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41.
Jianjun Xu 《Journal of fluorine chemistry》2004,125(5):725-730
High E/Z ratio (E/Z>75:25) 1-bromo-1-fluorostyrenes, which were prepared by isomerization of 1-bromo-1-fluorostyrenes (E/Z≈1:1), underwent the Heck reaction with methyl acrylate, and (2E, 4Z)-methyl 5-aryl-4-fluoropenta-2,4-dienoates were successfully isolated. Heck reactions of (Z)-1-bromo-1-fluorostyrenes also occur. However, the products are difficult to separate in a pure form, since they have an obvious tendency to isomerize on a silica gel column. 相似文献
42.
Novel enrofloxacin imprinted polymer applied to the solid-phase extraction of fluorinated quinolones from urine and tissue samples 总被引:1,自引:0,他引:1
A new molecularly imprinted polymer, prepared following a non-covalent approach, was synthesised using enrofloxacin as a template molecule. The imprinting effect of the polymer was verified by chromatographic evaluation and, interestingly, this evaluation also revealed that the imprinted polymer showed a high degree of cross-reactivity for ciprofloxacin, the major metabolite of enrofloxacin. The molecularly imprinted polymer was then applied as a selective sorbent in a two-step solid-phase extraction method focussing upon complex biological matrices, specifically human urine and pig liver. This two-step solid-phase extraction protocol, in which a commercial Oasis HLB cartridge and a molecularly imprinted solid-phase extraction cartridge were combined, allowed enrofloxacin and ciprofloxacin to be determined by liquid chromatography coupled to a UV detector at levels below the maximum residue limits established by the European Union. The quantification and detection limits in tissue samples of enrofloxacin and ciprofloxacin were established at 50 μg kg−1 and 30 μg kg−1, respectively. 相似文献
43.
(C6H5)3MX2 (M = As, Sb; X = OCOCF3 and M = Sb, Bi; X = SO3F, SO3CF3) compounds prepared by the interaction of triphenylmetal(V) substrates with (CF3CO)2O, (CF3SO2)2O and (FSO2)2O have been characterized by molecular weight determination, elemental and spectroscopic (IR, 1H and 19F NMR, mass) analyses. 相似文献
44.
Lifang Yang Haifeng He Hongqing Cao Xinhua Wan Qi-feng Zhou Department of Polymer Science & Engineering College of Chemistry & Molecular Engineering Peking University Beijing China 《高分子科学》2002,(5):401-407
Four new rod-coil diblock molecules, which had well-defined para-phenylene oligomers (PPP, from biphenyl toquinquephenyl) as rigid segments and poly(ethylene oxide) (PEO, M_w ca. 750) as flexible segments, were synhesized. Thechemical structure and the number of repeating unit in PEO coil and PPP rod were characterized by ~1H-NMR and MALDI-TOF mass spectromeny. The diblock oligomers showed good solubility in common organic solvents and aggregated in wateras characterized by a blue shift in UV-vis absorption spectra, a red shift in emission spectra, quenching of the fluorescenceand formation of the microfibrilla and fractal-like structures. The formation of different supramolecular structures meant thatthis effort might lead to commercial important highly organized functional materials. 相似文献
45.
Michael T. Mocella 《Journal of fluorine chemistry》2003,122(1):87-92
The semiconductor industry is now in the early stages of an unprecedented change in materials set for the integrated circuit (IC) interconnect structure. The traditional layers of aluminum conductors and silicon dioxide dielectrics are being replaced by copper thin films and a variety of low k candidates, respectively. In many cases, fluorine confers desirable properties on either the precursors or the final films. At the same time, fluorine presents some potentially adverse effects, which have led to a so-called “fear-of-fluorine” in interconnect applications. This paper will review the proposed uses of fluorinated compounds in the interconnect structures, covering both precursors and the resulting thin films. Both the status of technical studies, and the prospects for commercial implementation, will be addressed. 相似文献
46.
Yoshitsugu Kojima Takaaki Matsuoka Norio Sato Hideroh Takahashi 《Journal of polymer science. Part A, Polymer chemistry》1995,33(17):2935-2940
New conjugated oligomers were prepared by reacting phenylacetylene under high pressure of 0.11 to 0.92 GPa at 100–200°C for 0–5 h. The number-average molecular weight M?n, the weight-average molecular weight M?w, and the oligomer yield increased with pressure, tem-perature, and time. The average molecular weight of the oligomer showed the maximum value (M?n: 830, M?w: 2400) under 0.92 GPa, the maximum pressure, where phenylacetylene was oligomerized at a constant temperature. The structure of the oligomer was investigated from ESR, infrared, UV–VIS, field desorption mass (FDMS) spectra, and 13C NMR spec-trum. Analysis of the FDMS spectrum revealed that the molecular weight of the oligomer was multiple of the monomer. 13C NMR spectrum of the oligomer showed the absence of sp-carbon (? C?). We found that the oligomer had a cyclic structure. The cyclic oligomers of pentamer or more were new compounds. © 1995 John Wiley & Sons, Inc. 相似文献
47.
紫外光引发LDPE膜接枝含氟丙烯酸酯的研究 总被引:7,自引:0,他引:7
通过紫外光引发表面接枝聚合反应的方法 ,把含氟丙烯酸酯单体R 5 6 1 0引到LDPE薄膜上 .对经丁酮抽提后的接枝膜进行FTIR、ESCA、SEM和DSC等表征 ,证实含氟聚合物以化学键的方式接枝在LDPE基体膜上 .在一定范围内 ,增加紫外光强、引发剂和单体浓度以及反应温度等均有利于提高接枝率 .经计算R 5 6 1 0的紫外光引发接枝聚合反应总活化能为 5 4 2kJ mol.接枝膜的接触角随着接枝率的提高逐步增大 ,直至趋于恒定 .作者提出接枝膜存在一个在接触角测定时影响基体膜与探测水滴相互作用过程的边界层 .当接枝率较低、接枝层厚度小于边界层临界厚度时 ,基体LDPE影响接触角的大小 ,但随着接枝率提高 ,接枝层逐渐变厚 ,氟聚合物层对接触角的贡献逐渐占优势 ,导致接触角随之增大 .当接枝率超过一定值以后 ,接枝层厚度超过边界层临界厚度 ,接枝层对接枝膜的接触角起全部贡献 ,接触角测定值随之稳定 相似文献
48.
Bis(fluoroalkyl)acrylic and methacrylic phosphate monomers, their polymers and some of their properties 总被引:1,自引:0,他引:1
Christopher M. Timperley Robert E. Arbon Michael Bird Stuart A. Brewer Malcolm W. Parry David J. Sellers Colin R. Willis 《Journal of fluorine chemistry》2003,121(1):23-31
Ten fluoromonomers of structure (RFO)2P(O)OCH2CH2OC(O)CRCH2 were made in 30-64% yield by treating the chloridates (RFO)2P(O)Cl with HOCH2CH2OC(O)CRCH2 in chloroform in the presence of triethylamine [RF=CF3CH2, C2F5CH2, C3F7CH2, C4F9CH2, C4F9CH2CH2 or C6F13CH2CH2; R H or Me]. The chloromonomer (CCl3CH2O)2P(O)OCH2CH2OC(O)CHCH2 was obtained analogously in 29% yield. Polymerisation of the acrylate monomers, but not the methacrylate monomers, could be effected using α-azoisobutyronitrile as a radical initiator. Acrylic polymers having CF3CH2O, CCl3CH2O and C6F13CH2CH2O side-chains were obtained as translucent rubbers. Specimens of cotton fabric were treated with solutions of the polymers, and average water and oil repellency ratings measured. Fabric coated with the polymer with the C6F13CH2CH2O side-chain afforded protection from penetration of the test liquids. Treated fabrics were subjected to the limiting oxygen index (LOI) test according to BS EN ISO 4589-2 (1999): this test determines the point at which a material just burns in a volumetric flow of oxygen and nitrogen. The treated fabrics were more fire-resistant (LOI 22-29%) than the untreated fabric (LOI 18%). Fabric coated with the CCl3CH2O-based polymer can be considered fire-retardant (LOI 29%). The fluoromonomers were tested for anti-acetylcholinesterase activity and were found to be poor enzyme inhibitors; they are predicted to possess low acute toxicity. 相似文献
49.
Yu Xue Zexu Xue Wenwen Zhang Wenna Zhang Shuai Chen Kaiwen Lin Jingkun Xu 《Journal of polymer science. Part A, Polymer chemistry》2019,57(10):1041-1048
By employing planar thieno[3,2‐b]thiophene (TT) as end‐capped units and famous 3,4‐ethylenedioxythiophene (EDOT) or its all‐sulfur analog 3,4‐ethylenedithiathiophene (EDTT) as cores, two conjugated oligomer, TT‐EDOT‐TT and TT‐EDTT‐TT, have been synthesized and electropolymerized into electrochromic polymer films, P(TT‐EDOT‐TT) and P(TT‐EDTT‐TT), respectively. Due to strongly noncovalent inter/intramolecular interactions from S? S attraction of TT‐EDTT‐TT, it has twisted molecular configuration in contrast to planar TT‐EDOT‐TT. Spectroscopic, electrochemical, morphological as well as theoretical calculation studies of these oligomers or polymers were carried out to reveal the significant influence of such molecular geometry on their physicochemical and optoelectronic properties. According to electrochromic kinetics, P(TT‐EDTT‐TT) presented preferable electrochromic behavior such as the higher optical contrast (70.8%), favorable coloration efficiency (331.3 cm2 C?1) and fast response time (0.72 s). This research will help us deeply understand the effect of spatial organization of precursor molecules on the properties of electrochromic polymers and provides a promising strategy to develop high‐performance electrochromic materials. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 1041–1048 相似文献
50.
A palladium catalyzed cross-coupling of fluorinated benzothiadiazoles (FBTs) with allyl chlorides is reported. The significant feature of this method is synthetic simplicity, providing a straightforward access to unsymmetrical and symmetrical alkylated FBT derivatives that are of interest in organic electronic and optoelectronic materials. 相似文献