Qiuxiang Yin

Bio: Qiuxiang Yin is an academic researcher from Tianjin University. The author has contributed to research in topics: Solubility & Crystallization. The author has an hindex of 24, co-authored 193 publications receiving 1967 citations.

Effects of Solvent on Polymorph Formation and Nucleation of Prasugrel Hydrochloride

Abstract: Three intrinsic properties of solvent were used to evaluate the effects of solvent on polymorph formation of prasugrel hydrochloride. In situ Raman spectroscopy, FTIR, and powder X-ray diffraction were used to characterize two solvent-free polymorphs and five solvates of prasugrel hydrochloride, the two of which were reported for the first time. Reactive crystallization in 24 different pure solvents was studied at 313.15 K. It was found that polymorph formation of prasugrel hydrochloride directly depends on the solvents used in the experiments. Form I was obtained in solvents with low values of hydrogen bond donor ability (HBD), while form II was obtained in solvents with high values of HBD. The thermodynamic and kinetic reasons for the solvent effects were explained by using the solubility data and the nucleation experiments. The solubilities of forms I and II were experimentally determined by a gravimetric method, and an equation based on the linear free energy approach for predicting solubility was app...

Solubility of hydroquinone in different solvents from 276.65 K to 345.10 K

Abstract: Using a laser-monitoring observation technique, the solubility of hydroquinone in water, methanol, ethanol, 2-propanol, ethyl acetate, butyl acetate, and acetic acid were measured at temperatures ranging from 276.65 K to 345.10 K under the atmospheric pressure. The experimental solubility data was well-correlated with the data, calculated by means of a semiempirical equation.

Solubility and Thermodynamic Stability of the Enantiotropic Polymorphs of 2,3,5-Trimethyl-1,4-diacetoxybenzene

Abstract: The solubility data of two polymorphs of 2,3,5-trimethyl-1,4-diacetoxybenzene (TMHQ-DA) in ethanol, 1-propanol, 2-propanol, and 1-butanol at various temperatures were experimentally measured using gravimetrical method and correlated by the modified Apelblat model and the van’t Hoff equation, respectively. Differential scanning calorimetry (DSC) and thermogravimetry (TG) analyses were performed to investigate the thermodynamic stability and the transition of the two forms of TMHQ-DA. An enantiotropic relationship was found between TMHQ-DA Form A and TMHQ-DA Form B, and the transition point between them was experimentally determined to be 314.50 ± 1 K. A thermodynamic model for estimation of the transition point was also derived, and the estimated results are satisfactorily consistent with the experimental values. Finally, the accuracy of the transition point obtained in this research was validated by the polymorphic transformation experiments monitored using Raman spectroscopy.

Ab initio calculation of vibrational absorption and circular dichroism spectra using density functional force fields

Abstract: : The unpolarized absorption and circular dichroism spectra of the fundamental vibrational transitions of the chiral molecule, 4-methyl-2-oxetanone, are calculated ab initio. Harmonic force fields are obtained using Density Functional Theory (DFT), MP2, and SCF methodologies and a 5S4P2D/3S2P (TZ2P) basis set. DFT calculations use the Local Spin Density Approximation (LSDA), BLYP, and Becke3LYP (B3LYP) density functionals. Mid-IR spectra predicted using LSDA, BLYP, and B3LYP force fields are of significantly different quality, the B3LYP force field yielding spectra in clearly superior, and overall excellent, agreement with experiment. The MP2 force field yields spectra in slightly worse agreement with experiment than the B3LYP force field. The SCF force field yields spectra in poor agreement with experiment.The basis set dependence of B3LYP force fields is also explored: the 6-31G* and TZ2P basis sets give very similar results while the 3-21G basis set yields spectra in substantially worse agreements with experiment. jg

Observation of Single Colloidal Platinum Nanocrystal Growth Trajectories

Abstract: It is conventionally assumed that the growth of monodisperse colloidal nanocrystals requires a temporally discrete nucleation followed by monomer attachment onto the existing nuclei. However, recent studies have reported violations of this classical growth model, and have suggested that inter-particle interactions are also involved during the growth. Mechanisms of nanocrystal growth still remain controversial. Using in situ transmission electron microscopy, we show that platinum nanocrystals can grow either by monomer attachment from solution onto the existing particles or by coalescence between the particles. Surprisingly, an initially broad size distribution of the nanocrystals can spontaneously narrow. We suggest that nanocrystals take different pathways of growth based on their size- and morphology-dependent internal energies. These observations are expected to be highly relevant for other nanocrystal systems.

Handbook of Solubility Data for Pharmaceuticals

Abstract: Handbook of solubility data for pharmaceuticals , Handbook of solubility data for pharmaceuticals , کتابخانه دیجیتال جندی شاپور اهواز

Real-space identification of intermolecular bonding with atomic force microscopy

Abstract: Imaging Hydrogen Bonds The decoration of atomic force microscope tips with terminal CO molecules has afforded much higher resolution of the bonding of adsorbed molecules. Zhang et al. (p. 611, published online 26 September) show that this method, in combination with density function theory calculations, can image and characterize hydrogen-bonding contacts formed between 8-hydroxyquinoline molecules adsorbed on the (111) surface of copper under cryogenic conditions. At room temperature, a different bonding configuration was revealed that was the result of the molecules dehydrogenating on the copper surface and coordinating with surface copper atoms. An atomic force microscope tip bearing a single carbon monoxide molecule was used to resolve hydrogen-bonding contacts between molecules. We report a real-space visualization of the formation of hydrogen bonding in 8-hydroxyquinoline (8-hq) molecular assemblies on a Cu(111) substrate, using noncontact atomic force microscopy (NC-AFM). The atomically resolved molecular structures enable a precise determination of the characteristics of hydrogen bonding networks, including the bonding sites, orientations, and lengths. The observation of bond contrast was interpreted by ab initio density functional calculations, which indicated the electron density contribution from the hybridized electronic state of the hydrogen bond. Intermolecular coordination between the dehydrogenated 8-hq and Cu adatoms was also revealed by the submolecular resolution AFM characterization. The direct identification of local bonding configurations by NC-AFM would facilitate detailed investigations of intermolecular interactions in complex molecules with multiple active sites.