CAS: 1259-35-4; Tris(Perfluorophenyl)Phosphine

该化合物是高电子衰竭的磷离子,广泛用于有机金属化学和催化. 其强固的刘易斯酸性和不育性大宗使其在稳定低价金属中心和促进具有挑战性的转化方面特别有效, 如C-H活化和交叉反应. 电排的五氟联苯组增强了其氧化稳定性和抗拉链降解的能力,在苛刻的条件下可以产生强大的催化性性能. 这种离子在同质的催化中特别有用,因为其独特的电子特性可以进行选择性和高效的反应. 它与晚变金属的兼容性进一步扩大了其在合成和工业应用中的效用.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

CAS号344-04-7 溴五氟苯 | CAS号879-05-0 五氟苯基溴化镁 | CAS号7719-12-2 三氯化磷 | CAS号879-06-1 3-indole acetamide | CAS号3982-91-0 硫代磷酰氯 | CAS号22474-72-2 Difluorotris(pe... | CAS号344-04-7 溴五氟苯 | CAS号2729-11-5 Phosphine oxide... | CAS号6141-72-6 N-[bis(trifluor... | CAS号602-94-8 五氟苯甲酸 | CAS号5075-69-4 silver(I) n-butyrate

合成工艺路线路线简述

  • 合成目标产物 Tris(Pentafluorophenyl)Phosphine 主要起始原料 Bromopentafluorobenzene
  • (文献来源)合成步骤主要原料 Bromopentafluorobenzene
溴五氟苯置于magnesium,三溴化磷体系中,用 乙醚 用作溶剂,化学反应 1.0H,以31%的收率获得三(五氟苯基)膦
参考文献:三芳基甲硅烷基离子的新合成及其在二氢活化中的应用
标题:三芳基甲硅烷基离子的新合成及其在二氢活化中的应用
摘要:乱序:通过烷基二芳基甲硅烷基离子发生意外的取代基分布反应,导致取代基分布.从烷基二芳基硅烷开始,该反应为空间高度受阻的三芳基甲硅烷基离子提供了一种简便的合成方法.这些甲硅烷基离子可用于二氢活化反应中.
Doi:10.1002/anie.201106582

专利信息


专利号:US-11427530-B2
优先权日:2018-02-09
标 题 :Synthesis of 4-chlorokynurenines and intermediates
发明人:LEVIN DANIEL; LEEMING PETER; EISENREICH EMERICH; LIU XUEJUN KARL
权利人:VISTAGEN THERAPEUTICS INC
摘要:The invention relates to an overall enantio-specific synthesis of 4-chlorokynurenine compounds, in particular L-4-chlorokynurenine, with improved yields. Large-scale syntheses are disclosed. The invention also relates to novel intermediates in the synthesis of L-4-chlorokynurenine.

专利号:US-11794179-B2
优先权日:2016-08-24
标 题 :Synthesis and characterization of metathesis catalysts
发明人:JOHNS ADAM M
权利人:UMICORE AG & CO KG
摘要:This invention relates generally to olefin metathesis catalysts, to the preparation of such compounds, compositions comprising such compounds, methods of using such compounds, and the use of such compounds in the metathesis of olefins and in the synthesis of related olefin metathesis catalysts. The invention has utility in the fields of catalysis, organic synthesis, polymer chemistry, and in industrial applications such as oil and gas, fine chemicals and pharmaceuticals.

专利号:WO-2018191373-A1
优先权日:2017-04-12
标 题:Synthesis and characterization of metathesis catalysts
发明人:JOHNS ADAM
权利人:MATERIA INC
摘要:This invention relates generally to olefin metathesis catalysts, to the preparation of such compounds, compositions comprising such compounds, methods of using such compounds, and the use of such compounds in the metathesis of olefins and in the synthesis of related olefin metathesis catalysts. The invention has utility in the fields of catalysis, organic synthesis, polymer chemistry, and in industrial applications such as oil and gas, fine chemicals and pharmaceuticals.

专利号:US-4256649-A
优先权日:1977-10-20
标 题:Synthesis of olefinic oxides from olefin and oxygen
发明人:DYER PAUL N
权利人:AIR PROD & CHEM
摘要:Propylene oxide and other olefinic oxides are synthesized by reacting an olefin and oxygen in the presence of a catalytic amount of a complex. The complex is of the type L 2 MX 2 , L 2 M or L 2 MR where M is palladium, X is an acidic anion (preferably chloride); R is an olefinic group (preferably a propylene group) and L 2 consists of two monodentate ligands or a single bidentate ligand. n L 2 : n (a) is resistant to oxidation under the conditions of the process; n (b) is of the type AR 1 R 2 R 3 or R 4 R 5 AR 6 AR 7 R 8 where A is phosphorous or arsenic and R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined herein; n (c) (in the case of a monodentate ligand) has a cone angle not less than 170° when A is phosphorous and has a cone angle not less than 142° when A is arsenic; or n (d) in the case of a bidentate ligand) the monodentate equivalent of each part of the bidentate ligand has a cone angle of not less than 170° when A is phosphorous and of not less than 142° when A is arsenic. n Increased yields of olefinic oxide may be obtained by the introduction of hydrogen.

专利号:WO-2024019972-A1
优先权日:2022-07-18
标 题:A method for the synthesis of tris(ortho-carboranyl)borane
发明人:Martin Caleb; AKRAM MANJUR
权利人:UNIV BAYLOR
摘要:The described process synthesizes a halide-free single-site borane compound product tris( ortho -carboranyl)borane, or B o Cb 3 . B o Cb 3 has Lewis superacid properties. The compounds, B o Cb 3 , are thermally stable, and not reactive towards oxygen, but are sensitive to water. The characteristic high fluoride ion affinity is further translated to the catalytic C-F bond activation reactions of the unactivated alkyl fluorides towards the reduction and C-C bond forming reactions with silanes, and Fridel-Crafts type reactions with arenes. The potential of the synthesized Lewis acid as a catalysis is anticipated.

专利号:US-8231848-B1
优先权日:2012-04-10
标题:One-pot synthesis of chalcopyrite-based semi-conductor nanoparticles
发明人:REN YUHANG; SUN CHIVIN; SHUM KAI
权利人:REN YUHANG; SUN CHIVIN; SHUM KAI; SUN HARMONICS LTD
摘要:Ternary and quaternary Chalcopyrite CuInxGa1-xSySe2-y (CIGS, where 0≰x and y≰1) nanoparticles were synthesized from molecular single source precursors (SSPs) by a one-pot reaction in a high boiling solvent using salt(s) (i.e. NaCl as by-product) as heat transfer agent via conventional convective heating method. The nanoparticles sizes were 1.8 nm to 5.2 nm as reaction temperatures were varied from 150° C. to 190° C. with very high-yield. Tunable nanoparticle size is achieved through manipulation of reaction temperature, reaction time, and precursor concentrations. In addition, the method developed in this study was scalable to achieve ultra-large quantities production of tetragonal and quaternary Chalcopyrite CIGS nanoparticles.
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合成参考文献


摘要:Sumida, Y.; Ohmiya, H., Science of Synthesis Knowledge Updates, (2022) 3, 43.
摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 363.
摘要:Ghosh, B.; Maleczka, R. E., Jr., Science of Synthesis: Catalytic Reduction in Organic Synthesis, (2017) 1, 369.
摘要:Li, X.; Song, Q., Science of Synthesis: Knowledge Updates, (2024) 1, 319.
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