Issue 4, 2005

Investigation of two-photon absorption behavior in symmetrical acceptor–π–acceptor derivatives with dimesitylboryl end-groups. Evidence of new engineering routes for TPA/transparency trade-off optimization

Abstract

Investigations of the non-linear optical properties of a novel series of A–π–A quadrupoles, based on dimesitylboron end-groups, reveal the promising potential of elongated vinylboranes derivatives for combined enhanced two-photon absorption cross-section and improved transparency in the visible region. In addition, the excited state lifetime can be significantly enhanced in A–π–A′–π–A derivatives. This opens a new route towards optimized molecules for optical power limiting.

Graphical abstract: Investigation of two-photon absorption behavior in symmetrical acceptor–π–acceptor derivatives with dimesitylboryl end-groups. Evidence of new engineering routes for TPA/transparency trade-off optimization

Article information

Article type
Paper
Submitted
29 Oct 2004
Accepted
24 Dec 2004
First published
18 Jan 2005

Phys. Chem. Chem. Phys., 2005,7, 600-606

Investigation of two-photon absorption behavior in symmetrical acceptor–π–acceptor derivatives with dimesitylboryl end-groups. Evidence of new engineering routes for TPA/transparency trade-off optimization

M. Charlot, L. Porrès, C. D. Entwistle, A. Beeby, T. B. Marder and M. Blanchard-Desce, Phys. Chem. Chem. Phys., 2005, 7, 600 DOI: 10.1039/B416605A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements