Switching a pH indicator by a reversible photoacid: A quantitative analysis of a new two-component photochromic system. (February 2016)
- Record Type:
- Journal Article
- Title:
- Switching a pH indicator by a reversible photoacid: A quantitative analysis of a new two-component photochromic system. (February 2016)
- Main Title:
- Switching a pH indicator by a reversible photoacid: A quantitative analysis of a new two-component photochromic system
- Authors:
- Vallet, J.
Micheau, J.-C.
Coudret, C. - Abstract:
- Abstract: A UV/visible and pH-metric quantitative analysis of the spiropyran reversible photoacid1 -MEH allowed us to determine the pKa 's of the open and closed forms, the rate constants of relaxation, the quantum yield of decolouration and the UV/visible spectra of the protonated and deprotonated open and closed isomers. The coupling between1 -MEH and a selected pH-indicator acidochromic dye via proton exchange has also been analysed. The initial pH, stoichiometric ratio between the photoacid and the pH-indicator, light intensity and pKa range of the pH-indicator have been established to maximize the proton transfer from the photoacid donor to the pH-indicator acidochromic dye acceptor. When the pKa 's are matched, the two-component system behaves like a single photochromic dye. The proposed model explains why1 -MEH photo-switches BromoCresol Green but not Methyl-Orange. Graphical abstract: The coupling between a simple water soluble spiropyran reversible photoacid and a pH indicator has been quantitatively analysed. The initial pH, stoichiometric ratio, light intensity and pKa range have been determined to maximize the proton transfer from the photochromic donor to the pH-indicator acceptor. Highlights: A water soluble reversible photochromic spiropyran photoacid was parametrized. Numerical fit was used to propose a plausible chemical network. In silico optimization was used to optimize the photoacid to a pH sensitive dye. Experimental verification was then achieved withAbstract: A UV/visible and pH-metric quantitative analysis of the spiropyran reversible photoacid1 -MEH allowed us to determine the pKa 's of the open and closed forms, the rate constants of relaxation, the quantum yield of decolouration and the UV/visible spectra of the protonated and deprotonated open and closed isomers. The coupling between1 -MEH and a selected pH-indicator acidochromic dye via proton exchange has also been analysed. The initial pH, stoichiometric ratio between the photoacid and the pH-indicator, light intensity and pKa range of the pH-indicator have been established to maximize the proton transfer from the photoacid donor to the pH-indicator acidochromic dye acceptor. When the pKa 's are matched, the two-component system behaves like a single photochromic dye. The proposed model explains why1 -MEH photo-switches BromoCresol Green but not Methyl-Orange. Graphical abstract: The coupling between a simple water soluble spiropyran reversible photoacid and a pH indicator has been quantitatively analysed. The initial pH, stoichiometric ratio, light intensity and pKa range have been determined to maximize the proton transfer from the photochromic donor to the pH-indicator acceptor. Highlights: A water soluble reversible photochromic spiropyran photoacid was parametrized. Numerical fit was used to propose a plausible chemical network. In silico optimization was used to optimize the photoacid to a pH sensitive dye. Experimental verification was then achieved with standard pH indicators. … (more)
- Is Part Of:
- Dyes and pigments. Volume 125(2016)
- Journal:
- Dyes and pigments
- Issue:
- Volume 125(2016)
- Issue Display:
- Volume 125, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 125
- Issue:
- 2016
- Issue Sort Value:
- 2016-0125-2016-0000
- Page Start:
- 179
- Page End:
- 184
- Publication Date:
- 2016-02
- Subjects:
- Photochromism -- pH photocontrol -- Photoacid -- Chemical dynamics -- Coupled reactions -- Spiropyran
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2015.10.025 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2767.xml