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The solvation TCF, C. The results for Cl53 in acetonitrile and CO2 are shown in the left and right panels respectively.

The solvatochromic shifts of the dye Nile Red in a number of ionic hquids and organic solvents

The solvatochromic shifts of the dye Nile Red in a number of ionic liquids and organic solvents

The solvent accessibility of lysine residues in the Fc region of an antibody is illustrated by highlighting the lysine groups in solid gray. Some lysine e-amine groups are extremely accessible to conjugation, while others are only partially exposed, making them difficult to modify in bioconjugation reactions.

The solvent accessible areas . Solvent radius 15 A.

The solvent accessible surface . In the COSMO model, the SAS is then divided into a series of segments of area S and charge density cr, centered at a position R j.

The solvent accessible surface is defined by the centers of spheres rolled along the molecular contour surface, where the radius of the sphere is chosen according to the size of the solvent molecule.

The solvent and thermal focusing effect 0 High-volatile solute Low-volatile solute

The solvent can shift the fluorescence spectrum relative to the absorption spectrum. On the left we see that the absorption occru with the solvent . However, before fluorescence occurs, the solvent molecules relax into a new arrangement, and that arrangement is preserved during the subsequent radiative transition.

The solvent concentration field varies during polymer dissolution in a controlled release device. Before dissolution starts, there is no disentanglement in a swellable system .

The solvent dependence of the aromatic proton resonances of benzene,

The Solvent Excluding Surface of a particular solute is the envelope of the volume excluded to the solvent considered as a whole sphere that represents its charge density.

The solvent flush method.

The solvent is the majority component and the solute the minority component. Therefore, there will be more solvent atoms than solute atoms.

The solvent reorganization energies Es for proton transfer as a function of Ej for the nitrile solvents.

The solvent reorganization energies Es for proton transfer as a function of Et for the nitrile solvents.

The solvent selectivity triangle for separations on silica LD, localized dipole LB, localized base, ,

The solvent shift distributions for the two fluorescence transitions in indole at the air-water interface

The solvent-dependent effect of pressure on the competing and cycloadditions of tetracyanoethylene and 1,2-dimethylbutadiene at 40 C 9, 35 .

The solvent-free controlled thermolysis of gold thiolate complex producing gold nanoparticles stabilized by alkyl groups derived from the precursor.

The solvent-squeeze model for the shear-enhanced concentration fluctuations driven by stress-diffusion coupling. Based on Saito, S.

The solvents used for lead were ethyl ether or ethyl acetate .

The Solver Options dialog box.

The Solver Parameters dialog box.

The Solver window for the analysis of one equilibrium.



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