156 results about "Diphosphenes" patented technology

This disclosure provides for a process for preparing a catalyst system comprising a) contacting a metal compound, a diphosphino aminyl ligand metal complex, and a metal alkyl for a time period to form a mixture; and b) aging the mixture. The disclosure also provides for olefin oligomerization process comprising: a) contacting i) a metal compound, ii) a diphosphino aminyl ligand, and iii) a metal alkyl to form a mixture; b) aging the mixture; c) contacting the aged mixture with an olefin monomer; and d) forming an olefin oligomer product.

A metal complex comprising a metal compound complexed to a heteroatomic ligand, the metal complex having Structure X:wherein R1, R2, R3, and R4 are each independently an alkyl group, a cycloalkyl group, a substituted cycloalkyl group, an aromatic group, or a substituted aromatic group, R1c, R2c, R3c, R4c, and R5c are each independently hydrogen or an alkyl group, and MXp comprises a group IVB, VB, or VIB metal. A metal complex comprising a metal compound complexed to a diphosphino aminyl ligand comprising at least two diphosphino aminyl moieties and a linking group linking each aminyl nitrogen atom of the diphosphino aminyl moieties.

This invention relates to a method to selectively oligomerize olefins comprising contacting olefins with: 1) at least one diaryl-substituted diphosphine ligand; 2) a chromium metal precursor; and 3) optionally, one or more activators. In a particular embodiment, the method for selectively oligomerizing olefins includes trimerizing ethylene to selectively form 1-hexene.

The oligomerization of ethylene using a chromium catalyst having a bridged diphosphine ligand can produce a selective product distribution (to predominantly hexene or predominantly octene / hexene) when activated with an aluminoxane. The oligomerization reaction also produces polymer by product—particularly when the aluminoxane is provided in a non-aromatic solvent. The present invention mitigates this problem.

The present invention is a new non-cyanide alkaline copper plating bath, preparation and use method thereof. In the copper plating bath, using copper sulfate or basic copper carbonate as main salt, using hydroxy-ethylidene diphosphonic acid as main complexant, using trisodium citrate, potassium citrate or potassium sodium tartrate as auxiliary complexant, using sodium nitrate or potassium nitrate as conductive salt, using sodium hydroxide or potassium hydrate as pH value regulator; the operation conditions are: cathode current density is 0.5-3.0 A / dm [2], pH of plating bath controlled between 12 and 13, plating bath temperature is 50-70 DEG. Comparing with the prior known technology, the invention has following advantages or positive effects: simple plating bath formula, easy control and operation, wide temperature range of plating bath using, high current efficiency, fine crystallization coating, good appearance color, stable plating bath, strong uniform plating and covering ability, low cost, easy wastewater treatment. The invention can be used for pre copper plating or direct electro-coppering instead of virulent cyaniding electro-coppering process.

A novel developing solution for photoresists which is suitable for use as a developing solution for a photoresist formed on an aluminum-containing base formed on a wafer. It comprises an alkali builder, a calcium compound, and a chelating agent, the chelating agent being selected from the group consisting of 1-hydroxyethylidene-1,1-diphosphonic acid, aminotrimethylenephosphonic acid, 2-phosphonobutane-1,2,4-tricarboxylic acid, ethylenediaminetetramethylenphosphonic acid, diethylencetriaminepentamethylenephosphonic acid, hexamethylenediaminetetraethylenephosphonic acid, and diethylenetriaminepenta(methylenephosphonic acid).

The use of curable mixtures comprising(A) at least one phosphonic diester and / or at least one diphosphonic diester and(B) at least one compound containing at least two condensable silane groups,as coupling agents, particularly as coupling agents in laminates comprising at least one substrate, at least one coating, at least one adhesive layer, and at least one sheet, and also a new process for producing such laminates using the coupling agents, the laminates which are producible using the coupling agents, and thermally curable mixtures comprising the coupling agents and at least one thermally curable polyester (C).

The catalysts of formula (II): [Ru(L)m(L')wXY], wherein X and Y represent simultaneously or independently a hydrogen or halogen atom, a hydroxy group, or an alkoxy, carboxyl or other anionic radical, m is 1 or 2, w is 1 when m is 1 and w is 0 when m is 2, L is a phosphino-amine or phosphino-imine bidentate ligand and L' a diphosphine, are useful for the hydrogenation of substrates having a carbon-hetero atom double bond.

A manufacture method for synthesizing thiourea dioxide with high stability is the manufacturing method of a chemical product, which overcomes the disadvantages in other technologies and is confected by adopting the following raw materials: the molar ratio between thiourea and oxydol of 27.5 percent is 1:1.9 to 1:2.1; the mass ratio between polyethyleneglycol that is a stabilizing agent and hydroxyl ethidene diphosphonate tetrasodium is 1:1, and the quantity of polyethyleneglycol and hydroxyl ethidene diphosphonate tetrasodium can be 0.5 to 2.0 percent of the total quantity of thiourea; the mass ratio between postassium acetate that is an accelerant and ammonia bicarbonate is 2:3, and the quantity of postassium acetate and ammonia bicarbonate is 4.0 to 6.0 percent of the total auantity of thiourea. A method for preparing thiourea dioxide comprises the steps of confecting an accessory ingredient, catalysis synthesis, crystallization, dehydration, drying, and completing through packing. The main performance index of the product includes the aspects as follows: the main content of thiourea dioxide is more than or equals to 99.0 percent; residual thiourea is less than or equals to 0.1 percent, and sulphate is less than or equals to 0.17 percent; the iron content is less than or equals to 10ppm; the moisture content is less than or equals to 0.05 percent; the thermal stability is more than or equals to 55 minutes in water bath when the temperature is 95 DEG C. The manufacture method has the high yield of product and high thermal stability, effectively changes the product quality, and increases the safety performance of product transport and storage.

The present invention discloses a water treatment agent and its matched application method. It is made into the form of paste or slurry, and can be slowly and uniformly dissolved in the water completely, in addition to the water (including crystal water) said water treatment agent also contains corrosion inhibitor, antiscale, dispersing agent, sterilizing algaecide, thickening agent and pH regulating agent. The essential component of said water treatment agent is water, includes crystal water, and its cotent is 37%-50%, also contains water soluble zinc salt and hydroxyethylidene diphosphonate and its water-soluble salt. Said invention also provides its application method and steps.

The invention discloses a cloth cart. The cloth cart comprises a metal rotating shaft subjected to surface treatment. The surface treatment process includes the following steps that firstly, by mass, 1-2 parts of mercaptobenzothiazole, 0.9 part of nickel nitrate, 1.4 parts of 1-Hydroxyethylidene-1,1-diphosphonicacid, 2.3 parts of polyvinylpyrrolidone, 1.8 parts of dipyrazolone, 2.3 parts of 2,6-di-t-butyl-alpha-dimethylamino hydroquinone and 1.6 parts of tetramethyl ammonium bromide are added into 12 parts of deionized water and evenly stirred and mixed, and surface treatment working fluid is obtained; secondly, the surface treatment working fluid is heated to 53 DEG C; thirdly, the metal rotating shaft is put into the surface treatment working fluid to be steeped for 32 min, taken out and then dried. Due to the fact that the metal rotating shaft of the cloth cart is subjected to surface treatment, good rub resistance, corrosion resistance, rust resistance, heat resistance, cold resistance and weather resistance are achieved.

The invention relates to a chemically-bonded HEDP (1-hydroxy ethylidene-1, 1-diphosphonic acid) medium-temperature organic polysiloxane phosphate based proton exchange membrane. The membrane is prepared by the following steps: firstly, under protection of nitrogen, mixing dimethyl sulfoxide and HEDP, stirring to obtain clear and transparent mixture, and performing reflux reaction at 160 DEG C; removing the dimethyl sulfoxide after the solution is cooled to 110 DEG C to obtain 1,1-vinyl diphosphonic acid liquid; secondly, mixing 1, 1-vinyl diphosphonic acid, 3-(methacryloxy) propyl trimethoxyl silane, 2, 2'-azobisisobutyronitrile and ethanol, stirring at 60-80 DEG C to react, cooling to room temperature, adding diluted hydrochloric acid, and stirring to obtain clear and transparent sol; thirdly, performing gelation to the sol to obtain a gel membrane; and fourthly, drying the gel membrane to obtain the chemically-bonded HEDP medium-temperature organic polysiloxane phosphate based proton exchange membrane. The membrane has high proton conductivity under medium temperature and low humidity and has excellent flexibility and mechanical property.

The present invention relates to catalytic materials for hydrogenation or asymmetric hydrogenation. In particular, the invention relates to iron (II) complexes containing unsymmetrical tetradentate diphosphine (PNN′P) ligands with two different nitro gen donor groups useful for catalytic transfer hydrogenation or asymmetric transfer hydrogenation of ketones, aldehydes and imines.

The invention discloses a composite slow-release scale inhibitor suitable for a petrochemical wastewater reusing circulating water system. The composite slow-release scale inhibitor comprises 2-butane phosphate-1,2,4-tricarboxylic acid, hydroxy ethylidene diphosphonic acid, amino trimethylene phosphonic acid and zinc sulfate. After the composite slow-release scale inhibitor is adopted, by virtue of dynamic simulation experiment on oil refinery reuse water, the water quality inhibition rate is 86.18%; by virtue of the dynamic simulation experiment on ethylene plant reuse water, the water quality inhibition rate is 86.44%, and the scale inhibiting rate is 87.42%; the corrosion rate is reduced to 0.0168 mm / a and 0.0091 mm / a, which meets the anticorrosion requirement that the corrosion rate of China petrochemical circulating cooling water is less than 0.075 mm / a. Compared with the traditional polyphosphate carboxylate composite slow-release scale inhibitor, the composite slow-release scale inhibitor disclosed by the invention has the advantages of small addition amount and good corrosion inhibition effect and scale inhibition.

The present invention provides compounds of the formula wherein R is optionally substituted lower alkyl, cycloalkyl or aryl; R′ is alkyl or aryl; n is zero or an integer of 1 or 2; or an enantiomer thereof; or an enantiomeric mixture thereof. The compounds of formula (I) are bridged C2-symmetric biphenyldiphosphine analogs and, thus, may be employed as ligands to generate chiral transition metal catalysts which may be applied in a variety of asymmetric reactions. The compounds of the present invention are easily accessible in high diastereomeric and optical purity according to the methods disclosed herein.

The invention relates to a process for the preparation of diphosphonic acids by reaction of a carboxylic acid with a mixture of phosphorous acid and phosphorus oxychloride in defined molar ratios and in the absence of solvents. The invention futher relates to ibandronic acid monosodium salt in the amorphous form.

Disclosed is an improved carbonylation process for the production of carboxylic acids, carboxylic acid esters, and / or carboxylic acid anhydrides wherein a carbonylation feedstock compound selected from one or more organic oxygenates such as alcohols, ethers, and esters is contacted with carbon monoxide in the presence of a carbonylation catalyst and one or more onium compounds. The carbonylation process differs from known carbonylation processes in that a halide compound, other than the onium salt, such as a hydrogen halide (typically, hydrogen iodide) and / or an alkyl halide (typically, methyl iodide), extraneous or exogenous to the carbonylation process is not fed or supplied to the process. The process can be improved by using a bidentate ligand comprising two functional groups selected from tertiary amines and tertiary phosphines, such as 2,2′-bipyridine and diphosphine derivatives.

A process for the production of paroxetine is described, wherein N-substituted derivatives of 4-(p-fluorophenyl)-3-hydroxymethyl-1,2,3,6-tetrahydropyridine are treated according to the following sequence of reactions: (a) hydrogenation catalyzed by transition metal complexes with chiral diphosphinic ligands; (b) -OH derivatisation and nucleophilic substitution, the substituent being sesamol; (c) N-dealkylation. The process is highly stereospecific and brings about the formation of intermediates enriched with the desired isomeric components, which are converted into paroxetine in quantitative yields.

A novel multi-aryl bridged long-chain diphosphine ligand is disclosed. A semi-calix[4]arene is taken as a structural skeleton and subjected to double-side decoration, so that a novel phosphine-nitrogen ligand is designed and synthesized, and also the novel ligand and a palladium salt are used for in-situ catalysis of a Suzuki coupling reaction. The preparation method of the ligand comprises: synthesizing a semi-calix intermediate bis(5-tert-butyl-3-hydroxymethyl-2-methoxyphenyl)methane, brominating the intermediate and bridging with an intermediate 2-bromo-6-diphenylphosphanylpyridine to obtain the multi-aryl bridged long-chain diphosphine ligand. The advantages comprise that the novel diphosphine ligand employs the calixarene fragment as the main body, pyridine structure is used to stabilize the molecule and to adjust the molecular cavity, and the ligand is used to catalyze the Suzuki coupling reaction in the presence of trace palladium for carbon-carbon bond construction in organic synthesis. The ligand is stable in structure; the synthesis reaction is short in time, mild in condition, high in yield, easy for mass production and commercialization; and the catalyst use amount is small when the ligand is used for Suzuki coupling reactions, and it is expected that functional groups with specific function can be introduced for promoting synthesis of multiple medicaments.

The present invention relates to a computer electronic display screen cleaning agent, which comprises, by mass, 52-56 parts of biochemical fulvic acid, 54-58 parts of benzotriazole, 50-54 parts of 1-hydroxyethylidene-1,1-diphosphonicacid, 54-58 parts of alkanol phosphate ester, 50-54 parts of hydroxyethylenediamine, 54-58 parts of sodium ligninsulfonate, 50-54 parts of caprylic / capric triglyceride, 56-60 parts of benzoic acid, 50-54 parts of potassium dihydrogen phosphate, 54-58 parts of polyacrylamide, 50-54 parts of polyethylene glycol stearate, 54-58 parts of sodium humate, 50-54 parts of polyepoxysuccinic acid, 54-58 parts of mercaptobenzothiazole, 50-54 parts of isothiazolinone, 54-58 parts of cyclic silicone oil, 50-54 parts of lecithin, 54-58 parts of permethrin, 50-54 parts of butyl acetate, 54-58 parts of dodecyl dimethyl benzyl ammonium chloride, 50-54 parts of benzimidazole allyl thioether, 54-58 parts of aliette, 50-54 parts of a silver ion antibacterial agent, and 1000-2000 parts of water. The cleaning agent of the present invention has good cleaning ability.

Chiral diphosphines are constituted by an aromatic pentatomic biheterocyclic system, suitable to act as chiral ligands and complexes between the diphosphines and transition metals. They may be utilized as chiral catalysts in stereocontrolled reactions, such as diastereo- and enantioselective reduction reactions. Process is for the preparation of these chiral diphosphines; and process is for the preparation of these complexes and for their utilization as chiral catalysts in stereocontrolled reactions.

The invention relates to the synthesis and application technology field of compounds used for metal anticorrosion, and concretely discloses a novel rosin imidazoline corrosion inhibitor, a synthetic method and applications. The initial raw material of the provided compound is rosin acid, the raw material is single and the synthetic route operation is simple. The method for preparing a corrosion inhibitor from the synthesized compound is simple, the compound is dissolved in dimethyl formamide, then the obtained solution is dissolved in water, then 1-hydroxyethylidene-1,1-diphosphonic acid is added, and uniform stirring is carried out. The corrosion inhibitor is safe and environmentally friendly, and has excellent corrosion inhibition effects. The corrosion inhibitor can be used for oil and gas field ground gathering and storage and transportation pipes, prevents damage of corrosive gases to metal materials of steel and the like and reduces corrosion loss.

The invention relates to a composition comprising acid magnetic particles (p) based on an iron compound, the acid magnetic particles (p) being complexed by one or more gem-bisphosphonate compounds, of formula I X-L-CH(PO3H2)2 (I) in which L represents an organic group connecting the X group to the gem-bisphosphonate group -CH(PO3H2)2; X represents a chemical group capable of reacting with a biovector; all or some of the X groups of the particles optionally being coupled to a biovector. The invention relates also to a process for the preparation of the compositions and their use, in particular as contrast products for Magnetic Resonance Imaging (MRI).

A bis(aminostyryl)naphthalene compound represented by the general formula [I] or the like below. (where R2 and R3 each denotes an unsubstituted aryl group; R1 and R4 each denotes an aryl group having a specific substituent such as methoxy group; and R5 and R6 each denotes a cyano group or the like.)A process for producing a bis(aminostyryl)naphthalene compound represented by the general formula [I] by condensation of, for example, 4-(N,N-diarylamino)benzaldehyde with diphosphonic ester or diphosphonium.The bis(aminostyryl)naphthalene compound emits intense yellow or red light. The process permits efficient production of the bis(aminostyryl)naphthalene compound.

The invention discloses a phosphosilicate type rare earth ore flotation collector and a preparation method and an application thereof. The phosphosilicate type rare earth ore flotation collector is prepared from the following materials according to the mass ratio: 5 to 15 parts of octyl ether propyl-a-amino-1,1-diphosphonic acid, 60 to 80 parts of dist coconut fatty acid, 5 to 10 parts of hexadecyl sulfonate and 1 to 3 parts of Tween-60. The phosphosilicate type rare earth ore flotation collector has the advantages of high collecting capability, high concentrate recovery rate, low production cost, less consumption and good separation effect when the phosphosilicate type rare earth ore flotation collector is applied to the floatation of phosphosilicate type rare earth ore or xenotime.

Diphosphonates or their salts between acids and linear, branch substituted and non-substituted, cyclic, heterocyclic and aromatic amino alcohols are used to treat osteoporosis. Pharmaceutical compositions and therapeutic methods of treating osteoporosis are described.

Disclosed is a workshop floor cleaner. Raw materials of the cleaner include, by weight: 2.4 to 3.2 parts of benzene sulfonate, 2.5 to 6.5 parts of polyacrylamide, 1.3 to 4.2 parts of amido-sulfonic acid, 2 to 5 parts of sodium silicate, 2.5 to 3.2 parts of potassium chloride, 4.5 to 7.5 parts of aspartic acid, 2 to 3.5 parts of cleaning aids, 2.6 to 4.5 parts of fatty acid diethanolamide, 0.5 to 1.2 part of dehydroascorbate, 0.8 to 1.4 part of tertiary butylhydroquinone, 2.5 to 4.5 parts of naphthenic acid, 4.5 to 6 parts of triethylene glycol alkyl ether, 2 to 5 parts of benzotriazole, 0.2 to 1.5 part of molybdate and 8 to 14 parts of hydroxyethylidene diphosphonic acid. The workshop floor cleaner has the advantages that the cleaning effect of mineral oil, vegetable oil and mixed oil is fine, cleaning time is short, and labor force and working time are saved.

A scale inhibitor for mechanical equipment is prepared from the following raw materials, by weight, 8-15 parts of organic phosphonate, 4-7 parts of sodium dodecyl benzene sulfonat, 8-15 parts of 1-hydroxyethylidene-1,1-diphosphonicacid, 2-6 parts of magnesium nitrate, 3-7 parts of linseed oil, 2.5-6 parts of potassium pyrophosphate, 3.5-8 parts of chloramine, 1.2-4 parts of triethanolamine, 2.5-7 parts of n-propanol and 3.4-8 parts of a thickening agent. The invention has the following beneficial effects: the scale inhibitor can be used to delay formation of dirt and scale and form a protective layer to prevent expansion of dirt and is widely applied to metal equipment such as pipelines, heat exchangers, boilers and the like.