9 10 diphenylanthracene

Manufactured by Merck Group

Sourced in Japan, United Kingdom

9,10-diphenylanthracene is a fluorescent organic compound commonly used in laboratory settings. It is a crystalline solid that emits a blue-violet fluorescence when exposed to ultraviolet light. This compound is primarily utilized as a fluorescent probe or dye in various analytical and research applications.

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Lab products found in correlation

Pyrene, by Fujifilm (1 mentions) Anthracene, by Fujifilm (1 mentions) Dl camphor, by Merck Group (1 mentions) Naphthalene, by Merck Group (1 mentions) Chloroform, by Avantor (1 mentions) Ethyl acetate, by Avantor (1 mentions) Methanol, by Avantor (1 mentions) Ethanol, by Avantor (1 mentions) Chloroform d, by Thermo Fisher Scientific (1 mentions) N butyl lithium n buli, by Thermo Fisher Scientific (1 mentions) N octane, by Thermo Fisher Scientific (1 mentions) Hydrochloric acid (hcl), by Merck Group (1 mentions) Sodium thiosulfate, by Merck Group (1 mentions)

2 protocols using 9 10 diphenylanthracene

Synthesis and Characterization of Aromatic Compounds

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Section 1: naphthalene (Sigma-Aldrich, St. Louis, MO, USA), anthracene (FUJIFILM Wako Pure Chemical Corporation, Osaka, Japan), tetracene (Tokyo Chemical Company (TCI), Tokyo, Japan), pyrene (Wako).
Section 2: 9,10-diphenylanthracene (Sigma-Aldrich), 9,10-bis(phenylethynyl)anthracene (TCI), 2,7-di-tert-butyllpyrene (TCI), 1,3,6,8-tetraphenylpyrene (TCI), 5,12-bis(phenylethynyl)tetracene (Sigma-Aldrich).
Section 3: D-/L-camphor (Sigma-Aldrich), (R)-/(S)-(-)-1,1′-binaphthyl-2,2′-diyl hydrogen phosphate (TCI), (R)-/(S)-2,2′-dimethoxy-1,1′-binaphthyl (TCI), (R)-/(S)-2,2′-bis(methoxymethoxy)- 1,1’-binaphthyl (TCI).
Section 4: biphenyl (TCI), p-terphenyl (TCI), p-quaterphenyl (TCI), p-quinquphenyl (TCI), p-hexaphenyl (TCI), DMT (Exciton, Tokyo Instruments Inc (Tokyo, Japan)), Japanese vendor)), TMQ (Exciton), QUI (Exciton), Exalite 360 (Exciton), TBS (Exciton), [12 (link)] cycloparaphenylene (Kanto Chemicals, Tokyo, Japan).
Section 5: 9,9-dimethylfluorene (TCI), 9,9-dioctylfluorene (TCI), Exalite384 (Exciton), 9,9-dihexylfluorene trimer (American Dye Source (ADS), Quebec, Canada), 9,9-dihexylfluorene pentamer (ADS), 9,9-dihexylfluorene heptameter (ADS), Exalite 376 (Exciton), Exalite 404 (Exciton), Exalite 428 (Exciton), Exalite 416 (Exciton).

Fujiki M., Koe J.R., Mori T, & Kimura Y. (2018). Questions of Mirror Symmetry at the Photoexcited and Ground States of Non-Rigid Luminophores Raised by Circularly Polarized Luminescence and Circular Dichroism Spectroscopy: Part 1. Oligofluorenes, Oligophenylenes, Binaphthyls and Fused Aromatics. Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry, 23(10), 2606.

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Synthesis and Characterization Protocol

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Syntheses were carried out under a nitrogen atmosphere, unless stated otherwise. Glassware was dried before use. Solvents were dried over 4 Å molecular sieves for at least 24 h before use.
n-Butyllithium (n-BuLi, 2.5 M, in hexanes), chloroform-d (99.8 atom% D) and n-octane ($97%) were obtained from Acros, bromine (Br 2 , $99.99% trace metals basis), 9,10-diphenylanthracene, hydrochloric acid (HCl, 37%), magnesium silicide (Mg 2 Si, $99% trace metals basis, À20 mesh), molecular sieves (0.3 nm, rods), sodium sulfate (Na 2 SO 4 , anhydrous), and sodium thiosulfate (Na 2 S 2 O 3 , $98%, anhydrous) were obtained from Sigma Aldrich, chloroform, ethanol, ethyl acetate and methanol were obtained from VWR, TEM grids were obtained from EM Resolutions (Sheffield, United Kingdom), and XPS substrates from SSENS (Hengelo, The Netherlands).

Wilbrink JL ., Huang CC ., Dohnalova K , & Paulusse JMJ . (2020). Critical assessment of wet-chemical oxidation synthesis of silicon quantum dots. Faraday discussions, 222(0).

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