Titlebook: Rotational Dynamics of Small and Macromolecules; Proceedings of a Wor Th. Dorfmüller,R. Pecora Conference proceedings 1987 Springer-Verlag

Nonchalant

書目名稱Rotational Dynamics of Small and Macromolecules影響因子(影響力)




書目名稱Rotational Dynamics of Small and Macromolecules影響因子(影響力)學科排名




書目名稱Rotational Dynamics of Small and Macromolecules網絡公開度




書目名稱Rotational Dynamics of Small and Macromolecules網絡公開度學科排名




書目名稱Rotational Dynamics of Small and Macromolecules被引頻次




書目名稱Rotational Dynamics of Small and Macromolecules被引頻次學科排名




書目名稱Rotational Dynamics of Small and Macromolecules年度引用




書目名稱Rotational Dynamics of Small and Macromolecules年度引用學科排名




書目名稱Rotational Dynamics of Small and Macromolecules讀者反饋




書目名稱Rotational Dynamics of Small and Macromolecules讀者反饋學科排名

壓碎

The problem of internal motion of molecules in the liquid as seen from NMR relaxation studies,ry which gives the framework of the facts to be treated. A number of experimental results are presented for the following molecules: Methanol, acetic acid, DMSO, ethanol, i-propanol, toluene and propylene carbonate. It will be shown that the proton-proton distances in the molecule which result from

禁令

A comparative study of molecular rotation as studied by dynamic light scattering, fluorescence anissubstituted small molecules. The differences obtained by the three techniques are shown to result from the different components of the diffusion tensor observed by these methods. The simultaneous application of these techniques may allow us to better assess the rotational correlation times about all

insidious

真繁榮

Molecular order and dynamics of liquid crystal polymers studied by multipulse dynamic NMR techniqueuence, pulse separation and magnetic field orientation provides the large number of independent experiments necessary for a proper molecular characterization of the systems. Analysis of these experiments in terms of molecular order and dynamics is conveniently achieved by employing a density matrix

西瓜

The elastic trumbbell model for dynamics of stiff chains,one (λ.) to bending, dominate the relaxation spectrum of viscoelasticity and Kerr Effect. As the stiffness of the spring increases, the slowest relaxation mode Ψ. becomes dominant in the Kerr Effect case (K. ? K.), and the decay curves fit nearly single exponentials if Z ≥ 0.75. This, however, does

豐滿中國

Rotation of large molecular ions and transient dielectric relaxation effects, the slip limit are useful estimates of the rotation rate for large, symmetrically charged molecules, if there are no strong solvent interactions. For cases of strong interactions, the rotation rate reduces by a factor of 5–6. For the symmetric, anionic dye molecule resorufin, we successfully modele

折磨

surrogate

lipids