissociation constant of 2-ammonium-2-methyl-1,3-propanediol in water from 0 to 50 c and related thermodynamic quantities, J. Phys. Chem., 1962, 66, 308. [all data]

Hetzer, H.B.; Robinson, R.A.; Bates, R.G., Dissociation constant of t-butylammonium ion and related thermodynamic quantities from 5 to 35 c, J. Phys. Chem., 1962, 66, 2696. [all data]

Halle, J.-C.; Bates, R.G., Acidic Dissociation Constants of Malonic Acid in 50 Mass Percent Ethylene Carbonate + Water from 20 to 55 deg C, J. Chem. Soc., Faraday Trans. 1, 1976, 72, 2866-71. [all data]

Bates, R.G.; Pawlak, Z., Solvent effects on acid-base behavior: five uncharged acids in water + sulfolane solvents, J. Solution Chem., 1976, 5, 213. [all data]

Halle, J.-C.; Bates, R.G., Dissociation of acetic acid in 50 mass per cent ethylene carbonate + water from 20 to 55c, J. Solution Chem., 1975, 4, 1033. [all data]

Robinson, R.A.; Roy, R.N.; Bates, R.G., The system water + hydrochloric acid + ammonium chloride at 25c a study of harned's rule, J. Solution Chem., 1974, 3, 837-46. [all data]

Roy, R.N.; Robinson, R.A.; Bates, R.G., Thermodynamics of hydrobromic acid in water + 50 mass per cent methanol from e.m.f measurements at 278.15 to 333.15 k, J. Chem. Thermodyn., 1973, 5, 559-67. [all data]

Etz, E.S.; Robinson, R.A.; Bates, R.G., Dissociation constant of protonated tris(hydroxymethyl)aminomethane in n- methylpropionamide and related thermodynamic quantities from 10 to 55 c, J. Solution Chem., 1973, 2, 405. [all data]

Goldman, S.; Sagner, P.; Bates, R.G., Solute-solvent effects in the ionization of tris(hydroxymethyl)- acetic acid and related acids in water and aqueous methanol, J. Phys. Chem., 1971, 75, 826. [all data]

pool, K.H.; Bates, R.G., Thermodynamics of hydrochloric acid in 95 volume per cent (92.41 mass per cent) ethanol from e.m.f measurements at 5 to 50!31c, J. Chem. Thermodyn., 1969, 1, 21-9. [all data]

Schindler, P.; Robinson, R.A.; Bates, R.G., Solubility of tris(hydroxymethyl)aminomethane in water + methanol solvent mixtures and medium effects in the dissociation of the protonated base, J. Res. Natl. Bur. Stand., Sect. A, 1968, 72, 141-8. [all data]

Bates, S.A.; Rittby, C.M.L.; Graham, W.R.M., Fourier transform infrared isotopic study of linear CrC[sub 3]: Identification of the ν[sub 1](σ) mode, J. Chem. Phys., 2006, 125, 7, 074506, https://doi.org/10.1063/1.2234482 . [all data]

Bates, S.A.; Rittby, C.M.L.; Graham, W.R.M., Fourier transform infrared observation and density functional theory study of the AlC[sub 3] and AlC[sub 3]Al linear chains trapped in solid Ar, J. Chem. Phys., 2008, 128, 23, 234301, https://doi.org/10.1063/1.2938380 . [all data]

Bates, S.A.; Rhodes, J.A.; Rittby, C.M.L.; Graham, W.R.M., Fourier transform infrared observation of the ν[sub 1](σ) mode of linear CoC[sub 3] trapped in solid Ar, J. Chem. Phys., 2007, 127, 6, 064506, https://doi.org/10.1063/1.2756520 . [all data]

Bates, T.R.; Lin, S.-L.; Gibaldi, M., Solubilization and Rate of Dissolution of Drugs in the Presence of Physiologic Concentrations of Lysolecithin, J. Pharm. Sci., 1967, 56, 1492-1495. [all data]

Bates, T.R.; Gibaldi, M.; Kanig, J.L., Solubilizing Properties of Bile Salt Solutions I, J. Pharm. Sci., 1966, 55, 191-199. [all data]

Bates, T.R.; Gibaldi, M.; Kanig, J.L., Solubilizing Properties of Bile Salt Solutions II, J. Pharm. Sci., 1966, 55, 901-906. [all data]

Bates, T.R.; Young, J.M.; Wu, C.M.; Rosenberg, H.A., pH-Dependent Dissolution Rate of Nitrofurantoin from Commercial Suspensions, Tablets, and Capsules, J. Pharm. Sci., 1974, 63, 643-645. [all data]