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Hydrophobic flocculation flotation of rutile fines in presence of styryl phosphonic acid 被引量:10
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作者 Xiao-tao HUANG Wei XIAO +6 位作者 Hong-bo ZHAO Pan CAO Qi-xiu HU Wen-qing QIN Yan-sheng ZHANG Guan-zhou QIU Jun WANG 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2018年第7期1425-1433,共9页
The hydrophobic flocculation flotation of rutile fines in the presence of styryl phosphonic acid(SPA) was investigated by flotation tests, zeta-potential measurement, optical microscope observation, laser-based part... The hydrophobic flocculation flotation of rutile fines in the presence of styryl phosphonic acid(SPA) was investigated by flotation tests, zeta-potential measurement, optical microscope observation, laser-based particle size analysis, adsorption measurements and DLVO theory. The flotation tests indicated that rutile fines could be flocculated by SPA, and pH, shear force(stirring speed) and stirring time played significant roles in flocculation. The isoelectric point(IEP) and zeta-potential in whole range all moved to negative values as SPA was added according to the results from zeta-potential measurement. It was demonstrated that the primary reason for above was chemical adsorption. The laser-based particle size results showed the particle size at a stirring speed of 1800 r/min and 1000 mg/L SPA was the largest in all experiments. Furthermore, using the optical microscope observation and flotation tests, it was important for flotation of rutile fines to produce the flocculant. In the light of above-mentioned facts, floc flotation of rutile fines could be induced in the form of chemical adsorption by SPA to increase particle size. The data calculated from DLVO theory also indicated that chemical adsorption was the main reason for the formation of flocculant. 展开更多
关键词 hydrophobic flocculation flotation rutile fines styryl phosphonic acid(SPA) DLVO theory
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SYNTHESIS OF STYRYL-CAPPED POLYPROPYLENE via METALLOCENE-MEDIATED COORDINATION POLYMERIZATION: APPLY TO POLYPROPYLENE MACROMOLECULAR ENGINEERING 被引量:2
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作者 Hua-hua Huang Chuan-hui Zhang +2 位作者 Ya-wei Qin Hui Niu 董金勇 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2013年第4期550-562,共13页
In this paper, we review our recent progress in the synthesis and application of styryl-capped polypropylene (PP-t- St), an excellent reactive polyolefin that is both convenient and efficient in synthesis and facile... In this paper, we review our recent progress in the synthesis and application of styryl-capped polypropylene (PP-t- St), an excellent reactive polyolefin that is both convenient and efficient in synthesis and facile and versatile in application for preparing advanced polypropylene materials via macromolecular engineering. The synthesis of PP-t-St is made possible by a unique chain transfer reaction coordinated by a bis-styrenic molecule, such as 1,4-divinylbenzene (DVB) and 1,2-bis(4- vinylphenyl)ethane (BVPE), and hydrogen in typical C2-symmetric metallocene (e.g. rac-Me2Si(2-Me-4-Ph-Ind)2ZrC12, in association with methylaluminocene, MAO) catalyzed propylene polymerization. The regio-selective 2,1- insertion of the styrenic double bond in DVB or BVPE into the overwhelmingly 1,2-fashioned Zr-PP propagating chain enables substantial dormancy of the catalyst active site, which triggers selective hydrogen chain transfer that, with the formed Zr-H species ultimately saturated by the insertion of propylene monomer, results in an exclusive capping of the afforded PP chains by styryl group at the termination end. With a highly reactive styryl group at chain end, PP-t-St has been used as a facile building block in PP macromolecular engineering together with the employment of state-of-the-art synthetic polymer chemistry to fabricate broad types of new polypropylene architectures. 展开更多
关键词 POLYPROPYLENE Coordination polymerization styryl terminal group Macromolecular engineering.
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三氟甲基取代的4-苯乙烯基香豆素衍生物的合成
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作者 刘伟 陈芬芬 +1 位作者 韩小瑜 王永江 《浙江科技学院学报》 CAS 2023年第1期1-6,47,共7页
【目的】设计合成结构新颖的香豆素衍生物,有利于探索发现更多含香豆素骨架化合物的生物活性及应用价值,因而报道了一种三氟甲基取代的苯乙烯基香豆素衍生物的合成方法。【方法】采取不同取代基的3-氰基-4-甲基-香豆素和2,2,2-三氟-1-... 【目的】设计合成结构新颖的香豆素衍生物,有利于探索发现更多含香豆素骨架化合物的生物活性及应用价值,因而报道了一种三氟甲基取代的苯乙烯基香豆素衍生物的合成方法。【方法】采取不同取代基的3-氰基-4-甲基-香豆素和2,2,2-三氟-1-苯基乙烷-1-酮为反应起始原料,乙酸乙酯为反应溶剂,在室温条件下以DBU(1,8-二氮杂双环[5.4.0]十一碳-7-烯)为催化剂,经vinylogous-aldol(插烯羟醛)重排反应生成三氟甲基取代的苯乙烯基香豆素类化合物。【结果】产物经核磁1H NMR、13C NMR、19F NMR、高分辨质谱及X射线单晶衍射表征;制备了以E(反)式构型为主的8个三氟甲基取代的4-苯乙烯基香豆素化合物,产率最高可达95%。【结论】本研究结果为含氟苯乙烯基香豆素类化合物的合成提供了一种制备方法。 展开更多
关键词 三氟甲基 苯乙烯基 香豆素衍生物 插烯羟醛重排
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A novel method for synthesis of styryl phosphonate monoester and its application in La(Ⅲ) extraction 被引量:4
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作者 Kaihua Huang Yun Jia +2 位作者 Shuai Wang Jia Yang Hong Zhong 《Journal of Rare Earths》 SCIE EI CAS CSCD 2020年第6期649-656,共8页
Herein,styryl phosphonate monoester(SPE) was synthesized and first introduced as rare earth extractant.The solvent extraction of lanthanum(Ⅲ) from nitrate solution using styryl phosphonate mono-isooctyl ester(SPE108)... Herein,styryl phosphonate monoester(SPE) was synthesized and first introduced as rare earth extractant.The solvent extraction of lanthanum(Ⅲ) from nitrate solution using styryl phosphonate mono-isooctyl ester(SPE108),di-2-ethylhexyl phosphoric acid(D2 EHPA) and 2-ethylhexyl phosphonic acidmono-2-ethylhexyl ester(EHEHPA) as extractants was investigated.The effects of experimental parameters including equilibrium time,extractant concentration,aqueous pH,phase ratio and salt concentration on the extraction process were studied.The results indicate that the extraction ability and capacity of the extractants follow the order:SPE108> D2 EHPA> EHEHPA.What’s more,the extraction process is less affected by ammonium sulfate in the aqueous phase with SPE108.The results of the separation between lanthanum and adjacent lanthanides(Ce,Pr,Nd,Sm) show that SPE108 can separate lanthanides efficiently at low pH.The extraction mechanism of SPE108 is proved to be similar to D2 EHPA,and the density functional theory(DFT) calculation results infer that SPE108 exhibits superior extraction ability due to its strong electron-accepting ability. 展开更多
关键词 styryl phosphonate monoester Rare earth EXTRACTION EXTRACTANT
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Identification of Styryl Sulfonyl Fluoride as a Near-Perfect Michael Acceptor for Diversified Protein Bioconjugations
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作者 Qingsong Wu Qi Xue +8 位作者 Ji Li Qinheng Zheng Xinlu Zhao Wannan Li Shiming Sun Wanxing Sha Yang Yang Yi Yang Jie P.Li 《CCS Chemistry》 CSCD 2023年第10期2251-2263,共13页
Cysteine(Cys)-specific bioconjugation has widespread applications in the synthesis of protein conjugates,particularly for the functionalization of antibodies.Here,we report the discovery of transstyryl sulfonyl fluori... Cysteine(Cys)-specific bioconjugation has widespread applications in the synthesis of protein conjugates,particularly for the functionalization of antibodies.Here,we report the discovery of transstyryl sulfonyl fluoride(SSF)as a near-perfect Michael acceptor for Cys-specific protein bioconjugation.Compared to maleimides,which are predominantly used,SSF exhibited better chemoselectivity,selfstability,and conjugate stability while maintaining comparable reactivity.Using SSF-derived probes,proteins can be readily modified on the Cys residue(s)to install functionalities,for example,fluorescent dyes,toxins,and oligonucleotides,without influencing the activity.Further applications of SSF-derived serum-stable antibody-drug conjugates and PD-L1 nanobody-oligo conjugates demonstrate the great translational value of SSF-based bioconjugation in drug development and single-cell sequencing. 展开更多
关键词 styryl sulfonyl fluoride cysteine bioconjugation serum-stable ADC DNA-protein conjugates CITE-seq
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Solvent-free Rapid Synthesis of Styryl Dyes with Benzimidazole Nucleus Using Microwave Irradiation
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作者 Lan Ying WANG Xiao Gang ZHANG +1 位作者 Ying Qi JIA Zu Xun ZHANG 《Chinese Chemical Letters》 SCIE CAS CSCD 2003年第11期1116-1118,共3页
The reactions of 2-methylbenzimidazole or 2-methylbenzimidazolium iodide with aromatic aldehydes are accelerated under microwave irradiation by using Ac2O or piperidine as dehydrant or catalyst in the absence of any s... The reactions of 2-methylbenzimidazole or 2-methylbenzimidazolium iodide with aromatic aldehydes are accelerated under microwave irradiation by using Ac2O or piperidine as dehydrant or catalyst in the absence of any solvent. The approach provides an attractive and environmentally friendly pathway to several useful styryl dyes with benzimidazole nucleus. 展开更多
关键词 Microwave irradiation styryl dyes benzimidazole nucleus aromatic aldehydes.
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Pd-Catalyzed New Type of Cross-Coupling of RCOOH and Styryltrifluoroborates
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作者 Mohammad Al-Masum Musa Aman 《International Journal of Organic Chemistry》 CAS 2022年第4期181-188,共8页
The Palladium inserted hydridopalladium species represents as RCOOPdH. This work finds an interesting coupling of palladium inserted RCOOPdH species with potassium styryltrifluoroborates to synthesize new kinds of sty... The Palladium inserted hydridopalladium species represents as RCOOPdH. This work finds an interesting coupling of palladium inserted RCOOPdH species with potassium styryltrifluoroborates to synthesize new kinds of styryl ester compounds. Pd(OAc)<sub>2</sub> was most effective catalyst for this new cross-coupling reaction under microwave irradiation and gave styryl esters in good to moderate yields. 展开更多
关键词 styryl Ester Microwave Pd(OAc)2 as Catalyst Microwave Heating
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Multifunctional Langmuir-Blodgett film of an Amphiphilic Benziminazole Styryl Dye 被引量:1
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作者 ZHENG Jie LI Fu you +2 位作者 HUANG Chun hui YU An Chi ZHAO Xin Sheng 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2002年第3期325-329,共5页
An amphiphilic benziminazole styryl dye, 2 (4 dihexadecylaminostyryl)benziminazolium TCNQ -(DBTCNQ), was synthesized and successfully transferred onto the substrates by Langmuir Blodgett(LB) technique. H aggregates we... An amphiphilic benziminazole styryl dye, 2 (4 dihexadecylaminostyryl)benziminazolium TCNQ -(DBTCNQ), was synthesized and successfully transferred onto the substrates by Langmuir Blodgett(LB) technique. H aggregates were formed on the substrates. Its monolayer second order susceptibility[ χ (2) zzz = 109 p/mV) was determined with a polarized laser beam(Nd∶YAG, λ =1.064 μm). The photoelectrochemistry of the dye LB monolayer films was investigated in a traditional three electrode cell. The quantum efficiency of photoelectric conversion is 1.08% under favorable conditions [-200 mV, 0.5 mg/mL methylviologen diiodide(MV 2+ ) in 0.5 mol/L KCl electrolyte solution]. The experimental data indicate that the LB film exhibits multifunctional properties. 展开更多
关键词 MULTIFUNCTION Langmuir Blodgett films Benziminazole styryl dye
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A New Investigation of Mannich Reaction 被引量:1
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作者 Li Yuan MOU Zi Yun LIN +1 位作者 Li Ya ZHU Xiao Tian LIANG 《Chinese Chemical Letters》 SCIE CAS CSCD 2001年第6期471-474,共4页
During the synthesis of the derivatives of styryl ketonic Mannich bases, a side -product IM,other than the normal Mannich base MA, is obtained. Mannich reaction is further studied and the formation mechanism of produc... During the synthesis of the derivatives of styryl ketonic Mannich bases, a side -product IM,other than the normal Mannich base MA, is obtained. Mannich reaction is further studied and the formation mechanism of product IM is postulated and discussed on the basis of deuterium labelling. 展开更多
关键词 Mannich reaction side-product styryl ketonic Mannich bases MECHANISM
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3-Phenyl/Pyridinyl Derivatives of <i>Trans</i>-2-(aryl/heteryl)vinyl-3<i>H</i>-quinazolin-4-ones: Synthesis and Fluorescent Properties
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作者 Emiliya V. Nosova Tatyana V. Stupina +3 位作者 Galina N. Lipunova Marina S. Valova Pavel A. Slepukhin Valery N. Charushin 《International Journal of Organic Chemistry》 2012年第1期56-63,共8页
Novel 3-phenyl/pyridinyl-trans-2-(aryl/heteryl)vinyl-3H-quinazolin-4-ones 3a,b, 4a, 5a, 7a and their 6,7-difluoro de- rivatives 3c,d, 4b, 5b, 7b have been obtained by condensation of the correspondent 2-methylquinazol... Novel 3-phenyl/pyridinyl-trans-2-(aryl/heteryl)vinyl-3H-quinazolin-4-ones 3a,b, 4a, 5a, 7a and their 6,7-difluoro de- rivatives 3c,d, 4b, 5b, 7b have been obtained by condensation of the correspondent 2-methylquinazolin-4-ones 1, 6 with aromatic (heterocyclic) aldehydes in the presence of ZnCl2 (AcONa) or by the reaction of 2-methyl-3,1-benzoxazin-4- ones 2 with the Shiff bases. Effects of aryl(heteryl) substituents on photophysical properties of (aryl/heteryl) quinazolinylethenes have been studied. 展开更多
关键词 styryl Benzazines Fluorinated Quinazolin-4-Ones UV and FL Spectra X-Ray Trans-cis-Isomerisation 2-Methylquinazolinones 2-Methyl-3 1-benzoxazinones
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A new synthesis of cytotoxic (+)-7-epi-Goniofufurone
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作者 杨敏 李红明 +2 位作者 赵刚 俞庆森 丁渝 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2000年第2期225-231,共7页
Cytotoxic styryl lactone, ( + )-7-epi-Goniofufurone (1), has been prepared with a new route from 3-O-benzyl-1, 2-O-isopropylidene-5-C-phenyl-β-L-ido-pentofuranose (6), a derivative of (+)-glucose. Treatment of 14 wit... Cytotoxic styryl lactone, ( + )-7-epi-Goniofufurone (1), has been prepared with a new route from 3-O-benzyl-1, 2-O-isopropylidene-5-C-phenyl-β-L-ido-pentofuranose (6), a derivative of (+)-glucose. Treatment of 14 with HCl solution cleaved TBDMS and isopropylidene and simultaneously caused ring closure to afford 1 while treatment of 14 with Sc(OTf)3 only removed TBDMS to give 15. 展开更多
关键词 FURANS styryl lactone CYTOTOXICITY
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Synthesis and Properties of Crown Ether Benzotellurazole Heterocyclic Styryl Cyanines and Merocyanines
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作者 Ke Weijun Luo Xuehong +1 位作者 Liu Xiufang Xu Hansheng 《Wuhan University Journal of Natural Sciences》 CAS 1997年第4期75-78,共4页
Two Crown ether benzotellurastyryl cyanines and three crown ether benzotelluramerocyanines are synthesized via the key intermediate 3 methyl 5,6(15 crown 5) 2(β acetanilide)vinyl benzotellurazolium iodide.The ... Two Crown ether benzotellurastyryl cyanines and three crown ether benzotelluramerocyanines are synthesized via the key intermediate 3 methyl 5,6(15 crown 5) 2(β acetanilide)vinyl benzotellurazolium iodide.The reactive conditions are discussed.The influence of alkali( earth)metal ions on the visible absorption spectra of these two types of crown ether cyanines are also studied. 展开更多
关键词 active intermediate crown ether benzotellurazole styryl cyanine MEROCYANINE
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Adsorption mechanism of styryl phosphonate ester as collector in ilmenite flotation
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作者 Yan-ling XU Kai-hua HUANG +3 位作者 Hong-qiang LI Wei HUANG Cheng LIU Si-yuan YANG 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2022年第12期4088-4098,共11页
A styryl phosphonate ester(SPE) collector was used to improve the flotation performance of ilmenite, and the adsorption mechanism and model were revealed and established, respectively. Microflotation tests showed that... A styryl phosphonate ester(SPE) collector was used to improve the flotation performance of ilmenite, and the adsorption mechanism and model were revealed and established, respectively. Microflotation tests showed that SPE exhibited a stronger collecting ability for ilmenite than the traditional collector styrene phosphonic acid(SPA). Zeta potential measurements revealed that both SPE and SPA could negatively shift the zeta potential of ilmenite, while SPE had more effects than SPA, suggesting the stronger adsorption of SPE. The analysis of X-ray photoelectron spectroscopy confirmed the chemisorption of SPA and SPE onto the Fe/Ti sites of ilmenite. According to frontier orbital theory, the chemical activities of SPE are greater than those of SPA. The partial densities of states analysis indicated that the PO—H groups of the collectors could interact with the Ti/Fe atoms of the ilmenite surface to generate a stable four-membered ring. The bonding model of the collector and(104) ilmenite surface showed that the adsorption energy of SPE was higher than that of SPA. Overall, SPE presented a better collecting ability and interaction effect for ilmenite flotation than SPA, and had the potential to replace SPA in the industry. 展开更多
关键词 styryl phosphonate ester ILMENITE FLOTATION COLLECTOR X-ray photoelectron spectroscopy density functional theory adsorption mechanism
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苯乙烯喹啉衍生物的合成及抗癌活性 被引量:1
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作者 王明 侯宝龙 +2 位作者 闫佳旭 王翠玲 刘建利 《精细化工》 EI CAS CSCD 北大核心 2015年第10期1132-1136,共5页
以取代的苯胺和反式丁烯醛为原料,在盐酸中反应得到4个2-甲基喹啉衍生物,所得产物再与芳香醛在冰醋酸中回流反应合成了10个苯乙烯喹啉衍生物,收率为64%~78%。所得化合物的结构经1HNMR、MS、IR表征确认,并采用MTT法进行初步体外抗肿瘤活... 以取代的苯胺和反式丁烯醛为原料,在盐酸中反应得到4个2-甲基喹啉衍生物,所得产物再与芳香醛在冰醋酸中回流反应合成了10个苯乙烯喹啉衍生物,收率为64%~78%。所得化合物的结构经1HNMR、MS、IR表征确认,并采用MTT法进行初步体外抗肿瘤活性筛选。结果表明,化合物Ⅱc对A 549和HCT 116细胞均有较高的抑制活性,IC50值分别为9.77和9.66μmol/L,化合物Ⅱd对HCT 116细胞有较高的抑制活性,IC50值为9.80μmol/L。 展开更多
关键词 喹啉 苯乙烯基 2-甲基喹啉 抗癌活性 医药与日化原料
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2-苯乙烯基喹啉染料的无溶剂微波合成 被引量:11
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作者 李凤梅 王兰英 +1 位作者 王少康 张祖训 《有机化学》 SCIE CAS CSCD 北大核心 2004年第1期50-52,共3页
在微波促进无溶剂条件下 ,由 2 甲基喹啉与取代芳香醛在醋酐作用下合成了一系列 2 苯乙烯基喹啉染料 ,该法操作简便、收率高 .经元素分析 ,1HNMR ,MS 。
关键词 2—苯乙烯基喹啉染料 无溶剂微波合成 2—甲基喹啉 芳香醛 醋酐 结构
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苯乙烯基-β-萘噻唑染料电子光谱的含时密度泛函研究 被引量:17
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作者 陈沁闻 王兰英 +2 位作者 翟高红 文振翼 张祖训 《化学学报》 SCIE CAS CSCD 北大核心 2005年第1期39-43,F007,共6页
对苯乙烯基-β-萘噻唑染料系列用量子化学密度泛函方法(DFT)在 B3LYP/6-31g 水平上进行了几何构型全优化,探讨了苯环对位上不同的取代基 CH3, OCH3, N(CH3)2, 3,4-OCH2O, NO2等对分子电荷转移、前线轨道能量和电子光谱等性质的影响规律,... 对苯乙烯基-β-萘噻唑染料系列用量子化学密度泛函方法(DFT)在 B3LYP/6-31g 水平上进行了几何构型全优化,探讨了苯环对位上不同的取代基 CH3, OCH3, N(CH3)2, 3,4-OCH2O, NO2等对分子电荷转移、前线轨道能量和电子光谱等性质的影响规律, 在此基础上采用含时密度泛函方法(TD-DFT)计算了分子第一激发态的电子跃迁能, 得到最大吸收波长λmax. 计算结果表明, 上述 5 种取代基的引入, 均导致最大吸收波长红移. 与实验λmax 结果相比, 理论计算最大相对偏差为 0.0501, 最小相对偏差为 0.0085. 展开更多
关键词 电子光谱 密度泛函方法 取代基 B3LYP 电子跃迁能 激发态 几何构型 CH 最大吸收波长 噻唑
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黄皮种子中杀松材线虫成分分离及活性测定 被引量:17
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作者 马伏宁 万树青 +1 位作者 刘序铭 赵凤 《华南农业大学学报》 CAS CSCD 北大核心 2009年第1期23-26,共4页
采用药液浸渍法测定了黄皮Clausena lansium不同部位甲醇提取物对松材线虫Bursaphelenchus xylophilus的生物活性,在活性跟踪的基础上,通过萃取、柱层析、薄层制备、重结晶、核磁共振等方法对其有效成分进行了分离和结构鉴定.结果表明,... 采用药液浸渍法测定了黄皮Clausena lansium不同部位甲醇提取物对松材线虫Bursaphelenchus xylophilus的生物活性,在活性跟踪的基础上,通过萃取、柱层析、薄层制备、重结晶、核磁共振等方法对其有效成分进行了分离和结构鉴定.结果表明,黄皮不同部位甲醇提取物中种子提取物对松材线虫的毒杀活性最高,在1 mg/mL水溶液中处理72 h的校正死亡率为100%.各萃取相中石油醚相的活性最高,从石油醚相中分离、纯化获得一黄色晶体,经核磁共振检测分析为Lansiumamide B(N-甲基-N-顺-苯乙烯-肉桂酰胺).该化合物处理松材线虫24、48、72 h的LC50值分别为8.38、6.36、5.38 mg/L,表明该化合物是黄皮种子中主要杀松材线虫活性成分. 展开更多
关键词 松材线虫 黄皮 N-甲基-N-顺-苯乙烯-肉桂酰胺
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苯丙烯酸类衍生物和类似物的合成及其抗炎和抗癌活性研究(英文) 被引量:12
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作者 张琳萍 计志忠 《药学学报》 CAS CSCD 北大核心 1992年第11期817-823,共7页
近年研究表明,炎症和癌症都与花生四烯酸的代谢产物环氧酶和5-脂氧酶密切相关。据此选择对环氧酶或5-脂氧酶具有抑制作用的苯丙烯酸类化合物作为抗炎、抗癌先导化合物,并对其酯类衍生物及其苯乙烯酮类类似物进行初步探讨。本文作者设计... 近年研究表明,炎症和癌症都与花生四烯酸的代谢产物环氧酶和5-脂氧酶密切相关。据此选择对环氧酶或5-脂氧酶具有抑制作用的苯丙烯酸类化合物作为抗炎、抗癌先导化合物,并对其酯类衍生物及其苯乙烯酮类类似物进行初步探讨。本文作者设计并合成上述类型化合物共十九个,其中十五个为未见文献报道的新化合物,并经红外光谱、~1H-核磁共振光谱及元素分析等证实其化学结构。对所合成的化合物进行了抗炎及抗癌药理活性初步筛选。体内抗炎实验表明,所合成的苯丙烯酸类化合物Ⅰ_A,Ⅰ_B,Ⅰ_C人及其酯类衍生物Ⅱ_(2A),Ⅱ_(2C),Ⅱ_(5C)和苯乙烯酮类似物Ⅲ_C对巴豆油诱发的小鼠耳廓肿胀均有不同程度和抑制作用。体外抗癌作用初步筛选结果表明,化合物Ⅰ_B,Ⅱ_(5A),Ⅱ_(5C),及Ⅲ_D对HL-60人癌细胞均有较好的抑制作用。值得注意的是,化合物Ⅰ_B和Ⅱ_(5C)不仅对体外HL-60人癌细胞具有明显的抑制作用,而且对巴豆油所致小鼠炎症亦有较强的活性。深入的药理实验还在进行中。 展开更多
关键词 苯丙烯酸 苯乙烯酮 化合物 合成
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四甲川苯乙烯菁染料的合成及其激光性能 被引量:9
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作者 杨金龙 朱正华 姚祖光 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 1990年第3期286-289,共4页
合成了一系列四甲川苯乙烯菁染料。以Nd:YAG锁模激光倍频(532nm)作泵浦源,测定了染料的激光性能,包括激光调谐范围、中心激光波长、激光转换效率及稳定性。探讨了该类分子结构与其激光性能之间的关系。
关键词 四甲川苯乙烯菁染料 合成 激光性能
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三苯胺多枝化合物光谱性能的研究 被引量:4
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作者 杨天赦 杨平 +4 位作者 王筱梅 施琴芬 蒋宛莉 吴正颖 孙庭 《感光科学与光化学》 SCIE EI CAS CSCD 北大核心 2004年第1期4-12,共9页
研究了含三苯胺多枝化合物———4 正丁氧基苯乙烯三苯胺(T1)、双(4 正丁氧基苯乙烯)三苯胺(T2)和三(4 正丁氧基苯乙烯)三苯胺(T3)溶液的光谱行为.结果发现:在三苯胺对位进行单枝化(T1)、双枝化(T2)和三枝化(T3)后,摩尔吸光系数增大且... 研究了含三苯胺多枝化合物———4 正丁氧基苯乙烯三苯胺(T1)、双(4 正丁氧基苯乙烯)三苯胺(T2)和三(4 正丁氧基苯乙烯)三苯胺(T3)溶液的光谱行为.结果发现:在三苯胺对位进行单枝化(T1)、双枝化(T2)和三枝化(T3)后,摩尔吸光系数增大且最大吸收波长红移,但红移幅度依次减小,表明经多枝化处理后分子能带带隙趋于接近.在不同的溶剂中,T1—T3荧光行为有所不同:在环己烷中相对荧光强度的顺序为T3>T2>T1;随着溶剂极性增大,荧光强度顺序发生反转,为T1>T2>T3.量子产率数值(Φf)表明,随着溶剂的极性增大,T1和T2、T3的量子产率变化顺序也不同:T1的Φf值随溶剂极性的增大而增大,而T3的Φf值则基本是随着溶剂极性的增大而依次减小.造成这种差别的原因可能是ICT和TICT两发光态在极性不同的溶剂中相互转化、平衡移动所致. 展开更多
关键词 4-正丁氧基苯乙烯三苯胺 双(4-正丁氧基苯乙烯)三苯胺 三(4-正丁氧基苯乙烯)三苯胺 ICT态发光 TICT态发光
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