The polymerization of ethylene carbonate using different metal alkoxides results in poly(oxyethylene-ukthylene carbonate). Polymers containing low amounts of CO, or pure poly(oxyethylene) are formed with anionic and cationic initiators. Poly(ethy1ene carbonate) is not accessible from ethylene carbonate by variation of temperatures and concentration. The reason is not the low ceiling temperature. but the positive enthalpy of polymerization. A AH,-value of 125,6 kJ/mol was obtained from calorimetric investigations.
The anisotropy of structural distortion of the monoclinic polymorph of acetaminophen induced by hydrostatic pressure up to 4.0 GPa was studied by single-crystal X-ray diffraction in a Merrill-Bassett diamond anvil cell (DAC). The space group (P2(1)/n) and the general structural pattern remained unchanged with pressure. Despite the overall decrease in the molar volume with pressure, the structure expanded in particular crystallographic directions. One of the linear cell parameters (c) passed through a minimum as the pressure increased. The intramolecular bond lengths changed only slightly with pressure, but the changes in the dihedral and torsion angles were very large. The compressibility of the intermolecular hydrogen bonds NH...O and OH...O was measured. NH...O bonds were shown to be slightly more compressible than OH...O bonds. The anisotropy of structural distortion was analysed in detail in relation to the pressure-induced changes in the molecular conformations, to the compression of the hydrogen-bond network, and to the changes in the orientation of molecules with respect to each other in the pleated sheets in the structure. Dirichlet domains were calculated in order to analyse the relative shifts of the centroids of the hydrogen-bonded cycles and of the centroids of the benzene rings with pressure.
The rate of homogeneous nucleation in supersaturated vapors of water was studied experimentally using a thermal diffusion cloud chamber. Helium was used as a carrier gas. Our study covers a range of nucleation rates from 3x10(-1) to 3x10(2) cm(-3) s(-1) at four isotherms: 290, 300, 310, and 320 K. The molecular content of critical clusters was estimated from the slopes of experimental data. The measured isothermal dependencies of nucleation rate of water on saturation ratio were compared with the prediction of the classical theory of homogeneous nucleation, the empirical prediction of Wolk et al. [J. Chem. Phys. 117, 10 (2002)], the scaled model of Hale [Phys. Rev. A 33, 4156 (1986)], and the former nucleation onset data.
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