Issue 94, 2016, Issue in Progress

Synthesis, linear and nonlinear optical properties of a new dimethine cyanine dye derived from phenothiazine

Abstract

Dimethine cyanine dye (PTZIS) based on phenothiazine as the core donor and indolium salt as the acceptor has been synthesized and fully characterized. UV-Vis absorption and fluorescence properties of PTZIS were studied in different solvents. Absorption spectra revealed a large bathochromic shift of the intramolecular charge transfer (ICT) absorption band of PTZIS compared with those in the non-halogenated solvents. Also, the optical data of PTZIS showed a large Stokes shift compared with those in the non-halogenated solvents, indicating a great influence on the geometry of the emissive excited state. The nonlinear optical properties of PTZIS in ethanol solution at different concentrations and different laser powers have been studied using the Z-scan technique with a continuous wave (cw) argon ion laser at 514.5 nm. The closed aperture Z-scan data was used to estimate the nonlinear refractive index n2, while the open aperture scan provided the nonlinear absorption coefficient β. The values obtained are relatively very high and vary linearly with concentration.

Graphical abstract: Synthesis, linear and nonlinear optical properties of a new dimethine cyanine dye derived from phenothiazine

Supplementary files

Article information

Article type
Paper
Submitted
28 May 2016
Accepted
20 Sep 2016
First published
26 Sep 2016

RSC Adv., 2016,6, 91546-91556

Synthesis, linear and nonlinear optical properties of a new dimethine cyanine dye derived from phenothiazine

R. M. El-Shishtawy, F. A. M. Al-Zahrani, S. M. Afzal, M. A. N. Razvi, Z. M. Al-amshany, A. H. Bakry and A. M. Asiri, RSC Adv., 2016, 6, 91546 DOI: 10.1039/C6RA13839J

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