The Experts below are selected from a list of 69 Experts worldwide ranked by ideXlab platform
John M Plater - One of the best experts on this subject based on the ideXlab platform.
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liquid chromatography mass spectrometry analysis of Mauveine and phenosafranins in black precipitate from the bradford colour experience museum
Journal of Chemical Research-s, 2019Co-Authors: John M Plater, Andrea RaabAbstract:Mauveine chromophores and a family of phenosafranins have been extracted from the Colour Experience Museum black precipitate with boiling ethanol and separated by chromatography. Phenosafranin (287...
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liquid chromatography mass spectrometry analysis of Mauveine from the historical london suburb of sudbury w h perkin s home and factory and bradford
Journal of Chemical Research-s, 2017Co-Authors: John M Plater, Andrea RaabAbstract:Mauveine samples stored in museums in Sudbury, Bradford and Manchester are similar and are shown to be rich in Mauveine A and Mauveine B by liquid chromatography-mass spectrometry. By varying the a...
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who made Mauveine first runge fritsche beissenhirtz or perkin
Journal of Chemical Research-s, 2016Co-Authors: John M Plater, Andrea RaabAbstract:The oxidation of aniline or a mixture of aniline with o-toluidine and p-toluidine following Runge's original method as carefully as possible, using chloride of lime [Ca(OCl)2], produces a coloured ...
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Mauveine and the mauve shade six pence stamp
Journal of Chemical Research-s, 2016Co-Authors: John M Plater, Andrea RaabAbstract:British Victorian six pence lilac stamps (plates 5, 6, 8, and 9) have been analysed for Mauveine: six pence stamps (no hyphen and plates 8 or 9) were dyed with Mauveine, six-pence stamps with the h...
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syntheses and structures of pseudo Mauveine picrate and 3 phenylamino 5 2 methylphenyl 7 amino 8 methylphenazinium picrate ethanol mono solvate the first crystal structures of a Mauveine chromophore and a synthetic derivative
Journal of Chemical Research-s, 2015Co-Authors: John M Plater, William T A Harrison, Henry RzepaAbstract:We thank the EPSRC National Mass Spectrometry Service Centre (University of Swansea) for measuring mass spectra and the EPSRC National Crystallography Service Centre (University of Southampton) for collecting the diffraction data.
Andrea Raab - One of the best experts on this subject based on the ideXlab platform.
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liquid chromatography mass spectrometry analysis of Mauveine and phenosafranins in black precipitate from the bradford colour experience museum
Journal of Chemical Research-s, 2019Co-Authors: John M Plater, Andrea RaabAbstract:Mauveine chromophores and a family of phenosafranins have been extracted from the Colour Experience Museum black precipitate with boiling ethanol and separated by chromatography. Phenosafranin (287...
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synthesis and analysis by liquid chromatography mass spectrometry of a Mauveine composition similar to museum stored Mauveine
Journal of Chemical Research-s, 2018Co-Authors: M J Plater, Andrea RaabAbstract:Our proposal that museum-stored Mauveine was made by a modified method compared to Mauveine made by the William Henry Perkin patented method of 1856 is exemplified. An improved method of purificati...
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liquid chromatography mass spectrometry analysis of Mauveine from the historical london suburb of sudbury w h perkin s home and factory and bradford
Journal of Chemical Research-s, 2017Co-Authors: John M Plater, Andrea RaabAbstract:Mauveine samples stored in museums in Sudbury, Bradford and Manchester are similar and are shown to be rich in Mauveine A and Mauveine B by liquid chromatography-mass spectrometry. By varying the a...
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who made Mauveine first runge fritsche beissenhirtz or perkin
Journal of Chemical Research-s, 2016Co-Authors: John M Plater, Andrea RaabAbstract:The oxidation of aniline or a mixture of aniline with o-toluidine and p-toluidine following Runge's original method as carefully as possible, using chloride of lime [Ca(OCl)2], produces a coloured ...
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Mauveine and the mauve shade six pence stamp
Journal of Chemical Research-s, 2016Co-Authors: John M Plater, Andrea RaabAbstract:British Victorian six pence lilac stamps (plates 5, 6, 8, and 9) have been analysed for Mauveine: six pence stamps (no hyphen and plates 8 or 9) were dyed with Mauveine, six-pence stamps with the h...
Sergio Seixas J De Melo - One of the best experts on this subject based on the ideXlab platform.
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reconstructing the historical synthesis of Mauveine from perkin and caro procedure and details
Scientific Reports, 2017Co-Authors: Tânia F G G Cova, Alberto A C C Pais, Sergio Seixas J De MeloAbstract:Mauveine, an iconic dye, first synthesised in 1856 still has secrets to unveil. If nowadays one wanted to prepare the original Perkin’s Mauveine, what would be the procedure? It will be described in this work and lies on the use of a 1:2:1 (mole) ratio of aniline, p-toluidine and o-toluidine. This was found from a comparison of a series of products synthesized from different proportions of these starting materials, with a set of historical samples of Mauveine and further analysed with two unsupervised chemometrics methods.
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perkin s and caro s Mauveine in queen victoria s lilac postage stamps a chemical analysis
Chemistry: A European Journal, 2014Co-Authors: Maria Da Conceicao Oliveira, Ana Paula Soares Dias, Peter Douglas, Sergio Seixas J De MeloAbstract:Mauveine, a chemical icon, is no longer commercially available. If nowadays one wanted to have a sample of the original Perkin, or Caro, Mauveine, and see its colour, where would one find it? The answer is on UK Victorian 6d postage stamps from 1867–1880. This was found from a comparison with historical samples of Mauveine, from both William Perkin and a Heinrich Caro sample (here analysed for the first time). These have distinctly different compositions and this was used to identify the origin of Mauveine in the postage stamps, with evidence found for Mauveine made by both Perkin’s and Caro’s synthesis.
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revisiting perkin s dye s the spectroscopy and photophysics of two new Mauveine compounds b2 and c
Chemical Communications, 2007Co-Authors: Sergio Seixas J De Melo, S Takato, Micaela M Sousa, Maria Joao Melo, A J ParolaAbstract:Two new components have been identified in an early sample prepared according to the original recipe of Perkin, and perhaps even by Perkin himself around 1860 – a new isomer of Perkin's Mauveine B (designated as Mauveine B2) together with a new Mauveine compound (Mauveine C) – and these compounds were synthesized again using starting materials chosen to reproduce Perkin's original synthesis and isolated by HPLC-DAD, identified by 1H NMR, MS and their spectroscopic (UV/Vis and emission) and photophysical behaviour investigated.
William T A Harrison - One of the best experts on this subject based on the ideXlab platform.
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syntheses and structures of pseudo Mauveine picrate and 3 phenylamino 5 2 methylphenyl 7 amino 8 methylphenazinium picrate ethanol mono solvate the first crystal structures of a Mauveine chromophore and a synthetic derivative
Journal of Chemical Research-s, 2015Co-Authors: John M Plater, William T A Harrison, Henry RzepaAbstract:We thank the EPSRC National Mass Spectrometry Service Centre (University of Swansea) for measuring mass spectra and the EPSRC National Crystallography Service Centre (University of Southampton) for collecting the diffraction data.
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the isolation of n tert butyl p toluidine hydrochloride and the synthesis of Mauveine
Journal of Chemical Research-s, 2014Co-Authors: John M Plater, William T A HarrisonAbstract:Heating p-toluidine hydrochloride in tert-butanol gave a crystalline precipitate of N-tert-butyl-p-toluidine hydrochloride. This compound, now readily available by this simple procedure, was used t...
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synthetic derivatives of Mauveine
Journal of Chemical Research-s, 2013Co-Authors: John M Plater, William T A HarrisonAbstract:Oxidation of phenosafranin and an excess of aniline gave a novel hydroxylated derivative of pseudo-Mauveine. N-Methyl-p-toluidine and bis(4-methylphenyl)amine are efficient building blocks for maki...
Tânia F G G Cova - One of the best experts on this subject based on the ideXlab platform.
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reconstructing the historical synthesis of Mauveine from perkin and caro procedure and details
Scientific Reports, 2017Co-Authors: Tânia F G G Cova, Alberto A C C Pais, Sergio Seixas J De MeloAbstract:Mauveine, an iconic dye, first synthesised in 1856 still has secrets to unveil. If nowadays one wanted to prepare the original Perkin’s Mauveine, what would be the procedure? It will be described in this work and lies on the use of a 1:2:1 (mole) ratio of aniline, p-toluidine and o-toluidine. This was found from a comparison of a series of products synthesized from different proportions of these starting materials, with a set of historical samples of Mauveine and further analysed with two unsupervised chemometrics methods.