Fluorimetric studies of solutions of pyronin dyes

equilibrium constants in water and partition coefficients in organic-solvent-water systems

Mohamed El Baraka, Michel Deumié, Pierre Viallet, Theodore Lampidis

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

The cytotoxic pyronin dyes provide simplified models for the xanthene squeleton of popular rhodamines. Kinetic analysis of fluorescence spectra of pyronin Y (PY) and pyronin B (PB) aqueous solutions allows us to study the reversible equilibria between R+ zwitterions (λ Fluo, max=566 nm (PY), 570 nm (PB)) and colorless ROH xanthydrols (λFluo, max=463 nm (PY), 467 nm (PB)) formed through ion-pair reactions with nucleophile OH-. The rate and equilibrium constants of R+ hydrolysis by OH- in water gives pKR+(S0)= -2.6 for the two pyronins while fluorescent species are too short lived for any shift in the equilibrium to be detected in the S1 state. Covalent ROH species are stable in basic solutions and poor ion solvating solvents; the reaction of R+ with OH- is slow in neutral solutions. For further understanding and applications of pyronins on biomembranes, biphasic mixtures of an organic solvent (OS) with water (W) provide partition coefficients P and extraction percentages E of the different species in the OS phase. In the n-octanol-water (ratio 1:1) system, R+ and ROH co-exist in both phases, resulting in Pion=1.8 (PY) and 2.6 (PB) at physiological pH with EROH=0.09 (PY) and 0.16 (PB); most pyronin exists as R+ in water owing to its pKR+ but the presence of the octanol phase shifts the equilibrium toward ROH. The ROH structure presents other features of interest because of its oxidization by air into RO xanthone in aprotic non-polar solvents. In the OS-W system (1:1) where OS is cyclohexane, the partitioning of pyronins between the OS and W phases is strongly one sided with R+ remaining in water RO(λFluo, max=365-366 nm) completely trapped in the cyclohexane. The E percentages differ for PY and PB since ERO(PY)=0.8 but only 0.3 for PB. The implication of hydrophobic interactions and hydrogen-bonded (solvated) water in OS is also discussed.

Original languageEnglish
Pages (from-to)295-311
Number of pages17
JournalJournal of Photochemistry and Photobiology, A: Chemistry
Volume56
Issue number2-3
DOIs
StatePublished - Feb 15 1991

Fingerprint

Pyronine
Equilibrium constants
Organic solvents
partitions
Coloring Agents
Dyes
dyes
Water
coefficients
water
Cyclohexane
Xanthenes
cyclohexane
Nucleophiles
Ions
1-Octanol
Octanols
Rhodamines
Phase shift
zwitterions

ASJC Scopus subject areas

  • Bioengineering
  • Physical and Theoretical Chemistry

Cite this

Fluorimetric studies of solutions of pyronin dyes : equilibrium constants in water and partition coefficients in organic-solvent-water systems. / El Baraka, Mohamed; Deumié, Michel; Viallet, Pierre; Lampidis, Theodore.

In: Journal of Photochemistry and Photobiology, A: Chemistry, Vol. 56, No. 2-3, 15.02.1991, p. 295-311.

Research output: Contribution to journalArticle

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abstract = "The cytotoxic pyronin dyes provide simplified models for the xanthene squeleton of popular rhodamines. Kinetic analysis of fluorescence spectra of pyronin Y (PY) and pyronin B (PB) aqueous solutions allows us to study the reversible equilibria between R+ zwitterions (λ Fluo, max=566 nm (PY), 570 nm (PB)) and colorless ROH xanthydrols (λFluo, max=463 nm (PY), 467 nm (PB)) formed through ion-pair reactions with nucleophile OH-. The rate and equilibrium constants of R+ hydrolysis by OH- in water gives pKR+(S0)= -2.6 for the two pyronins while fluorescent species are too short lived for any shift in the equilibrium to be detected in the S1 state. Covalent ROH species are stable in basic solutions and poor ion solvating solvents; the reaction of R+ with OH- is slow in neutral solutions. For further understanding and applications of pyronins on biomembranes, biphasic mixtures of an organic solvent (OS) with water (W) provide partition coefficients P and extraction percentages E of the different species in the OS phase. In the n-octanol-water (ratio 1:1) system, R+ and ROH co-exist in both phases, resulting in Pion=1.8 (PY) and 2.6 (PB) at physiological pH with EROH=0.09 (PY) and 0.16 (PB); most pyronin exists as R+ in water owing to its pKR+ but the presence of the octanol phase shifts the equilibrium toward ROH. The ROH structure presents other features of interest because of its oxidization by air into RO xanthone in aprotic non-polar solvents. In the OS-W system (1:1) where OS is cyclohexane, the partitioning of pyronins between the OS and W phases is strongly one sided with R+ remaining in water RO(λFluo, max=365-366 nm) completely trapped in the cyclohexane. The E percentages differ for PY and PB since ERO(PY)=0.8 but only 0.3 for PB. The implication of hydrophobic interactions and hydrogen-bonded (solvated) water in OS is also discussed.",
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