Accelerating charge transfer in a triphenylamine-subphthalocyanine donor-acceptor system

Anaïs Medina1, Christian G Claessens, G M Aminur Rahman

  • 1Departamento de Química Orgánica, C-1, Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.

Chemical Communications (Cambridge, England)
|April 2, 2008
PubMed
Summary

Researchers created a new boron(III) subphthalocyanine molecule with a triphenylamine group. This novel electron donor-acceptor system shows promise for advanced electronic applications.

Related Concept Videos

Aryldiazonium Salts to Azo Dyes: Diazo Coupling01:11

Aryldiazonium Salts to Azo Dyes: Diazo Coupling

The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para position.
Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.