74331-74-1Relevant articles and documents
ORGANIC ELECTROLUMINESCENCE ELEMENT AND MATERIAL
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, (2020/05/16)
PROBLEM TO BE SOLVED: To provide a phosphorescent metal complex emitting blue light, which shows a low drive voltage, high emission efficiency, high color purity of emission and a long emission life when used for an element, and to provide an organic electroluminescence element containing the above metal complex. SOLUTION: The present invention provides a compound represented by general formula (I): ML1mL2n, and an organic electroluminescence element containing the above compound. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2020,JPOandINPIT
A light emitting device for emitting compd. (by machine translation)
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Paragraph 0104; 0114, (2016/10/20)
The invention discloses a, R 2 is, optionally substituted phenyl, the substituent Alkoxypyrimidinyl and optionally can be from Pirimidinyl substd., cyano, aryl and/or has heteroaryloxazolidinone; R 3 is, optionally substituted carbosorylethyl, optionally substituted dihydrobenzo carbosorylethyl, optionally [...] substd., optionally [...] substd. phenazinyl and optionally can be substituted with from, heteroaryl, compound represented by eq. 1. In another embodiment, the organic light emitting diode device including a compound of eq. 1. Selected drawing: fig. 1 (by machine translation)
CO extrusion in homogeneous gold catalysis: Reactivity of gold acyl species generated through water addition to gold vinylidenes
Bucher, Janina,St?sser, Tim,Rudolph, Matthias,Rominger, Frank,Hashmi, A. Stephen K.
supporting information, p. 1666 - 1670 (2015/01/30)
Herein, we describe a new gold-catalyzed decarbonylative indene synthesis. Synergistic σ,π-activation of diyne substrates leads to gold vinylidene intermediates, which upon addition of water are transformed into gold acyl species, a type of organogold compound hitherto only scarcely reported. The latter are shown to undergo extrusion of CO, an elementary step completely unknown for homogeneous gold catalysis. By tuning the electronic and steric properties of the starting diyne systems, this new reactivity could be exploited for the synthesis of indene derivatives in high yields.
General and selective head-to-head dimerization of terminal alkynes proceeding via hydropalladation pathway
Jahier, Claire,Zatolochnaya, Olga V.,Zvyagintsev, Nickolay V.,Ananikov, Valentine P.,Gevorgyan, Vladimir
supporting information; experimental part, p. 2846 - 2849 (2012/07/17)
A general highly regio- and stereoselective palladium-catalyzed head-to-head dimerization reaction of terminal acetylenes is presented. This methodology allows for the efficient synthesis of a variety of 1,4-enynes as single E stereoisomers. Computational studies reveal that this dimerization reaction proceeds via the hydropalladation pathway.
Ortho, ortho′-Substituted KITPHOS monophosphines: Highly efficient ligands for palladium-catalyzed C-C and C-N bond formation
Doherty, Simon,Knight, Julian G.,McGrady, John P.,Ferguson, Alexandra M.,Ward, Nicholas A. B.,Harrington, Ross W.,Clegg, William
supporting information; experimental part, p. 201 - 211 (2010/06/20)
ortho, ortho′-Substitution of the phosphinoalkyne-derived aryl ring in KITPHOS (11-dicyclohexylphosphino-12-phenyl-9,10-ethenoanthracene) monophosphines enhances the performance of this class of ligand in palladium-catalyzed Suzuki-Miyaura cross-couplings and BuchwaldHartwig aminations, compared with their unsubstituted and mono-substituted counterparts. An alternative complementary synthesis of KITPHOS monophosphines has been developed and two new members of this family, 2,6-Me2-KITPHOS [11-dicyclohexylphosphino-12-(2,6-dimethylphenyl)-9,10-ethenoanthracene] and 2,6-(MeO)2-KITPHOS [11-dicyclohexylphosphino-12-(2,6-dimethoxyphenyl)-9,10-ethenoanthracene], have been prepared; palladium complexes of both are highly efficient catalysts for C - C and C - N bond formation with a range of electron-rich and electron-poor aromatic chlorides as well as heteroaryl chlorides.
Arylethynyl derivatives of the dihydroazulene/vinylheptafulvene photo/thermoswitch: Tuning the switching event
Broman, Soren Lindbaek,Petersen, Michael Axman,Tortzen, Christian G.,Kadziola, Anders,Kilsa, Kristine,Nielsen, Mogens Brondsted
body text, p. 9165 - 9174 (2010/08/21)
A selection of dihydroazulene (DHA) photoswitches incorporating an arylethynyl-substituent in the seven-membered ring was prepared by palladium-catalyzed Sonogashira cross-coupling reactions employing a suitable bromo-functionalized DHA. Shielding of the
A comparison of linear optical properties and redox properties in chalcogenopyrylium dyes bearing ortho-substituted aryl substituents and tert-butyl substituents
Panda, Jagannath,Virkler, Peter R.,Detty, Michael R.
, p. 1804 - 1809 (2007/10/03)
A series of thiapyrylium pentamethine dyes (4 and 12-15) bearing 2,2′-di-tert-butyl-6,6′-diphenyl, 2,2′-di-tert-butyl-6,6′-bis(2,6-dimethylphenyl), 2,2′-di-tert-butyl-6,6′-bis(2-methylphenyl), 2,2′,6,6′-tetrakis(2,6-dimethylphenyl), and 2,2′,6,6′-tetrakis(2-methylphenyl) substituents, respectively, were prepared and their linear optical properties and electrochemical redox properties were measured and compared to thiapyrylium pentamethine dyes 3 and 5. The tert-butyl and 2,6-dimethylphenyl substituents give nearly identical chromophores with respect to values of λmax, molar extinction coefficients (ε), bandwidths at half-height (ν1/2), and lack of absorption in the visible spectrum. The 2-methylphenyl substituent imparts linear optical properties that are intermediate between those of the tert-butyl and phenyl substituents. The 2,6-dimethylphenyl and 2-methylphenyl substituents impart greater oxidative stability based on anodic shifts in oxidation potential.
Dimeric α-lithio-2,6-dimethylstyrene
Knorr, Rudolf,Behringer, Claudia,Noeth, Heinrich,Schmidt, Martin,Lattke, Ernst,Raepple, Edith
, p. 585 - 592 (2007/10/03)
Improved preparations of 2,6-dimethylstyrene (5) and its abromo derivative (10) are described. The Br/Li exchange reaction of 10 provides single crystals of the title compounds 11 or 12, which were characterized as disolvated dimers by X-ray analyses. A similar dimer persists in diethyl ether, tertbutyl methyl ether, and toluene at all accessible temperatures, with significant lithiation NMR shifts (relative to 5) partially due to charge delocalization from the sp2-carbanionic center. Some NMR coupling constants are typical of the dimeric aggregate. The configurational (E,Z) lability is quantified in toluene solution. VCH Verlagsgesellschaft mbH.
Aromatic stabilization of the triarylborirene ring system by tricoordinate boron and facile ring opening with tetracoordinate boron
Eisch, John J.,Shafii, Babak,Odom, Jerome D.,Rheingold, Arnold L.
, p. 1847 - 1853 (2007/10/02)
To remove uncertainties in the apparent C=C and B-C bond lengths of the borirene ring, as previously estimated from an X-ray crystallographic analysis of trimesitylborirene, the unsymmetrically substituted 2-(2,6-dimethylphenyl)-1,3-dimesitylborirene was
Dissociative ionization of aryl-substituted vinyl bromides in the gas phase: Experimental and computational evidence for the formation of stable α-arylvinyl cations both by direct means and spontaneous exothermic isomerization of unstable isomeric ions
Apeloig, Yitzhak,Franke, Wilfried,Rappoport, Zvi,Schwarz, Helmut,Stahl, Daniel
, p. 2770 - 2780 (2007/10/02)
The kinetic energy release T which accompanies the Br· loss from ionized (E)- and (Z)-β-bromostyrenes (5 and 6) in the gas phase is higher by 0.7 ± 0.03 kcal mol-1 than that from the molecular ion of α-bromostyrene (4). Together with both colli
