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1656 results about "Bipyridine" patented technology

Bipyridines also known as bipyridyls, dipyridyls, and dipyridines, are a family of chemical compounds with the formula (C₅H₄N)₂, consisting of two pyridyl (C₅H₄N) rings. Pyridine is an aromatic nitrogen-containing heterocycle that forms complexes with most transition metals. It interacts with metals mainly as a σ-donating Lewis base.

Non-cyanide silver plating bath composition

Disclosed is an electroplating solution for the deposition of silver; said solution containing silver in the form of a complex of silver with hydantoin or a substituted hydantoin compound; said solution also containing an excess of the hydantoin or substituted hydantoin compound employed, together with an effective quantity of a nonprecipitating electrolyte salt, and also an effective quantity of 2,2′ dipyridyl for the purpose of obtaining a mirror-bright to brilliant deposit.
Owner:TECHNIC INC

Copper (i) complexes for optoelectronic devices

ActiveUS20130150581A1Short possible emission decay timeDiminished roll-off behaviorFinal product manufactureGroup 5/15 element organic compoundsSolubilityChlorobenzene
The invention relates to neutral mononuclear copper (I) complexes for emitting light and with a structure according to formula (A) in which: M represents: Cu(I); L∩L represents: a single, negatively charged, bidentate ligand; N∩N represents: a diimine ligand (substituted with R and FG), in particular a substituted 2,2′-bipyridine derivative (bpy) or a substituted 1,10-phenanthroline derivative (phen); R represents: at least one sterically demanding substituent for preventing the planarisation of the complex in the excited state; FG=functional group, and represents: at least one second substituent for increasing solubility in organic solvents. The substituent can also be used for electron transport or alternatively for hole transport, said functional group being bound to the diimine ligands either directly or by means of suitable bridges; and the copper (I) complex: having a ΔE(S1−T1) value of less than 2500 cm−1 between the lowest excited singlet state (S1) and the triplet state (T1) which lies below; having an emission lifespan of at most 20 μs; having an emission quantum yield of greater than 40%, and a solubility of at least 1 g / L in organic solvents, in particular polar organic hydrocarbons such as acetone, methyl ethyl ketone, benzene, toluene, chlorobenzene, dichlorobenzene, dichloromethane, chloroform, dichloroethane, tetrachloroethylene, alcohols, acetonitrile or water.
Owner:SAMSUNG DISPLAY CO LTD

Preparation method of copper-coated tungsten composite powder

The invention discloses a preparation method of copper-coated tungsten composite powder, belonging to the technical field of powder metallurgy. Corresponding tungsten powder and blue vitriod are employed according to the weight ratio of composite powder to be prepared and the tungsten powder is pre-treated; copper sulphate and seignette sol are dissolved into solution; bipyridine is added and NaOH is used to adjust pH value to 12-14; an appropriate amount of formaldehyde solution and the tungsten powder are added; the mixture is heated and then stirred continuously in constant-temperature bathing at 30-60 DEG C until the tungsten powder is red; the tungsten powder is washed, dried, reduced and annealed, thereby obtaining copper-coated tungsten composite powder. The preparation method of copper-coated tungsten composite powder has wide application range and is applicable to tungsten-powder coating coppers with different finenesses and shapes. The preparation method of copper-coated tungsten composite powder prepares copper-coated tungsten composite powder in different content ratios according to different requirements. The copper-coated tungsten composite powder obtained by the method of the invention has excellent sintering activity, thereby improving the combination property of tungsten copper alloy.
Owner:UNIV OF SCI & TECH BEIJING

Transition metal complex based on semirigid bipyridine bisamide organic ligand and terephthalic acid as well as synthetic method and application of transition metal complex

The invention discloses a transition metal complex based on a semirigid bipyridine bisamide organic ligand and terephthalic acid as well as a synthetic method and application of the transition metal complex. The molecular formula of the transition metal complex is as follows: [Zn(3-bpah)(1,4-BDC)).H2O; [Cd(3-bpah)(1,4-BDC)(H2O)], wherein 3-bpah is N,N'-bi(3-pyridine acylamino)-1 2-cyclohexane. The method comprises the steps of mixing Zb<2+> nitrate or Cd<2+> chloride, the semirigid bipyridine bisamide ligand, terephthalic acid and deionized water, adjusting the pH value of the mixture, pouring the mixture into a high-pressure reaction kettle, performing heat preservation in hydrothermal condition, cooling the mixture to room temperature, and airing the mixture, so as to obtain the target complex. The transition metal complex as well as the synthetic method and application of the transition metal complex have the advantages that the synthetic method is simple, the synthetic yield is high, the synthesized complex has high fluorescence-emission property, fluorescent selectivity to different solvent molecules, and fluorescence identification and detection properties for environmental pollutant nitrobenzene, and can be used as fluorescent material.
Owner:BOHAI UNIV

Alkaline ionic liquid and its prepn process and application

The present invention is one kind of alkaline ionic liquid and its preparation process and application in Pd catalyzed C-C and C-N coupling reaction, and belongs to the field of new material and fine chemical technology. The alkaline ionic liquid consists of two parts, cation A+ and anion B-. The cation A+ precursor is imidazole, pyridine, etc; and the anion B- is alkaline group X- or non-alkaline group Y-. The alkaline ionic liquid is prepared through the first quaternizing with alkyl halide as the quaternizing reagent to obtain ion type halide; and the subsequent ion exchange to obtain the target alkaline ionic liquid. The alkaline ionic liquid of the present invention may act as acid-binding agent and can avoid formation of sticky inorganic salt to facilitate reuse.
Owner:EAST CHINA NORMAL UNIVERSITY

Carbazole compound and organic light-emitting device using same

There are provided a novel carbazole compound and an organic light-emitting device having an optical output with extremely high efficiency and luminance and having extremely high durability. Specifically, there are provided a novel carbazole compound represented by the general formula (1):wherein Ar represents a substituted or unsubstituted bipyridine group, a substituted or unsubstituted terpyridine group, or a substituted or unsubstituted 4,5-diazafluorene group and is bonded to any of the eight available carbon atoms on the carbazole skeleton, and an organic light-emitting device using the carbazole compound.
Owner:CANON KK

Osmium complexes and related organic light-emitting devices

Osmium complexes having the formula [Os(II) (N—N)2L—L]2+ 2A− (or A2−), or [Os(II) N—N(L—L)2]2+ 2A− (or A2−), where N—N is a bipyridine or phenanthroline ligand, L—L is a π-acid bidentate ligand, and A is counter ion.
Owner:UNIV OF WASHINGTON

Phosphorescent Osmium (II) complexes and uses thereof

There is disclosed herein phosphorescent compounds, uses thereof, and devices including organic light emitting diode (OLEDs) including such compounds. Compounds of interest include: wherein A is Os or Ru The anionic chelating chromophores NˆN, which are formed by connecting one pentagonal ring structure containing at least two nitrogen atoms to a hexagonal pyridine type of fragment via a direct carbon-carbon linkage. L is a neutral donor ligand; the typical example includes carbonyl, pyridine, phosphine, arsine and isocyanide; two neutral L's can also combine to produce the so-called chelating ligand such as 2,2′-bipyridine, 1,10-phenanthroline and N-heterocyclic carbene (NHC) ligand, or bidentate phosphorous ligands such as 1,2-bis(diphenylphosphino)ethane, 1,2-bis(diphenylphosphino)benzene. L can occupy either cis or trans orientation. When L occupies the trans position, the preferred structure contains both the hexagonal fragment of NˆN as well as its pentagonal fragment located at the trans position respect to their counterparts of the second NˆN chromophore. When L occupies the cis position, the preferred structure consists of the pentagonal unit of NˆN chromophores residing opposite to the L. X,1 X2 and X3 independently are C or N; when X2 is N, R1 is omitted, when X3 is N, R2 is omitted, R1 is H, C1-C8 alkyl, C1-C8 substituted phenyl or C1-C4 perfluoroalkyl, R2 is H, F or cyano substituent, X4 is either C or N; X4 may locate at any position of the hexagonal ring, when X4 is N and R3 and R4 are not linked to X4, R3 is H, methyl or C1-C3 small alkyl, R4 is H, methyl or C1-C3 small alkyl, or R3 and R4 together form an additional conjugated unit with structure
Owner:TAO YE +3

Redox polymers for use in analyte monitoring

Polymers for use as redox mediators in electrochemical biosensors are described. The transition metal complexes attached to polymeric backbones can be used as redox mediators in enzyme based electrochemical sensors. In such instances, transition metal complexes accept electrons from, or transfer electrons to, enzymes at a high rate and also exchange electrons rapidly with the sensor. The transition metal complexes include at least one substituted or unsubstituted biimidazole ligand and may further include a second substituted or unsubstituted biimidazole ligand or a substituted or unsubstituted bipyridine or pyridylimidazole ligand.
Owner:ABBOTT DIABETES CARE INC
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