1979
DOI: 10.1021/j100469a012
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Absolute luminescence yield of cresyl violet. A standard for the red

Abstract: Publication costs assisted by the Petroleum Research Fund and the National Science Foundation We measure ( for the oxazine dye cresyl violet to be 0.54s in methanol, at 22 °C, for excitation from 540 to 640 nm. With a mean emission wavelength near 638 nm, this should be a useful luminescence quantum yield standard for the red. We judge our absolute accuracy to be well within 10% and probably better than 5%. The yield is rather insensitive to conditions even including choice of solvent. It is constant from extr… Show more

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Cited by 383 publications
(264 citation statements)
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“…Luminescence data were recorded on a Perkin--Elmer LS--luminescence spectrometer, in CHCl 3 (1 × 10 --5 M) and in solid state measurements were made using finely pulverized KBr dispersions of the sample in 5 mm quartz tubes at room temperature. Luminescence quantum yields were obtained at room temperature using the optically dilute method (A < 0.1) in degassed chloroform (quantum yields standard were perylene in methanol (Ф fl = 0.92), 24 rhodamine B in ethanol (Ф fl = 0.70), 33 and cresyl violet in ethanol (Ф fl = 0.54) 34 and using an excitation wavelength of 434, 510 and 540 nm, respectively nm). The emission lifetime measurements were carried out with a Lifespec--red picosecond fluorescence lifetime spectrometer from Edinburgh Instruments.…”
Section: Methodsmentioning
confidence: 99%
“…Luminescence data were recorded on a Perkin--Elmer LS--luminescence spectrometer, in CHCl 3 (1 × 10 --5 M) and in solid state measurements were made using finely pulverized KBr dispersions of the sample in 5 mm quartz tubes at room temperature. Luminescence quantum yields were obtained at room temperature using the optically dilute method (A < 0.1) in degassed chloroform (quantum yields standard were perylene in methanol (Ф fl = 0.92), 24 rhodamine B in ethanol (Ф fl = 0.70), 33 and cresyl violet in ethanol (Ф fl = 0.54) 34 and using an excitation wavelength of 434, 510 and 540 nm, respectively nm). The emission lifetime measurements were carried out with a Lifespec--red picosecond fluorescence lifetime spectrometer from Edinburgh Instruments.…”
Section: Methodsmentioning
confidence: 99%
“…45 Both systems were excited at 2.30 eV (540 nm) with their absorbances matched at the excitation wavelength. Differences in solvent refractive indices as well as spectrometer sensitivities were taken into account.…”
Section: Optical Measurementsmentioning
confidence: 99%
“…In the case of GePc the strong overlap between the lowest energy absorption band and the fluorescence emission may cause optical artifacts arising from inner filter and/or trivial reabsorption effects; therefore, in order to minimise such effects, the GePc solutions were always kept at an optical density lower than 0.05 at both the excitation and maximum absorption wavelengths. The quantum yield of GePc fluorescence was calculated by comparison of the area below the corrected emission spectrum for a 0.01 gM phthalocyanine solution in chloroform with that of cresyl violet chosen as a fluorescence standard (quantum yield 0.54 in methanol; Magde et al, 1979).…”
Section: Experimental Photodynamic Therapymentioning
confidence: 99%