38378-77-7

Upstream product

• 38366-38-0 9,10-dioxo-9,10-dihydroanthracene-1,8-dicarboxylic acid 
• 82-43-9 1,8-dichloroanthraquinone 
• 544-92-3 copper(I) cyanide 
• 10208-16-9 1,8-diacetylanthracene 
• 120-12-7 anthracene 
• 14381-66-9 1,8-dichloroanthracene 
• 93655-34-6 dimethyl anthracene-1,8-dicarboxylate 
• 117-10-2 1,8-dihydroxy-9,10-anthracenedione 
• 64817-82-9 1,8-dihydroxy-9,10-dihydroanthracene 
• 94803-05-1 1,8-diacetylanthraquinone 
• 90866-50-5 1,8-dicyanoanthraquinone 
• 92967-66-3 anthracene-1,8-dicarbonitrile 

Downstream Products

• 38378-71-1 9,10-Ethanoanthracen-1,8-dicarbonsaeure 
• 103259-25-2 N,N',N''-tris(4-methylphenyl)-1,8,16-triptycenetricarboxamide 
• 34824-20-9 1,8-bis(hydroxymethyl)anthracene 
• 103006-32-2 Anthracen-1,8-bis-carbohydrazid-bis-benzolsulfonyl 
• 1397271-05-4 C₆₈H₅₆F₆N₄O₈ 
• 1397271-09-8 C₇₀H₅₄N₂O₈ 
• 1397270-95-9 C₂₃H₁₆O₄ 

Relevant academic research and scientific papers

Solid-state esterification via ionic-to-covalent bond transformation in ionic molecular crystals consisting of disubstituted anthracene anion-cation combinations

Thermal solid-state reactions involving ionic-to-covalent bond transformation were achieved in the ionic molecular crystals of 1,8-bis[(pyridin-1-ium-1-yl)methyl]anthracene anthracene-1,8-dicarboxylate to produce the cyclic diester. The crystal structure given by X-ray diffraction analysis showed that the electrostatic interaction between the benzyl pyridinium cation and the carboxylate anion successfully works to locate these reaction sites close to each other and that there are channels for crystalline solvents and the liberated pyridine to escape. There by, the cyclic diester was selectively formed by the crystal-to-crystal reaction, which was proven by powder XRD profiles and optical microscopic and SEM images of the crystals before and after the reaction. This is the first thermal crystal-to-crystal condensation reaction. Another ionic molecular crystal of 1,8-bis[(pyridin-1-ium-1-yl)methyl]anthracene anthraquinone-1,8-dicarboxylate was also studied. There in, the corresponding cyclic diester was also obtained, but the crystals were transformed to amorphous solid by the reaction.

Fluorescent molecule for identifying mercury ions as well as preparation method and application

The invention discloses a fluorescent molecule for identifying mercury ions as well as a preparation method and application. Polycyclic aromatic hydrocarbons including a naphthalene ring or an anthracene ring and the like are used as starting raw materials and different identification sites are connected through a series of organic synthetic reaction (including substitution and addition) to obtainmolecular-tweezers-shaped main body compounds with different identification properties. The fluorescent molecule can be used for detecting the mercury ions and the problem that guest molecules cannotbe easily effectively identified through an existing molecule device is solved.

A host-guest system based on collagen-like triple-helix hybridization

A strategy inspired by tweezer receptors has been employed to develop a new host-guest system. The hybridization into a collagen-like triple helix is the driving force for the recognition that occurs with high affinity and selectivity. Several systems have been screened to find the best host-guest pair and this strategy may be implemented for tag fused protein recognition.

Symmetrically Trisubstituted Triptycenes

A simple synthesis of 1,8,13- and 1,8,16-trisubstituted triptycenes is described.Diels-Alder reaction of 1,8-disubstituted anthracenes with ortho-substituted benzynes gave 15 new triptycene compounds as mixtures of the syn (1,8,13) and anti (1,8,16) trisu