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Triphenylphosphine-catalyzed isomerization of alkynyl ketones in aqueous solution 被引量:1
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作者 Qing Fa Zhou Fei Yang +1 位作者 Qing Xiang Guo Song Xue 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第9期1029-1032,共4页
An efficient isomerization of alkynyl ketones to (E,E)-diene ketones was developed. The reaction catalyzed by 20 mol% triphenylphosphine in aqueous media gave the desired products in good yields.
关键词 triphenylphosphine ISOMERIZATION Alkynyl ketones Water
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An efficient chemoselective synthesis of O-vinylaryl systems using acetylenic esters and dihydroxybenzenes in the presence of triphenylphosphine or alkyl isocyanides 被引量:1
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作者 Robabeh Baharfar Mohammad Javad Taghizadeh +1 位作者 Majid Ahmadian Seyed Meysam Baghbanian 《Chinese Chemical Letters》 SCIE CAS CSCD 2010年第2期175-178,共4页
The addition of 2,4-dihydroxyaceto(and benzo)phenone to propiolic ester is catalyzed by triphenylphosphine or tert-butyl isocyanide to form O-vinyl aryl derivatives in fairly good yields.
关键词 2 4-Dihydroxyaceto(and benzo)phenone triphenylphosphine Propiolic ester tert-Butyl isocyanide
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Synthesis,Structural Characterization and Catalytic Activity of Copper(Ⅰ)Complexes with Triphenylphosphine and Pyridine Derivatives 被引量:2
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作者 刘桂艳 徐颖 刘成鑫 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2016年第5期740-746,共7页
Two new Cu(Ⅰ) complexes [CuCl(3-PyOH)(PPh_3)_2](1) and [Cu_2(μ-Cl)_2(4-Stpy)(Ph_3P)_3](2)(PyOH = hydroxypyridine; stpy = styrylpyridine) with triphenylphosphine and pyridine derivatives have been s... Two new Cu(Ⅰ) complexes [CuCl(3-PyOH)(PPh_3)_2](1) and [Cu_2(μ-Cl)_2(4-Stpy)(Ph_3P)_3](2)(PyOH = hydroxypyridine; stpy = styrylpyridine) with triphenylphosphine and pyridine derivatives have been synthesized and characterized by elemental analysis and X-ray single-crystal diffraction. Compound 1 crystallizes in monoclinic, space group P2_1/c with a = 9.8945(7), b = 37.266(2), c = 10.9461(7) A, β = 116.0750(10)°, V = 3625.3(4) A^3, Z = 4, D_c = 1.350 Mg/cm^(-3), μ = 0.801 mm^(-1), F(000) = 1528, the final R = 0.0320 and w R = 0.0729 for 18568 observed reflections(I 〉 2σ(I)), R(all data) = 0.0413, wR(all data) = 0.0769, completeness to theta of 25.01 is 99.9% and GOF = 1.037. Compound 2 crystallizes in monoclinic, space group P2_1/c with a = 11.290(3), b = 20.388(5), c = 24.092(6) A, β = 102.028(4)°, V = 5424(2) A^3, Z = 4, D_c = 1.428 Mg/cm^(-3), μ = 1.016 mm^(-1), F(000) = 2408, the final R = 0.0568 and w R = 0.1486 for 27644 observed reflections(I 〉 2σ(I)), R(all data) = 0.0716, wR(all data) = 0.1592, completeness to theta of 25.01 is 99.9% and GOF = 1.056. Two new Cu(I) complexes have been utilized as catalysts for N-arylation of imidazole and both showed good catalytic activity. 展开更多
关键词 copper(I) complex triphenylphosphine pyridine derivatives N-arylation imidazole
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Triphenylphosphine Stabilized Silver Carboxylates
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作者 JianLinHAN YingZhongSHEN YiPAN 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第4期443-444,共2页
A series of novel triphenylphosphine stabilized silver carboxylates, potential precursors for CVD growth of ultrafast interconnection link in microelectronic devices, have been prepared and characterized.
关键词 CVD precursor INTERCONNECT triphenylphosphine silver carboxylate.
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Synthesis and Structural Characterization of a New One-dimensional Infinite Chain of Silver(I) Complex with Triphenylphosphine
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作者 LIUBing ZHOUGuo-Wei +3 位作者 FUMing-Lai CAILi-Zhen GUOGuo-Cong HUANGJin-Shun 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2004年第6期547-550,共4页
The reaction of triphenylphosphine with AgNO3 yielded an unusual nitrate anion bridging one-dimensional infinite chain [Ag(PPh3)NO3] in which the silver(I) atom is three-coordinated by one P atom of triphenylphosphine... The reaction of triphenylphosphine with AgNO3 yielded an unusual nitrate anion bridging one-dimensional infinite chain [Ag(PPh3)NO3] in which the silver(I) atom is three-coordinated by one P atom of triphenylphosphine and two O atoms of two bridging nitrate anions to form a scalene triangle. The complex [Ag(PPh3)NO3] crystallizes in the monoclinic system, space group P21/c with a = 10.281(2), b = 18.596(5), c = 9.180(2) , = 90.60(1), V = 1755.1(7) 3, Z = 4, Mr = 432.15, Dc = 1.635 g/cm3, F(000) = 864 and = 1.254 mm-1. The final R = 0.0606 and wR = 0.1400 for 2188 observed reflections with I > 2(I) out of 3057 unique ones (Rint = 0.0539). IR and elemental analysis of the complex are characterized. 展开更多
关键词 SILVER triphenylphosphine infinite chain organic hybrid crystal structure
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A NOVEL SYNTHETIC METHOD AND STRUCTURE OF TETRAKIS(BENZOATE)BIS(TRIPHENYLPHOSPHINE OXIDE)DICOPPER(II).OXIDATIVE ADDITION OF DIBENZOYL ON METALLIC COPPER
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作者 Rui Na YANG Bao Yu XUE and Dou Man JIN Henan Institute of Chemistry,Zhengzhou 450003 KOZO KOZAWA and TOKIKO UCHIDA Science University of Tokyo,Noda,Chiba 278,Japan 《Chinese Chemical Letters》 SCIE CAS CSCD 1992年第9期737-740,共4页
Dibenzoyl peroxide undergoes oxidative addition on metallic copper with triphenylphosphine in a mixed solvent(acetone,dichloromethane and trichloromethane),and affords the binuclear copper complex (Cu(C_6H_5COO)_2(OPP... Dibenzoyl peroxide undergoes oxidative addition on metallic copper with triphenylphosphine in a mixed solvent(acetone,dichloromethane and trichloromethane),and affords the binuclear copper complex (Cu(C_6H_5COO)_2(OPPh_3))_2.Crystals are monoclinic,space group A_2/a,with cell parameters,a=24.337(3),b=10.566(1),c=21.579(2),β= 93.18(1)°, V=5540(1)~3,Z=4,R=0.042,and Rw=0.044 for 5872 observed reflections. Each copper ion is coordinated by four bridging benzoato ligands and one triphenylphosphine oxide group to form binuclear complexes. 展开更多
关键词 BENZOATE)BIS A NOVEL SYNTHETIC METHOD AND STRUCTURE OF TETRAKIS OXIDATIVE ADDITION OF DIBENZOYL ON METALLIC COPPER triphenylphosphine OXIDE)DICOPPER II
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Asymmetric Tetrahedral Cadmium Complex:Bis[triphenylphosphine]cadmium(Ⅱ)Diiodide
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作者 Gou Shao-Hua Lu Jian-Ping +1 位作者 Zeng Qin-Dao You Xiao-Zeng(Coordination Chemistry Institute and State Key Laborataory of Coordination Chemistry,Nanjing University, Hanjing 210093)Yu Kai-Bei(Chengdu Center of Analysis and Determination, Academia Sinica,Cheng 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 1996年第4期270-272,共3页
The structure of the title complex, [Cd (PPh_3)_2I_2], was determined by X-ray diffraction with crystallographic data as follows: C_36H_30CdI_2P_2, Mr=890. 75, monoclinic, space group P2_1/a, a=18. 367(3), b=10. 300(3... The structure of the title complex, [Cd (PPh_3)_2I_2], was determined by X-ray diffraction with crystallographic data as follows: C_36H_30CdI_2P_2, Mr=890. 75, monoclinic, space group P2_1/a, a=18. 367(3), b=10. 300(3), c=19.339 (3) A, β=111. 68(1)°; V=3400(1) A ̄3, Z=4, D_x= 1. 74 g/cm ̄3, P=25. 5 cm ̄(-1),F(000)=1720, R=0. 0470, R_w=0. 049. The coordination polyhedron of each Cd atom is a distorted tetrahedron consisting of two P atoms from two triphenylphosphine groups and two iodine anions. The molecule has no C_2 symmetry with two unequal Cd -P bonds due to the presence of the bulky size of triphosphine. 展开更多
关键词 crystal structure Cd(Ⅱ) complex triphenylphosphine
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Triphenylphosphine and sodium iodide: a new catalyst combination to rival precious metal complexes in visible light photoredox catalysis 被引量:3
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作者 Adam Noble Varinder K.Aggarwal 《Science China Chemistry》 SCIE EI CAS CSCD 2019年第9期1083-1084,共2页
Photoredox catalysis has changed the landscape of modern synthetic organic chemistry by prompting a dramatic increase in research activity into reactions that proceed through free radical intermediates.
关键词 triphenylphosphine sodium IODIDE VISIBLE light PHOTOREDOX CATALYSIS
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Phase separation morphology and mode II interlaminar fracture toughness of bismaleimide laminates toughened by thermoplastics with triphenylphosphine oxide group 被引量:3
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作者 SUN ShuJun GUO MiaoCai +1 位作者 YI XiaoSu ZHANG ZuoGuang 《Science China(Technological Sciences)》 SCIE EI CAS CSCD 2017年第3期444-451,共8页
Toughness improvement of bismaleimide(BMI)resin is very important for its application in composite materials.Blending with
关键词 THERMOPLASTIC phase separation BLENDS triphenylphosphine oxide BISMALEIMIDE ex-situ toughening interlaminar fracture toughness
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An effcient,rapid and facile procedure for conversion of aldoximes to nitriles using triphenylphosphine and N-halo sulfonamides 被引量:3
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作者 Ramin Ghorbani-Vaghei Lotf Shiri Arash Ghorbani-Choghamarani 《Chinese Chemical Letters》 SCIE CAS CSCD 2013年第12期1123-1126,共4页
N,N,N',N'-Tetrabromobenzene-1,3-disulfonamide (TBBDA)/triphenylphosphine and N,N,N',N'-tetra- chlorobenzene-1,3-disulfonamide (TCBDA)/triphenylphosphine have been introduced as highly efficient systems for the... N,N,N',N'-Tetrabromobenzene-1,3-disulfonamide (TBBDA)/triphenylphosphine and N,N,N',N'-tetra- chlorobenzene-1,3-disulfonamide (TCBDA)/triphenylphosphine have been introduced as highly efficient systems for the versatile conversion of aldoxime derivatives into nitriles. The process reported here is operationally simple and reactions have been mildly performed in dichloromethane at room temperature. 展开更多
关键词 Aldoxime Nitrile N N N' N'-Tetrabromobenzene-1 3- disulfonamide N N N' N'-Tetrachlorobenzene-1 3- disulfonamide triphenylphosphine (PPh3)
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STUDIES ON THE EXTRACTION MECHANISM OF GOLD (Ⅲ) FROM HYDROCHLORIC ACID MEDIUM BY TRIPHENYLPHOSPHINE OXIDE (TPPO) 被引量:3
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作者 龚钰秋 夏世华 杨健 《Chinese Science Bulletin》 SCIE EI CAS 1986年第16期1112-1116,共5页
In studies on the extraction chemistry of gold, the extractants of alcohols, ethers, ketones and amines are widely used. The neutral extractants tributylphosphate (TBP) and trioctylphosphine oxide (TPPO) have been wid... In studies on the extraction chemistry of gold, the extractants of alcohols, ethers, ketones and amines are widely used. The neutral extractants tributylphosphate (TBP) and trioctylphosphine oxide (TPPO) have been widely applied. A few experiments on the synthesis of solid complexes of transition metal ions with TPPO have been car- 展开更多
关键词 STUDIES ON THE EXTRACTION MECHANISM OF GOLD TPPO FROM HYDROCHLORIC ACID MEDIUM BY triphenylphosphine OXIDE
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Triphenylphosphine-Catalyzed Michael Addition of Alcohols to Acrylic Compounds 被引量:1
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作者 刘海灵 江焕峰 王玉刚 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2007年第7期1023-1026,共4页
A facile triphenylphosphine-catalyzed Michael addition of alcohols to acrylic compounds was described. The reaction was carried out in open air at refluxing temperature in the presence of 10 mol% PPh3. Michael additio... A facile triphenylphosphine-catalyzed Michael addition of alcohols to acrylic compounds was described. The reaction was carried out in open air at refluxing temperature in the presence of 10 mol% PPh3. Michael addition of saturated and unsaturated alcohols to acrylonitrile or acrylates has been examined. The reaction gave β-alkoxy derivatives with isolated yields of 5%-79%. PPh3 is cheaper and more stable than those trialkylphosphines previously used for the similar reactions, and the products can be easily separated from the reaction mixture via distillation. 展开更多
关键词 Michael addition triphenylphosphine ORGANOCATALYSIS alcohol acrylic compound
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Triphenylphosphine as Reducing Agent for Copper(II)-catalyzed AGET ATRP 被引量:1
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作者 柏良久 Wen-xiang Wang +2 位作者 Ming-hua Wang Jin-ming Sun 陈厚 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2015年第9期1260-1270,共11页
Triphenylphosphine (TPP) was used as reducing agent to continuously generate the Cu(I) activator in copper(II)- catalyzed activators generated by electron transfer atom transfer radical polymerization (AGET ATR... Triphenylphosphine (TPP) was used as reducing agent to continuously generate the Cu(I) activator in copper(II)- catalyzed activators generated by electron transfer atom transfer radical polymerization (AGET ATRP). For example, the polymers prepared with a molar ratio of [MMA]0/[EBiB]0/[CuC12]o/[PMDETA]0/[TPP]o = 500/1/0.1/0.5/0.5 had controlled molecular weights and low molecular weight distribution (Mw/Mn) values (-1.2). TPP as a commercial reducing agent provides a convenient copper-catalyzed AGET ATRP procedure for the preparation of well-defined polymers. 展开更多
关键词 ATRP AGET ATRP Reducing agent triphenylphosphine (TPP).
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Three-component reaction of triphenylphosphine,dialkyl but-2-ynedioate and arylidene pivaloylacetonitrile for diastereoselective synthesis of densely substituted 2,3-dihydrofurans
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作者 Wen-Jie Qi Ying Han +1 位作者 Chang-Zhou Liu Chao-Guo Yan 《Chinese Chemical Letters》 SCIE CAS CSCD 2017年第2期442-445,共4页
The three-component reaction of triphenylphosphine,dialkyl but-2-ynedioate and arylidene pivaloylacetonitrile in dry methylene dichloride at room temperature resulted in unexpected densely substituted 1-(triphenyl-λ... The three-component reaction of triphenylphosphine,dialkyl but-2-ynedioate and arylidene pivaloylacetonitrile in dry methylene dichloride at room temperature resulted in unexpected densely substituted 1-(triphenyl-λ^5-phosphanylidene)ethyl)-2,3-dihydrofurans in satisfactory yields with high diastereoselectivity.The relative configuration of the 2,3-dihydrofurans was elucidated by determination of single crystal structures. 展开更多
关键词 Multicomponent reaction triphenylphosphine But-2-ynedioate Pivaloylacetonitrile 2 3-Dihydrofuran
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Enhancing the activity,selectivity,and recyclability of Rh/PPh_(3) system‐catalyzed hydroformylation reactions through the development of a PPh_(3)‐derived quasi‐porous organic cage as a ligand 被引量:4
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作者 Wenlong Wang Cunyao Li +7 位作者 Heng Zhang Jiangwei Zhang Lanlu Lu Zheng Jiang Lifeng Cui Hongguang Liu Li Yan Yunjie Ding 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2021年第7期1216-1226,共11页
In contrast to heterogeneous network frameworks(e.g.,covalent organic frameworks and metal‐organic frameworks)and porous organic polymers,porous organic cages(POCs)are soluble molecules in common organic solvents tha... In contrast to heterogeneous network frameworks(e.g.,covalent organic frameworks and metal‐organic frameworks)and porous organic polymers,porous organic cages(POCs)are soluble molecules in common organic solvents that provide significant potential for homogeneous catalysis.Herein,we report a triphenylphosphine‐derived quasi‐porous organic cage(denoted as POC‐DICP)as an efficient organic molecular cage ligand for Rh/PPh_(3) system‐catalyzed homogeneous hydroformylation reactions.POC‐DICP not only displays enhanced hydroformylation selectivity(aldehyde selectivity as high as 97%and a linear‐to‐branch ratio as high as 1.89)but can also be recovered and reused via a simple precipitation method in homogeneous reaction systems.We speculate that the reason for the high activity and good selectivity is the favorable geometry(cone angle=123.88°)and electronic effect(P site is relatively electron‐deficient)of POC‐DICP,which were also demonstrated by density functional theory calculations and X‐ray absorption fine‐structure characterization. 展开更多
关键词 HYDROFORMYLATION triphenylphosphine Porous organic cages Chemical selectivity Linear‐regioselectivity
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Effect of loading on the Ni_2P/Al_2O_3 catalysts for the hydrotreating reactions 被引量:4
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作者 Junen Wang Shaozhong Li +3 位作者 Jun Xu Hui Chen Jiangyu Yuan Jianyi Shen 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2015年第4期441-447,共7页
The 80%Ni2P/Al2O3 catalysts were prepared by the phosphidation of corresponding 80%Ni/Al2O3 with triphenylphosphine in liquid phase and compared with the 60%Ni2P/Al2O3 for hydrotreating reactions. Both the60%Ni2P/Al2O... The 80%Ni2P/Al2O3 catalysts were prepared by the phosphidation of corresponding 80%Ni/Al2O3 with triphenylphosphine in liquid phase and compared with the 60%Ni2P/Al2O3 for hydrotreating reactions. Both the60%Ni2P/Al2O3 and 80%Ni2P/Al2O3 in comparison exhibited the small and uniform Ni2 P particles(6.3 and8.4 nm,respectively),high CO uptakes(305 and 345 μmol/g,respectively) and thus high activities for the hydrotreating reactions. After the hydrotreating reactions,the small and uniform Ni2 P particles were remained,although the CO uptakes on the used 60%Ni2P/Al2O3 and 80%Ni2P/Al2O3 were greatly decreased(to 68 and95 μmol/g,respectively) due to the incorporation of S into the Ni2 P surfaces. The 80%Ni2P/Al2O3 was found to be significantly more active than the 60%Ni2P/Al2O3 due to that the 80%Ni2P/Al2O3 possessed more,and more active Ni2 P sites than the 60%Ni2P/Al2O3,probably due to the less S incorporated in the 80%Ni2P/Al2O3 than in the 60%Ni2P/Al2O3 during the hydrotreating reactions. 展开更多
关键词 Supported Ni2P Liquid phase phosphidation triphenylphosphine Microcalorimetric adsorption of CO Hydrotreating reactions
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Optimization of MgO/Al_2O_3 ratio for the maximization of active site densities in the Ni_2P/MgAlO catalysts for the hydrotreating reactions 被引量:3
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作者 Junen Wang Xiaogan Wang +2 位作者 Yamei Yuan Abdalla Shuaib Jianyi Shen 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2016年第4期571-576,共6页
The Ni2P/MgAlO catalysts with different MgO/Al2O3 ratios were prepared by the phosphidation of corresponding Ni/MgAlO catalysts with triphenylphosphine in liquid phase. It was found that the MgO/Al2O3 ratio affected t... The Ni2P/MgAlO catalysts with different MgO/Al2O3 ratios were prepared by the phosphidation of corresponding Ni/MgAlO catalysts with triphenylphosphine in liquid phase. It was found that the MgO/Al2O3 ratio affected the Ni2P/MgAlO catalysts significantly. The Ni2P/MgAlO catalyst with the MgO/Al2O3 ratio of 3 (w/w) exhibited the highly dispersed Ni2P particles (similar to 9 nm) with the highest CO uptake (344 mu mol/g) and thus the highest activities for the hydrotreating reactions. However, based on the CO uptakes on the used catalysts, the TOF values for the hydrodesulphurization of dibenzothiophene as well as those for the hydrogenation of tetralin on all the Ni2P/MgAlO catalysts were respectively similar, indicating that the MgO/Al2O3 ratio did not affect the intrinsic activities of Ni2P supported on the MgAlO support for the hydrotreating reactions. (C) 2016 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved. 展开更多
关键词 Supported Ni2P Liquid phase phosphidation triphenylphosphine Microcalorimetric adsorption of CO Hydrotreating reactions
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(31)~P NMR and ESI-MS Studies on Some Intermediates of the Peptide Coupling Reagents Triphenyl-chlorophosphoranes 被引量:1
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作者 GuoTANG GuiJiZHOU +1 位作者 FengNI LiMingHU 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第3期385-388,共4页
The intermediates of the Appel coupling reagents were studied in acetonitrile, dimethoxyethane and dioxane by P NMR, C NMR spectrum and ESI-MS. In dioxane a new high 31 13 coordinated phosphorous compound with P NMR s... The intermediates of the Appel coupling reagents were studied in acetonitrile, dimethoxyethane and dioxane by P NMR, C NMR spectrum and ESI-MS. In dioxane a new high 31 13 coordinated phosphorous compound with P NMR shift at -39 ppm was observed. The ESI-MS 31 showed that it could be a penta-coordinated phosphorous compound containing dioxane. The carboxyl activated intermediates were also studied in three solvents. 展开更多
关键词 triphenylphosphine HEXACHLOROETHANE (31)~PNMR ESI-MS penta-coordinated phosphorous compound.
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Synthesis and Crystal Structure of 2-(4’-Methylphenoxy)-5,8,9-trimethyl-3-phenyl Thieno[3′,2′:5,6]pyrido[4,3-d]pyrimidin-4-(3H)-one Hydrochloride 被引量:1
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作者 LIU Jian-Chao HE Hong-Wu DING Ming-Wu 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2006年第5期577-581,共5页
The title compound 2-(4'-methylphenoxy)-5,8,9-trimethyl-3-phenyl thieno[3',2':5,6] pyrido[4,3-d]pyrimidin-4(3H)-one hydrochloride (C26H23Cl4N3O2S, Mr = 583.33) has been determined by single-crystal X-ray dif... The title compound 2-(4'-methylphenoxy)-5,8,9-trimethyl-3-phenyl thieno[3',2':5,6] pyrido[4,3-d]pyrimidin-4(3H)-one hydrochloride (C26H23Cl4N3O2S, Mr = 583.33) has been determined by single-crystal X-ray diffraction. The crystal belongs to monoclinic, space group P21/c with a = 14.8442( 11 ), b = 11.5131 (8), c = 17.2010(13) A, β = 113.7250(10)°, V = 2691.3(3) ,A^3, Z = 4, Dc = 1.440 g/cm^3, S = 1.094,μ = 0.547 mm^-1, F(000) = 1200, the final R = 0.0571 and wR = 0.1458. X-ray analysis reveals that the title compound combines with a molecule of dichloromethane by an intramolecular hydrogen bond. The thienopyridine ring is almost coplanar, and the dihedral angle between the thiophene plane and the pyridine plane is 0.6°. 展开更多
关键词 thieno[3' 2':5 6]pyrido[4 3-d]pyrimidin-4(3H)-one triphenylphosphine IMINOPHOSPHORANE crystal structure
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Synthesis and Structural Characterization of Organophosphorus Ylide-1-(3-nitrophenyl)-2-(triphenyl phosphoranylidene)ethanone 被引量:1
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作者 ALIREZA Dadrass ALI Ramazani +6 位作者 AHMAD Poursattar Marjani HOJJATOLLAH Rahchamani HASSAN Nasri Koureh ALI Souldozi SEPIDEH Samiee KATARZYNA lepokura TADEUSZ Lis 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2015年第3期373-378,共6页
The title compound Ph3P=C(H)C(O)PhNO2 (L) has been prepared by the addition of triphenylphosphine in acetone as solvent to 2-bromo-1-(3,nitrophenyl)ethanone followed by the addition of alkaline solution of sod... The title compound Ph3P=C(H)C(O)PhNO2 (L) has been prepared by the addition of triphenylphosphine in acetone as solvent to 2-bromo-1-(3,nitrophenyl)ethanone followed by the addition of alkaline solution of sodium hydroxide. The yellow crystals of the title ylide were grown in methanol/chloroform solution by drop method without stirring at room temperature. The solid state structure of ylide has been established by X-ray crystallography analysis. In the molecule of the title compound, the geometry around the P atom is nearly tetrahedral and the O atom is in synperiplanar orientation to the P atom. The nitrophenyl ring is twisted with respect to the plane of the carbonyl group through an angle of 36.6(1)°. The crystal (C26H20NO3P, Mr = 425.40) belongs to the monoclinic system, space group P21/n with a = 10.889(3), b = 14.467(3), e = 13.872(4)A, β = 103.08(3)°, V = 2128.6(10) A3, Z= 4, T= 100(2) K, R = 0.059 and wR = 0.163 for 3984 observed reflections with I〉 2σ(I). 展开更多
关键词 crystal structure phosphorus yUde 2-bromo-1-(3-nitrophenyl)ethanone triphenylphosphine
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