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102 results about "Thiocarbonate" patented technology

Thiocarbonate describes a family of anions with the general chemical formula CS₃₋ₓO²⁻ₓ (x = 0, 1, or 2). Like the carbonate dianion, the thiocarbonates are planar, with carbon at the center. The average bond order from C to S or O is 1 ¹⁄₃. The state of protonation is usually not specified. These anions are good nucleophiles and good ligands.

2-(2'-hydroxyphenyl) benzothiazole chelated zinc derivative as well as preparation method and application thereof

The invention relates to a 2-(2'-hydroxyphenyl) benzothiazole chelated zinc derivative as well as a preparation method and an application thereof, belonging to the field of organic electroluminescentluminescent materials. The preparation method of the derivative comprises the following steps: firstly, introducing different substituent groups with electron-withdrawing or electron-donating capability in a benzothiazole benzene ring or a hydroxyphenyl benzene ring of a 2-(2'-hydroxyphenyl) benzothiazole matrix to obtain a substituted 2-(2'-hydroxyphenyl) benzothiazole ligand; coordinating with diatomic zinc to form a corresponding complex, and the like. The substituted 2-(2'-hydroxyphenyl) benzothiazole ligand can be prepared by a plurality of reactions, such as substituted aniline acylation, hydroxyl protection, hydroxyl thiocarbonate, Jacobson cyclization while hydroxyl deprotection, and the like or prepared by a direct reaction of O-amino thiophenol and substituted ortho-hydroxybenzoic acid. When applied to an organic electroluminescent luminescent device as an electronic transmission layer, the derivative has favorable electronic transmission performance and has performance superior to the most common electronic transmission material 8-hydroxyquinoline aluminum.
Owner:DALIAN UNIV OF TECH

Method for treating purification copper-removing slag of nickel electrolysis anode solution

The invention discloses a method for treating the purification copper-removing slag of a nickel electrolysis anode solution. The method comprises the following steps: treating the copper-removing slag generated in the nickel thiocarbonate method copper-removing process with a copper-containing solution to leach nickel in the copper-removing slag, obtain copper-removing slag of which copper-nickel ratio is above 150 and convert the leachate to a nickel-containing solution, then using the nickel-containing solution to react with a thiocarbonate solution and prepare nickel thiocarbonate, and using the prepared nickel thiocarbonate to remove copper in the nickel electrolysis anode solution. In the copper-removing process, only copper in the nickel electrolysis anode solution is required to be removed completely without considering the copper-nickel ratio of the copper-removing slag. A lot of copper-removing agent is added to ensure that even the highest concentration of copper in the solution can be removed completely. Therefore, the copper concentration of the solution is not required to be accurately controlled before the copper-removing process and the operations are performed easily. Meanwhile, a lot of copper-removing agent is added and the copper-removing solution with extremely lower copper concentration can be obtained, compared with the copper-removing effect by adding a defined amount of the copper-removing agent. As whether nickel exceeds the standard is not considered, the copper-removing operation can be easily controlled.
Owner:CENT SOUTH UNIV

Colorimetric fluorescence probes used for analyzing mercury ions, and preparation method and application of colorimetric fluorescence probe

The invention relates to high-selectivity mercury ion colorimetric fluorescence probes. Specifically, the probes provided by the invention are thiocarbonate compounds, and the compounds can be used as the mercury ion colorimetric fluorescence probes for detecting mercury ions. The structure formula of the compounds is described in the description. The probes can realize at least one of the technical effects of realizing high selective identification of the mercury ions, more rapidly responding to the mercury ions, being good in water solubility, being stable in properties and being stored for a long time, and having higher anti-interference ability.
Owner:UNIV OF JINAN

Preparation method and application of heavy metal contaminated soil/bottom mud stabilizer

The invention relates to the technical fields of soil remediation and environmental protection, in particular to a heavy metal contaminated soil/bottom mud stabilizer. The heavy metal contaminated soil/bottom mud stabilizer is prepared from soluble ferric salt, dibutyl dithiophosphate and butyl dithiocarbonate in proportion. A heavy metal repair agent is low in cost, can effectively eliminate harm of heavy metal ions in soil, and has relatively good stabilizing effect on arsenic and other heavy metals in arsenic-containing composite heavy metal contaminated bottom mud under an acid condition, so that the defect that an existing product is poor in stabilizing effect on the arsenic-containing composite heavy metal contaminated bottom mud is overcome. The heavy metal contaminated soil/bottom mud stabilizer can be applied to stabilizing treatment of heavy metal contaminated muddy bottom of arsenic, lead, cadmium, copper, zinc and chromium. The heavy metal contaminated soil/bottom mud treated by the stabilizer can be used for roadbed building filler. The heavy metal contaminated soil/bottom mud stabilizer has the effects of protecting the environment, changing waste into things of value and increasing a waste utilization rate, and has a considerable economic value.
Owner:湖南新九方科技有限公司

Sacrificial materials

Various embodiments disclosed relate to sacrificial materials and methods of using the same. Various embodiments provide objects having the sacrificial material at least partially removed therefrom, and methods of making the same. Various embodiments provide sacrificial adhesives, sacrificial mechanical connectors, and methods of using the same. The sacrificial material can include a polymer including a repeating unit including a substituted or unsubstituted (C2-C20)hydrocarbylene and at least one of carboxylate, carbonate, carbamate, thiocarbonate, and thiocarbamate. The method can include exposing the sacrificial material to at least one of heat and acid, such that at least some of the sacrificial material degrades. The method can include removing at least some of the degraded sacrificial material.
Owner:UNIV OF MASSACHUSETTS

Method for preparing thionocarbamate and trithiocarbonate

The invention discloses a method for preparing thionocarbamate and trithiocarbonate. The method comprises the following steps: carrying out an esterification reaction on alkyl xanthate salt and a halogenation reagent to obtain alkyl xanthate ester; carrying out an aminolysis reaction on the alkyl xanthate ester and fatty amine to obtain a thionocarbamate and mercaptan compound mixture; and carrying out an addition reaction on the thionocarbamate and mercaptan compound mixture and carbon disulfide in the presence of caustic alkali, and carrying out solid-liquid separation to obtain a liquid phase which is the thionocarbamate product and a solid phase which is the trithiocarbonate product. The products prepared through the preparation method have high yield and high purity, and the method allows the two high-efficiency collectors comprising thionocarbamate and trithiocarbonate to be simultaneously produced, and has the advantages of easiness in separation of the products, high atom economy property, low production cost, and easiness in realization of industrial production.
Owner:CENT SOUTH UNIV

Terminal alkynyl containing RAFT chain transfer agent and preparation method and application thereof

The invention belongs to the field of organic synthesis and discloses a terminal alkynyl containing RAFT chain transfer agent and a preparation method and application thereof.The RAFT chain transfer agent has a structure shown in the description.The preparation method comprises the steps that tert-butyl mercaptan serves as a start raw material and reacts with carbon disulfide under the action of alkali to form trithiocarbonate; under the alkaline catalytic action, the obtained trithiocarbonate reacts with bromo propionate, and after acidification, terminal carboxylgroup containing RAFT chain transfer agent is obtained; the terminal carboxylgroup containing RAFT chain transfer agent is re-crystalized through n-hexane, and then under the action of EDC.HC1 and DMAP, the terminal carboxylgroup containing RAFT chain transfer agent and propargyl alcohol generate terminal alkynyl containing trithiocarbonate.The rough product is subjected to extraction and column chromatography, and then the product is obtained.The terminal alkynyl containing RAFT chain transfer agent can achieve RAFT polymerization and click reaction and prepare block polymer with specific structures and functions.
Owner:FOSHAN CENT FOR FUNCTIONAL POLYMER MATERIALS & FINE CHEM
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