共查询到19条相似文献,搜索用时 149 毫秒
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探索了以苯胺和对硝基氯苯为原料合成4,4′-二氨基二苯胺(3)的最佳反应条件,重要中间体和目标产物经元素分析和IR表征。3是合成苯胺低聚体或共聚物的最基本原料。 相似文献
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以苯胺为原料,经重氮化、偶合、还原得到4-羟基-5-乙氧基苯胺。合成中,通过保险粉还原偶氮化合物的方法在芳香环上引进氨基,不仅产物收率高(总收率86%,较文献提高了26.3%),而且还原产物容易分离,粗品纯度可达95%。本合成路线中间体均不经提纯,且氨基的引入中避免了贵金属的加氢还原,是一条适合大规模生产4-羟基-5-乙氧基苯胺的新合成工艺路线。 相似文献
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以2,2’-联吡啶膦盐为吸电子基团,4-咔唑苯甲醛为供电子基团,经无溶剂Wittig反应,合成了一种新型的含顺式π共轭结构联吡啶——顺-6-苯基-4’-{4-[4-(1H-咔唑)乙烯基]苯基}-2,2’-联吡啶(3),其结构经IR,1H NMR,ESI-MS,元素分析及X-ray单晶衍射表征。3属三斜晶系,空间群Pī,晶胞参数a=9.533(5),b=12.352(5),c=13.446,α=91.483(5)°,β=14.221(5)°,γ=9.483°,V=1 534(1)3,Z=2,Dc=1.246 g·cm-3,R1=0.0673,ωR2=0.179 5。并利用UV-Vis和单光子荧光光谱研究了3的光学性能。结果表明,3的λmax位于289 nm和345 nm;在苯,二氯甲烷,乙醇和DMF中的λem分别位于418 nm,449 nm,456 nm和466 nm。 相似文献
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1,4-双{2-[4-[2-苯并恶唑)苯基]乙烯基}苯及衍生物的合成 总被引:4,自引:0,他引:4
通过Wittig-Horner反应,以对苯二甲醛和2—(4-氯甲基苯基)苯并恶唑为主要 原料,合成了八个新型1,4-双{2-[4-(2—苯并恶唑)苯基]乙烯基}苯及衍生物.通 过IR,^1H NMR,UV-vis和元素分析等方法确认了它们的化学结构,分析数据表明各 标题化合物分子结构中的C=C双键均为反式结构特. 相似文献
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A novel fluorene derivative containing triphenylamine groups, 2,7-bis[4-(diphenylamino)-phenyl]fluorene (C49H36N2 , Mr= 652.80), was synthesized via Suzuki coupling reaction (yield: 19%) and its crystal structure was determined by single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1 with a = 9.320(4), b = 11.250(6), c = 17.369(6) , α = 88.035(3), β = 86.450(5), γ = 73.524(5)°, V = 1742.8(13) 3 , Z = 2, Dc = 1.244 g/cm 3 , μ(MoKα) = 0.072 mm -1 , F(000) = 688, S = 1.095, the final R = 0.0616 and wR = 0.1878. It presents a linear framework constituted by a linkage of fluorene as a bridge and two triphenylamine groups. Its spectral and electrochemical properties were studied by UV-Vis absorption, fluorescence spectroscopy and cyclic voltammetry (CV). This compound can emit intense blue fluorescence with a peak wavelength of 446 nm and a full width at half maximum (FWHM) of 38 nm under UV excitation at 350 nm in film. The highest occupied molecular orbital (HOMO) energy level, the lowest unoccupied molecular orbital (LUMO) energy level and optical band gap (Eg) of the title compound are -5.46, -2.57 and 2.89 eV, respectively. 相似文献
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In this study, 3-(4-{3-[3-(dimethylamino)phenoxy]propoxy}phenyl)propan-1-ol, 3-(4-{3-[3-(diethylamino)phenoxy]propoxy}phenyl)propan-1-ol and axially disubstituted silicon naphthalocyanines (SiNc) bearing electropolymerizable bis-[(4-{3-[3-(dimethylamino)phenoxy]propoxy}phenyl)propanoxy] and bis-[(4-{3-[3-(diethylamino)phenoxy]propoxy}phenyl)propanoxy] units were synthesized for the first time. Aggregation behavior of SiNcs was examined in different solvents and concentrations in DMSO. In all solvents and concentrations, SiNcs were non-aggregated. Also, electrochemical studies of SiNcs were investigated by cyclic and square wave voltammetry. While SiNcs gave only naphthalocyanine-based reduction process during the cathodic potential scans, they were electropolymerized on the working electrode during the anodic potential scan because of the oxidative electropolymerization of (4-{3-[3-(dimethylamino)phenoxy]propoxy}phenyl)propanoxy and (4-{3-[3-(diethylamino)phenoxy]propoxy}phenyl)propanoxy groups on the substituents of the complexes. 相似文献
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叔丁基[1-(对溴苯基)环丁基]氨基甲酸酯与N-甲基-N-甲氧基-苄酰胺在正丁基锂的作用下,经Weinreb酮合成法合成了抗癌药物二氮杂萘衍生物的关键中间体——叔丁基{1-[(对苯乙酰基)苯基]环丁基}氨基甲酸酯,收率33%,其结构经1H NMR确证。 相似文献
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