109-69-3 + 616-47-7 = 79917-90-1 反应条件:1.1 5 D,80 °C 标题:Cross-Linked Candida Antarctica Lipase B Is Active In Denaturing Ionic Liquids 作者:Toral,Antonio Ruiz; Et Al 参考文献:Enzyme And Microbial Technology 日期:2007 卷标:40(5) 页码:1095-1099]
119393-94-1 = 79917-90-1 反应条件:1.1 Reagents: Benzoyl Peroxide Solvents: Tetrahydrofuran; Rt -> Reflux; Rt1.2 Reagents: Sodium Bicarbonate; 15 Min,Rt1.3 Solvents: Ethanol; 30 Min,Rt1.4 Reagents: Dimethyl Sulfoxide Solvents: Water-D21.5 Reagents: Sodium Chloride Solvents: Diethyl Ether,Ethanol 标题:Oxidative Desulfurization Of Azole-2-Thiones With Benzoyl Peroxide: Syntheses Of Ionic Liquids And Other Azolium Salts 作者:Wolfe,Derek M.; Et Al 参考文献:European Journal Of Organic Chemistry 日期:2007 卷标:(17) 页码:2825-2838]
109-69-3 = 79917-90-1 反应条件:1.1 15 Min,120 °C 标题:Preparation And Physicochemical Characterization Of Deep Eutectic Solvents And Ionic Liquids For The Potential Absorption And Biodegradation Of Styrene Vapors 作者:Candia-Lomeli,M.; Et Al 参考文献:Journal Of Hazardous Materials 日期:2023 卷标:441]
109-69-3 = 79917-90-1 反应条件:1.1 Solvents: Acetonitrile; Rt; 72 H,75 - 80 °C 标题:Polymorphism And Particle Formation Pathway Of Carbamazepine During Sonoprecipitation From Ionic Liquid Solutions 作者:Prasad,Rupanjali; Et Al 参考文献:Crystal Growth & Design 日期:2020 卷标:20(8) 页码:5169-5183]
109-69-3 + 35487-17-3 = 79917-90-1 反应条件:1.1 Solvents: Toluene; 0 °C; 24 H,0 °C -> 110 °C; 12 H,-20 °C 标题:Synthesis And Antiproliferative Activity Of Ammonium And Imidazolium Ionic Liquids Against T98G Brain Cancer Cells 作者:Kaushik,Nagendra Kumar; Et Al 参考文献:Molecules 日期:2012 卷标:17 页码:13727-13739]
109-69-3 + 35487-17-3 = 79917-90-1 反应条件:1.1 Overnight,Rt; 7 H,Reflux 标题:Disproportionation Of Light Paraffins 作者:Schmidt,Roland; Et Al 参考文献:Energy & Fuels 日期:2008 卷标:22(3) 页码:1812-1823]
109-69-3 + 693-98-1 = 79917-90-1 反应条件:1.1 Solvents: Acetonitrile; 48 H,Reflux 标题:Direct Conversion Of Propylene Oxide To 3-Hydroxy Butyric Acid Using A Cobalt Carbonyl Ionic Liquid Catalyst 作者:Rajendiran,Senkuttuvan; Et Al 参考文献:Catalysts 日期:2017 卷标:7(8) 页码:228/1-228/6]
71614-56-7 = 79917-90-1 反应条件:1.1 Rt 标题:A Novel And Green Method For The Synthesis Of Ionic Liquids Using The Corresponding Acidic Ionic Liquid Precursors And Dialkyl Carbonate 作者:Xiao,Wenjun; Et Al 参考文献:Chemistry Letters 日期:2010 卷标:39(10) 页码:1112-1113]
616-47-7 = 79917-90-1 反应条件:1.1 Solvents: Acetonitrile; 70 °C; 72 H,70 °C 标题:Interaction Of Electron Beam With Ionic Liquids And Its Application For Micropatterning 作者:Rola,Krzysztof P.; Et Al 参考文献:European Polymer Journal 日期:2021 卷标:156]
616-47-7 = 79917-90-1 反应条件:1.1 Reagents: 1,1,1-Trifluoroethane; 48 H,70 °C 标题:Microwave-Assisted Synthesis Of Imidazole Ionic Liquids 作者:Zhou,Jing; Et Al 参考文献:Yingyong Huagong 日期:2009 卷标:38(1) 页码:58-60]
39678-28-9 = 79917-90-1 反应条件:1.1 Solvents: Ethanol,Water; 90 Min,35 °C 标题:An Efficient Ultrasonic-Assisted Synthesis Of Imidazolium And Pyridinium Salts Based On The Zincke Reaction 作者:Zhao,Sanhu; Et Al 参考文献:Ultrasonics Sonochemistry 日期:2010 卷标:17(4) 页码:685-689]
= 79917-90-1 反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Water; 0 °C; 1 H,0 °C -> Rt1.2 10 Min,150 °C 标题:Rapid Continuous-Flow Water-Free Synthesis Of Ultrapure Ionic Liquids Assisted By Microwaves 作者:Cao,Lei; Et Al 参考文献:Organic Process Research & Development 日期:2022 卷标:26(1) 页码:207-214]
= 79917-90-1 反应条件:1.1 Reagents: Ammonium Chloride Solvents: Water; 24 H,110 °C 标题:A General And Direct Synthesis Of Imidazolium Ionic Liquids Using Orthoesters 作者:Kim,Do Joong; Et Al 参考文献:Green Chemistry 日期:2014 卷标:16(9) 页码:4098-4101]
616-47-7 = 79917-90-1 [标题:Reaction Conditions 标题:Preparation Of Chitin Nanofiber-Reinforced Xanthan Gum Hydrogels 作者:Kawano,Akito; Et Al 参考文献:Journal Of Polymers And The Environment 日期:2019 卷标:27(4) 页码:671-677]
109-69-3 = 79917-90-1 反应条件:1.1 72 H,75 °C 标题:The Effect Of Ionic Liquids On The Conductivity Of Electrospun Polyacrylonitrile Membranes 作者:Savest,Natalja; Et Al 参考文献:Journal Of Electrostatics 日期:2016 卷标:83 页码:63-68]
109-69-3 + 616-47-7 = 79917-90-1 反应条件:1.1 72 H,75 - 80 °C 标题:Thermo-Solvatochromism Of Chloro-Nickel Complexes In 1-Hydroxyalkyl-3-Methyl-Imidazolium Cation Based Ionic Liquids 作者:Wei,Xianjun; Et Al 参考文献:Green Chemistry 日期:2008 卷标:10(3) 页码:296-305]
120-94-5 + 616-47-7 = 79917-90-1 反应条件:1.1 Solvents: Acetonitrile; 60 °C; 60 °C; 3 D,70 °C 标题:Rapid,High-Yield Fructose Dehydration To 5-Hydroxymethylfurfural In Mixtures Of Water And The Noncoordinating Ionic Liquid [bmim][otf] 作者:Ghatta,Amir Al; Et Al 参考文献:Chemsuschem 日期:2019 卷标:12(19) 页码:4452-4460]
80432-08-2 = 79917-90-1 反应条件:1.1 Reagents: Sodium Chloride Solvents: Water; 2 H,Rt 标题:Ionic Liquid Ion Exchange: Exclusion From Strong Interactions Condemns Cations To The Most Weakly Interacting Anions And Dictates Reaction Equilibrium 作者:Naert,Pieter; Et Al 参考文献:Green Chemistry 日期:2018 卷标:20(18) 页码:4277-4286
氯丁烷置于n-甲基咪唑体系中,用98%的收率获得产物氯化(1-丁基-3-甲基咪唑) 参考文献:Method For Prepararing Alkoxyamines From Nitroxides 标题:Method For Prepararing Alkoxyamines From Nitroxides 摘要:该发明涉及一种在两相介质中制备烷氧胺的方法.该方法包括混合离子液体,有机溶剂,金属盐,金属配体,卤代碳氢zx化合物和亚硝基,在20oc至90oc的温度下将反应介质保持在搅拌状态,直到亚硝基被消除,然后沉淀,回收有机相,可选地用水洗涤,然后通过在减压下蒸发有机溶剂来分离烷氧胺.
专利号:US-10260154-B2 优先权日:2015-08-01 标 题:Method for the synthesis of layered luminescent transition metal dichalcogenide quantum dots 发明人:MANIKOTH SHAIJUMON MANCHERI; DAMIEN DIJO; Gopalakrishnan Deepesh 权利人:INDIAN INSTITUTE OF SCIENCE EDUCATION AND RES THIRUVANANTHAPURAM IISER TVM 摘要:The invention discloses a method for the synthesis of monodispersed luminescent quantum dots of transition metal dichalcogenides (TMDC), single- or few-layered, using a single-step electrochemical exfoliation that involves dilute ionic liquid and water. The method disclosed helps to obtain nanoclusters of TMDC of desired size including small sizes ranging up to 6 nm, by varying the concentration of the electrolyte and the applied DC voltage. The invention further discloses a method by which mono- or few-layered luminescent transition metal dichalcogenides can be directly deposited onto conducting substrates in a uniform manner. The monodispersed single- or few-layered luminescent TMDC and electro-deposited substrates exhibit improved electronic conductivity and new active sites, making them suitable as high-performance electrocatalysts in hydrogen evolution reactions in solar water-splitting applications and also as electrodes for solar cell applications.
专利号:WO-2023036838-A1 优先权日:2021-09-07 标题:Process for preparing starting compounds intended for the synthesis of an ammine metal borohydride 发明人:HAJIYEV PARVIZ; NGUYEN HUYNH DUC 权利人:COMMISSARIAT ENERGIE ATOMIQUE 摘要:Process for preparing a metal hydride of formula AxMHx+m and a borane compound BH3, starting from a product of formula AxM(BNH)x+m, wherein: A is an alkali metal, M is a metal different from an alkali metal, 0 ≤ x ≤10, in particular 0 ≤ x ≤ 2 m>0, the process comprising: aT) reacting the metal hydride of formula AxM(BNH)x+m with ammonia such as obtain an ammoniated product of formula AxM(NH2)x+m and a hydrogenated boron nitride compound BNH, a' 2) the hydrogenation of the ammoniated product of formula AxM(NH2)x+m such as to obtain an metal hydride of formula AxMHx+m, the process further comprising the separation of the hydrogenated boron nitride compound BNH from the ammoniated product of formula AxM(NH2)x+m before step a' 2) or from the metal hydride of formula AxMHx+m after step a' 2), and b) the synthesis of the borane compound BH3, from the hydrogenated boron nitride compound BNH, the synthesis comprising: - a digestion reaction of the boron nitride compound BNH in a gaseous atmosphere containing, even consisting in, an anhydrous hydrogen halide acid gas comprising at least one halogen element Y, such as to produce a boron halide BY3, Y being preferably chlorine Cl, - a hydrodehalogenation of the boron halide, in a hydrogen gas atmosphere to obtain the borane compound BH3.
专利号:WO-2023036831-A1 优先权日:2021-09-07 标 题:Process for preparing starting compounds intended for the synthesis of an ammine metal borohydride 发明人:HAJIYEV PARVIZ; NGUYEN HUYNH DUC 权利人:COMMISSARIAT ENERGIE ATOMIQUE 摘要:Process for preparing a metal hydride of formula AxMHx+m and a borane compound BH3, starting from a product of formula AxM(BNH)x+m, wherein: A is an alkali metal, M is a metal different from an alkali metal, 0 ≤ x ≤10, in particular 0 ≤ x ≤ 2 m>0, the process comprising: a) contacting the product of formula AxM(BNH)x+m with a catalyst comprising a transition metal in solution in an aprotic polar solvent, such as to separate the metal hydride of formula AxMHx+m and a hydrogenated boron nitride compound BNH, b) the synthesis of the borane compound BH3, from the hydrogenated boron nitride compound BNH, the synthesis comprising: - a digestion reaction of the boron nitride compound BNH in a gaseous atmosphere containing, even consisting in, an anhydrous hydrogen halide acid gas comprising at least one halogen element Y, such as to produce a boron halide BY3, Y being preferably chlorine Cl, - a hydrodehalogenation of the boron halide, in a hydrogen gas atmosphere to obtain the borane compound BH3.
专利号:US-8637695-B2 优先权日:2011-12-30 标 题:Synthesis of organohalosilane monomers from conventionally uncleavable Direct Process Residue 发明人:LEWIS KENRICK MARTIN; NEELY JOHN DAVID 权利人:LEWIS KENRICK MARTIN; NEELY JOHN DAVID; MOMENTIVE PERFORMANCE MAT INC 摘要:Disclosed herein is a catalytic process for the synthesis of organohalosilane monomers from tetraorganodihalodisilanes and other compounds that are not cleaved during the conventional hydrochlorination of Direct Process Residue. The process is characterized by the use of a catalyst containing (1) one or more heterocyclic amines and/or one or more heterocyclic ammonium halides, and (2) one or more quaternary Group 15 onium compounds.
专利号:US-2005087449-A1 优先权日:2002-03-04 标题:Electrochemical synthesis of ammonia 发明人:DENVIR ADRIAN; MURPHY OLIVER J; CISAR ALAN; ROBERTSON PRISCILLA; USELTON KYLE 摘要:A method for electrochemical synthesis of ammonia gas comprising providing an electrolyte between an anode and a cathode, providing hydrogen gas to the anode, oxidizing negatively charged nitrogen-containing species present in the electrolyte at the anode to form an adsorbed nitrogen species, and reacting the hydrogen with the adsorbed nitrogen species to form ammonia. Preferably, the hydrogen gas is provided to the anode by passing the hydrogen gas through a porous anode substrate. It is also preferred to produce the negatively charged nitrogen-containing species in the electrolyte by reducing nitrogen gas at the cathode. However, the negatively charged nitrogen-containing species may also be provided by supplying a nitrogen-containing salt, such as lithium nitride, into the molten salt electrolyte mixture in a sufficient amount to provide some or all of the nitrogen consumed in the production of ammonia.
专利号:US-8541571-B2 优先权日:2008-03-03 标题:Homogeneous synthesis of cellulose ethers in ionic liquids 发明人:MOELLMANN EUGEN; HEINZE THOMAS; LIEBERT TIM; KOEHLER SARAH 权利人:MOELLMANN EUGEN; HEINZE THOMAS; LIEBERT TIM; KOEHLER SARAH; SE TYLOSE GMBH & CO KG 摘要:The invention is directed to a simple and new method for the homogeneous synthesis of cellulose ethers. Ionic liquids are not only used as solvent, but also as reaction media for the homogeneous etherification of cellulose. The dissolved cellulose is treated with the etherification agent in the absence of organic and/or inorganic bases and in the absence and/or in the presence of moderate amounts of water. The obtained cellulose ethers show new distributions of substitution on the polymer chain, resulting in new properties and applications.
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合成参考文献
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