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硫脲型有机催化剂在Schiff碱合成反应中的应用 被引量:3
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作者 马润霞 王小平 《广东化工》 CAS 2016年第4期77-78,共2页
硫脲型催化剂可促进席夫碱合成反应的有效进行,并且硫脲型催化剂毒性较低甚至无毒,符合绿色化学的发展要求。因此,硫脲型催化剂在Schiff碱合成反应中有着十分重要的作用。文章介绍了硫脲型有机催化剂和Schiff碱合成反应及其应用,并展望... 硫脲型催化剂可促进席夫碱合成反应的有效进行,并且硫脲型催化剂毒性较低甚至无毒,符合绿色化学的发展要求。因此,硫脲型催化剂在Schiff碱合成反应中有着十分重要的作用。文章介绍了硫脲型有机催化剂和Schiff碱合成反应及其应用,并展望了其应用前景。 展开更多
关键词 硫脲 有机催化剂 schiff合成 应用
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煤基固体酸催化合成席夫碱反应 被引量:1
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作者 吴之强 徐泽杨 +3 位作者 毕淑娴 詹海鹃 马保军 刘万毅 《应用化学》 CSCD 北大核心 2017年第5期563-571,共9页
以煤基活性炭(AC)和苯胺(ANI)为原料,通过原位-溶液聚合法制备了煤基固体酸催化剂AC@PANI-SO_3H(APS),利用扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)、X射线光电子能谱(XPS)和热重分析(TG)等技术手段对催化剂进行了结构和性能的... 以煤基活性炭(AC)和苯胺(ANI)为原料,通过原位-溶液聚合法制备了煤基固体酸催化剂AC@PANI-SO_3H(APS),利用扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)、X射线光电子能谱(XPS)和热重分析(TG)等技术手段对催化剂进行了结构和性能的表征。研究了该催化剂在微波辐射下催化合成Schiff碱化合物的活性,并对其催化工艺条件进行了优化考察。结果表明,催化剂用量5%(以每摩尔邻苯二胺用量为基准),反应时间3~20 min,溶剂选用乙醇(Et OH),Schiff碱化合物产率可达80%~93%,说明该催化剂在微波催化合成席夫碱反应中变现出良好的催化活性,反应时间短,工艺简单操作,且催化剂能重复使用5次。通过红外发现,催化剂重复5次后活性下降的主要原因是固体酸表面键合的磺酸基官能团消失,从而导致活性降低。 展开更多
关键词 固体酸 schiff合成 微波辐射 工艺优化
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STUDIES ON SCHIFF BASE COMPLEXES——Ⅳ. SYNTHESIS AND CRYSTAL STRUCTURE OF Fe (SALDPT) SAL
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作者 汪信 William T.Pennington James C.Fanning 《无机化学学报》 SCIE CAS CSCD 北大核心 1989年第3期46-53,共8页
制备了Fe(saldpt)sal单晶并作了晶体结构分析。晶体数据:单斜,空间群P2_1/C(#14),a=12.486(5),b=18.502(8),c=10.870(5)A,β=104.23(3)°,V=2434(2)A^3,Z=4,D_c=1.
关键词 铁配合物 schiff合成 晶体结构
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2-乙酰吡啶缩羟乙基乙二胺锌配合物的合成及晶体结构研究
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作者 郭亚宁 《宝鸡文理学院学报(自然科学版)》 CAS 2011年第3期41-44,共4页
目的合成一种新Schiff碱锌配合物。方法以2-乙酰吡啶,羟乙基乙二胺和金属Zn(II)离子为原料合成一种新的Schiff碱金属锌配合物,用X-射线单晶衍射法对其结构进行表征。结果标题化合物属于三斜晶系,空间群P1,晶胞参数a=0.814 3(10)nm,b=0.9... 目的合成一种新Schiff碱锌配合物。方法以2-乙酰吡啶,羟乙基乙二胺和金属Zn(II)离子为原料合成一种新的Schiff碱金属锌配合物,用X-射线单晶衍射法对其结构进行表征。结果标题化合物属于三斜晶系,空间群P1,晶胞参数a=0.814 3(10)nm,b=0.917 91(12)nm,c=1.267 69(14)nm,α=74.256 0(10)°,β=75.117(2)°,γ=71.838 0(10)°,V=0.851 0(18)nm3,Dc=1.517 g/cm3,Z=2,μ=1.695 mm-1,F(000)=400,R=0.030 9,wR=0.069 4。结论该化合物结构中锌原子分别与5个N原子配位,呈正方锥体构型。化合物分子通过N1-H1…O1和O1-H1A…S1分子间氢键及π…π堆积作用自组装成二维网络结构。这些分子间作用力对晶体的组成、稳定性及结晶起了重要的作用。其结果为进一步研究该类化合物的结构及结构与性质等方面的关系提供基础数据。 展开更多
关键词 schiff碱锌配合物合成 2-乙酰吡啶 晶体结构
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Synthesis of Schiff bases of naphtha[1,2-d]thiazol-2-amine and metal complexes of 2-(2'-hydroxy)benzylideneaminonaphthothiazole as potential antimicrobial agents 被引量:4
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作者 AZAM Faizul SINGH Satendra +1 位作者 KHOKHRA Sukhbir Lal PRAKASH Om 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2007年第6期446-452,共7页
Objective: A series of 2-benzylideneaminonaphthothiazoles were designed and synthesized incorporating the lipophilic naphthalene ring to render them more capable of penetrating various biomembranes. Methods: Schiff ... Objective: A series of 2-benzylideneaminonaphthothiazoles were designed and synthesized incorporating the lipophilic naphthalene ring to render them more capable of penetrating various biomembranes. Methods: Schiff bases were synthesized by the reaction of naphtha[1,2-d]thiazol-2-amine with various substituted aromatic aldehydes. 2-(2'-Hydroxy)ben- zylideneaminonaphthothiazole was converted to its Co(Ⅱ), Ni(Ⅱ) and Cu(Ⅱ) metal complexes upon treatment with metal salts in ethanol. All the compounds were evaluated for their antibacterial activities by paper disc diffusion method with Gram positive Staphylococcus aureus and Staphylococcus epidermidis and Gram negative Escherichia coli and Pseudomonas aeruginosa bacteria. The minimum inhibitory concentrations of all the Schiff bases and metal complexes were determined by agar streak dilution method. Results: All the compounds moderately inhibited the growth of Cram positive and Gram negative bacteria. In the present study among all Schiff bases 2-(2'-hydroxy)benzylideneaminonaphthothiazole showed maximum inhibitory activity and among metal complexes Cu(Ⅱ) metal complex was found to be most potent. Conclusion: The results obtained validate the hypothesis that Schiff bases having substitution with halogens, hydroxyl group and nitro group at phenyl ring are required for the antibacterial activity while methoxy group at different positions in the aromatic ring has minimal role in the inhibitory activity. The results also indicated that the metal complexes are better antibacterial agents as compared to the Schiff bases. 展开更多
关键词 schiff bases Metal complexes ANTIMICROBIAL
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Synthesis and Structure of Chromium Complexes with New Tetradentate Schiff Base N202-Type Ligand
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《Journal of Chemistry and Chemical Engineering》 2012年第3期259-262,共4页
In this research two chromium(II][) and (VI) complexes of tetradentate Schiff bases have been prepared by condensing of salicylaldehyde with 4-methyl 1,2-phenylenediamine. Schiff base complexes of chromium(Ill) ... In this research two chromium(II][) and (VI) complexes of tetradentate Schiff bases have been prepared by condensing of salicylaldehyde with 4-methyl 1,2-phenylenediamine. Schiff base complexes of chromium(Ill) have been employed to design and synthesize polynuclear complexes. So they have played an important role in molecular magnetism. Synthesized complexes were characterized by elemental analysis, IR, molar conductivity and NMR. The free ligands were alsc characterized by 1H, 13C NMR spectra. The 13C NMR and IR spectra of free ligand and the complexes are compared and discussed. 展开更多
关键词 Tetradentate schiffbase chromium(VI) SALICYLALDEHYDE 4-methyl 1 2-phenylene diamine.
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Cyanide-bridged complexes based on dinuclear Cu(Ⅱ)-M(Ⅱ) [M=Pb and Cu] building blocks: Synthesis, crystal structures and magnetic properties 被引量:3
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作者 WANG HaiLong WANG Kang +3 位作者 CAO Wei BAI Ming BIANYongZhong JIANG JianZhuang 《Science China Chemistry》 SCIE EI CAS 2012年第6期978-986,共9页
Four cyanide-bridged heterometallic complexes { [CuPb(L1)][FenI(bpb)(CN)2] }2-(C104)2.2H20.2CH3CN (1), { [CuPb(LI)]2[FeII (CN)6](HzO)z}'10H20 (2), {[Cu2(L2)][Fent(bpb)(CN)2]2}'2H20'2CH3OH (... Four cyanide-bridged heterometallic complexes { [CuPb(L1)][FenI(bpb)(CN)2] }2-(C104)2.2H20.2CH3CN (1), { [CuPb(LI)]2[FeII (CN)6](HzO)z}'10H20 (2), {[Cu2(L2)][Fent(bpb)(CN)2]2}'2H20'2CH3OH (3) and {[Cu2(L2)]3[FeIII(CN)6]z(H20)2}-10H20 (4) have been synthesized by treating K[Fem(bpb)(CN)2] [bpb2-=l,2-bis(pyridine-2-carboxamido)benzenate] and K3[Feln(CN)]6 with dinuc[ear compartmental macrocyclic Schiff-base complexes [CuPh(LI)].(C104)2 or [Cu2(L2)]-(CIO4)2, in which H2LJ was derived from 2,6-diformyl-4-methyl-phenol, ethylenediamine, and diethylenetriamine in the molar ratio of 2:1:1 and H2L2 from 2,6-diformyl-4-methyl-phenol and propylenediamine in the molar ratio of 1:1. Single crystal X-ray diffraction analysis reveals that compound 1 displays a cyclic hexanuclear heterotrimetallic molecular structure with alternating [Fem(bpb)(CN)2]- and [CuPb(L+)]2+ units. Complex 2 is of a neutral dumb-bell-type pentanuclear molecular configuration consisting of one [Fe(CN)6]4- anion sandwiched in two [CuPu(L1)]2+ cations, and the pentanuclear moieties are further connected by the hydro- gen bonding to give a 2D supramolecular framework. Heterobimetallic complex 3 is a tetranuclear molecule composed of a centrosymmetric [Cuz(L2)]2+ segment and two terminal cyanide-containing blocks [Fetn(bpb)(CN)2]-. Octanuclear compound 4 is built from two [Fe(CN)6]3- anions sandwiched in the three [Cu2L2]2+ cations. Investigation of their magnetic properties reveals the overall antiferromagnetic behavior in the series of complexes except 2. 展开更多
关键词 cyanide-bridged complex crystal structures magnetic properties
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