@article {4885,
	title = {Prediction of the thermal conductivity of gases based on the Rainwater-Friend theory and a new corresponding states function},
	journal = {Physica a-Statistical Mechanics and Its Applications},
	volume = {275},
	number = {1-2},
	year = {2000},
	note = {ISI Document Delivery No.: 270GXTimes Cited: 14Cited Reference Count: 52},
	month = {Jan},
	pages = {48-69},
	type = {Article},
	abstract = {The Rainwater-Friend theory is used for the evaluation of the initial density dependence of the thermal conductivity of the noble gases using accurate realistic potentials. This theory, which was originally developed for spherically symmetric potentials, is adapted for the calculation of the initial density dependence of the translational contribution of the thermal conductivity of polyatomic gases. The internal state contribution is evaluated using a combination of Mason-Monchick theory and hard-sphere Enskog theory. At high density, beyond the range of the Rainwater-Friend theory, a deviation thermal conductivity function has been presented. With the help of this function, an easily usable corresponding-states function for the calculation of the thermal conductivity of supercritical gases has been developed, which is valid over a wide temperature range and for pressures up to 400 MPa. (C) 2000 Elsevier Science B.V. All rights reserved.},
	keywords = {ARGON, CARBON-DIOXIDE, high-pressure thermal conductivity, INITIAL DENSITY-DEPENDENCE, NOBLE-GASES, PHYSICAL-PROPERTIES, POLYATOMIC GASES, POTENTIAL-ENERGY CURVE, Rainwater-Friend theory, second, TEMPERATURE, thermal conductivity, thermal conductivity virial coefficient, TRANSPORT-PROPERTIES, ZERO DENSITY},
	isbn = {0378-4371},
	url = {<Go to ISI>://000084528200005},
	author = {Najafi, B. and Araghi, R. and Rainwater, J. C. and Alavi, S. and Snider, R. F.}
}
@article {4364,
	title = {Improved initial density dependence of the viscosity and a corresponding states function for high pressures},
	journal = {Physica a-Statistical Mechanics and Its Applications},
	volume = {260},
	number = {1-2},
	year = {1998},
	note = {ISI Document Delivery No.: 135WLTimes Cited: 24Cited Reference Count: 50},
	month = {Nov},
	pages = {31-48},
	type = {Article},
	abstract = {The initial density correction to gaseous viscosity using accurate realistic potentials of the noble gases is evaluated using the Rainwater-Friend theory. It is shown that this theory works satisfactorily for densities up to about 2 mol dm(-3). Due to the superimposability of the noble gas potential functions, a universal function of the reduced second viscosity virial coefficient is obtained over the entire reduced temperature range. At densities beyond the range of the theory, a variant of the excess viscosity is developed, by which the viscosity of the different gases can be easily calculated above the critical temperature for pressures up to 900 MPa. The accuracy of this method is within the experimental uncertainties. (C) 1998 Elsevier Science B.V. All rights reserved.},
	keywords = {11 POLYATOMIC GASES, ARGON, COEFFICIENT, COEFFICIENTS, EQUILIBRIUM, high-pressure excess viscosity, NOBLE-GASES, ORGANIC VAPORS, PHYSICAL-PROPERTIES, Rainwater-Friend theory, second viscosity virial, TEMPERATURE, THERMAL-CONDUCTIVITY, TRANSPORT-PROPERTIES, VISCOSITY},
	isbn = {0378-4371},
	url = {<Go to ISI>://000076825600004},
	author = {Najafi, B. and Ghayeb, Y. and Rainwater, J. C. and Alavi, S. and Snider, R. F.}
}
@article {2854,
	title = {TETRAPHENYLCYCLOPENTADIENYL NITROSYL COMPLEXES OF MOLYBDENUM AND TUNGSTEN},
	journal = {Organometallics},
	volume = {12},
	number = {4},
	year = {1993},
	note = {ISI Document Delivery No.: KX233Times Cited: 8Cited Reference Count: 40},
	month = {Apr},
	pages = {1029-1037},
	type = {Article},
	abstract = {{Sequential treatment Of M(CO)6 (M = MO, W) in THF with Cp(phi)Li (Cp(phi) = eta5-C5Ph4H) and Diazald (N-methyl-N-nitroso-p-toluenesulfonamide) affords good yields of Cp(phi)M(NO)(CO)2 which convert to Cp(phi)M(NO)Cl2 upon treatment with PCl5 in Et2O. Dialkyl compounds of the type Cp$\#$M(NO)R2 (R = CH2SiMe3, CH2Ph) are readily preparable from these dichloro precursors by straight forward metathesis reactions. Finally, molybdenum dinitrosyl complexes of the type Cp(phi)Mo(NO)2X (X = Cl, Ph) are obtained when Cp(phi)Mo(NO) (CO)2 is reacted with [NO] [PF6] in CH2Cl2 and the resulting [Cp(chi)Mo(NO)2]PF6 intermediate salt is treated in situ with a source of X-. All new complexes have been characterized by conventional means, and an X-ray crystallographic analysis of CP(phi)W(NO)(CH2SiMe3)2 has been performed. Crystal data for Cp(phi)W(NO)(CH2SiMe3)2: triclinic, space group P1BAR},
	keywords = {CHEMISTRY, CHROMIUM, CYCLOPENTADIENYL, PHYSICAL-PROPERTIES, REDUCTION},
	isbn = {0276-7333},
	url = {<Go to ISI>://A1993KX23300017},
	author = {Legzdins,Peter and Reina, R. and Shaw, M. J. and Batchelor, R. J. and Einstein, F. W. B.}
}
@article {7157,
	title = {LIPOPHILIC COORDINATION-COMPOUNDS - ALUMINUM, GALLIUM, AND INDIUM COMPLEXES OF 1-ARYL-3-HYDROXY-2-METHYL-4-PYRIDINONES},
	journal = {Inorganic Chemistry},
	volume = {30},
	number = {3},
	year = {1991},
	note = {ISI Document Delivery No.: EW602Times Cited: 58Cited Reference Count: 31},
	month = {Feb},
	pages = {509-515},
	type = {Article},
	abstract = {{A series of 1-aryl-3-hydroxy-2-methyl-4-pyridinones and tris(1-aryl-3-hydroxy-2-methyl-4-pyridinonato) aluminum(III), -gallium(III), and -indium(III) complexes have been prepared and completely characterized. The pyridinones have a variety of aryl substituents at the ring nitrogen atom (phenyl, p-tolyl, p-methoxyphenyl, p-nitrophenyl). The complexes have been studied by a number of techniques including n-octanol/water partitioning, potentiometry, and single-crystal X-ray diffraction. The uncomplexed ligands have log (n-octanol/water partition coefficients) (log p) greater than 1, except for the p-nitrophenyl case; the log p values are significantly higher in the complexes (> 2, except for the p-nitrophenyl cases). The complexes of 3-hydroxy-2-methyl-1-phenyl-4-pyridinone with aluminum (III), gallium (III), and indium (III) have been characterized by potentiometric (glass electrode) titration. The equilibria have been examined at 25.0 +/- 0.1-degrees-C (and 37.0 +/- 0.1-degrees-C for Al) at an ionic strength of mu- = 0.15. This ligand forms Ml(n) complexes (n = 1-3) of high stability; at 25-degrees-C the overall stability constants beta-3 for the 3:1 complexes are 10(30.7) (M = Al3+), 10(36.3) (Ga3+), and 10(31.1) (In3+). At ligand to metal ratios greater-than-or-equal-to 1, the ligands prevent M(III) hydrolysis at millimolar concentrations, even under slightly basic conditions, and the effective formation constants (beta-3eff) for the metal ions at physiological pH are 10(24.7) (M = Al3+), 10(30.3) (Ga3+), and 10(25.1) (In3+). Crystals of the ML3.5.5H2O complexes C39H36MN3O6.5.5H2O) (where M is Al or Ga, respectively, and L is the anion of 3-hydroxy-2-methyl-1-p-tolyl-4-pyridinone) are isomorphous and isostructural, crystallizing in the trigonal space group p3BAR1c with Z = 4},
	keywords = {3-HYDROXY-4-PYRIDINONES, 4-PYRIDONE EXTRACTANTS, PHYSICAL-PROPERTIES},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1991EW60200031},
	author = {Zhang, Z. H. and Rettig, S. J. and Orvig, Chris}
}
