Patent classifications
C07F9/6596
FUSED POLYCYCLIC COMPOUND AND LIGHT EMITTING DEVICE INCLUDING THE SAME
A light emitting device includes an emission layer disposed between electrodes. The emission layer includes a host and a delayed fluorescence dopant. The delayed fluorescence dopant includes a fused polycyclic compound represented by Formula 1:
##STR00001##
MOTOR OIL BLENDS VOID OF ZPPD AND METHODS FOR REDUCING ENGINE WEAR VIA MOTOR OIL BLENDS VOID OF ZPPD
An environmentally-improved motor oil blend and related methods for properly lubricating components of an engine and favorably modifying a plastic response of components of the engine, the blend being free of zinc di-alkyl-di-thiophosphates (ZDDP) and free of zinc di-thiophosphate (ZDTP), comprising: a motor oil selected from the motor oil group consisting of Group I, Group II, Group III, Group IV, and Group V motor oils; a motor oil additive comprising alpha-olefins and hydroisomerized hydro-treated severe hydrocracked base oil; ZDDP omitted from the chemical constituents of the motor oil; and ZDTP omitted from the chemical constituents of the motor oil.
Method for preparing sensitizing material and organic light emitting diode
A method for preparing a sensitizing material and an organic light emitting diode are provided, the method including: adding C.sub.24H.sub.16Br.sub.2P.sub.2 and dichloromethane to a hydrogen peroxide solution to react therewith, dissolving a reactant in a dichloromethane solution and subjecting the solution to a purification with a first silica gel column; adding a purified product, a predetermined electron donor material, palladium acetate, and tri-tert-butylphosphine tetrafluoroborate in sodium tert-butoxide and toluene to react; extracting with dichloromethane and purified by a second silica gel column.
NON-AQUEOUS ELECTROLYTE, POWER STORAGE DEVICE USING SAME, AND LITHIUM SALT USED FOR SAME
A nonaqueous electrolytic solution having an electrolyte salt dissolved in a nonaqueous solvent, the nonaqueous electrolytic solution containing a lithium salt having a specific α,β-dihydroxy carboxylic acid ester structure, phosphono hydroxy carboxylic acid structure, alkoxycarbonyl hydroxy carboxylic acid structure, or formyloxy structure; an energy storage device using the nonaqueous electrolytic solution; and a lithium salt used for the nonaqueous electrolytic solution. This nonaqueous electrolytic solution makes it possible not only to improve the electrochemical characteristics when the energy storage device is used at a high temperature and a high voltage and to improve the capacity retention rate after high-voltage and high-temperature storage, but also to suppress gas generation.
NON-AQUEOUS ELECTROLYTE, POWER STORAGE DEVICE USING SAME, AND LITHIUM SALT USED FOR SAME
A nonaqueous electrolytic solution having an electrolyte salt dissolved in a nonaqueous solvent, the nonaqueous electrolytic solution containing a lithium salt having a specific α,β-dihydroxy carboxylic acid ester structure, phosphono hydroxy carboxylic acid structure, alkoxycarbonyl hydroxy carboxylic acid structure, or formyloxy structure; an energy storage device using the nonaqueous electrolytic solution; and a lithium salt used for the nonaqueous electrolytic solution. This nonaqueous electrolytic solution makes it possible not only to improve the electrochemical characteristics when the energy storage device is used at a high temperature and a high voltage and to improve the capacity retention rate after high-voltage and high-temperature storage, but also to suppress gas generation.
Organic electroluminescence device and polycyclic compound for organic electroluminescence device
An organic electroluminescence device and a polycyclic compound used for the organic electroluminescence device are provided. The polycyclic compound according to an embodiment of the inventive concept is represented by Formula 1. In Formula 1, Y is B, P═O, or P═S, and X is SiR.sub.3R.sub.4, or GeR.sub.5R.sub.6. At least one of R.sub.1 or R.sub.2 is NAr.sub.2Ar.sub.3. ##STR00001##
Organic electroluminescence device and polycyclic compound for organic electroluminescence device
An organic electroluminescence device and a polycyclic compound used for the organic electroluminescence device are provided. The polycyclic compound according to an embodiment of the inventive concept is represented by Formula 1. In Formula 1, Y is B, P═O, or P═S, and X is SiR.sub.3R.sub.4, or GeR.sub.5R.sub.6. At least one of R.sub.1 or R.sub.2 is NAr.sub.2Ar.sub.3. ##STR00001##
ADDUCTS OF TRIPHENYLPHOSPHINE AND TRIPHENYLPHOSPHITE AND THEIR USE FOR THE BROMINATION OF PRIMARY ALCOHOLS
The present invention relates to the use of novel adducts of general formula (I) TPP.sub.xTPOP.sub.(1-x), wherein TPP is triphenylphosphine, TPOP is triphenylphosphite and x is a real number between 0.05 and 0.9. These novel adducts are useful for the bromination of primary alcohols, in particular for the bromination of primary alcohols.
METHOD FOR PRODUCING InP QUANTUM DOT PRECURSOR AND METHOD FOR PRODUCING InP-BASED QUANTUM DOT
The present invention relates to a method for producing an InP-based quantum dot precursor from a phosphorus source and an indium source, in which a silylphosphine compound represented by the following Formula (1) with a content of a compound represented by the following Formula (2) of 0.3 mol % or less is used as the phosphorus source. Further, the present invention provides a method for producing an InP-based quantum dot comprising heating an InP quantum dot precursor to a temperature of 200° C. or more and 350° C. or less to obtain an InP quantum dot.
##STR00001##
(R is as defined in the specification.)
Compound, organic electroluminescent device and display device
The present disclosure relates to a compound, an organic electroluminescent device, and a display device. The compound has a structure of formula (I) ##STR00001## X is selected from a C atom, a Si atom, a B atom, or a P atom; Y.sub.1 to Y.sub.4 are each independently selected from a C atom or an N atom; A and B are each independently selected from any one or more of a substituted or unsubstituted C6-C40 aryl group and a substituted or unsubstituted C4-C40 heteroaryl group; R.sub.1 is selected from carbonyl, C1-C9 alkyl, a substituted or unsubstituted C6-C18 aryl group, and a substituted or unsubstituted C4-C30 heteroaryl group; and R.sub.2 and R.sub.3 are each independently selected from any one of a C1-C9 alkyl group, a substituted or unsubstituted C6-C18 aryl group, and a substituted or unsubstituted C4-C30 heteroaryl group, and n is selected from 0 or 1.