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61.
Gao Pei‐Sen Zhang Jin‐Lei Li Ning Zheng Zhan Jiang Yuan Yang Gao Zi‐Wei Zhang Weiqiang Xu Li‐Wen 《应用有机金属化学》2018,32(3)
Catalytic allylic γ‐substitution with Morita‐Baylis‐Hillman (MBH) adducts for creating a new family of unsymmetrical dicarbonyl compounds was presented in this work, in which a variety of allylated amide products were achieved in good yields and high regioselectivity with excellent linear‐to‐branched ratios. Especially, it was found that the Pd/HZNU‐Phos complex exhibited remarkably high activity (with a TON up to 16800) in this transformation between dicarbonyl amides and MBH adducts. In addition, the possibly multisite interaction between multifunctional Pd/HZNU‐Phos catalyst system and substrates might responsible for its exceptionally high efficiency in this reaction. 相似文献
62.
Bismuth tellurate nanospheres have been successfully synthesized by a facile hydrothermal route. X-ray diffraction (XRD) shows that the nanospheres are composed of orthorhombic Bi2Te2O7 phase. Scanning electron microscopy (SEM) displays that the diameter of the nanospheres is 100–500 nm. The bismuth tellurate nanospheres (BTS) modified glassy carbon electrode (GCE) has been prepared for the electrochemical detection of L-cysteine (L-CySH). A pair of semi-reversible CV peaks at +0.14 V and–0.84 V, respectively are observed. The BTS modified GCE displays high electrocatalytic activity toward L-CySH and exhibits a linear relationship in the range of 0.0001–2 mM with a detection limit of 0.046 μM in KCl solution. The broad linear range, low detection limit, good reproducibility and stability make the BTS modified GCE valuable for the practical application. 相似文献
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64.
CeO2-MnOx催化剂形貌对低浓度甲烷催化燃烧反应性能的影响 总被引:1,自引:0,他引:1
采用水热合成法制备了船形、扁球形及纳米片CeO2-MnOx复合氧化物。并运用低温N2吸脱附、XRD、SEM、TEM、H2-TPR、拉曼光谱、XPS等表征技术对不同形貌CeO2-MnOx复合氧化物的结构与其低浓度CH4催化燃烧反应性能之间的关系进行了关联。结果表明,CeO2-MnOx复合氧化物的形貌与其催化性能密切相关。其中,扁球形CeO2-MnOx复合氧化物的氧空位、Ce3+含量及表面吸附活性氧物种最多,其CH4催化燃烧反应活性最高,540℃时,可将CH4完全转化;其次是船形CeO2-MnOx复合氧化物催化剂,540℃时其CH4转化率为94.05%;与前两者相比,纳米片CeO2-MnOx复合氧化物催化剂的氧空位及表面吸附活性氧物种较少,活性较差,相同反应温度下,其CH4转化率仅为89.68%。 相似文献
65.
The assembly of alternating DNA and positively charged poly‐(dimethyldiallylammonium chloride) (PDDA) multilayer films by electrostatic layer‐by‐layer adsorption has been studied. Real time surface plasmon resonance (BIAcore) technique was used to characterize and monitor the formation of multilayer films in solution in real time continuously. The results indicate that the uniform multilayer can be obtained on the poly‐(ethylenimine) (PEI) coated substrate surface. The kinetics of the adsorption of DNA on PDDA surface was also studied by real‐time BIAcore technique, and the observed rate constant was calculated using a Langmuir model (kobs = (1.28 ± 0.08) × 10?2s?1). 相似文献
66.
Der‐Jang Liaw Pei‐Nan Hsu Wen‐Hsiang Chen Been‐Yang Liaw 《Journal of polymer science. Part A, Polymer chemistry》2001,39(20):3498-3504
A series of new soluble poly(amide‐imide)s were prepared from the diimide‐dicarboxylic acid 2,2‐bis[4‐(4‐trimellitimidophenoxy)phenyl]hexafluoropropane with various diamines by direct polycondensation in N‐methyl‐2‐pyrrolidinone containing CaCl2 with triphenyl phosphite and pyridine as condensing agents. All the polymers were obtained in quantitative yields with inherent viscosities of 0.52–0.86 dL · g?1. The poly(amide‐imide)s showed an amorphous nature and were readily soluble in various solvents, such as N‐methyl‐2‐pyrrolidinone, N,N‐dimethylacetamide (DMAc), N,N‐dimethylformamide, pyridine, and cyclohexanone. Tough and flexible films were obtained through casting from DMAc solutions. These polymer films had tensile strengths of 71–107 MPa and a tensile modulus range of 1.6–2.7 GPa. The glass‐transition temperatures of the polymers were determined by a differential scanning calorimetry method, and they ranged from 242 to 279 °C. These polymers were fairly stable up to a temperature around or above 400 °C, and they lost 10% of their weight from 480 to 536 °C and 486 to 537 °C in nitrogen and air, respectively. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3498–3504, 2001 相似文献
67.
Yong Nie Chun‐Hua Hu Xue Li Wei Yong Jian‐Min Dou Jie Sun Ruo‐Shui Jin Pei‐Ju Zheng 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(8):897-899
Each of the title compounds, 8‐methoxy‐7,7‐bis(triphenylphosphine‐P)‐8,9:10,11‐di‐μH‐7‐platina‐nido‐undecaborane dichloromethane hemisolvate, [Pt(CH14B10O)(C18H15P)2]·0.5CH2Cl2, (I), 8‐isopropoxy‐7,7‐bis(triphenylphosphine‐P)‐8,9:10,11‐di‐μH‐7‐platina‐nido‐undecaborane dichloromethane solvate, [Pt(C3H18B10O)(C18H15P)2]·CH2Cl2, (II), and 9‐isopropoxy‐7,7‐bis(triphenylphosphine‐P)‐8,9:10,11‐di‐μH‐7‐platina‐nido‐undecaborane dichloromethane solvate, [Pt(C3H18B10O)(C18H15P)2]·CH2Cl2, (III), has an 11‐vertex nido polyhedral skeleton, with the 7‐platinum centre ligating to two exo‐polyhedral PPh3 groups and an alkoxy‐substituted polyhedral borane ligand. Compounds (II) and (III) are isomers. The Pt—B distances are in the range 2.214 (7)–2.303 (7) Å for (I), 2.178 (16)–2.326 (16) Å for (II) and 2.205 (6)–2.327 (6) Å for (III). 相似文献
68.
69.
模式识别—人工神经网络在化学中的若干新应用 总被引:2,自引:0,他引:2
本文通过我们应用模式识别-人工神经网络方法预报新化合物、熔盐相图以及复杂化学反应体系的研究,展示应用模式识别-人工神经网络方法与物理化学理论相结合,研究化学现象的可能性和应用价值。 相似文献
70.