Competitive Halide Binding by Halogen Versus Hydrogen Bonding: Bis‐triazole Pyridinium

The binding of F^?, Cl^?, Br^?, and I^? anions by bis‐triazole‐pyridine (BTP) was examined by quantum chemical calculations. There is one H atom on each of the two triazole rings that chelate the halide via H bonds. These H atoms were replaced by halogens Cl, Br, and I, thus substituting H bonds by halogen bonds. I substitution strongly enhances the binding; Br has a smaller effect, and Cl weakens the interaction. The strength of the interaction is sensitive to the overall charge on the BTP, rising as the binding agent becomes singly and then doubly positively charged. The strongest preference of a halide for halogenated as compared to unsubstituted BTP, as much as several orders of magnitude, is observed for I^?. Both unsubstituted and I‐substituted BTP could be used to selectively extract F^? from a mixture of halides.     

Shock tube study of dissociation and relaxation in 1,1-difluoroethane and vinyl fluoride

This paper reports measurements of the thermal dissociation of 1,1-difluoroethane in the shock tube. The experiments employ laser-schlieren measurements of rate for the dominant HF elimination using 10% 1,1-difluoroethane in Kr over 1500-2000 K and 43 < P < 424 torr. The vinyl fluoride product of this process then dissociates affecting the late observations. We thus include a laser schlieren study (1717-2332 K, 75 < P < 482 torr in 10 and 4% vinyl fluoride in Kr) of this dissociation. This latter work also includes a set of experiments using shock-tube time-of-flight mass spectrometry (4% vinyl fluoride in neon, 1500-1980 K, 500 < P < 1300 torr). These time-of-flight experiments confirm the theoretical expectation that the only reaction in vinyl fluoride is HF elimination. The dissociation experiments are augmented by laser schlieren measurements of vibrational relaxation (1-20% C(2)H(3)F in Kr, 415-1975 K, 5 < P < 50 torr, and 2 and 5% C(2)H(4)F(2) in Kr, 700-1350 K, 6 < P < 22 torr). These experiments exhibit very rapid relaxation, and incubation delays should be negligible in dissociation. An RRKM model of dissociation in 1,1-difluoroethane based on a G3B3 calculation of barrier and other properties fits the experiments but requires a very large DeltaE(down) of 1600 cm(-1), similar to that found in a previous examination of 1,1,1-trifluoroethane. Dissociation of vinyl fluoride is complicated by the presence of two parallel HF eliminations, both three-center and four-center. Structure calculations find nearly equal barriers for these, and TST calculations show almost identical k(infinity). An RRKM fit to the observed falloff again requires an unusually large DeltaE(down) and the experiments actually support a slightly reduced barrier. These large energy-transfer parameters now seem routine in these large fluorinated species. It is perhaps a surprising result for which there is as yet no explanation.     

Dissociation of 1,1,1-trifluoroethane behind reflected shock waves: shock tube/time-of-flight mass spectrometry experiments

The dissociation of 1,1,1,-trifluoroethane, a potential non-RRKM reaction, has been studied at 600 and 1200 Torr and high temperatures (1500-1840 K) using a new shock tube/time-of-flight mass spectrometer (ST/TOF-MS). These data obtained by an independent method are in good agreement with the laser schlieren, LS, experiments of Kiefer et al. [J. Phys. Chem. A 2004, 108, 2443-2450] and extend the range of that experimental dataset. The data have been simulated by both standard RRKM calculations and the non-RRKM model reported by Kiefer et al. but with = 750 cm(-1). Both the RRKM and non-RRKM calculations provide equally good fits to the ST/TOF-MS data. Neither model simulates the combined ST/TOF-MS and LS datasets particularly well. However, the non-RRKM model predicts a pressure dependency closer to that observed in the experiments than the RRKM model.     

Reaction of hydrogen atoms with propyne at high temperatures: an experimental and theoretical study

The kinetics of the reaction of hydrogen atoms with propyne (pC3H4) was experimentally studied in a shock tube at temperatures ranging from 1200 to 1400 K and pressures between 1.3 and 4.0 bar with Ar as the bath gas. The hydrogen atoms (initial mole fraction 0.5-2.0 ppm) were produced by pyrolysis of C2H5I and monitored by atomic resonance absorption spectrometry under pseudo-first-order conditions with respect to propyne (initial mole fraction 5-20 ppm). From the hydrogen atom time profiles, overall rate coefficients k(ov) identical with -([pC3H4][H])(-1) x d[H]/dt for the reaction H + pC3H4 --> products ( not equal H) were deduced; the following temperature dependence was obtained: kov = 1.2 x 10(-10) exp(-2270 K/T) cm(3) s(-1) with an estimated uncertainty of +/-20%. A pressure dependence was not observed. The results are analyzed in terms of statistical rate theory with molecular and transition state data from quantum chemical calculations. Geometries were optimized using density functional theory at the B3LYP/6-31G(d) level, and single-point energies were computed at the QCISD(T)/cc-pVTZ level of theory. It is confirmed that the reaction proceeds via an addition-elimination mechanism to yield C2H2 + CH3 and via a parallel direct abstraction to give C3H3 + H2. Furthermore, it is shown that a hydrogen atom catalyzed isomerization channel to allene (aC3H4), H + pC3H4 --> aC3H4 + H, is also important. Kinetic parameters to describe the channel branching of these reactions are deduced.     

Throughput performance of cooperative spectrum sensing network with improved energy detectors and SC diversity over fading channels

Wireless Networks - This paper proposes a novel cooperative spectrum sensing network (CSSN) with improved energy detector (IED) based cognitive radio (CR) users. Every CR user is furnished with...     

Algebraic Connectivity of Connected Graphs with Fixed Number of Pendant Vertices

In this paper, we consider the following problem. Over the class of all simple connected graphs of order n with k pendant vertices (n, k being fixed), which graph maximizes (respectively, minimizes) the algebraic connectivity? We also discuss the algebraic connectivity of unicyclic graphs.     

A 8–12 GHz, 44.3 dBm RF output class FF−1 DPA using quad-mode coupled technique for new configurable front-end 5G transmitters

Analog Integrated Circuits and Signal Processing - This paper presents a high-efficiency Class $${\mathrm{FF}}^{-1}$$ DPA using the quad-mode coupled technique for new configurable front-end 5G...     

Minimizing Laplacian spectral radius of unicyclic graphs with fixed girth

In this paper we consider the following problem: Over the class of all simple connected unicyclic graphs on n vertices with girth g (n, g being fixed), which graph minimizes the Laplacian spectral radius? Let U _n,g be the lollipop graph obtained by appending a pendent vertex of a path on n ? g (n > g) vertices to a vertex of a cycle on g ? 3 vertices. We prove that the graph U _n,g uniquely minimizes the Laplacian spectral radius for n ? 2g ? 1 when g is even and for n ? 3g ? 1 when g is odd.