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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 44 (1972), S. 253-259 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 5 (1976), S. 751-763 
    ISSN: 1572-8927
    Keywords: Aqueous solutions ; thermal expansibilities ; alcohols ; ethers ; solute-water interactions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The temperature dependence of limiting apparent molal volumes Φ°υ in water for some alcohols (methanol, ethanol, 1-propanol, 2-butanol, 3-pentanol, 3-hexanol, 2,5-hexanediol, cyclopentanol, cyclohexanol, cycloheptanol, and 1,4-cyclohexanediol) and ethers (trimethylene oxide, tetrahydrofuran, tetrahydropyran, 1,3-dioxolane, 1,3-dioxane, 1,4-dioxane, 1,3-dioxepane, 1,3,5-trioxane, dimethoxymethane, 1,2-dimethoxyethane, diethoxymethane, and diethyl ether) has been studied in the temperature range 10–50°C by means of an automatic digital-readout dilatometer. Values of the thermal expansion coefficient α* = (1/Φ°υ)(∂Φ°υ/∂T)p have been obtained at several temperatures and discussed together with literature data on expansibilities of related compounds. The data show a wide spectrum of values of α* at low temperatures which is narrowed at the higher ones. The expansibilities of monofunctional alcohols increase with increasing temperature; the opposite effect is observed for polyhydric alcohols. The α*'s of ethers are very slightly temperature dependent and are much higher, at low temperature, than those of alcohols having the same ratio ofn o/nc. These results are discussed in terms of solutewater interactions, and a possible interpretation is put forward.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-8927
    Keywords: Apparent molal heat capacities ; aqueous solutions ; solute-water interactions ; ethers ; aminoethers ; aminoalcohols ; diamines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Apparent molal heat capacities of 20 organic uncharged compounds in aqueous solution have been determined at 25 and 40°C. The substances studied include mono- and polyfunctional ethers, and bifunctional open-chain compounds like aminoalcohols, aminoethers, and diamines. The results obtained support the presence of interaction between water and the hydrophilic groups −O−, −NH2, −NH−, and $$\begin{array}{*{20}c} \backslash \\ / \\ \end{array} N - $$ , and evidence indicates that these interactions strongly depend on the molecular structure of the compound containing the functional group.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-8927
    Keywords: Apparent molal compressibilities ; aqueous solutions ; solute-water interactions ; cyclic alcohols ; cyclic ethers ; water structure ; open-chain alcohols ; linear diethers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The limiting apparent molal adiabatic and isothermal compressibilities in aqueous solutions of alcohols and ethers at various temperatures have been determined by means of ultrasonic velocity measurements. The following compounds have been considered: secondary cyclic and open-chain alcohols (cyclopentanol, cyclohexanol, cycloheptanol, 2-butanol, 3-pentanol, 3-hexanol, 4-heptanol; cyclic ethers of the types (CH2)3On (n=1, 2, 3), (CH2)nO2 (n=3, 4, 5), and (CH2)nO (n=3, 4, 5); and the linear diethers dimethoxymethane, diethoxymethane, and 1,2-dimethoxyethane. The results indicate that both alcohols and ethers cause the water near the solute to become more resistant to pressure than the bulk. This is in agreement with the prediction of a mixture model for water.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-8927
    Keywords: Enthalpy of solution ; water ; octan-1-ol ; organic solutes ; microheterogeneity, microphase transition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Limiting enthalpies of solution δsolnH°(oct/w) of several monofunctionalcompounds (tetrahydropyran, diethylamine, pyrrolidine, piperidine,1-methylpiperidine) in water–octan-1-ol mixtures with water content ranging from zero tosaturation have been determined at 25°C. The observed phenomenology hasbeen interpreted by supposing that the solvent medium undergoes a microphasetransition at water mole fraction of about 0.08. In the water-poor region theexperimental behavior is consistent with the presence of water molecules inprevailingly monodispersed form, while in the water-rich region the formationof organized pseudomicellar water aggregates is suggested. Two different simplemodels have also been proposed to describe quantitatively the observed trendsof δsolnH°(oct/w) vs. mole fraction of water.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1572-8927
    Keywords: Group contributions ; partial molar heat capacity ; partial molar volume ; free energy of hydration ; enthalpy of hydration ; dilute aqueous solutions ; non-electrolytes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermodynamic properties ΔG h o,ΔH h o, and ΔC p,h oassociated with the transfer of non-ionic organic compounds from gas to dilute aqueous solution and the limiting partial molar properties C p o ,2 and V2 2 of these compounds in water are described through a simple scheme of group contributions. A distinction is made between groups made only of carbon and hydrogen, and functional groups i.e. groups containing at least one atom different from carbon and hydrogen. Each group is assigned a contribution, for each property, through a least squares procedure which utilizes only molecules containing at most one functional group. Finally, for compounds containing more than one functional group, correction parameters are evaluated as the differences between the experimental values and those calculated by means of the group contributions. The different behavior of hydrophilic compared with hydrophobic groups is discussed for the various properties. A rationale for the correction parameters, i.e. for the effects of the interactions among hydrophilic groups on the thermodynamic properties, is attempted.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1572-8927
    Keywords: Apparent molal heat capacity ; aqueous solution ; piperidines ; morpholines ; piperazines ; heat capacity of protonation ; solute-water interaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Apparent molal heat capacities $$\Phi _{C_p } $$ of some piperidine, morpholine, and piperazine derivatives in aqueous solution have been determined by adiabatic calorimetry in the temperature range 20–55°C and in the molality range 0.2–1m. Comparison of experimental $$\Phi _{C_p } $$ values with those calculated through group contributions, found for monofunctional compounds, indicates strong interactions between the hydrophilic centers. An interpretation is given of the possible mechanism of this interaction. Also, values of ΔC p for the addition reaction of proton to nitrogen centers of mono- and bifunctional organic compounds are examined.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1572-8927
    Keywords: Thermodynamics of oxygen binding ; Co(II) oxygen-carrier complexes ; macrocyclic ligands ; tetraazacyclopentadecane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Aqueous solutions containing Co2+ and the macrocyclic ligand 1,4,8,12-tetraazacyclopentadecane (L) are able to bind reversibly molecular oxygen to form the species Co2L2O 2 4+ between pH 5 and 7. This species at pH greater than 8 is replaced by the complex Co2L2O2 (OH) 2 2+ whose concentration in the solution increases to about pH 10.5. At pH greater than 10.5, Co(II) exists totally in this μ-peroxobisydroxo complex. Both the above mentioned oxygenated forms suffer a relatively slow irreversible oxidation to Co(III). From oxygen binding curves, approximate values of the equilibrium constants were calculated for the addition of oxygen to CoL2+ to form the μ-peroxo and the μ-peroxo-bishydroxo complexes. The enthalpies of formation of this latter complex starting from both Co2+ or CoL2+ have been obtained by means of calorimetric measurements. The effects of the size of the macrocyclic ligand on the affinity and the enthalpy of oxygen binding have been considered.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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