## Abstract In this paper we examine the theory and method for obtaining rotational diffusion coefficients for peptides in dilute solution from ^13^Cβnmr spinβlattice relaxation data. We show that even for the case of nearly equal observed relaxation times of chemically and magnetically nonequivale
Picosecond transient grating study of the rotational diffusion of a ruthenium complex in solution
β Scribed by Arthur Henseler; Eric Vauthey
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 697 KB
- Volume
- 228
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The rotational diffusion time of ruthenium( II)-bis( 2,2'-bipyridine) (2,2'-biquinoleine) has been measured in polar solvents of different viscosity. The rotational dynamics can be explained in terms of the Stokes-Einstein-Debye hydrodynamics theory under stick boundary condition by considering the rotating body as a prolate spheroid enclosing the complex. This overestimates the intrinsic molecular volume by a factor of 1.5. The difference can be accounted for by solvent molecules intercalated in the inter&and space and stabilized by electrostatic interaction with the charge of the metal atom.
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The rotational dynamics of nile red has been studied in polar protic, polar aprotic and non-polar solvents. In the non-polar and the aprotic solvents, with the exception of long alkanenitriles, the rotation dynamics is consistent with the prediction of the Stokes-Einstein-Debye hydrodynamics theory
A method for measuring the translational diffusion coefficient of a photochemically stable molecule by the transient grating method is proposed. For obtaining optical modulation, the difference between the optical properties of the ground and the excited triplet states is utilized. This method is ap