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Bis(trifluoromethylsulfonyl)phenylamines as Internal Donors for Ziegler-Natta Polymerization Catalysts 被引量:5
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作者 Li Huashu Yi Jianjun Cui Chunming 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2008年第3期51-54,共4页
Several bis(trifluoromethylsulfonyl)phenylamines have been synthesized and used as internal donors for the preparation of heterogeneous Ziegler-Natta catalysts for propylene polymerization. These new cata- lysts are... Several bis(trifluoromethylsulfonyl)phenylamines have been synthesized and used as internal donors for the preparation of heterogeneous Ziegler-Natta catalysts for propylene polymerization. These new cata- lysts are highly active and stereospecific in combination with an external donor for the polymerization of propylene. The activity of these catalysts is dramatically influenced by the electronic capability of the phenyl substituents on the sulfonyl phenylamines. Therefore, the performances of the catalysts can be modified by adjusting the electronic property of the phenyl substituents of the sulfonyl phenylamines. 展开更多
关键词 Ziegler-Natta catalyst PROPYLENE sulfonyl phenylamines internal electron donor POLYPROPYLENE
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Theoretical Studies on the N-Phenylpyrrolidine Formation Mechanism Based on the Reaction of Phenylamine with 1,4-Butanediol
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作者 罗芳 孙仁安 +3 位作者 许长志 石雷 李春梅 闫杰 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2008年第4期416-420,共5页
The reaction mechanism of phenylamine reacting with 1,4-butanediol to give N- phenylpyrrolidine was investigated with traditional transition state theory. Based on the experimental results, two reaction channels were ... The reaction mechanism of phenylamine reacting with 1,4-butanediol to give N- phenylpyrrolidine was investigated with traditional transition state theory. Based on the experimental results, two reaction channels were discussed. The geometries of their reactants, products, intermediates and transition states were optimized. The possible transition State and activation energy were determined by vibrational analysis and IRC verification. And finally, the main reaction channel was given. 展开更多
关键词 phenylamine 1 4-BUTANEDIOL N-phenylpyrrolidine transition state DFT
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(4-Ferrocenylethyne) phenylamine on Graphene as the Signal Amplificator to Determinate Dopamine and Acetaminophen Simultaneously
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作者 Linping Wang Meiling Liu Yue Meng Haitao Li Youyu Zhang Shouzhuo Yao 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2013年第6期845-854,共10页
A novel (4-ferrocenylethyne) phenylamine functionalized graphene sheets (FEPA-GR), coupling with chitosan (CS) were used as a signal amplification platform for simultaneous and sensitive determination of dopami... A novel (4-ferrocenylethyne) phenylamine functionalized graphene sheets (FEPA-GR), coupling with chitosan (CS) were used as a signal amplification platform for simultaneous and sensitive determination of dopamine (DA) and acetaminophen (AC). In this work, FEPA used as electron transfer mediator can be immobilized on GR surface via strong π-π stacking interaction between the conjugate chain of FEPA and GR, which effectively prevents FEPA electron mediator leaking from the electrode surface and amplified the signal. Transmission electron microscopy, FT-IR spectroscopy, UV-vis spectroscopy and electrochemical experiments results are all demonstrated the strong π-π stacking interaction between FEPA and GR. The resulted biosensor exhibited a fast response, remarkable electrocatalytic activity, perfect anti-interference ability and good stability for simultaneous detection of DA and AC. Under the optimum conditions, the oxidation peak currents of DA and AC were linearly correlated to their concentrations in the range of 2.0-135.0 μmol·L-1 and 0.3--80.0μmol·L 1, respectively. The lower detection limits for DA and AC were 0.30 and 0.05 μmol·L-1, respectively. The feasibility of the proposed method was validated by successfully applied to the simultaneous determination of DA and AC in serum samples with the standard addition method. 展开更多
关键词 simultaneous electrochemical detection (4-ferrocenylethyne) phenylamine π-π stacking
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Generation of halogenated angucyclinones with cytotoxicity activities against human cancer cell lines based on biosynthesis and chemical conversion
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作者 Hua Xiao Guiyang Wang +5 位作者 Mengyuan Li Huichun Zhao Xinyi Qi Jian Huang Donghui Yang Ming Ma 《Chinese Journal of Natural Medicines》 2025年第12期112-121,共10页
Halogen substituents play a crucial role in the structural diversity and biological activity of natural products,and the synthesis of halogenated molecules remains an area of significant research interest.This study d... Halogen substituents play a crucial role in the structural diversity and biological activity of natural products,and the synthesis of halogenated molecules remains an area of significant research interest.This study describes the generation of 15 new halogenated angucyclinones through the incorporation of halogen-containing phenylamines into a biosynthetic C-ringcleaved angucyclinone under mild conditions.The newly synthesized compounds feature halogen substituents encompassing all four halogen atoms(F,Cl,Br,I),with some compounds containing multiple halogen types.Structural elucidation was accomplished through ultraviolet(UV),infrared spectroscopy(IR),mass spectrometry(MS),and nuclear magnetic resonance(NMR)spectroscopic analyses,expanding the structural diversity of angucyclinonetype polyketides.Cytotoxicity evaluations revealed that eight compounds demonstrated moderate cytotoxic activities against four human tumor cell lines,with half maximal inhibitory concentration(IC_(50))values ranging from 3.35±0.37 to 16.02±6.60μmol·L-1.These findings highlight the significant potential of combining biosynthetic and chemical approaches in generating bioactive halogenated molecules. 展开更多
关键词 Angucyclinone CYTOTOXICITY HALOGENATION Nonenzymatic conversion phenylamine
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Preparation of the Heat Resistant Adhesive of NBR Modified BMI 被引量:1
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作者 黄志雄 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2002年第1期69-71,共3页
A Kind of homogeneous resin , which can be used as thermal resistant adhesive and matrix for composite, was prepared by bis (4-maleimidophenyl) methane ( BMI), 4,4’ -diaminodiphenylmethane( DDM), aniline (An), phenol... A Kind of homogeneous resin , which can be used as thermal resistant adhesive and matrix for composite, was prepared by bis (4-maleimidophenyl) methane ( BMI), 4,4’ -diaminodiphenylmethane( DDM), aniline (An), phenol type epoxy resin ( F-51 ) and nitrile -butadiene rubber ( NRR) through solution copolymer-ization . The reaction from prepolymerization to curing of the resin system was studied. And the factors such as raw material ratio and curing temperature, which affect thermal resistance and adhesives of cured product, were also analyzed. SEM and IR spectra were utilized to discuss the mechanisms of toughness and reaction of modified BMI. 展开更多
关键词 ADHESIVE phenylamine phenoltype epoxy resin nitrile-butaiene rubber
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The Reaction of Acenaphthene with Nitrobenzene
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作者 Wu Lin Li Hong +4 位作者 Chen Shao-feng Qin Yi-min Zong Zhi-ming Wei Xian-yong Zou Guo-lin 《Wuhan University Journal of Natural Sciences》 CAS 2002年第2期227-230,共4页
The reaction of acenaphthene with nitrobenzene was investigated in the presence of AlCl3. The results showed that the reaction proceeded via carboncation-electrophilic substitution reaction and free radical substituti... The reaction of acenaphthene with nitrobenzene was investigated in the presence of AlCl3. The results showed that the reaction proceeded via carboncation-electrophilic substitution reaction and free radical substitution reaction pathway. The products of acenaphthenyl phenylamine and biacenaphthyl could be synthesized by this reaction. The influence of the amount of AlCl3 and the temperature on the components of products were also studied in this reaction. 展开更多
关键词 ACENAPHTHENE NITROBENZENE carboncation free radical reaction mechanism acenaphthenyl phenylamine biacenaphthyl
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An Efficient Approach to 6, 7-Disubstituted-1H-quinoxalin-2-ones
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作者 Xun LI Qing Ping HU +1 位作者 Xue Gui CUI Dong Hua WANG College of Pharmacy, Shandong University, Jinan 250100 College of Pharmaceuticals and Biotechnology, Tianjin University, Tianjin 300072 《Chinese Chemical Letters》 SCIE CAS CSCD 2004年第12期1400-1402,共3页
A novel approach to the synthesis of 6, 7-disubstituted-1H-quinoxalin-2-ones is described.The title compounds were regioselectively prepared by starting from substituted phenylamines andchloroacetyl chloride through t... A novel approach to the synthesis of 6, 7-disubstituted-1H-quinoxalin-2-ones is described.The title compounds were regioselectively prepared by starting from substituted phenylamines andchloroacetyl chloride through the efficient sequence of acylation, nitration, reduction, intramolecular alkylation, and oxidation. 展开更多
关键词 6 7 -Disubstituted-1H-quinoxalin-2-ones REGIOSELECTIVE substituted phenylamine.
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A new approach for one-pot,green synthesis of new polycyclic indoles in aqueous solution
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作者 Mohsen Ameri Alireza Asghari +1 位作者 Ali Amoozadeh Mohammad Bakherad 《Chinese Chemical Letters》 SCIE CAS CSCD 2017年第5期1031-1034,共4页
Electro-oxidation of phenylamine derivatives(1a and 1b) have been studied in the presence of pyrazolidine-3,5-dione(3) as a nucleophile in phosphate buffer solution mixed with ethanol,using voltammetric and spectr... Electro-oxidation of phenylamine derivatives(1a and 1b) have been studied in the presence of pyrazolidine-3,5-dione(3) as a nucleophile in phosphate buffer solution mixed with ethanol,using voltammetric and spectroscopic techniques.The obtained results indicated that the oxidized form of phenylamines(2a and 2b) participate in Michael addition type reactions with pyrazolidine-3,5-dione(3) and via ECECCCCC mechanisms convert to the corresponding new polycyclic indoles(12a and 12b).In the present study,new polycyclic indole derivatives were synthesized with good yields and high purity using a facile,one-pot and environmentally friendly electrochemical method,without any chemical catalysts,toxic solvents and hard conditions. 展开更多
关键词 Electro-oxidation phenylamine Polycyclic indoles Environmentally friendly ECECCCCC mechanism
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