Topic
Xanthene
About: Xanthene is a research topic. Over the lifetime, 2132 publications have been published within this topic receiving 34803 citations. The topic is also known as: Xanthene & dibenzo[a,e]pyran.
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TL;DR: In this article, commercial dye samples and three liquid wastes from organic pigment and dye manufacture have been characterized without prior chromatography by thermospray ionization and low energy collision-activated dissociation of protonated molecules using a triple quadrupole mass spectrometer.
Abstract: Sixteen commercial dye samples and three liquid wastes from organic pigment and dye manufacture have been characterized without prior chromatography by thermospray ionization and low energy collision-activated dissociation of protonated molecules using a triple quadrupole mass spectrometer. Many samples contained precursors of the dyes and other by-products of the synthesis. Many of these components were identified by collision-activated dissociation experiments and by inspection of the chemistry of dye manufacture. Detection limits of 20–200 ng in the positive ion mode were obtained for seven dyes of the anthraquinone, triarylmethane, xanthene, coumarin, azo and sulfonated azo dye classes. Under conditions of negative ionization, detection limits for an anthraquinone dye and a sulfonated azo dye were about one order of magnitude higher.
43 citations
TL;DR: In this article, a new basic ionic liquid from ethan-1,2-diylbis (hydrogen sulfate) and 1,8-diazobicyclo[5.4.0]undec-7-ene was suggested.
43 citations
TL;DR: In this paper, a series of hole-transporting molecules based on spiro(fluorene-9,9′-xanthene) were designed and synthesized by a copper-catalyzed modified Ullmann reaction.
43 citations
TL;DR: Tetrahydrobenzo[c]xanthenes-11-ones was synthesized by a three component reaction of α-naphthol, aromatic aldehyde and dimedone using Ceric ammonium nitrate as a suitable eco-friendly catalyst.
43 citations
TL;DR: In this paper, a simple, efficient, and environmentally benign route was developed for the preparation of 14-aryl or alkyl-14H-dibenzo[a,j]xanthene, 1,8-dioxo-octahydroxanthene and 12-aryl.
Abstract: A simple, efficient, and environmentally benign route was developed for the preparation of 14-aryl or alkyl-14H-dibenzo[a,j]xanthene, 1,8-dioxo-octahydroxanthene and 12-aryl—8,9,10,12-tetrahydrobenzo[a]xanthene-11-ones from condensation of various aldehydes with (i) β-naphthol, (ii) cyclic 1,3-dicarbonyl compounds and (iii) β-naphthol and cyclic 1,3-dicarbonyl compounds, using novel polymeric catalyst [poly(AMPS-co-AA)] under solvent-free conditions. Use of easily available catalyst, shorter reaction times, better yields, simplicity of the reaction, heterogeneous system, and easy work-up are the advantages of the present method.
43 citations