- A silicon-containing compound and comprising the silicon-containing compound of the organic electroluminescent device (by machine translation)
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Provides improved emission efficiency silicon-containing compound and comprising the silicon-containing compound of the organic electroluminescent device. According to the present invention contemplates silicon-containing compound by the following formula 1 expressed. Type 1 . (by machine translation)
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Paragraph 0219-0222; 0224
(2019/04/15)
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- Solid-state valence tautomeric octahedral {CoII[(BQ-N-Cat)]2}0 complex formation via ligand-centered phenolic C-O bond breaking and Co-O bond making
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Ligand H4LO(AP/AP) underwent ligand-centered C-O bond cleavage during a complexation reaction with Co(ii)-salt. The thus formed octahedral {CoII[(BQ-N-Cat)]2}0 complex showed valence tautomerization in the solid state. While the process was triggered by the presence of lattice solvent, the nature of the solvent molecule has less effect on the process.
- Mondal, Manas Kumar,Tiwari, Archana,Mukherjee, Chandan
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supporting information
p. 11995 - 11998
(2016/10/09)
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- Method for the preparation of diphenyl ether compounds
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The invention relates to a method for preparing a diphenyl ether compound. The method is characterized by comprising the following technical steps of: (1) adding a halogenated benzene derivative and a bis(pinacolato)diboron into a reaction vessel, adding copper chloride or aluminum chloride and 1,2-bi(diphenylphosphine) ethane as a catalyst, then adding alkaline and an organic solvent, and reacting at 25-160 DEG C for 6-24 hours; and (2) after extracting a reaction solution obtained from the step (1) by using ethyl acetate, purifying by a 200-300 meshes silica gel column, pre-eluting the silica gel column by using 20-50 mL of normal hexane, eluting by adopting an eluent at a flow speed of 1-2 mL/min for 3-6 hours, and removing the solvent to obtain the diphenyl ether compound. The method for preparing the diphenyl ether compound, disclosed by the invention, no only overcomes the disadvantage of the use of phenolic substances in a reaction process, but also has the advantages of mild reaction condition and high yield.
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Paragraph 0038-0040
(2016/12/01)
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