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卤代芳烃

卤代芳烃的相关文献在1988年到2022年内共计140篇,主要集中在化学、化学工业、环境科学基础理论 等领域,其中期刊论文71篇、会议论文1篇、专利文献46381篇;相关期刊47种,包括商业文化、四川职业技术学院学报、西北师范大学学报(自然科学版)等; 相关会议1种,包括中国化学会第九届全国络合催化学术讨论会等;卤代芳烃的相关文献由376位作者贡献,包括员汝胜、朱本占、毛莉等。

卤代芳烃—发文量

期刊论文>

论文:71 占比:0.15%

会议论文>

论文:1 占比:0.00%

专利文献>

论文:46381 占比:99.85%

总计:46453篇

卤代芳烃—发文趋势图

卤代芳烃

-研究学者

  • 员汝胜
  • 朱本占
  • 毛莉
  • 王乐乐
  • 魏英聪
  • 余训民
  • 李海燕
  • 李红喜
  • 柯方
  • 蔡春
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 符鑫博
    • 摘要: 通过Buchwald-Hartwig偶联反应形成碳氮键是有机合成领域中构建碳氮键的重要方法之一.本文对近几年关于卤代芳烃和胺类化合物的Buchwald-Hartwig偶联反应来构建碳-氮键的报道进行了综述,主要包括氯代芳烃和胺的Buchwald-Hartwig偶联反应、溴代芳烃和胺的Buchwald-Hartwig偶联反应、碘代芳烃和胺的Buchwald-Hartwig偶联反应.
    • 陈宁; 张松林
    • 摘要: 报告了一种通过Cu(Ⅲ)-CF_(3)化合物在无任何额外添加剂的条件下对芳基碘化物(以及其他卤化物)进行常见且简单的三氟甲基化的研究方法,这种方法涉及Cu(Ⅲ)-CF_(3)化合物夺取碘原子的关键步骤。这导致芳基自由基和Cu(Ⅱ)双-CF_(3)中间体的产生,相互反应生成Ar-CF_(3)产物。反应产率普遍在85%~100%和良好的官能团耐受性。其他相关的卤化物,包括杂芳基、苄基、乙烯基和炔丙基卤化物的反应产率也在50%以上。目前Cu(Ⅲ)-CF_(3)化合物夺取碘原子的反应性尚不清楚。
    • 许秀枝; 张帆; 黄胜; 张志强; 柯方
    • 摘要: 通过在可见光下卤代芳烃的羟基化反应合成一系列苯酚类化合物.反应用单质碘作光催化剂,在室温下反应获得较好收率的产物,生成目标产物最高产率可达到92%,该体系对氯代芳烃同样具有较好的催化活性.此方法具有便宜、易处理、对环境无污染的优点,为酚类化合物的合成提供了一种简便经济的方法.运用此策略,以5-乙酰-4-溴-2-甲氧基苄基二异丙基氨基二硫代甲酸酯合成的5-乙酰-4-羟基-2-甲氧基苄基二异丙基氨基二硫代甲酸酯,具有明显的抗增殖作用.
    • 沈棣; 潘国军; 苏超; 芦逵
    • 摘要: 橙酮是植物体内的一种次生代谢产物,属于特殊的黄酮类化合物,具有广泛的生理活性.卤代芳烃类化合物是偶联反应的重要中间体之一,常用于 Suzuki及 Heck等偶联反应.本研究以3种橙酮化合物为原料,探讨橙酮类化合物5位、7位溴代的高效合成方法.%Aurones are secondary metabolites in plants.They are also flavonoids with a wide variety of biological activities.Halogenated aromatic compounds are widely used in Suzuki reaction and Heck reaction as important intermediates.In this research,three kinds of aurone stemnucleuses were taken as starting materials to discuss the efficient synthetic method for the preparation of 5-bromo and 7-bromo aurones.
    • 朱本占; 谢琳娜; 沈忱; 高慧颖; 朱丽雅; 毛莉
    • 摘要: 卤代芳烃是一类在环境中广泛存在的化合物,因其可能导致人体及生态系统的潜在环境风险而被公众日益关注.最近,高级氧化过程作为一种“环境绿色友好”的技术被用于处理和降解这类难降解持久性有机污染物.我们先前意外发现,卤代醌的典型代表物四氯苯醌与过氧化氢反应不仅会生成-OH,还会产生专一依赖于·OH的两次化学发光.进一步研究发现,对产生·OH的高级氧化体系而言,不仅四氯苯醌的前体五氯酚和其他卤代酚能产生化学发光,其余所有经测试的卤代芳烃也能产生化学发光.在此基础上,对19种氯酚同系物产生化学发光的结构-效应关系进行了系统研究,结果发现:氯原子取代数目越多化学发光越强.有趣的是,氯酚的化学发光还与生成的氯代醌中间体以及半醌自由基呈良好相关性.基于上述结果,我们认为反应生成了某种醌中间体以及激发态多羰基产物,正是它们导致了化学发光.进而开发出一种快速灵敏的化学发光分析手段,不仅可检测和定量痕量的卤代芳烃,还可为预测其毒性以及实时监测降解动力学提供有用信息.%The ubiquitous distribution of halogenated aromatic pollutants (XAr)coupled with their carcinogenicity has raised public concerns on their potential risks to both human health and the ecosystem.Recently,advanced oxidation processes (AOPs) have been employed as an "environmental-green" technology for treatment and degradation of such recalcitrant and highly toxic XAr.During our study on the molecular mechanism of metal-independent hydroxyl radicals (ˉOH) production by halogenated quinones and H2O2,we unexpectedly find that an unprecedented ·OH-dependent two-step intrinsic chemiluminescene (CL) can be produced by H2O2 and tetrachloro-p-benzoquinone,which is the major carcinogenic metabolite of the widely-used wood preservative pentachlorophenol.We further find that ˉOH-producing AOPs-mediated degradation of pentachlorophenol and all other XAr could produce intrinsic CL that is directly dependent on the formation of the extremely reactive ·OH.A systematic structure-activity relationship study for all 19 chlorinated phenols demonstrates that the CL increases with an increasing number of chlorine-substitution in general.More interestingly,a relatively good correlation is noticed that not only between CL intensity and chlorinated quinoid intermediates,but also between CL emission and semiquinone radicals.Taken together,we propose that ·OH-dependent formation of quinoid intermediates,quinone-1,2-dioxetane and electronically excited carbonyl species is responsible for this unusual intrinsic CL production.A rapid,sensitive,simple,and effective CL method has been developed to not only detect and measure trace amount of XAr in real environment,but also to provide useful information for predicting the toxicity or monitoring the degradation kinetics of XAr.These findings may have broad chemical,environmental and biological implications for future studies on remediation of other halogenated persistent organic pollutants by AOPs.
    • 王一冰; 郭晓宁; 吕曼乾; 翟兆洋; 王英勇; 郭向云
    • 摘要: 卤代苯与酚类化合物反应制取二芳基醚是现代有机合成中的一个重要反应.传统的二苯醚合成方法是铜催化卤代苯与酚类化合物的Ullmann型C-O偶联反应,但是这种方法需要苛刻的反应条件.后来,人们发现了Pd(0)和Cu(Ⅰ)基催化剂,但是前者成本较高,且需要使用昂贵的配体,因此其应用受到了限制,而铜作为一种成本较低的催化剂受到了越来越多的关注.铜催化剂可以分为均相和非均相两大类.均相铜催化剂使用的是铜盐,并且需要加入配体,成本较高,且不易分离和循环利用.非均相铜催化剂研究较多的是CuO,Cu2O及Cu纳米颗粒,其中Cu2O纳米颗粒催化剂对Ullmann型C-O偶联反应具有很高的催化活性,但是它在潮湿的空气中容易被氧化,因此需要寻找一种合适的载体防止Cu2O纳米颗粒被氧化.SiC具有优良的化学稳定性及导电导热性能,并且作为载体己经成功应用到很多热催化及光催化反应中.本文以高比表面积的SiC为载体,以二乙二醇作为溶剂和还原剂,采用传统的两步液相还原法制备了Cu2O/SiC催化剂,并通过X射线衍射、X射线光电子能谱、扫描电子显微镜(SEM)、透射电子显微镜(TEM)和H2程序升温还原等方法对Cu2O/SiC催化剂进行了表征.SEM和TEM结果表明,Cu2O纳米颗粒均匀分散在SiC表面,同时上述表征结果都表明Cu在SiC上主要以Cu2O的形式存在.将制备的Cu2O/SiC催化剂用于催化卤代芳烃与酚类的Ullmann C-O偶联反应中.以碘苯和苯酚的Ullmann C-O偶联反应为模型实验,考察了反应温度、反应时间、溶剂、碱的种类及用量和催化剂用量等条件的影响,得到了碘苯与苯酚UllmannC-O偶联反应的最优反应条件为:卤代芳烃14 mmol,酚类14 mmol,1.0当量的Cs2CO3,Cu2O/SiC(5 wt%) 10 mg,四氢呋喃10mL,在Ar气氛下150°C反应3h.在该条件下,二苯醚收率达到97%,转化频率(TOF)高达1136 h-1.Cu2O/SiC催化剂对Ullmann C-O偶联反应具有很好的普适性,并且对Ullmann C-S偶联反应也表现出很高的活性,TOF高达1186h-1.以碘苯和苯酚的Ullmann C-O偶联反应为基准实验,对催化剂的循环稳定性进行了考察.Cu2O/SiC催化剂五次循环后二苯醚的收率从97%降低至64%,这主要是由于活性组分Cu2O的流失所致.%A Cu2O/SiC heterogeneous catalyst was prepared via a two-step liquid-phase method using diethylene glycol as both the solvent and the reducing agent.The catalyst was characterized using X-ray diffraction,X-ray photoelectron spectroscopy,scanning electron microscopy (SEM),transmission electron microscopy (TEM),and H2 temperature-programmed reduction.All the results indicate that Cu is present on the SiC support primarily as Cu2O.The SEM and TEM results show that cubic Cu2O nanoparticles are uniformly dispersed on the β-SiC surface.The reaction conditions,namely the temperature,reaction time,and amounts of base and catalyst used,for the Ullmann-type C-Ocross-coupling reaction were optimized.A model reaction was performed using iodobenzene (14.0 mmol) and phenol (14.0 mmol) with Cu2O/SiC (5 wt% Cu) as the catalyst,Cs2CO3 (1.0 equiv.) as the base,and tetrahydrofuran as the solvent at 150 °C for 3 h;a yield of 97% was obtained and the turnover frequency (TOF) was 1136 h-1.The Cu2O/SiC catalyst has a broad substrate scope and can be used in Ullmann-type C-O cross-coupling reactions of aryl halides and phenols bearing a variety of different substituents.The catalyst also showed high activity in the Ullmann-type C-S cross-coupling of thiophenol with iodobenzene and substituted iodobenzenes;a TOF of 1186 h-1 was achieved.The recyclability of the Cu2O/SiC catalyst in the O-arylation of phenol with iodobenzene was investigated under the optimum conditions.The yield decreased from 97% to 64% after five cycles.The main reason for the decrease in the catalyst activity is loss of the active component,i.e.,Cu2O.
    • 杨琴
    • 摘要: C-N偶联反应是合成芳香胺的重要手段,咪唑、脂肪胺和氨常用作该反应的氮源.氨是最简单的氮化合物,应用在该反应中不仅廉价而且更加绿色环保.然而,由于氨结构以及偶联后产物结构使其存在一定的挑战性.各种催化体系的出现实现了以氨为氮源的C-N偶联反应.综述钯和镍在均相、多相体系中催化氨为氮源的C-N偶联合成苯胺类化合物的反应.这类金属催化剂催化活性较高,但存在进一步偶联生成二级胺的问题,且催化剂成本偏高.铜作为廉价金属在C-N偶联反应中的应用一直受到关注,重点介绍各种常见的铜盐、铜纳米材料和负载型铜催化剂等在氨为氮源的C-N偶联反应中的应用.%C-N coupling reaction is an important route for synthesis of aromatic amines.Imidazoles,aliphatic amines and ammonia are usually used as nitrogen sources for the coupling.As the simplest nitrogen compounds,ammonia is of low cost and environmentally-benign for this reaction.But due to the structure of ammonia and the resultant coupling product,using ammonia as nitrogen source is of challenge.Emerging of various catalytic systems makes it feasible C-N coupling reaction using ammonia as nitrogen source.The researches on C-N coupling reaction catalyzed by palladium,nickel and copper in homogeneous and heterogeneous phase,using ammonia as nitrogen source,were reviewed in this paper.These catalytic systems exhibit high catalytic activity,but some systems result in further coupling to form secondary amines byproducts,such as diphenylamines or triphenylamines,and palladium and nickel catalysts are of high cost.As an inexpensive metal,use of copper catalyst in C-N coupling reaction attracts much attention.Application of copper salts,nanoparticle copper and supported copper as the catalysts for C-N reaction using ammonia as nitrogen source was reviewed in detail.
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