The ground state for sticky disks

It is proven that the ground state of the two-dimensional sticky potential is the triangular lattice.Research supported in part by NSF grant MCS 78-01520-A01.     

Dye laser excitation of the fluorosulfate radical: Origin band excitation

Discrete visible fluorescence is observed from excitation of the fluorosulfate radical by means of a dye laser. The frequency of the dye laser is chosen to coincide with each of the two components of the origin band observed at 19 383 and 19 354 cm^?1. Ground-state fundamentals are assigned for the radical and evidence is provided to suggest that the ground state of the radical may not have C_3v symmetry.     

Temperature derivatives at constant volume of the elastic constants of the alkali halides

Values of dC/dT)_V have been computed from experimental dC/dT)_P and dC/dP)_T for the three elastic constants (expressed as $\text{B}{}_{\mathrm{T}}\text{, C}{}_{44}\text{and}\text{(C}{}_{11}\text{?C}{}_{12}\text{)}\text{2)}$ of each of the 16 Li, Na, K, and Rb halides. The dC/dT)_V measure the explicit dependence of C on T, the effect of thermal expansion having been removed. The dC/dT)_V are all small (compared with dC/dT)_P), are all negative, and vary quite systematically and smoothly with anion, with cation and with the three elastic constants. Negative dB_T/dT)_V is accounted for both thermodynamically and by available lattice dynamical calculations. dC/dT)_V for shear constant is expressed in terms of two vibrational mode parameters, whose values can then be estimated from the observed value, and the trend of dC/dT)_V with Debye temperature.     

Research Note

Formulas are derived for consistent evaluation of permutationally totally symmetric and determinantally antisymmetric powers of generalized combinations in which irreducible representations may occur with either positive or negative weights.     

Reactivity of tetrahydrochromeno[2,3‐b]indoles: chromic indicators of cyanide

The synthesis and reactivity of a tetrahydrochromeno[2,3‐b]indoles are reported. Evidence for reversible ring‐opening is based on H/D exchange and trapping experiments. These compounds readily undergo reaction with tetra‐n‐butylammonium cyanide. The cyanide reaction is 10–100× faster when the solution is irradiated with 350 nm light. Reaction with trimethylsilyl cyanide occurs only with UV irradiation demonstrating photoreactivity. The rate of tetrahydrochromeno[2,3‐b]indole ring‐opening is greater for (i) Me substitution at the hemiaminal carbon (compared to Ph), and (ii) substitution of fluorine at the 9‐position of the indole. Under acidic conditions, the ring‐opened indolium ion is observed. Copyright © 2013 John Wiley & Sons, Ltd.     

The level shift operator and its effect on line shapes in vibronically perturbed spectra

This paper discusses the role of the level shift operator in vibronically mixed molecular resonances. The effect of this operator on the shapes of resonances is particularly important when the resonances contain resolved structure.     

13C NMR Assignments of Artemisinin,Desoxyartemisinin and Artemether

The ¹³C nmr assignments for all carbons except the methylene groups were made for artemisinin (1), artemether (2) and desoxyartemisinin (3). The assignments were based on chemical shift theory and confirmed by selective band decoupling experiments.     

An experimental and modeling study of the autoignition of 3-methylheptane

An experimental and kinetic modeling study of the autoignition of 3-methylheptane, a compound representative of the high molecular weight lightly branched alkanes found in large quantities in conventional and synthetic aviation kerosene and diesel fuels, is reported. Shock tube and rapid compression machine ignition delay time measurements are reported over a wide range of conditions of relevance to combustion engine applications: temperatures from 678 to 1356 K; pressures of 6.5, 10, 20, and 50 atm; and equivalence ratios of 0.5, 1.0, and 2.0. The wide range of temperatures examined provides observation of autoignition in three reactivity regimes, including the negative temperature coefficient (NTC) regime characteristic of paraffinic fuels. Comparisons made between the current ignition delay measurements for 3-methylheptane and previous results for n-octane and 2-methylheptane quantifies the influence of a single methyl substitution and its location on the reactivity of alkanes. It is found that the three C₈ alkane isomers have indistinguishable high-temperature ignition delay but their ignition delay times deviate in the NTC and low-temperature regimes in correlation with their research octane numbers. The experimental results are compared with the predictions of a proposed kinetic model that includes both high- and low-temperature oxidation chemistry. The model mechanistically explains the differences in reactivity for n-octane, 2-methylheptane, and 3-methylheptane in the NTC through the influence of the methyl substitution on the rates of isomerization reactions in the low-temperature chain branching pathway, that ultimately leads to ketohydroperoxide species, and the competition between low-temperature chain branching and the formation of cyclic ethers, in a chain propagating pathway.     

Element neighbourhoods in twofold triple systems

The method of differences is used to establish that every 2-regular multigraph onv– 10,2 (mod 3) points occurs as the neighbourhood graph of an element in a twofold triple system of orderv, with two exceptions: C₂C₃and C₃C₃.Dedicated to Professor Hanfried Lenz on the occasion of his seventieth birthday     

Algebraic properties of discrete box splines

The central objective of this paper is to discuss linear independence of translates of discrete box splines which we introduced earlier as a device for the fast computation of multivariate splines. The results obtained here allow us to draw conclusions about the structure of such discrete splines which have, in particular, applications to counting the number of nonnegative integer solutions of linear diophantine equations.