Class / Patent application number | Description | Number of patent applications / Date published |
556081000 | Germanium, tin, or lead containing (Ge, Sn, or Pb) | 24 |
20130023685 | METHOD FOR PRODUCING METAL COMPOUNDS - The invention relates to processes for preparing metal(IV) compounds which are suitable especially as catalysts for preparation of polyesters, polyurethanes and polysiloxanes, and to the use of the metal compounds for preparation of polyesters, polyurethanes or polysiloxanes. | 01-24-2013 |
20140142332 | PROCESS OF PREPARING GRIGNARD REAGENT - A novel process of preparing a Grignard reagent is disclosed. The process is effected by electrochemically reacting a Grignard precursor with an electrode which comprises a metal for forming the Grignard reagent, in the presence an electrolyte solution that comprises a room temperature ionic liquid (RTIL). Electrochemical cells and systems for performing the process, and uses thereof in various applications are also disclosed. | 05-22-2014 |
20160251383 | METHODS FOR PRODUCING SINGLE CRYSTAL MIXED HALIDE PEROVSKITES | 09-01-2016 |
556083000 | Plural heavy metals bonded directly to the same chalcogen (e.g., two germaniums bonded directly to the same oxygen, etc.) | 2 |
20100292496 | Process for Production of Alkyl Tin Alkoxide Compound, and Process for Production of Carbonic Acid Ester Using the Compound - The present invention provides a process for producing: a compound represented by XOR | 11-18-2010 |
20130165681 | Catalyst, Method of Preparing the Same, and Method of Preparing Aromatic Carbonate From Dialkyl Carbonate Using the Same - The present invention provides a catalyst for synthesizing an aromatic carbonate, a method of preparing the same, and a method of preparing an aromatic carbonate from dialkyl carbonate using the catalyst. The catalyst has a unit structure of Formula | 06-27-2013 |
556087000 | Carbon bonded directly to the metal | 18 |
20090156852 | Organometallic compounds - Organometallic compounds suitable for use as vapor phase deposition precursors for Group IV metal-containing films are provided. Methods of depositing Group IV metal-containing films using certain organometallic precursors are also provided. Such Group IV metal-containing films are particularly useful in the manufacture of electronic devices. | 06-18-2009 |
20090275770 | NOVEL TIN AMINO-ALKOXIDE COMPLEXES AND PROCESS FOR PREPARING THEREOF - The present invention relates to novel tin amino-alkoxide complexes and a method for preparing the same, precisely novel tin amino-alkoxide complexes represented by formula 1 and useful as a precursor for tin and tin oxide thin films and a precursor for the production of nano-sized tin and tin oxide particles and a method for preparing the same. In formula 1, A is linear or branched (C2-C10) alkylene substituted or not substituted with halogen; R | 11-05-2009 |
20110313183 | METHOD FOR PREPARATION OF N-METHYL-3-(2-TRIBUTYLSTANNYLPHENOXY)-3-PHENYLPROPANAMINE, AND USE THEROF - A method for preparation of N-methyl-3-(2-tributylstannylphenoxy)-3-phenylpropanamine is provided, which includes formation of N-methyl-3-(2-tributylstannylphenoxy)-3-phenylpropanamine, useful as a precursor of a norepinephrine transporter (NET) contrast label [ | 12-22-2011 |
20160023988 | FLUORESCENT PROBE - A compound represented by the formula (I) (R | 01-28-2016 |
20160176812 | CONVERSION OF ALKANES TO ORGANOSELENIUMS AND ORGANOTELLURIUMS | 06-23-2016 |
20190144472 | METHOD OF FORMING TIN-CONTAINING MATERIAL FILM AND METHOD OF SYNTHESIZING A TIN COMPOUND | 05-16-2019 |
556088000 | Chalcogen bonded directly to the metal | 5 |
20100041908 | PROCESS FOR PRODUCING DIALKYL TIN DIALKOXIDES - An object of the present invention is to provide a process for producing a dialkyl tin compound from a composition of deactivated forms of a dialkyl tin catalyst, and to provide a process for producing the dialkyl tin catalyst from the dialkyl tin compound and using the dialkyl tin catalyst to produce a carbonic acid ester. According to the present invention, a process for producing a dialkyl tin compound is provided that subjects a composition of the deactivated forms of the dialkyl tin catalyst, formed when producing an ester compound, to an alkyl group redistribution reaction and/or dealkylation reaction. | 02-18-2010 |
556089000 | Plural chalcogens bonded directly to the metal | 4 |
20080275262 | Process for Production of Alkyltin Alkoxides - A process for the production of alkyltin alkoxides which comprises subjecting at least one alkyltin compound selected from among organotin compounds having tin-oxygen-tin linkages as the starting compound and a hydroxyl compound as the reactant to dehydration to obtain an alkyltin alkoxide corresponding to the starting compound and the reactant, characterized by continuously feeding the starting compound and the reactant into a reactor, discharging a water-containing low boiling point component from the reactor, and continuously withdrawing a reaction fluid containing an alkyltin alkoxide as the bottom from the reactor. | 11-06-2008 |
20100160662 | Method for Separating Out and Recovering Dialkyltin Dialkoxide - For an alkyltin alkoxide catalyst composition used in carbonate production, there is a problem that the alkyltin alkoxide catalyst composition is thermally decomposed by being heated in the production process, changing into an undistillable alkyltin alkoxide catalyst composition containing a high boiling deactivated component and an active component. The present invention provides a method for separating out and recovering the active component from the alkyltin alkoxide catalyst composition as a useful dialkyltin dialkoxide. According to the present invention, there is disclosed a method in which such an undistillable alkyltin alkoxide catalyst composition containing a high boiling deactivated component and an active component is reacted with an alcohol and/or a carbonate, so as to obtain a reaction liquid containing a product originating from the active component, and then the reaction liquid is subjected to distillation, so as to separate out and recover a dialkyltin dialkoxide from the product originating from the active component. | 06-24-2010 |
556093000 | Having -C(=X)X-, are the same or diverse chalcogens, attached indirectly to the metal by nonionic bonding (e.g., dialkyl tin thioglycollic acid esters, etc.) | 2 |
20100298589 | Alkyltin Sulfanyl Diester Thiols - Disclosed herein are compounds of the formula: | 11-25-2010 |
20140357883 | METHYLTIN MERCAPTIDE DERIVATIVE AND METHOD FOR PREPARING THE SAME - A compound represented by formula I or II and a method for preparing the same. The method includes: a) adding isooctyl mercaptopropionate to a reactor, adding dropwise an aqueous solution of methyltin chloride, stirring and allowing for a complete reaction, and adding aqueous ammonia, an aqueous solution of sodium hydroxide, an aqueous solution of sodium bicarbonate, an aqueous solution of sodium carbonate, or a solution of an organic base to regulate the pH value of a resulting mixture from a starting value of between 2 and 8 to an end value of between 6 and 10 for a primary stage of esterification; and b) allowing a product obtained from step a) to proceed to a secondary stage of the esterification, allowing the product to stand until phases are separated, collecting and washing an organic phase using deionized water, allowing a resulting mixture to stand until phases are separated. | 12-04-2014 |
556095000 | The compound consists of the metal, carbon and hydrogen or the metal, carbon, hydrogen and halogen (e.g., tetraalkylleads, etc.) | 7 |
20110282087 | Regioselective catalytic conversion of hydrocarbons to versatile synthetic reagents via C-H bond functionalization - The present invention provides a novel and improved method of functionalizing a C—H bond of an arene compound comprising the step of reacting an organometallic compound having a group 14 element with the arene compound having at least one hydrogen bonded to a carbon in the presence of a catalyst. | 11-17-2011 |
20140012027 | Method for Producing Fluorine-Containing Substituted Compound and Fluorine-Containing Substituted Compound - A method for producing a fluorine-containing substituted compound, the method including: introducing an organofluorine compound and an organolithium compound into a microreactor provided with a flow path capable of mixing a plurality of liquids, to thereby obtain a reaction product; and introducing, into the microreactor, the reaction product and an electrophile exhibiting electrophilic effect on the reaction product, to thereby obtain a fluorine-containing substituted compound. | 01-09-2014 |
20160108067 | Method for Producing Fluorine-Containing Substituted Compound and Fluorine-Containing Substituted Compound - A method for producing a fluorine-containing substituted compound, the method including: introducing an organofluorine compound and an organolithium compound into a microreactor provided with a flow path capable of mixing a plurality of liquids, to thereby obtain a reaction product; and introducing, into the microreactor, the reaction product and an electrophile exhibiting electrophilic effect on the reaction product, to thereby obtain a fluorine-containing substituted compound. | 04-21-2016 |
20160145276 | TRACELESS DIRECTING GROUPS IN RADICAL CASCADES: FROM OLIGOALKYNES TO FUSED HELICENES WITHOUT TETHERED INITATORS - The present disclosure is directed to a traceless directing group in a radical cascade. The chemo- and regioselectivity of the initial attack in skipped oligoalkynes is controlled by a propargyl alkoxy moiety. Radical translocations lead to the boomerang return of radical center to the site of initial attack where it assists to the elimination of the directing functionality via β-scission in the last step of the cascade. In some aspects, the reaction of the present invention is catalyzed by a stannane moiety, which allows further via facile reactions with electrophiles as well as Stille and Suzuki cross-coupling reactions. This selective radical transformation opens a new approach for the controlled transformation of skipped oligoalkynes into polycyclic ribbons of tunable dimensions. | 05-26-2016 |
556096000 | Preparing by utilizing a magnesium containing material (e.g., Grignard reagent, etc.) | 1 |
20130281725 | Process For Preparing Monoalkyltin Trihalides and Dialkyltin Dihalides - The invention provides a process for producing monoalkyltin trihalide or a mixture of monoalkyltin trihalide and dialkyltin dihalide by: (a) contacting dialkyltin dihalide with an alkylation agent and, optionally, tin tetrahalide, to form a tetraalkyltin mixture comprising tetraalkyltin, trialkyltin halide, and dialkyltin dihalide; (b) reacting the tetraalkyltin mixture with tin tetrahalide to form a monoalkyltin trihalide mixture comprising monoalkyltin trihalide, dialkyltin dihalide and optionally triaklyltin halide; (c) processing the monoalkyltin trihalide mixture to separately recover the monoalkyltin trihalide and a dialkyltin dihalide stream optionally containing trialkyltin halide; and (d) recycling at least a portion of the dialkyltin dihalide stream recovered in step (c) to the contacting step (a). | 10-24-2013 |
556098000 | Preparing by reacting free heavy metal or heavy metal containing alloy with hydrocarbyl halide (e.g., reacting Pb-Na alloy with hydrocarbyl chloride, etc.) | 1 |
556099000 | Additional heavy metal containing material or aluminum containing material utilized | 1 |
20150045571 | Method for Preparing an Organofunctional Compound - Claimed is a method for making an organofunctional compound of formula R | 02-12-2015 |
556103000 | Purification or recovery | 1 |
20090131704 | Process for the Preparation of Monoalkyltin Trihalides and Dialkyltin Dihalides - The present invention relates to a process for the production of monoalkyltin trihalides of the formula RSnHal | 05-21-2009 |
556105000 | Containing -C(=X)X-, wherein the X's are the same or diverse chalcogens | 1 |
20150291422 | QUANTUM DOT STABILIZED BY HALOGEN SALT AND METHOD FOR MANUFACTURING THE SAME - A quantum dot stabilized by a halogen salt includes a compound of Group 13 and Group 15, a compound of Group 12 and Group 16 or a compound of Group 14 and Group 16. The quantum dot has a crystalline structure and at least a portion of a surface of the quantum dot is combined with a halogen salt. Thus, the quantum dot has a high stability in an air. | 10-15-2015 |