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11.
Ecaterina Stela Dragan Marcela Mihai Anton Airinei 《Journal of polymer science. Part A, Polymer chemistry》2006,44(20):5898-5908
The thermochemical transformation of electrostatically formed complexes of methyl orange (MO) with polycations containing primary amine groups such as ammonium salts afforded new polymers with a high concentration of covalently bound 4‐N,N‐dimethylaminoazobenzene groups in the side chain. Poly(allylamine hydrochloride) and poly(β‐aminoethylene acrylamide hydrochloride) were employed as support polycations for MO. The transformation of sulfonate–ammonium ion pairs into sulfonamide bonds, via heating at an elevated temperature, was supported by the polymer properties before and after the thermal treatment. The polymer structure changes were monitored with elemental analysis, Fourier transform infrared, 1H NMR, and ultraviolet–visible absorption spectroscopy, and thermogravimetric analysis. The spacer length between the backbone and azobenzene structures used as side chains strongly influenced the polymer properties before and after the heat‐induced reaction. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5898–5908, 2006 相似文献
12.
维生素B类药物在薄层原位的近红外付立叶变换表面增强拉曼光谱 总被引:3,自引:0,他引:3
维生素B类药物在薄层原位的近红外付立叶变换表面增强拉曼光谱汪瑗,于秉正张煦(首都师范大学分析测试中心北京100037)(北京大学分析测试中心北京)关键词维生素B_1,维生素B_2,薄层色谱,表面增强拉曼散射,近红外付立叶变换拉曼光谱将薄层色谱(TLC)... 相似文献
13.
Shiraz A. Markarian Liana S. Gabrielyan Karine R. Grigoryan 《Journal of solution chemistry》2004,33(8):1005-1015
FT IR ATR spectra of urea/dimethyl sulfoxide and urea/diethyl sulfoxide mixtures in the S=O and N—H stretching vibration regions at different molar ratios have been measured. On the basis of the band deconvolution data, various types of intermolecular associated forms, including dimers and hydrogen-bonded urea–sulfoxide complexes, have been revealed. The latter has been confirmed also by ab initio calculations. 相似文献
14.
S Çak?r E Co?kunP Naumov E Biçer? Bulut H ?çbudakO Çak?r 《Journal of Molecular Structure》2002,608(1):101-107
Aspartame adduct of copper(II) chloride Cu(Asp)2Cl2·2H2O (Asp=aspartame) is synthesized and characterized by elemental analysis, FT IR, UV/vis, ESR spectroscopies, TG, DTG, DTA measurements and molecular mechanics calculations. Aqueous solution of the green solid absorbs strongly at 774 and 367 nm. According to the FT IR spectra, the aspartame moiety coordinates to the copper(II) ion via its carboxylate ends, whereas the ammonium terminal groups give rise to hydrogen bonding network with the water, the chloride ions or neighboring carboxylate groups. The results suggest tetragonally distorted octahedral environment of the copper ions. 相似文献
15.
Ilaria Serafini Livia Lombardi Claudia Fasolato Manuel Sergi Francesca Di Ottavio Fabio Sciubba 《Natural product research》2019,33(7):1040-1051
AbstractIn this paper, the application of a multi-analytical approach for the characterisation of synthetic and natural dyes in a historical textile is presented. The work is focused on a historical dress of a Sicilian noblewoman, dating from about 1865–1870. Firstly, SERS on fibre was performed, in order to individuate the classes of dyes employed. The SERS spectra suggested the presence of two main dyes: mauveine and orcein. In order to confirm these preliminary results, two different extraction protocols were applied. The extracts obtained were analysed by ESI-MS, MALDI-ToF and UHPCL-MS analyses, confirming the SERS results. In particular, the application of the ammonia mild extraction technique allowed to selectively extract the phenoxazonic dyes, separating them already in the extraction step from the synthetic ones. Thanks to this multi-analytical approach, this dress could be considered as one of the first examples of employment of synthetic dyes in association with natural ones. 相似文献
16.
The spectral evolution of the surface-enhanced Raman scattering (SERS) of 4-tert-butylbenzylmer-captan(4-tBBM)on gold nanopanlcles assembly under laser irradiation is reported.The reIative intensities of typical peaks in the spectrum of 4-tBBM gradually change with irradiation time.Comparison of the rate of spectral changes under several experimental conditions indicates that the surface plasmon resonance(SPR)induced heat in the gold nanoparticles assembly is the origin of the spectraI evolution.During the process of self-assembly,4-tBBM molecules do not form a compact ordered monolayer because of the spatial hindrance of the 4-tert-butyl end group.The heat induced by laser irradiation drives the 4-tBBM molecules to rearrange to a more stable orientation. 相似文献
17.
《中国科学B辑(英文版)》2007,(4)
The spectral evolution of the surface-enhanced Raman scattering (SERS) of 4-tert-butylbenzylmer-captan (4-tBBM) on gold nanoparticles assembly under laser irradiation is reported. The relative intensities of typical peaks in the spectrum of 4-tBBM gradually change with irradiation time. Comparison of the rate of spectral changes under several experimental conditions indicates that the surface plasmon resonance (SPR) induced heat in the gold nanoparticles assembly is the origin of the spectral evolution. During the process of self-assembly, 4-tBBM molecules do not form a compact ordered monolayer because of the spatial hindrance of the 4-tert-butyl end group. The heat induced by laser irradiation drives the 4-tBBM molecules to rearrange to a more stable orientation. 相似文献
18.
Mauricio Alcolea Palafox Nerea Iza Manuel Gil Jos Luís Núez 《International journal of quantum chemistry》2002,89(1):25-47
A quantum chemical study of several complex monocyclic 4‐benzoyl‐4‐phenyl‐β‐lactam derivatives was carried out using cyclobutane, azetidine, 2‐azetidinone, 1‐methyl‐2‐azetidinone, and 3‐methyl‐2‐azetidinone as model compounds. The optimum geometry was obtained for the different conformations. The planarity of the ring was discussed in terms of the influence of the substituents on the amide resonance. To better analyze the amide resonance and the activity of the β‐lactam ring, a vibrational study was also carried out. To examine the influence of solvent polarity on the carbonyl bands, the Fourier transform–infrared (FT‐IR) spectra of the β‐lactam monocyclic derivatives were recorded in CCl4, C6H6, and CHCl3 solutions. The normal vibrations of the β‐lactam ring in the model compounds were characterized and used in the analysis of the β‐ring of more complex derivatives. © 2002 Wiley Periodicals, Inc. Int J Quantum Chem, 2002 相似文献
19.
IntroductionTheincreasingcommercialvalueoftransitionmetalcomplexesofxanthateshasarousedconsiderableinterestintheirchemistry .Whiletheiranalyticalapplicationsarewellknown ,1theyarenowfindingextensiveuseinvulcan izationofrubber ,frothfloatationprocessforconcentrationofsulphideores ,asantioxidants ,lubricants ,2 ,3andhavebeenfoundtopossessfungicidalandinsecticidalactivi ties .4 Recently ,molecularrecognitionbetweenhostandguestmolecules ,inclusionphenomenaandnoncovalentmolecularinteractionarefunda… 相似文献
20.
研究了水-乙腈混合溶液中SO4●-自由基氧化酪氨酸的反应.实验结果表明,SO4●-自由基氧化酪氨酸的反应机制不因乙腈的加入而改变,但所产生的瞬态粒子的动力学行为受到较大影响.随介质中乙腈体积分数的增加,SO4●-的衰变速率减慢而酪氨酸中性自由基(TyrO●)的衰变速率加快.我们认为这两种自由基所呈现出来的相反的溶剂效应是由于其所带电荷的不同.随介质中乙腈体积分数的增加,SO4●-氧化酪氨酸的反应速率减慢.这一实验结果意味着,在有机溶剂存在的情况下TyrO●/ TyrOH的氧化还原电势可能发生了变化,从而旁证了关于TyrO●/ TyrOH的氧化还原电势因酪氨酸从游离状态变到肽或蛋白质中而发生变化的推测. 相似文献