Abstracts - faqs.org

Abstracts

Chemicals, plastics and rubber industries

Search abstracts:
Abstracts » Chemicals, plastics and rubber industries

Cyclodextrin cavity size effect on the complexation and rotational dynamics of the laser dye 2,5-diphenyl-1,3,4-oxadiazole: From singly occupied complexes to their nanotubular self-assemblies

Article Abstract:

The steady-state (SS) and time-resolved (TR) fluorescence spectroscopy are used to study the general complexation scheme as well as the dynamic features of the supramolecular structures resulting from the interaction of the laser dye 2,5-diphenyl-1,3,4-oxadiazole (PPD) with the naturally occurring [alpha]-, [beta]- and [gamma]-cyclodextrins in water. The results have supported that two distinct dimeric forms of PPD play the role of the shaft between adjacent units.

Author: Pistolis, George, Balomenou, Ioanna
Publisher: American Chemical Society
Publication Name: Journal of Physical Chemistry B
Subject: Chemicals, plastics and rubber industries
ISSN: 1520-6106
Year: 2006
Usage, Fluorescence spectroscopy, Azo compounds

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Molecular recognition kinetics of beta-cyclodextrin for several alcohols by ultrasonic relaxation method

Article Abstract:

Ultrasonic absorption coefficients alpha were measured in the frequency range 0.8-9Mhz by a resonance method in which three cells with 3,5 and 7 Mhz x-cut fundamental x-cuts crystals were investigated. The result indicates that the isometric effect of the guests on the dynamic interaction with beta-cyclodextrin was considered and it is deducted form the experimental results that the hydrophobicity is very sensitive for recognition.

Author: Nishikawa, Sadakatsu, Ugawa, Takaho, Fukahori, Takanori
Publisher: American Chemical Society
Publication Name: Journal of Physical Chemistry B
Subject: Chemicals, plastics and rubber industries
ISSN: 1520-6106
Year: 2001
Relaxation phenomena, Relaxation (Physics), Alcohols

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Complexation dynamics of xanthone and thioxanthone to (beta)-cyclodextrin derivatives

Article Abstract:

The relocation of the excited triplet-state ketones from the cyclodextrins (CD) cavity to the aqueous phase was followed for studying the complexation dynamics of xanthone and thioxanthone to substituted (beta)-cyclodextrin derivatives. Results suggest that the ground-state complexation efficiency and the binding dynamics of a neutral guest molecule is affected by the substitution on the rim of (beta)-CD.

Author: Okano, L.T., Barros, T.C., Chou, D.T.H., Bennet, A.J., Bohne, C.
Publisher: American Chemical Society
Publication Name: Journal of Physical Chemistry B
Subject: Chemicals, plastics and rubber industries
ISSN: 1520-6106
Year: 2001
Chemistry, Physical and theoretical, Physical chemistry, Ketones, Aqueous solution reactions

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Subjects list: Research, Cyclodextrins, Chemical properties
Similar abstracts:
  • Abstracts: Surface effects on aqueous ionic solvation: a molecular dynamics simulation study of NaCl at the air/water interface from infinite dilution to saturation
  • Abstracts: Cross polarization and cross relaxation from laser-polarized xenon to surface species. Variable temperatures study of the cross-relaxation dynamics in the hyperpolarized xenon-induced enhancement of surface nuclei
  • Abstracts: Ultrafast nonradiative relaxation dynamics of eumelanin. Binding of ochratoxin a derivatives to human serum albumin
  • Abstracts: Numerical and analytical studies of the electrical conductivity of a concentrated colloidal suspension. Charge-tunable optical properties in colloidal semiconductor nanocrystals
  • Abstracts: Semiconductors' photo electrochemistry: a kinetic and thermodynamic analysis in the light of equilibrium and nonequilibrium models
This website is not affiliated with document authors or copyright owners. This page is provided for informational purposes only. Unintentional errors are possible.
Some parts © 2025 Advameg, Inc.