Abstracts - faqs.org

Abstracts

Chemicals, plastics and rubber industries

Search abstracts:
Abstracts » Chemicals, plastics and rubber industries

Structural studies of copper(II)-amine terminated dendrimer complexes by EXAFAS

Article Abstract:

The interaction of amine-terminated polyamido(amine), PAMAM, dendrimer with copper(II) ions determined by extended X-ray absorption fine structure (EXAFS) is reported. The results suggest that the model consisting of the copper(II) ion forming five- and six- membered rings by chelating with the primary amine, amide, and tertiary amine nitrogen doors of the PAMAM dendrimer could describe the experimental EXAFS data well.

Author: Tran, M. Linh, Gahan, Lawrence R., Gentle, Ian R.
Publisher: American Chemical Society
Publication Name: Journal of Physical Chemistry B
Subject: Chemicals, plastics and rubber industries
ISSN: 1520-6106
Year: 2004
Amines

User Contributions:

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

CAPTCHA


Electrochemical actuation of growing copper dendrimers in water

Article Abstract:

The observation of electrochemical actuation in growing dendritic fibers made of self-assembled copper nanostructures, on the metallic cathode of an ordinary aqueous electrochemical cell is reported. The extent of actuation is found to be dependent on the applied voltage, the concentration of [Cu.sup.2+] ions in the solution, and also on ions such as [Na.sup.+], which did not get deposited at the cathode.

Author: Paul, Anumita, Panda, Biswa Ranjan, Rao, Pinjala Nagaraju, Chattopadhyay, Arun
Publisher: American Chemical Society
Publication Name: Journal of Physical Chemistry B
Subject: Chemicals, plastics and rubber industries
ISSN: 1520-6106
Year: 2006
Water, Electrochemical analysis, Chemical properties, X-ray analysis

User Contributions:

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

CAPTCHA


Light-harvesting in carbonyl-terminated phenylacetylene dendrimers: The role of delocalized excited states and the scaling of light-harvesting efficiency with dendrimer size

Article Abstract:

Steady-state and time-resolved optical spectroscopy was employed to study the photophysics of a family of conjugated phenylacetylene (PA) light-harvesting dendrimers. It was found that this class of molecules has several unique photophysical properties that affect their utility as light-harvesting compound.

Author: Bardeen, Christopher J., Tai Sang Ahn, Thompson, Alexis L., Bharathi, P., Muller, Astrid
Publisher: American Chemical Society
Publication Name: Journal of Physical Chemistry B
Subject: Chemicals, plastics and rubber industries
ISSN: 1520-6106
Year: 2006
Science & research, Research, Optical properties, Acetylene, Energy transformation

User Contributions:

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

CAPTCHA


Subjects list: Copper compounds, Structure, Dendrimers
Similar abstracts:
  • Abstracts: Intramolecular charge transfer in 1:1 Cu(II)/pyrenylcyclam dendrimer complexes. Effect of temperature and pressure in the photocatalytic oxidation of n-octanol on partially desilanized hydrophobic TiO2 suspended in aerated supercritical CO2
  • Abstracts: Orientational dynamics of beta-cyclodextrin inclusion complexes. Electrochemistry of guest molecules in thiolated cyclodextrin self-assembled monolayers: an implication for size-selective sensors
  • Abstracts: Effects of the confined synthesis on conjugated polymer transport properties. Organization of a polar molecule at the air-water interface
  • Abstracts: Structural changes in self-assembled monolayers initiated by ultraviolet light. Synthesis, characterization, and applications of dendrimer-encapsulated nanoparticles
  • Abstracts: Nanostructure formation in polyelectrolyte-surfactant complexes. A new and simple means for self-assembled nanostructure: Facilitated by buffer layer
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.