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Articles 61 - 64 of 64
Full-Text Articles in Chemistry
Alkali Oxides. Analysis Of Bonding And Explanation Of The Reversal Of Ordering Of The 2Σ And 2Π States, Janet N. Allison, Robert J. Cave, William A. Goddard Iii
Alkali Oxides. Analysis Of Bonding And Explanation Of The Reversal Of Ordering Of The 2Σ And 2Π States, Janet N. Allison, Robert J. Cave, William A. Goddard Iii
All HMC Faculty Publications and Research
We analyze the bonding in alkali oxides, MO, for M = Li, Na, K, Rb, and Cs. Using ab initio correlated wave functions we find that the ground state is ²II for M = Li, Na, and K and that the ground state is ²Ʃ^+ for M = Rb and Cs. The origin of this effect is explained.
A Survey Of Ligand Effects Upon The Reaction Entropies Of Some Transition Metal Redox Couples, Edmund L. Yee, Robert J. Cave, Kendall L. Guyer, Paul D. Tyma, Michael J. Weaver
A Survey Of Ligand Effects Upon The Reaction Entropies Of Some Transition Metal Redox Couples, Edmund L. Yee, Robert J. Cave, Kendall L. Guyer, Paul D. Tyma, Michael J. Weaver
All HMC Faculty Publications and Research
The reaction entropies ∆S°_rc of a number of transition metal redox couples of the form M(III)/(II) in aqueous solution have been determined using nonisothermal electrochemical cells in order to explore the effect of varying the ligand structure upon the nature of the ion-solvent interactions. Examinations of six aquo couples of the form M(OH_2)_n&3+/2+ with varying metal M yielded ∆S°_rc values in the range 36-49 eu. In order to scrutinize the effect of replacing aquo with ammine and simple anionic ligands, Ru(III)/(II) couples were employed since the relative substituion inertness of both oxidation states allowed ∆S …
The Kinetics Of Solvent Reorientation In Hydroxylated Solvents From The Exciting-Wavelength Dependence Of Chromophore Emission Spectra, John Milton, Robert M. Purkey, William C. Galley
The Kinetics Of Solvent Reorientation In Hydroxylated Solvents From The Exciting-Wavelength Dependence Of Chromophore Emission Spectra, John Milton, Robert M. Purkey, William C. Galley
WM Keck Science Faculty Papers
The disappearance of the exciting-wavelength dependence of the phosphorescence spectra of polar, aromatic chromophores in supercooled glycol–water mixtures is utilized to monitor the kinetics of solvent reorientation. Reorientation times in the nanosecond to second range are obtained for (3:2 v/v) glycerol–water and (1:1 v/v) ethylene glycol–water at 140–240 °K. The results suggest that the process is one involving a cluster of solvent molecules and in which the chromophore plays a relatively passive role. Steady-state data and direct measurements of phosphorescence shifts as a function of time indicate that the solvent reorientation process is nonexponential in nature. The decay function derived …
A Theoretical Model For Gas Separation In A Glow Discharge: Cataphoresis, Fredrick H. Shair, Donald S. Remer
A Theoretical Model For Gas Separation In A Glow Discharge: Cataphoresis, Fredrick H. Shair, Donald S. Remer
All HMC Faculty Publications and Research
A theoretical model for transient and steady-state cataphoresis is developed starting with the macroscopic equations of continuity. After a brief breakdown period, the impurity ions are assumed to be closely coupled with their neutral counterparts. The basic assumptions in the model are that after breakdown, the level of ionization of the impurity, and the axial electric field remain constant; it is demonstrated that under these conditions a system involving rapid ionization-recombination reactions is equivalent to a system in which no reaction occurs, but in which the "effective'' ion mobility is a product of the true ion mobility and the fraction …