22612-93-7

Upstream product

• 6372-63-0 9,10-dihydro-9,10-ethano-anthracen-11-one 
• 2732-95-8 dibenzobicyclo<2.2.2>octane-cis-2,3-diol 
• 20678-93-7 (E)-Dihydroxy-11,12 Ethano-9,10 dihydro-9,10 Anthracene 
• 120-12-7 anthracene 
• 1521-59-1 9,10-dihydro-9,10-ethano-anthracen-11-ol 
• 5675-70-7 cis-9,10-dihydro-9,10-ethanoanthracene-11,12-diol cyclic carbonate 

Downstream Products

• 2732-95-8 cis-2,3-Dihydroxy-dibenzo-bicyclo<3,2,1>octadien 
• 613-31-0 9,10-dihydroanthracene 
• 144-62-7 oxalic acid 
• 120-12-7 anthracene 
• 1428896-96-1 C₃₂H₂₈Br₂N₂Ni 
• 1428896-98-3 C₃₄H₃₂Br₂N₂Ni 

Relevant academic research and scientific papers

Effects of backbone substituent and intra-ligand hydrogen bonding interaction on ethylene polymerizations with Α-diimine nickel catalysts

The design of transition metal catalysts and the development of new catalyst design strategies for olefin polymerization have received substantial attention in the field of polyolefin research. In this paper, we initially reported backbone substituent eff

ORGANIC COMPOUND, ORGANIC LIGHT EMITTING DIODE HAVING THE SAME, AND ORGANIC LIGHT EMITTING DEVICE

The present disclosure relates to an organic compound having the following structure, and an organic light emitting diode (OLED) and an organic light emitting device comprising the same. The organic compound is applied to a light-emitting layer, so that the driving voltage of the OLED and the organic light-emitting device is reduced, and the light-emitting efficiency and the color purity of the OLED and the organic light-emitting device are improved.

N- Heterocyclic carbene palladium complex with butterfly structure and application thereof (by machine translation)

N - Heterocyclic carbene palladium complex, with a butterfly structure prevents aromatic amine from encircling carbon-nitrogen bond upset, and in a steric hindrance C11 framework structure to inhibit C12 coupling reaction, between nitrogen-containing heterocyclic chlorine and low-activity nitrogen-containing heterocyclic boronic acid and reaction can be carried out β - under mild conditions of air and water at the same time to ensure higher reaction yield, The present invention also greatly improves the reaction activity, Suzuki - Miyaura of the catalyst. (by machine translation)

Photogeneration of heptacene in a polymer matrix

Heptacene (1) was generated by the photodecarbonylation of 7,16-dihydro-7,16-ethanoheptacene-19,20-dione (2) in a polymer matrix using a UV-LED lamp (395 ± 25 nm). Compound 1 showed a long wavelength absorption band extending from 600 to 825 nm (λmax ～760 nm) and was found to be stable up to 4 h in the polymer matrix. However, irradiation of a solution of 2 in toluene produced only oxygen adducts. Copyright

Transition metal mediated exo selective Diels-Alder reactions: Preparation of 2-cobalt-substituted 1,3-dienes containing C2 symmetric 2,3-dibenzobicyclo[2.2.2]octanedione dioxime equatorial ligands and their use in thermal and Lewis acid catalyzed 4 + 2 cycloadditions

The preparation of C2 symmetric 2,3-dibenzobicyclo[2.2.2]octanedione dioxime is reported. This ligand is then used in the preparation of a (pyridine)(glyoxime)2cobalt(III) chloride complex. The chloride is reduced to a cobaloxime anion which reacted with allenic electrophiles to produce (pyridine)(glyoxime)2cobalt-1,3-dienyl complexes. Thermal and Lewis acid catalyzed Diels-Alder reactions of these dienyl complexes as well as the complexes with glyoxime = diphenylglyoxime and dimethylglyoxime are reported. In most cases these Diels-Alder reactions are anti (exo) selective, and in many cases diastereoselectivities are >20:1. Cycloadduct demetalation reactions are also reported which preserve cycloaddition stereochemistry and provide cobalt complexes which can be recycled into the starting dienyl complex.