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  Partner: UNT College of Arts and Sciences
 Language: English
 Collection: UNT Scholarly Works
Anomalous diffusion and environment-induced quantum decoherence

Anomalous diffusion and environment-induced quantum decoherence

Date: July 1996
Creator: Bonci, Luca; Grigolini, Paolo & Laux, Adam
Description: This article discusses anomalous diffusion and environment-induced quantum decoherence. Abstract: We study the anomalous diffusion resulting from the standard map in the so-called accelerating state, and we observe that it is determined by unusually large times of sojourn of the classical trajectories in the fractal region at the border between the chaotic sea and the acceleration island. The quantum-mechanical breakdown of this property implies a coherence among so slightly different values of momentum as to become much more robust against environment fluctuations than the quantum localization corresponding to normal diffusion.
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Anomalous diffusion associated with nonlinear fractional derivative Fokker-Planck-like equation: Exact time-dependent solutions

Anomalous diffusion associated with nonlinear fractional derivative Fokker-Planck-like equation: Exact time-dependent solutions

Date: August 2000
Creator: Bologna, Mauro; Tsallis, Constantino & Grigolini, Paolo
Description: This article discusses anomalous diffusion associated with nonlinear fractional derivative Fokker-Planck-like equation. Abstract: We consider the d=1 nonlinear Fokker-Planck-like equation with fractional derivatives (∂/∂t)P(x,t) = D(∂ƴ/∂xƴ)[P(x,t]v. Exact time-dependent solutions are found for v = (2 - y)/(1 + y)(-∞ < y ⩽ 2). By considering the long-distance asymptotic behavior of these solutions, a connection is established, namely, q = (y + 3)/(Y + 1)(0 < y ⩽ 2), with the solutions optimizing the nonextensive entropy characterized by index q. Interestingly enough, this relation coincides with the only already known for Lévy-like superdiffusion (i.e., v = 1 and 0 < y ⩽ 2). Finally, for (y,v) = (2,0) the authors obtain q=5/3, which differs from the value q = 2 corresponding to the y = 2 solutions available in the literature (v < 1 porous medium equation), thus exhibiting nonuniform convergence.
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Application of the Correlation Consistent Composite Approach (ccCA) to Third-Row (Ga-Kr) Molecules

Application of the Correlation Consistent Composite Approach (ccCA) to Third-Row (Ga-Kr) Molecules

Date: January 19, 2008
Creator: DeYonker, Nathan J.; Mintz, Benjamin; Cundari, Thomas R., 1964- & Wilson, Angela K.
Description: This article discusses the application of the correlation consistent composite approach (ccCA). Abstract: The correlation consistent composite approach (ccCA) has been applied to the G3/05 training set of 51 energetic properties for the atoms and molecules that contain the 4p elements, Ga-Kr. When atomic and molecular first-order spin orbit coupling corrections are added to open shell atoms and molecules, the ccCA has a mean absolute deviation from experiment (MAD) of 0.95 kcal mol-1, an improvement of 0.10 kcal mol-1 over G3 and G3X model chemistries. The performance of the ccCA on third-row-containing atoms and molecules is, therefore, commensurate in accuracy with previous studies on lighter main group elements H-Ar. While the typical methods used to compute theoretical molecular spin orbit corrections may go against the spirit of "black box" model chemistries, such corrections may be necessary for molecules containing heavy elements such as Ga-Kr. For example, when second-order spin orbit corrections are added to the atomic and molecular energies, the ccCA MAD is reduced to 0.88 kcal mol-1.
Contributing Partner: UNT College of Arts and Sciences
Are Net Discount Rates Stationary?: Some Further Evidence

Are Net Discount Rates Stationary?: Some Further Evidence

Date: September 1994
Creator: Haslag, Joseph H.; Nieswiadomy, Michael L. & Slottje, Daniel J.
Description: This article discusses net discount rates. Abstract: Gamber and Sorensen provide evidence suggesting that the net discount ratio experienced a level shift in the mean between 1977 and 1981. If such a shift occurred, the nonlinearity in the data shows up as a failure to reject the null hypothesis that a unit root is present; that is, the series is I(1). In this reply, evidence is presented - the Phillips-Perron test and a univariate version of the Stock-Watson q-test - suggesting that the net discount ratio is stationary. Hence, the mean is constant. In addition, if one extends the analysis to include the 1989 through 1993 period, the net discount ratio appears to be reverting.
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Are Net Discount Ratios Stationary?: The Implications For Present Value Calculations

Are Net Discount Ratios Stationary?: The Implications For Present Value Calculations

Date: September 1991
Creator: Haslag, Joseph H.; Nieswiadomy, Michael L. & Slottje, Daniel J.
Description: Abstract: This article analyzes the relationship between real interest rates and real growth rates in wages. The stationary of these time series has been discussed in the literature. However, since the net discount ratio, (1 + gτ)/(1 + rτ), is a nonlinear transformation, it is not necessarily stationary even if the interest rate and growth rate in wages series are each stationary. On the other hand, the net discount ratio may be stationary even if the interest rate and growth rate series are both non-stationary. The significant finding of this article is that this ratio is stationary. This conclusion appears robust since it holds for at least four different Treasury securities analyzed: three month, six month, one year, and three year. Therefore, a real net discount ratio, (1 + gτ)/(1 + rτ), can be used with confidence in constructing present value forecasts of expected earnings.
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Aromatic C-H Activation and Catalytic Hydrophenylation of Ethylene by TpRu{P(OCH2)3CEt} (NCMe)Ph

Aromatic C-H Activation and Catalytic Hydrophenylation of Ethylene by TpRu{P(OCH2)3CEt} (NCMe)Ph

Date: June 5, 2008
Creator: Foley, Nicholas A.; Ke, Zhuofeng; Gunnoe, T. Brent; Cundari, Thomas R., 1964- & Petersen, Jeffrey L.
Description: This article discusses aromatic C-H activation and catalytic hydrophenylation of ethylene by TpRu{P(OCH2)3CEt} (NCMe)Ph. Abstract: The complexes TpRu{P(OCH2)3CEt}(L)R {L = PPh3 or NCMe; R = Cl, OTf (OTf = trifluoromethane-sulfonate), or Ph; Tp = hydridotris(pyrazolyl)borate} and TpRu{P(OCH2)3CEt} (ɳ3-C3H4Me) were synthesized and isolated. TpRu{P(OCH2)3CEt} (NCMe)Ph was found to initiate C-H activation of benzene and to catalyze the hydrophenylation of ethylene to produce ethylbenzene. Ethylene C-H activation to ultimately produce TpRu{P(OCH2)3CEt} (ɳ3-C3H4Me) kinetically competes with the catalytic hydrophenylation of ethylene. Computational studies were undertaken on reactions in the proposed catalytic ethylene hydrophenylation cycle as well as key side reactions.
Contributing Partner: UNT College of Arts and Sciences
Arylpalladium Phosphonate Complexes as Reactive Intermediates in Phosphorus-Carbon Bond Forming Reactions

Arylpalladium Phosphonate Complexes as Reactive Intermediates in Phosphorus-Carbon Bond Forming Reactions

Date: January 21, 2009
Creator: Kohler, Mark C.; Grimes, Thomas V.; Wang, Xiaoping; Cundari, Thomas R., 1964- & Stockland, Robert A., Jr.
Description: This article discusses arylpalladium phosphonate complexes as reactive intermediates in phosphorus-carbon bond forming reactions. Abstract: Phosphorus-carbon bond formation from discrete transition metal complexes have been investigated through a combination of synthetic, spectroscopic, crystallographic, and computational methods. Reactive intermediates of the type (diphosphine)Pd(aryl)P(O)(OEt)2) have been prepared, characterized, and studied as possible intermediates in metal-mediated coupling reactions. Several of the reactive intermediates were characterized crystallographically, and a discussion of the solid state structures is presented. In contrast to other carbon-heteroelement bond forming reactions, palladium complexes containing electron-donating substituents on the aromatic fragment exhibited faster rates of reductive elimination. Large bit angle diphosphine ligands induced rapid rates of elimination, while bipyridine and small bite angle diphosphine ligands resulted in much slower rates of elimination. An investigation of the effect of typical impurities on the elimination reaction was carried out. While excess diphosphine, pyridine, and acetonitrile had little effect on the observed rate, the addition of water slowed the phosphorus-carbon bond forming reaction. Coordination of water to the complex was observed spectroscopically and crystallographically. Computational studies were utilized to probe the reaction pathways for P-C bond formation via Pd catalysis.
Contributing Partner: UNT College of Arts and Sciences
Atomic resolution ultrahigh vacuum scanning tunneling microscopy of epitaxial diamond (100) films

Atomic resolution ultrahigh vacuum scanning tunneling microscopy of epitaxial diamond (100) films

Date: May 1, 1995
Creator: Stallcup, Richard E.; Aviles, A. F. & Pérez, José M.
Description: In this article, the authors report atomic resolution images of chemical vapor deposition grown epitaxial diamond (100) films obtained in ultrahigh vacuum (UHV) with a scanning tunneling microscope. A (2X1) dimer surface reconstruction and amorphous atomic regions are observed. The (2X1) unit cell is measured to be 0.51±0.01X0.25±0.01 nm2. The amorphous regions are identified as carbon. A radial structure 1.5 nm in diameter is observed on a plane at a 20° slope to the (2X1) surface. Tunneling current versus voltage spectra in UHV and Raman spectra are also obtained.
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Atomic structure of steps and defects on the clean diamond (100)-2 X 1 surface studied using ultrahigh vacuum scanning tunneling microscopy

Atomic structure of steps and defects on the clean diamond (100)-2 X 1 surface studied using ultrahigh vacuum scanning tunneling microscopy

Date: December 9, 2002
Creator: Stallcup, Richard E. & Pérez, José M.
Description: In this article, the authors report ultrahigh vacuum scanning tunneling microscopy studies of the clean nonhydrogen-terminated diamond (100)-2 X 1 surface showing single- and double-layer steps that are rebonded. The main defects observed are single, multiple, and row dimer vacancies, and antiphase boundaries. Buckling of dimers is not observed, consistent with symmetric dimers.
Contributing Partner: UNT College of Arts and Sciences
The Autecology of the Fío-Fío (Elaenia Albiceps Lafresnaye and D'Orbigny) in Subantarctic Forests of the Cape Horn Biosphere Reserve, Chile

The Autecology of the Fío-Fío (Elaenia Albiceps Lafresnaye and D'Orbigny) in Subantarctic Forests of the Cape Horn Biosphere Reserve, Chile

Date: 2007
Creator: Brown, Clare E.; Anderson, Christopher B.; Ippi, Silvina; Sherriffs, Margaret; Charlin, Rina; McGehee, Steven M. et al
Description: This article discusses the autecology of the fío-fío. Abstract: As the most diverse and abundant terrestrial vertebrates in the Cape Horn Archipelago, birds potentially play key roles in the ecology of subantarctic ecosystems. However, the lack of long-term ornithological studies in southern South America has previously hindered the identification of relevant aspects of the autecology of even the most common species. One abundant species in the austral summer is the fío-fío's ecology in the CHBR by determining: a) longevity and site fidelity, b) arrival-departure dates, c) abundance of adults and juveniles, d) diet and e) morphology. A total 827 fío-fíos were banded during the study period. Of the 67 recaptures, it was possible to determine that fío-fíos may live at least up to 7 years. Fío-fíos arrived as early as 28 October and left as late as 15 April with juveniles fledging in January. In the austral archipelago, the fío-fío's diet consisted of 10 invertebrate orders and at least 5 plant species. Males had significantly longer tails and wings than females, while females were significantly heavier in the pre-fledging season (Oct-Dec). This study provides new information on the autecology of fío-fío in the world's southernmost forests.
Contributing Partner: UNT College of Arts and Sciences