Modulating Thermal Properties of Polymers through Crystal Engineering

Crystal engineering has exclusively focused on the development of advanced materials based on small organic molecules. We now demonstrate how the cocrystallization of a polymer yields a material with significantly enhanced thermal stability but equivalent mechanical flexibility. Isomorphous replacement of one of the cocrystal components enables the formation of solid solutions with melting points that can be readily fine-tuned over a usefully wide temperature range. The results of this study credibly extend the scope of crystal engineering and cocrystallization from small molecules to polymers

Measurement and correlation of the solubility of telmisartan (form A) in nine different solvents from 277.85 to 338.35 K

The solubility of telmisartan (form A) in nine organic solvents (chloroform, dichloromethane, ethanol, toluene, benzene, 2-propanol, ethyl acetate, methanol and acetone) was determined by a laser monitoring technique at temperatures from 277.85 to 338.35 K. The solubility of telmisartan (form A) in all of the nine solvents increased with temperature as did the rates at which the solubility increased except in chloroform and dichloromethane. The mole fraction solubility in chloroform is higher than that in dichloromethane, which are both one order of magnitude higher than those in the other seven solvents at the experimental temperatures. The solubility data were correlated with the modified Apelblat equation and λh equations. The results show that the λh equation is in better agreement with the experimental data than the Apelblat equation. The relative root mean square deviations (σ) of the λh equation are in the range from 0.004 to 0.45 %. The dissolution enthalpies, entropies and Gibbs energies of telmisartan in these solvents were estimated by the Van’t Hoff equation and the Gibbs equation. The melting point and the fusion enthalpy of telmisartan were determined by differential scanning calorimetry

High-pressure phase transitions in tetrakis(trimethylsilyl)silane Si[Si(CH3)(3)](4)

The compound tetrakis(trimethylsilyl)silane S-i[Si(CH3,)(3)](4) (TSi) has been studied at room temperature for pressures up to 2 1.5(1) GPa, using X-ray powder diffraction with synchrotron radiation. Three different phases are reported in the investigated pressure range. The c.c.p.-type structure is stable up to a pressure of 0.19(1) GPa (Fm (3) over barm, a = 13.52110)Angstrom, V = 2471.95(1)Angstrom(3), Z = 4 at 0.02(1)GPa). It shows a severe orientational disorder of the molecules. At pressures 0.19(1)-0.71(1)GPa a monoclinic phase (HP1) is found with space group P2(1)/n and Z=8 (a = 17.746(1)Angstrom, b = 16.098(1)Angstrom, c= 16.871(1)Angstrom, gamma = 111.437(5)degrees and V = 4486.3(8) Angstrom(3) at 0.24(1)GPa). Another monoclinic phase (HP2) exists at pressures 0.52(1)-8.67(5)GPa. This phase has a smaller unit cell than the HP1 phase with Z(.)=2 (a =8.3778(8)Angstrom, b=9.1050(7)Angstrom, c= 13.3024(8)Angstrom, gamma= 111.63(1)degrees and V = 943.22(6) Angstrom(3) at 1.73(2)GPa). The pressure dependencies of the unit-cell volumes are successfully described by Mumaghan or Vinet-type equations of state. The structures at different pressures and temperatures of TSi and related compounds are described as distorted superstructures of the c.c.p. arrangement. The occurrence of different superstructures is rationalized as the result of an optimized packing of ordered molecules of various shapes

A rational approach to screen for hydrated forms of the pharmaceutical derivative magnesium naproxen using liquid-assisted grinding

Variation of water content in liquid-assisted grinding was utilised to mechanochemically screen for different hydrated forms of magnesium naproxen directly from a mixture of magnesium oxide and naproxen. Structure determination from powder and single crystal X-ray diffraction data, supported by solid-state NMR and synchrotron radiation diffraction experiments, revealed a monohydrate coordination polymer, a discrete tetrahydrate complex, and provided a preliminary structural model for a highly hydrated salt