Stable vesicles composed of cationic and anionic single-tailed-surfactant were prepared, and their image obtained by electron microscopy with negative staining technique. Significant fluorescence enhancement for acridine orange in vesicle with regards to water has been observed. In heterogeneous vesicle solution composed of mixed cationic and anionic surfactants for the energy transfer between acridine orange (D) and pyronine (A), the Förster dipole-dipole model was valid, and it is interesting to note that the energy transfer rate constant (kET) was smaller than that in homogeneous aqueous solution. On the inside and outside of the stable vesicle, immiscible water solution of acridine orange and pyronine could be obtained, and the distance calculated from the energy transfer between D and A separated by the bilayer membrane implied that the location of ionic dye molecules was in the Gouy-Chapman layers of the vesicles. Furthermore, due to the electrostatic absorption of the dye molecules to charged headgroups of surfactants, acridine orange and pyronine accumulated and aggregated to the vesicle bilayer membrane. 相似文献
Over the past decade, liquid-phase epitaxy (LPE) has become an established technique for the growth of HgCdTe. This article reviews one of the successful LPE technologies developed for HgCdTe, specifically, “infinite-melt” vertical LPE (VLPE) from Hg-rich solutions.
In spite of the relatively low solubility of Cd in Hg-rich solutions and the relatively high Hg pressure at the usual growth temperatures, this approach has been found to offer superior results for growth of HgCdTe suitable for various compositions and layer structures.
An historical perspective and the current status of VLPE technology are presented. Particular emphasis is placed on the important role of the thermodynamic parameters (phase diagram), on control of stoichiometry (defect chemistry) and on impurity doping (distribution coefficient) for growth of HgCdTe layers from Hg solutions. Critical material characteristics, such as transport properties, minority-carrier lifetime, morphology and crystal structure, are also discussed. 相似文献
The criteria for the onset of thermocapillary convection in a horizontal radiating fluid layer heated by an incident thermal radiative energy source are determined. The fluid layer is an absorbing and isotropically scattering medium confined between a free upper surface and an insulated rigid lower surface. Linear analysis is performed on the continuity, momentum, energy, and approximate radiative equations. The resulting disturbance equations are solved using a numerical optimization technique to obtain the eigenvalues governing the onset of convective motion. The influence of thermal radiation on the critical Marangoni number is examined. Attention is drawn to the physical significance of the heat transfer mode, gravitational force, the scattering effect, and the surface radiative properties. The conditions leading to the onset of convection are presented as functions of the optical thickness, scattering albedo, Planck number, surface emissivities, and transmissivities. 相似文献
Various acidic anhydrides including cantharidin were converted into corresponding aminobenzylcantharidinimide 3a and analogous imides 3b~k (at the ortho, meta, and para positions) with 35%~87% yields by reacting with aminobenzylamines and triethylamine. The two methyl side chains of cantharidinimides 3ao , 3am , and 3ap, and related imides had more than two chiral centers; the lone pair of electrons of nitrogen displayed a different chemical shift and coupling constant in H‐NMR spectra when the amino group of benzylamine was in the ortho position. These cantharidinimides had parent aniline, pyridine, and naphthalene plane structures, and the primary amine nucleophilicity and basicity might reflect the inductive electron’s negative effect on chemical shifts. We prepared cantharidinimides by heating the reactants cantharidin 1a , aliphatic and aromatic acid anhydrides, primary benzylic amines, and aniline derivatives to ca. 200 °C with 3 mL of dry toluene, and 1~2 mL of triethylamine in high‐pressure sealed tubes (Buchi glasuster 0032) to produce cantharidinimides and their analogues in good yields. The para‐aminobenzylic imides showed greater inhibition of nitric oxide (NO) synthesis by NO synthase (NOS) than did ortho‐ and meta‐aminobenzylic imides. Compound 3fp , para‐aminobenzylic norbonane‐imide, had the most potent effect on inducible NOS among the tested compounds and showed 35% inhibition. 相似文献
Aurora kinase family is one of the emerging targets in oncology drug discovery and several small molecules targeting aurora
kinases have been discovered and evaluated under early phase I/II trials. Among them, PHA-739358 (compound 1r) is a 3-aminopyrazole
derivative with strong activity against Aurora A under early phase II trial. Inhibitory potency of compound 1r (the benzylic
substituent at the pro-R position) is 30 times over that of compound 1s (the benzylic substituent at the pro-S position).
In present study, the mechanism of how different configurations influence the binding affinity was investigated using molecular
dynamics (MD) simulations, free energy calculations and free energy decomposition analysis. The predicted binding free energies
of these two complexes are consistent with the experimental data. The analysis of the individual energy terms indicates that
although the van der Waals contribution is important for distinguishing the binding affinities of these two inhibitors, the
electrostatic contribution plays a more crucial role in that. Moreover, it is observed that different configurations of the
benzylic substituent could form different binding patterns with protein, thus leading to variant inhibitory potency of compounds
1r and 1s. The combination of different molecular modeling techniques is an efficient way to interpret the chirality effects
of inhibitors and our work gives valuable information for the chiral drug design in the near future. 相似文献