Dissociation Quotients for Citric Acid in Aqueous Sodium Chloride Media to 150°C

The three molal dissociation quotients for citric acid were measured potentiometrically with a hydrogen-electrode concentration cell from 5 to 150°C in NaCl solutions at ionic strengths of 0.1, 0.3, 0.6, and 1 molal. The molal dissociation quotients and available literature data at infinite dilution were fitted by empirical equations in the all-anionic form involving an extended Debye-Hückel term and up to five adjustable parameters involving functions of temperature and ionic strength. This treatment yielded the following thermodynamic quantitites for the first dissociation equilibrium at 25°C: logK _1a=−3.127±0.002, ΔH _1a ^o =4.1±0.2 kJ-mol⁻¹, ΔS _1a ^o =−46.3±0.7 J-K⁻¹-mol⁻¹, and ΔCp _1a ^o =−162±7 J-K⁻¹-mol⁻¹; for the second acid dissociation equilibrium at 25°C: logK _2a =−4.759±0.001, ΔH _2a ^o =2.2±0.1, ΔS _2a ^o =−83.8±0.4, and ΔCp _2a ^o =−192±15, and for the third dissociation equilibrium at 25°C: logK _3a=−6.397±0.002, ΔH _3a ^o =−3.6±0.2, ΔS _3a ^o =−134.5±0.7, and ΔCp _3a ^o =−231±7.     

Spin exchange interaction through phenylene-ethynylene bridge in diradicals based on iminonitroxide and nitronylnitroxide radical derivatives. 1. Experimental investigation of the through-bond spin exchange coupling

A series of bis-iminonitroxide diradical derivatives of different lengths and geometry have been prepared that incorporate a conjugated phenylene-ethynylene bridge as a rigid spacer. This paper describes the synthesis of these new components and their main characterizations. An unexpected singlet ground state and substituent effects on the singlet-triplet gap have been found for substituted "m-phenylene"-based diradicals. The effects of the pi-conjugation on the intramolecular through-bond spin coupling have been investigated by changing the length of the spacer within linear derivatives. The EPR studies demonstrate the intramolecular magnetic coupling between the radical spins within all compounds. This result is very attractive and unusual, given the large distance between the radicals from 15 A in the dimer to 36 A in the pentamer.     

Structural isomerism in crystals of redox-active secondary ortho-diamides: the role of competing intra- and intermolecular hydrogen bonds in directing crystalline topologies

The solid-state chemistry of a series of seven ortho-bis(alkylamido)ethylenedithiotetrathiafulvalene derivatives EDT-TTF-(CONHR)2 (R=Me, 1; Et, 2; Pr, 3; Bu, 4; Pent, 5; Hex, 6; and Bz, 7), in their neutral and one-electron-oxidized, radical cation states, was investigated with an eye on the topology of intra- and intermolecular hydrogen-bond motifs. In the case of neutral, monomolecular solids, an intramolecular N--H.O hydrogen bond seals a constrained seven-membered ring for 1, 2, 3, and 7, which is disrupted in butyl derivative 4 in favor of an antiparallel ladder at the expense of any intramolecular hydrogen bond. In the solid-state, the competition between intra- and intermolecular hydrogen bonding observed in solution depends on the packing of the molecules. Electrocrystallization of methyl derivative 1 with ReO4- or ClO4-, two anions of different volumes but otherwise identical charge and symmetry, revealed a fine sensitivity of the constrained seven-membered ring to the internal chemical pressure exerted by the anion. [1]2 *+ReO4 (sigmaRT=8.5 S cm(-1), activation energy Delta=600 K at high temperature) and beta"-[1]2 *+ClO4 (sigmaRT=0.03 S cm(-1), Delta=1600 K; under pressure at room temperature, the conductivity increases by three orders of magnitude up to 17 kbar with a linear variation of the activation energy with pressure, Delta=aP with a=0.202 10(6) K kbar(-1)) have vastly different architectures, dimensionalities, electronic structures, and collective properties, a consequence of the presence of the closed or open structural isomers in one or the other. This exemplifies the flexibility of functionalized TTF derivatives, even when the functional group is directly attached to the electro-active core. This allows an analogy to be drawn with tetrafunctionalized metallocenes, in which such flexibility has already been observed. The experimental data are supported by theoretical calculations of the energy profile of a model molecule on rotation of the amido groups.     

Singular crystalline beta'-layered topologies directed by ribbons of self-complementary amide...amide ring motifs in [EDT-TTF-(CONH(2))(2)](2)X (X = HSO(4)(-), ClO(4)(-), ReO(4)(-), AsF(6)(-)): coupled activation of ribbon curvature, electron interactions, and magnetic susceptibility

The deliberate design of a series of single crystals of conducting two-dimensional radical cation salts of o-bis(amide)-appended ethylenedithiotetrathiafulvalene, beta'-[EDT-TTF-(CONH(2))(2)](2)X (X = HSO(4)(-), ClO(4)(-), ReO(4)(-), or AsF(6)(-)) and of their parent monocomponent solid EDT-TTF-(CONH(2))(2) is demonstrated and allows us to reach a level of prediction of the structure of molecular conductors. Their conductivity is activated with a gap of 1650 K and a sizable room-temperature conductivity of 0.15 S.cm(-)(1) (for X = ClO(4)(-)) and a singular spin susceptibility for a beta'-type salt that, in addition, changes very remarkably with the anion. The key design element is that of a recurrent, puckered ribbon constructed out of self-complementary, hydrogen-bonded amide...amide ring motifs whose minute modulations of curvature and shape throughout the series have been shown to correlate to very remarkable differences in the intrastack beta(HOMO)(-)(HOMO) interaction energies and changes in the density of states at the Fermi level and on to important differences of spin susceptibility behavior in a system where electron correlations are significant. The coupled activation of structure, electron interactions, and magnetic susceptibility discovered and discussed throughout the paper is unprecedented and is seen as a genuine expression of interfacial hydrogen-bond interactions onto the collective electronic properties.     

Heterogeneity in styrene-butadiene latex films

Low-Tg styrene-butadiene (SB) latex films were investigated by noncontact atomic force microscopy and scanning electric potential microscopy, revealing a number of different morphologies and electric potential patterns across films cast from the same SB latex dispersions under the same conditions. Surface leveling and charge dispersion throughout the films are, thus, restrained even at temperatures above Tg and the minimum film-formation temperature. An unprecedented electric pattern is observed, in which the particle cores are more positive than the contacting particle outer layers. Different packing patterns, including cubic and hexagonal arrays, coexist in neighboring areas. Zonal centrifugation of the SB latex in sucrose density gradient shows that particles cover a broad range of densities. Thus, film surface heterogeneity is at least partly due to particle heterogeneity. Fractal dimensions of topographic profiles are lower than those of the electric potential profiles, showing that charge mobility is much more restrained than polymer chain motion at the film surface and that it imposes a limit to the charged chain-ends motion.     

On the complexity of the Unit Commitment Problem

Annals of Operations Research - This article analyzes how the Unit Commitment Problem (UCP) complexity evolves with respect to the number n of units and T of time periods. A classical reduction...     

The effect of subcritical carbon dioxide on the dissolution of cellulose in the ionic liquid 1-ethyl-3-methylimidazolium acetate

The ionic liquid (IL) 1-ethyl-3-methylimidazolium acetate ([emim][OAc]) readily dissolves high concentrations of cellulose. However, the high viscosity of [emim][OAc] (162 cP at 20 °C) could limit its use as a solvent for cellulose. Dissolved CO₂ has been shown to decrease the viscosity of ILs. In this study, a 50 psi CO₂ environment was applied for the dissolution of cellulose in [emim][OAc] to determine if the cellulose dissolution could be enhanced. Dissolution profiles of 4 wt% cellulose dissolved in [emim][OAc] were obtained over a 24 h period. A 75% increase in the amount of dissolved cellulose was observed with the application of a 50 psi CO₂ environment.     

Kinetic Study on Models of the Tetrabutqxyzirconium-Catalyzed Reaction Between α, ω -Dicarboxypolyamide-11 and α, ω -Dihydroxypolyoxyethylene

The kinetics of the tetrabutoxyzirconium-catalyzed esterifications between 11-dodecylamideundecanoic acid and 1-dodecanol, 2-tridecanol, a-dodecyl-ω-hydroxypolyoxyethylene are studied and compared to that of α, ω-dicarboxypolyamide-l 1 and α, ω-dihydroxypolyoxyethylene. The reaction with 2-tridecanol is characterized by an autoacceleration phenomenon. In the other cases the reaction rate is not greatly affected by catalyst concentration. An explanation involving the formation of catalyst condensates at the very beginning of the reaction is put forward.