Abstracts - faqs.org

Abstracts

Chemistry

Search abstracts:
Abstracts » Chemistry

Analysis of the interactions responsible for long-range through-bond-mediated electronic coupling between remote chromophores attached to rigid polynorbornyl bridges

Article Abstract:

The distance and strength of an electronic interaction determined the extent of through-bond (TB) couplings. The McConnell model was preferred over both the photoelectron spectroscopy and electron transmission spectroscopy in determining bridge-length effects on anionic and cationic splittings. However, the application of natural bond orbitals (NBO) in polynorbornyl TB coupling showed that the splitting pathway followed a nonexponential distance dependence, whichresulted in more accurate analyses. In addition, NBOs were used in nonperturbative and ab initio calculations regarding TB coupling.

Author: Jordan, Kenneth D., Paddon-Row, Michael N.
Publisher: American Chemical Society
Publication Name: Chemical Reviews
Subject: Chemistry
ISSN: 0009-2665
Year: 1992
Semiconductors, Photoelectron spectroscopy

User Contributions:

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

CAPTCHA


Photoinduced electron transfer in supramolecular systems for artificial photosynthesis

Article Abstract:

Porphyrin-containing supramolecular systems are being developed to perform photoinduced charge separation reactions that imitate plant transformation of solar to chemical energy. Improvements in the electron-transfer (ET) process involve structural control of temperatures and donor-acceptor distances. Moreover, interacting solvent properties and electronic coupling strength influence the rate and energetics of ET processes.

Author: Wasielewski, Michael R.
Publisher: American Chemical Society
Publication Name: Chemical Reviews
Subject: Chemistry
ISSN: 0009-2665
Year: 1992
Photosynthesis research, Porphyrins

User Contributions:

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

CAPTCHA


Noncovalent binding between guanidinium and anionic groups: Focus on biological-and synthetic-based arginine/guanidinium interactions with phosph[on]ate and sulf[on]ate residues

Article Abstract:

Review of work pertaining to noncovalent binding interactions involving primarily the cationic guanidinium group and the anionic sulfonate and phosphonate groups is presented. Noncovalent binding interactions are used in spectroscopic, biomimetic, molecular interaction modeling, and bioinformatics tools among others, that are greatly varied and used in a wide variety of fields.

Author: Lindner, Wolfgang, Schug, Kevin A.
Publisher: American Chemical Society
Publication Name: Chemical Reviews
Subject: Chemistry
ISSN: 0009-2665
Year: 2005
Science & research, All Other Basic Organic Chemical Manufacturing, Industrial Organic Chemicals, Guanidine, Anions, Chemical properties, Guanidines

User Contributions:

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

CAPTCHA


Subjects list: Research, Methods, Charge transfer, Chemical bonds
Similar abstracts:
  • Abstracts: Explosives detection: a challenge for physical chemistry. High resolution spectroscopy in the gas phase: even large molecules have well-defined shapes
  • Abstracts: Strong closed-shell interactions in inorganic chemistry. Polyoxometalates: very large clusters - nanoscale magnets
  • Abstracts: Inorganic mimics of ribonucleases and ribozymes: from random cleavage to sequence-specific chemistry to catalytic antisense drugs
  • Abstracts: A critical appraisal of the evolution of N-nitrosoureas as anticancer drugs. Electron transfer at semiconductor electrode-liquid electrolyte interfaces
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.