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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.


Papers
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Journal ArticleDOI
TL;DR: The title compound, C34H35O2N3, was synthesized by the reaction of 2-[3,6-bis(diethylamino)-9H-xanthen-9-yl]benzoyl chloride with aniline.
Abstract: In the crystal structure of the title compound, C31H37N3O2, the dihedral angle between the planes of the xanthene ring system and the spiro­lactam ring is 90.3°.

4 citations

Journal ArticleDOI
TL;DR: Several poly(arylene ether nitrile) (PAEN) copolymers containing multi-methyl and cardo xanthene groups were synthesized by nucleophilic substitution reaction of 2,6-difluorobenzonitrile with varying molar ratios of 9,9-bis(3,5-dimethyl-4-hydroxyphenyl)xanthene (BDMHPX) and hydroquinone (HQ) in N-methyl-2-pyrrolidone (NMP) in the presence of anhydrous
Abstract: Several poly(arylene ether nitrile) (PAEN) copolymers containing multi-methyl and cardo xanthene groups were synthesized by nucleophilic substitution reaction of 2,6-difluorobenzonitrile with varying molar ratios of 9,9-bis(3,5-dimethyl-4-hydroxyphenyl)xanthene (BDMHPX) and hydroquinone (HQ) (80/20–40/60) in N-methyl-2-pyrrolidone (NMP) in the presence of anhydrous potassium carbonate. These new PAENs had inherent viscosities between 0.56 and 0.68 dL g–1, and their weight-average molecular weights and number-average molecular weights were in the range of 33,300–36,500 g mol−1 and 17,300–18,400 g mol−1, respectively. All polymers were amorphous and soluble in dipolar aprotic solvents such as NMP and N,N-dimethylacetamide and even in THF and chloroform at room temperature. These PAENs showed glass transition temperatures (Tgs) between 248°C and 289°C, and the Tg values were found to increase with increase of the BDMHPX content in the polymeric main. Thermogravimetric analysis showed that all PAENs were stab...

4 citations

Journal ArticleDOI
01 May 1958-Nature
TL;DR: The ability of colloidal electrolytes to change the colour of oppositely charged dyes is well known as discussed by the authors, and it has been used to observe micelle formation in the presence of ionized dyes.
Abstract: THE ability of colloidal electrolytes to change the colour of oppositely charged dyes is well known. One of the earliest systematic studies was that of Hartley1, and later Harkins and others showed that the colour change could be used to observe micelle formation2. Similar colour changes can sometimes be caused by non-ionic soaps in solutions of ionized dyes of either charge, but a more striking effect is found with some non-ionic soaps and certain xanthene dyes in the undissociated form. Instead of the usual band shift of between 10 and 20 mµ to the red, there is a more or less complete removal of the main absorption band and discharge of visible colour. Discharge also occurs if water-miscible organic solvents are added, or if the dye is dissolved in the pure solvent.

4 citations

Journal Article
TL;DR: In this paper, an efficient and eco-friendly method for the one-pot synthesis of 14-aryl-14H-dibenzo [a,i]xanthene-8,13-dione derivatives has been developed in the presence of Fe3O4@SiO2 core-shell nanoparticles.
Abstract: An efficient and eco-friendly method for the one-pot synthesis of 14-aryl-14H-dibenzo [a,i]xanthene-8,13-dione derivatives has been developed in the presence of Fe3O4@SiO2 core-shell nanoparticles. The multi-component reactions of 2-hydroxy-1,4naphthoquinone, β-naphthol and aldehydes were efficiently catalyzed using novel nano-scale materials under reflux conditions. The present method offers several advantages such as environmentally benign, simple work-up, excellent yield of products, short reaction times, little catalyst loading and facile catalyst separation. The nanomagnetic catalyst could be readily recovered using a simple external magnet and reused several times without any significant loss in activity. The catalyst was fully characterized by FT-IR, SEM, XRD, EDX and VSM analysis.

4 citations

Patent
03 Feb 2005
TL;DR: In this article, a diagnostic agent for positron emission tomography (PET) and methods for use of such agents for imaging of human or animal tissue are described, wherein the primary active component of such agent is a radiolabeled halogenated xanthene or halogenation of xanthenes derivative.
Abstract: New diagnostic agents for positron emission tomography (PET) and methods for use of such agents for imaging of human or animal tissue are described, wherein a primary active component of such agents is a radiolabeled halogenated xanthene or halogenated xanthene derivative. Preferably, the radiolabeled halogenated xanthene is radiolabeled Rose Bengal or a functional derivative of Rose Bengal.

4 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202354
2022136
202182
202091
201986
201891