Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5269223 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
A straightforward synthesis of fluorescent tris-meta-substituted triphenylamines (m-TPAs) is presented. These new fluorophores display a unique feature that is a remarkably high Stokes shift up to 250Â nm, as compared to their para counterparts. Although the meta substitution is made at the expense of the quantum yield, the latter is maintained at an appreciable level (5%) making the m-TPAs a new class of fluorophores adaptable to a large range of applications from biology to materials science.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Guillaume Bordeau, Rémy Lartia, Marie-Paule Teulade-Fichou,