Spiropyran-Merocyanine Equilibrium in Presence of Organic Acids and Bases
- 1 June 2005
- journal article
- research article
- Published by Taylor & Francis in Molecular Crystals and Liquid Crystals
- Vol. 431 (1) , 337-344
- https://doi.org/10.1080/15421400590946712
Abstract
Manipulation of the rate of thermal reversion of N-functionalized merocyanines (MC) to the corresponding spiropyran isomers in the dark, was demonstrated by using both organic acid and base additives. In the presence of organic bases, increase or decrease of the rate of reaction was dependent on the solvent used. When organic acids were used, in all cases the reaction rate decreased when compared with the system containing no acid. Similar behavior was also observed in polymer films. This approach is of interest for applications in the design of optical switches and memory with enhanced stability of the stored information.Keywords
This publication has 8 references indexed in Scilit:
- Modulation of the Spiropyran−Merocyanine Reversion via Metal-Ion Selective Complexation: Trapping of the “Transient” cis-MerocyanineChemistry of Materials, 2001
- Thermal Reversion Mechanism of N-Functionalized Merocyanines to Spiropyrans: A Solvatochromic, Solvatokinetic, and Semiempirical StudyThe Journal of Physical Chemistry A, 2000
- Stabilization of the merocyanine form of photochromic compounds in fluoro alcohols is due to a hydrogen bondChemical Communications, 1998
- Effects of metal ion complexation on the spiropyran–merocyanine interconversion: development of a thermally stable photo-switchChemical Communications, 1998
- Improvement of the properties of a functional organized thin film by the introduction of nanoparticles part I. Retardation of photo-isomerization rate of a spiropyran-containing Langmuir-Blodgett film by the incorporation of SiO2 nanoparticlesColloids and Surfaces A: Physicochemical and Engineering Aspects, 1996
- Photoreversible optical nonlinearities of polymeric films containing spiropyran with long alkyl chainsApplied Physics Letters, 1996
- The Esterification of Trifluoroacetic Acid: A Variable Temperature NMR Kinetics StudyJournal of Chemical Education, 1996
- The esterification of trifluoroacetic acid: An NMR kinetics experimentJournal of Chemical Education, 1985