Issue 2, 2003

New near infrared-sensitive photochromic fluorescing molecules

Abstract

The synthesis of new photochromic 2-indolylfulgide dicyanomethylene derivatives is described and their structures confirmed by X-ray crystallography, NMR, mass spectroscopy and elemental analysis. The molecules exhibit two thermally stable isomeric forms, which are only optically interconverted. The ring-open form absorbs between 400 and 550 nm, while the ring-closed form absorbs in the 650 to 700 nm region. The cyclized form emits fluorescence in the near infrared, with a 0.18 quantum yield. The spectroscopic characteristics described make this molecule suitable for optical switching and optical storage devices.

Graphical abstract: New near infrared-sensitive photochromic fluorescing molecules

Supplementary files

Article information

Article type
Paper
Submitted
06 Jul 2002
Accepted
18 Nov 2002
First published
16 Dec 2002

J. Mater. Chem., 2003,13, 286-290

New near infrared-sensitive photochromic fluorescing molecules

Y. Liang, A. S. Dvornikov and P. M. Rentzepis, J. Mater. Chem., 2003, 13, 286 DOI: 10.1039/B206577K

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