607-61-4

Upstream product

• 61736-92-3 anthracene-1,8-disulphonic acid 
• 16294-34-1 1,8-dimethoxyanthracene 
• 120-12-7 anthracene 
• 1963-82-2 1,8-diacetoxy-9,10-anthraquinone 
• 117-10-2 1,8-dihydroxy-9,10-anthracenedione 

Downstream Products

• 31999-55-0 1,8-diacetoxyanthracene 

Relevant academic research and scientific papers

A new fluorescent as well as chromogenic chemosensor for anions based on an anthracene carbamate derivative

A new fluorescent as well as chromogenic anion sensor, 1,8-anthradiol bis(N-phenylcarbamate) 2, was synthesized. It exhibits new selective red-shifted absorption and fluorescence bands with F- and AcO-, which could be attributed to the anthracene moiety directly involved in the bonding interaction with the anions.

1,8-Dioxyanthracene-Derived Crown Ethers: Synthesis, Complexation with Paraquat and Assembly of a Tetracationic Cyclophane-Crown Ether Based [2]Catenane

1,8-Dioxyanthracene-based bisarylene crown ethers, composed of ethylene glycol chains and aromatic moieties, have been synthesized. Complexation studies revealed that these crown ethers could form 1:1 complexes with methyl viologen dication (N,N′-dimethyl

An easy and multigram scale synthesis of anthracene-1,8-ditriflate

1,8-Ditriflated anthracene was prepared by an easy and straightforward approach that enables its reproducible synthesis on a 10 gram scale. Its symmetric/unsymmetric diethynylations by using the Sonogashira cross-coupling reactions were also demonstrated. Georg Thieme Verlag Stuttgart.

ESR Spectroscopic Detection of Intramolecular Interactions in Radical Cations of Poly(α-methoxy)triptycenes

-Cycloaddition of 1,4-benzoquinone to the di- and tetra(α-methoxy)anthracenes 11 yields the diketones 12 which undergo an acid-catalyzed rearrangement to the triptycene hydroquinones 13.Methylation of 13 affords the poly(α-methoxy)triptycenes 4.Aluminium chloride in nitromethane oxidizes the triptycenes 4 to the radical cations 4+* having one 1,4-dialkoxybenzene ring (4b+*, 4c+*, 4e+*) or two (4a+*) or three (4d+*), respectively, of such potential radical centers.The protons of the radical center give rise to hyperfine splittings which are very similar to those found in the ESR spectra of simple cis-1,4-dialkoxybenzene radical cations.The other aromatic protons, but not the bridgehead protons, exhibit a long range hyperfine coupling of 0.011 mT.Selective line broadening in the ESR spectrum of the radical cation 4a+* indicates that intramolecular electron transfer between the 1,4-dimethoxybenzene moieties occurs at a moderate rate.The deceleration of the exchange rate compared to the rate expected for a free radical cation is interpreted in terms of ion pairing.