38 research outputs found
Structure-property relationships in protic ionic liquids : a study of solvent-solvent and solvent-solute Interactions
The ionic nature of a functionalized protic ionic liquid cannot be rationalized simply through the differences in aqueous proton dissociation constants between the acid precursor and the conjugate acid of the base precursor. The extent of proton transfer, i.e. the equilibrium ionicity, of a tertiary ammonium acetate protic ionic liquid can be significantly increased by introducing an hydroxyl functional group on the cation, compared to the alkyl or amino-functionalized analogues. This increase in apparent ionic nature correlates well with variations in solvent-solute and solvent-solvent interaction parameters, as well as with physicochemical properties such as viscosity
Structure-property relationships in protic ionic liquids : A thermochemical study
How does cation functionality influence the strength of intermolecular interactions in protic ionic liquids (PILs)? Quantifying the energetics of PILs can be an invaluable tool to answer this fundamental question. With this in view, we have determined the standard molar enthalpy of vaporization, Delta H_vap , and the standard molar enthalpy of formation, Delta H_f, of three tertiary ammonium acetate PILs with varying cation functionality, and of their corresponding precursor amines, through a combination of Calvet-drop microcalorimetry, solution calorimetry, and ab-initio calculations. The obtained results suggest that these PILs vaporize as their neutral acid and base precursors. We also found a strong correlation between Delta H_vap of the PILs and of their corresponding amines. This suggests that, within this series of PILs, the influence of cation modification on their cohesive energies follows a group additivity rule. Finally, no correlation between the Delta H_vap of PILs and the extent of proton transfer, as estimated from the difference in aqueous pKa between the precursor acid and the conjugate acid of the precursor base, was observed
Crystallization of 4ā²-Hydroxyacetophenone from Water: Control of Polymorphism via Phase Diagram Studies
The preparation of polymorphs and solvates and the characterization
of their stability domains have received considerable attention in
recent years, due to the importance of these studies for fundamental
research and for the production of new materials for task-specific
applications. In this work, the selective and reproducible crystallization
of different solid forms of 4ā²-hydroxyacetophenone (HAP) from
water was investigated, through the determination of a temperatureāconcentration
(<i>T</i>ā<i>c</i><sub>HAP</sub>) phase
diagram. This determination was mainly based on gravimetric solubility
measurements, slurry tests, and metastable zone width (MZW) studies
with thermometric and turbidity detection. The experimental conditions
for the formation of five different HAP phases by cooling crystallization
could be established: the previously characterized anhydrous forms
I and II and the hydrate HAPĀ·1.5H<sub>2</sub>O (H1), and two
new hydrates, one of stoichiometry HAPĀ·3H<sub>2</sub>O (H2) and
another (H3) which proved too unstable for a stoichiometry determination.
The crystallization precedence of the various phases, their approximate
lifetimes, and transformation sequences could also be elucidated.
It was finally found that for a specific <i>T</i>ā<i>c</i><sub>HAP</sub> domain the crystallization of HAP solid
phases was mediated by a colloidal dispersion. Preliminary dynamic
light scattering experiments indicated that this dispersion consisted
of particles with diameters in the range of 100ā800 nm
A new polymorph of 4ā²-hydroxyvalerophenone revealed by thermoanalytical and X-ray diffraction studies
A new polymorph of 1-(4-hydroxyphenyl)pentan-1-one (4ā²-hydroxyvalerophenone, HVP) was identified by using differential scanning calorimetry, hot stage microscopy, and X-ray powder diffraction. This novel crystal form (form II) was obtained by crystallization from melt. It has a fusion temperature of Tfus = 324.3 Ā± 0.2āK and an enthalpy of fusion ĪfusHmo = 18.14Ā±0.18ākJĀ·molā1. These values are significantly lower than those observed for the previously known phase (form I, monoclinic, space group P21/c, Tfus = 335.6 Ā± 0.7āK; ĪfusHmo = 26.67Ā±0.04ākJĀ·molā1), which can be prepared by crystallization from ethanol. The results here obtained, therefore, suggest that form I is thermodynamically more stable than the newly identified form II and, furthermore, that the two polymorphs are monotropically related
Polymorphism in 4āHydroxybenzaldehyde: A Crystal Packing and Thermodynamic Study
A procedure for the selective and
reproducible preparation of the
two known 4-hydroxybezaldehyde polymorphs was developed, based on
the investigation of their relative stabilities by differential scanning
calorimetry and solubility studies. From the obtained results, the
stability domains of the two forms could be quantitatively represented
in a Ī<sub>f</sub><i>G</i><sub>m</sub><sup>Ā°</sup>ā<i>T</i> phase
diagram. The system was found to be enantiotropic: form II is more
stable than form I up to 277 Ā± 1 K; above this temperature, the
stability order is reversed, and the fusion of form I subsequently
occurs at 389.9 Ā± 0.2 K. Analysis of the crystal structures revealed
that in both polymorphs the 4-hydroxybezaldehyde molecule exhibits
the OH and CĀ(O)H substituents in a <i>Z</i> conformation,
which, according to B3LYP/6-31GĀ(d,p) calculations, is more stable
than the <i>E</i> conformation by only 0.4 kJĀ·mol<sup>ā1</sup>. The two forms are monoclinic, space group <i>P</i>2<sub>1</sub>/<i>c</i>, <i>Z</i>ā²/<i>Z</i> = 1/4, and have essentially identical densities at ambient
temperature (1.358 gĀ·cm<sup>ā3</sup> for form I; 1.357
gĀ·cm<sup>ā3</sup> for form II), but differ in their packing.
These differences are discussed, and the dissimilarities in the interactions
sustaining the packing are highlighted using Hirshfeld surfaces. Finally,
the relative stability and volumetric properties of both forms are
analyzed by molecular dynamics simulations
All-Atom Force Field for Molecular Dynamics Simulations on Organotransition Metal Solids and Liquids. Application to M(CO)<sub><i>n</i></sub> (MĀ = Cr, Fe, Ni, Mo, Ru, or W) Compounds
A previously developed OPLS-based
all-atom force field for organometallic
compounds was extended to a series of first-, second-, and third-row
transition metals based on the study of MĀ(CO)<i><sub>n</sub></i> (M = Cr, Fe, Ni, Mo, Ru, or W) complexes. For materials that are
solid at ambient temperature and pressure (M = Cr, Mo, W) the validation
of the force field was based on reported structural data and on the
standard molar enthalpies of sublimation at 298.15 K, experimentally
determined by Calvet-drop microcalorimetry using samples corresponding
to a specific and well-characterized crystalline phase: Ī<sub>sub</sub><i>H</i><sub>m</sub><sup>Ā°</sup> = 72.6 Ā± 0.3 kJĀ·mol<sup>ā1</sup> for CrĀ(CO)<sub>6</sub>, 73.4 Ā± 0.3 kJĀ·mol<sup>ā1</sup> for MoĀ(CO)<sub>6</sub>, and 77.8 Ā± 0.3 kJĀ·mol<sup>ā1</sup> for WĀ(CO)<sub>6</sub>. For liquids, where problems of polymorphism
or phase mixtures are absent, critically analyzed literature data
were used. The force field was able to reproduce the volumetric properties
of the test set (density and unit cell volume) with an average deviations
smaller than 2% and the experimentally determined enthalpies of sublimation
and vaporization with an accuracy better than 2.3 kJĀ·mol<sup>ā1</sup>. The Lennard-Jones (12-6) potential function parameters
used to calculate the repulsive and dispersion contributions of the
metals within the framework of the force field were found to be transferable
between chromium, iron, and nickel (first row) and between molybdenum
and ruthenium (second row)
Driving Force for the Thermally Induced Solid State Polymerization of Alkali Metal Halogenoacetates:Ā A Thermochemical Analysis
Kinetics and Mechanism of the Thermal Dehydration of a Robust and Yet Metastable Hemihydrate of 4āHydroxynicotinic Acid
Hydrates
are the most common type of solvates and certainly the
most important ones for industries such as pharmaceuticals which strongly
rely on the development, production, and marketing of organic molecular
solids. A recent study indicated that, in contrast with thermodynamic
predictions, a new hemihydrate of 4-hydroxynicotinic acid (4HNAĀ·0.5H<sub>2</sub>O) did not undergo facile spontaneous dehydration at ambient
temperature and pressure. The origin of this robustness and the mechanism
of dehydration were investigated in this work, through a combined
approach which involved kinetic studies by thermogravimetry (TGA),
crystal packing analysis based on X-ray diffraction data, and microscopic
observations by hot stage microscopy (HSM), scanning electron microscopy
(SEM), and atomic force microscopy (AFM). The TGA results indicated
that the resilience of 4HNAĀ·0.5H<sub>2</sub>O to water loss is
indeed of kinetic origin, c.f., due to a significant activation energy, <i>E</i><sub>a</sub>, which increased from 85 kJĀ·mol<sup>ā1</sup> to 133 kJĀ·mol<sup>ā1</sup> with the increase in particle
size. This <i>E</i><sub>a</sub> range is compatible with
the fact that four moderately strong hydrogen bonds (typically 20ā30
kJĀ·mol<sup>ā1</sup> each) must be broken to remove water
from the crystal lattice. The dehydration kinetics conforms to the
Avrami-Erofeev A2 model, which assumes a nucleation and growth mechanism.
Support for a nucleation and growth mechanism was also provided by
the HSM, SEM, and AFM observations. These observations further suggested
that the reaction involves one-dimensional nucleation, which is rarely
observed. Finally, a statistical analysis of Arrhenius plots for samples
with different particle sizes revealed an isokinetic relationship
between the activation parameters. This is consistent with the fact
that the dehydration mechanism is independent of the sample particle
size
From Molecules to Crystals: The Solvent Plays an Active Role Throughout the Nucleation Pathway of Molecular Organic Crystals
Crystallization is indisputably one
of the oldest and most widely
used purification methods. Despite this fact, our current understanding
of the early stages of crystallization is still in its infancy. In
this work dynamic light scattering and proton nuclear magnetic resonance
were used to investigate the changes occurring in 4ā²-hydroxyacetophenone
colloidal particles, as they form in a supersaturated aqueous solution
and evolve toward anhydrous or hydrate materials during a cooling
crystallization process. In the concentration range probed, the particles
are initially composed by both solute and water. If the outcome of
crystallization is an anhydrous phase, a complete loss of solvent
from the particles is progressively observed up to the onset of crystal
precipitation. These findings provide unique experimental evidence
that the role of solvent in the formation of crystals can go well
beyond influencing the self-assembly and clustering of solute molecules
prior to nucleation