Related Experiment Video
Updated: Oct 4, 2026

Spatial Separation of Molecular Conformers and Clusters
Published on: January 9, 2014
Acceptor strength and solvent polarity govern charge separation in TCBD- and DCNQ-functionalized isoindigo
Chamari V Ileperuma1, Youngwoo Jang1, Yogajivan Rout2
1Department of Chemistry, University of North Texas, 1155 Union Circle, #305070, Denton, TX, 76203-5017, USA. Francis.DSouza@UNT.edu.
Abstract:
Far-red-capturing, strong electron-acceptor-bearing isoindigo push-pull systems have been shown to undergo ultrafast charge transfer, leading to charge separation.
More Related Videos
08:54Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid
Published on: January 25, 2020
06:44From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
Published on: March 24, 2018
Related Concept Videos
Intermolecular Forces
Ion Exchange
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Ion-Exchange Chromatography
Diels–Alder Reaction: Characteristics of Dienophiles
Characteristics of Dienophiles
Generally, the best dienophiles are alkenes containing electron-withdrawing substituents such as carbonyl, nitrile, and nitro groups. The feasibility of a Diels–Alder reaction depends on...
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry