109results about "Sodium organic compounds" patented technology

Metal films are deposited with uniform thickness and excellent step coverage. Copper metal films were deposited on heated substrates by the reaction of alternating doses of copper(I) NN′-diispropylacetamidinate vapor and hydrogen gas. Cobalt metal films were deposited on heated substrates b the reaction of alternating doses of cobalt(II) bis(N,N′-diispropylacetamidinate) vapor and hydrogen gas. Nitrides and oxides of these metals can be formed by replacing the hydrogen with ammonia or water vapor, respectively. The films have very uniform thickness and excellent step coverage in narrow holes. Suitable applications include electrical interconnects in microelectronics and magnetoresistant layers in magnetic information storage devices.

The invention relates to trans carotenoid compounds and salts thereof as well as compositions thereof, methods for making them, and uses thereof. These compounds are useful in improving diffusivity of oxygen between red blood cells and body tissues in mammals including humans.

Sulfonate salts have the formula: R1COOCH2CH2CF2CF2SO3−M+ wherein R1 is alkyl, aryl or hetero-aryl, M+ is a Li, Na, K, ammonium or tetramethylammonium ion. Onium salts, oxime sulfonates and sulfonyloxyimides derived from these salts are effective photoacid generators in chemically amplified resist compositions.

Sulfonate salts have the formula: HOCH2CH2CF2CF2SO3−M+ wherein M+ is a Li, Na, K, ammonium or tetramethylammonium ion. Onium salts, oxime sulfonates and sulfonyloxyimides derived from these salts are effective photoacid generators in chemically amplified resist compositions.

Disclosed is a coordination polymer crystal with porous metal-organic frameworks (MOFs), in which, while a crystal state of the coordination polymer crystal is maintained, an additional material selected from the group consisting of an organic compound, a metal cluster, and an organometallic compound is chemically bonded to the coordination polymer crystal. Therefore it is possible easily adsorb and store more guest molecules regardless of a change in an ambient temperature or pressure due to the chemically bonded additional material.

Sulfonate salts have the formula: R1SO3—CH(Rf)-CF2SO3−M+ wherein R1 is alkyl or aryl, Rf is H or trifluoromethyl, and M+ is a Li, Na, K, ammonium or tetramethylammonium ion. Onium salts, oximesulfonates and sulfonyloxyimides and other compounds derived from these sulfonate salts are effective photoacid generators in chemically amplified resist compositions.

Sulfonate salts have the formula: CF3—CH(OH)—CF2SO3−M+ wherein M+ is a Li, Na, K, ammonium or tetramethylammonium ion. Because of inclusion within the molecule of a hydroxyl group which is a polar group, the sulfonic acids are effective for restraining the length of acid diffusion through hydrogen bond or the like. The photoacid generators that generate these sulfonic acids perform well during the device fabrication process including coating, pre-baking, exposure, post-exposure baking, and developing steps. The photoacid generators are little affected by water left on the wafer during the ArF immersion lithography.

Disclosed is a coordination polymer crystal with porous metal-organic frameworks (MOFs), in which, while a crystal state of the coordination polymer crystal is maintained, an additional material selected from the group consisting of an organic compound, a metal cluster, and an organometallic compound is chemically bonded to the coordination polymer crystal. Therefore it is possible easily adsorb and store more guest molecules regardless of a change in an ambient temperature or pressure due to the chemically bonded additional material.

The invention provides a process for synthesizing metalloporphyrin, in particular a process for synthesizing metallic aryl porphyrin and mu-oxygen bimetallic aryl porphyrin from pyrrole and aromaticity aldehyde as raw material by using zinc salt as template center through the steps of, synthesizing aryl porphine and zinc aryl porphyrin mixture, reacting the aryl porphine and zinc aryl porphyrin mixture with other metal salt under acidity or neutrality conditions to obtain metallic aryl porphyrin, synthesizing mu-oxygen bimetallic aryl porphyrin through one-step reaction under alkaline condition.

Sulfonate salts have the formula:R1SO3—CH(Rf)—CF2SO3−M+wherein R1 is alkyl or aryl, Rf is H or trifluoromethyl, and M+ is a Li, Na, K, ammonium or tetramethylammonium ion. Onium salts, oximesulfonates and sulfonyloxyimides and other compounds derived from these sulfonate salts are effective photoacid generators in chemically amplified resist compositions.

The invention relates to trans carotenoid compounds and salts thereof as well as compositions thereof, methods for making them, and uses thereof. These compounds are useful in improving diffusivity of oxygen between red blood cells and body tissues in mammals including humans.

The invention relates to trans carotenoid salt compounds, methods for making them, methods for solubilizing them and uses thereof. These compounds are useful in improving diffusivity of oxygen between red blood cells and body tissues in mammals including humans.

The present invention belongs to the field of chemical synthesis technology, and is synthesis and product of 1-methyl cyclopropenyl sodium as the precursor of novel preservative 1-methyl cyclopropene and used in developing efficient and low-toxic fruit and vegetable preservative. The present invention synthesizes 1-methyl cyclopropenyl sodium with amino sodium. During use, 1-methyl cyclopropenyl sodium reacts with water produced in the breathe of fruits to produce 1-methyl cyclopropene capable of inhibiting the synthesis of ethylene of fruits. The synthesis process of the present invention is simple and suitable for industrial production, and has low cost and no environmental pollution.

Sulfonate salts have the formula: CF3—CH(OH)—CF2SO3−M+ wherein M+ is a Li, Na, K, ammonium or tetramethylammonium ion. Because of inclusion within the molecule of a hydroxyl group which is a polar group, the sulfonic acids are effective for restraining the length of acid diffusion through hydrogen bond or the like. The photoacid generators that generate these sulfonic acids perform well during the device fabrication process including coating, pre-baking, exposure, post-exposure baking, and developing steps. The photoacid generators are little affected by water left on the wafer during the ArF immersion lithography.

The claimed invention meets these and other objects by providing a method of preparing a metal salt of a dialkyl ester of 5-sulfoisophthalic acid. Broadly speaking, the method provides for the contacting of a dialkyl ester of 5-sulfoisophthalic acid with a metal cation in a buffered reaction mixture to form the metal salt of the dialkyl ester. The reaction mixture is buffered, at least in part, by the acetate of the metal cation. The method according to invention also encompasses various methods of preparing the dialkyl ester of 5-sulfoisophthalic acid.

The invention relates to trans carotenoid compounds and salts thereof as well as compositions thereof, methods for making them, and uses thereof. These compounds are useful in improving diffusivity of oxygen between red blood cells and body tissues in mammals including humans.

The invention relates to a method for preparing thermal-reversible cross-linking polyisobutene rubber capable of being processed repeatedly. According to a rubber matrix, a bromination poly(isobutene-co-p-methylstyrene) copolymer containing benzyl bromide functional groups is adopted, and the benzyl bromide functional groups generate a cross-linking reaction with a cross-linking agent easily; dimeric cyclopentadiene carboxylic acid sodium salt or dimeric cyclopentadiene carboxylic acid kali salt is adopted, by the adoption of a blended vulcanization mode, the thermal-reversible cross-linking agent generates an esterification reaction with the rubber matrix to form a dicyclopentadiene cross-linking bridge key, and then the rubber is prepared after hot press is performed. The prepared rubber is equivalent to traditional vulcanized rubber in stretchability and heat resistance, the tensile strength of the rubber is stabilized to be about 70% of original performance, the elongation at break is stabilized to be about 60% of original performance, rubber raw materials can be obviously saved, meanwhile, leftover materials can be reprocessed to be finished products, reutilization of the leftover materials is achieved, in this way, the utilization rate of resources is increased, and environmental friendliness and saving are achieved.

The present invention relates to a bile salt adjuvant for animals for improving fat utilization efficiency in the bodies of the animals, and to animal feed comprising same. More particularly, the present invention relates to a bile salt adjuvant for animals comprising sodium stearoyl-2-lactylate. The adjuvant is used in animal feed to improve fat utilization efficiency in the bodies of livestock when ingested by said livestock, thereby reducing the amount of fat required to be used in animal feed and improving productivity.

Anionic polymerization initiators useful in the preparation of polymers having a protected amine functional group. The amine functionality includes a first protecting group, which can be aralkyl, methyl, allyl or tertiary alkyl group. The other of the amine protecting groups can be the same as the first protecting group. Alternatively, the second protecting group can be different from the first protecting group, in which case it is selected to have differential stability to agents used to remove the aralkyl, methyl, allyl or tertiary alkyl protecting group.

The invention relates to a synthetic method for preparing nitrogen heterocyclic compound metal salt and nitrogen heterocyclic compound metal salt heterocyclic compound complex. Under a solvent-free condition, nitrogen heterocyclic compounds are mixed with corresponding metal hydrides, and ball milling is carried out to obtain corresponding nitrogen heterocyclic compound metal salt; under the solvent-free condition, ball milling of a mixture of the nitrogen heterocyclic compounds, the corresponding metal hydrides, and heterocyclic compound ligands according to a certain ratio is carried out, or ball milling of a mixture of the nitrogen heterocyclic compound metal salt and a certain amount of heterocyclic compound ligands is carried out, so as to obtain nitrogen heterocyclic compound metal salt heterocyclic compound complex. The ball milling temperature is generally between -100 DEG C and 300 DEG C; the rotating speed is between 10 rpm and 500 rpm; the ball milling time is generally controlled to be 1-300 hours. The preparation method has the advantages of simplicity, practicality, no solvent, no reaction balance point, reaction thoroughness, reaction process monitorability, and easy amplification.

This invention relates to a method for producing low-zinc rongalite. The method comprises: mixing water and zinc powder, beating, adding SO2, reacting to obtain zinc hydrosulfite, placing in a reaction pot, adding formaldehyde and zinc powder, reacting to obtain alkaline sodium formaldehyde sulfoxylate, precipitating, removing the supernatant, adding NaOH, reacting to obtain sodium formaldehyde sulfoxylate, filtering, standing for settlement, cooling, adjusting the pH value, performing ultrafiltration, mixing, adding NaOH, sending into an evaporator, evaporating to obtain melt of low-zinc sodium formaldehyde sulfoxylate, cooling, solidifying, and pulverizing to obtain the final product. The obtained low-zinc rongalite can satisfy the requirements of pharmaceutical and plastic industries. The zinc content is less than or equal to 50 ppm. The low-zinc rongalite has such advantages as high purity, high stability, low production cost and convenient usage.

A method for preparing an ionic compound by mixing at least one compound of formula CxAy-zH2O (1) with at least one hydrogen donor and heating the mixture obtained is provided. The said ionic compound remains in a physical state selected from the group consisting of liquid and semisolid at a temperature below 150° C., preferably below 125° C.

The invention provides a dihydroporphin compound as well as a preparation method and application thereof, and relates to the technical field of medicines. The dihydroporphin compound is a compound represented by a formula I, or a salt thereof, or a stereoisomer thereof, or a hydrate thereof, or a solvate thereof, or a prodrug thereof. The compound disclosed by the invention has a good effect when being used as a photosensitizer for photodynamic tumor treatment or a sound-sensitive agent for sonodynamic tumor treatment, and can be used for preparing medicines for treating tumors. Meanwhile, the compound disclosed by the invention is good in safety and small in toxic and side effects, and has a good application prospect.

The present invention is a phosphorylcholine-containing chemical compound represented by the following formula (1) or (2).(CH3)3N+CH2CH2PO4−CH2COOH   (1)(CH3)3N+CH2CH2PO4−CH2COONa   (2)The object of the present invention is to provide a new phosphorylcholine-containing compound that is useful as a surface treatment agent or a source material of a surface treatment agent. Another object is to provide a manufacturing method that has a high industrial utility value.

The invention relates to trans carotenoid salt compounds, methods for making them, methods for solubilizing them and uses thereof. These compounds are useful in improving diffusivity of oxygen between red blood cells and body tissues in mammals including humans.

The invention relates to a method for preparing low-zinc low-iron clear rongalite, which comprises the steps that: rongalite solution is used as a raw material and quinoline organic precipitator is used for precipitating zinc and ferrous ions in the solution before concentration; then, sampling and filtering are carried out, ammonia-ammonium chloride with the pH of 10 is used for buffering the solution with Eriochrome black T as a visualization reagent, and the content of the residual zinc ions in filtrate is measured by colorimetry; after the measured value meets the control requirement of 1 to 3mg / L, stirring is stopped, after precipitation and aging are carried out for 2 to 3 hours, precipitates are filtered away and then the filtrate is colorless and transparent; then, cooling for crystallization, crushing and packaging are carried out for obtaining the products of the clear rongalite with zinc and ferrous contents lower than 10PPm after the filtrate is concentrated to the content of over 98 percent at a vacuum level ranging from minus 0.085 to minus 0.095mPa and temperature lower than 75 DEG C. The invention has the advantages that the products prepared by the method have good stability and zinc and ferrous contents of lower than 10PPm, thus meeting special requirements on rongalite products by industries such as medicine and rubber, etc.

The invention relates to a process for preparing an alcoholic solution of an alkali metal alkoxide from alkali metal hydroxide and alcohol in a reaction column, the alcohol and the alkali metal hydroxide being conducted in countercurrent, which is characterized in that a reflux ratio of at least 0.05 is established in the reaction column.