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排序方式: 共有402条查询结果,搜索用时 15 毫秒
1.
由环氧乙烷及烯丙基缩水甘油醚合成含双键侧基的聚氧乙烯用苯乙烯接枝共聚,接枝效率可达50%左右.接枝产物经纯化,用IR及~1H NMR表征.该产物与LiClO_4的络合物有较高的室温导电率,其PEO含量在70%及EO/Li=20/1时,25℃的导电率接近10~(-4)S/cm.此外,该接枝共聚物有较高的乳化能力.在Williamson固液反应中具有良好的相转移催化作用. 相似文献
2.
Jordi Faraudo Alex Travesset 《Colloids and surfaces. A, Physicochemical and engineering aspects》2007,300(3):287-292
In this paper, we argue that many of the fascinating electrostatic effects that take place in amphiphilic systems are strongly related to the particular organization of the oxygen atoms within each individual molecule. In particular, we focus on two effects: charge inversion and dielectric overscreening. For that purpose, we present molecular dynamics simulations of phosphatidic acid (DMPA2−) in the presence of divalent counterions. Our results show that the many oxygens present in DMPA2− cooperatively create strong binding sites for counterions, which in some cases lead to charge inversion. We also present an analysis of the role of interfacial water and relate our analysis to the phenomenon of dielectric overscreening. Several experimental implications are discussed in the conclusions. 相似文献
3.
两亲性丙烯酸酯共聚物的聚合研究 总被引:1,自引:0,他引:1
利用过氧化苯甲酰为引发剂探讨了甲基丙烯酸β-羟乙酯和丙烯酸长链烷基酯的自由基共聚合。重点讨论了合成条件如溶剂、沉淀剂、引发剂用量、单体配比、反应时间等对共聚反应的影响以及各种聚合条件对该共聚物的组成、结构和性能的影响。并用IR,GPC,^13CNMR等手段对共聚物进行了表征。 相似文献
4.
5.
Katja Jankova 《Journal of fluorine chemistry》2005,126(2):241-250
Block copolymers based on poly(pentafluorostyrene), PFS, in various numbers and of different lengths, and polystyrene are prepared by atom transfer radical polymerization (ATRP). Di- and triblock copolymers with varying amounts of PFS were synthesized employing either 1-phenylethylbromide or 1,4-dibromoxylene as initiators for ATRP. Diverse bromo(ester) (macro)initiators were also devised and involved in the formulation of fluorinated pentablock as well as amphiphilic triblock copolymers with a central polyether segment. Amphiphilic star-shaped fluoropolymers, hydrophobic fluorinated nanoparticles, or segmented fluorinated star-shaped block copolymers are further designed by use of different multifunctional initiators. The composition of the novel materials with PFS is determined by combination of SEC and 1H NMR. Glass transition temperatures and thermal stabilities of the hydrophobic star-shaped PFSs on a six arm dipentaerythritol core are investigated in a wide range of molecular masses and further discussed. 相似文献
6.
The reaction of the ortho-alkynylarylimines 1 with allyltributylstannane and allyl chloride in the presence of allylpalladium chloride dimer (5 mol %) and Cu(OAc)2 (20 mol %) in CH3CN at 50 °C gave the 1,4-diallyl-1,2-dihydroisoquinolines 2 in good yields. Most probably, the reaction proceeds through tandem bis-allylation of the imine-alkyne functional groups with bis-π-allylpalladium. 相似文献
7.
Résumé La courbe représentant, en fonction de la concentrationc, la tension interfaciale entre le toluène et une solution aqueuse d'un copolymère á blocs amphiphile á séquence hydrophile polyélectrolyte (polystyrène-b-polyvinyl-2-pyridine quaternisée au bromure d'éthyle) est foncièrement différente de celle que l'on obtient avec les détergents classiques.Les longues séquences polyélectrolytes ancrées á l'interface y établissent entre les deux phases une différence de potentiel électrique bien supérieure á celle que l'on obtient avec les détergents classiques. Il en résulte que le système reste éloigné de l'équilibre thermodynamique. Comme les énergies d'activation des processus d'adsorption et de désorption sont de nature différente, les courbes (,c) etablies en concentration croissante et décroissante sont non seulement distinctes, mais de caractères différents.
Summary Plotting the water toluene interface tension against the concentrationc, one gets quite different behaviours using classical detergents (Sodium laurylsulfate) or ampholytic block copolymers with polyelectrolytic hydrophilic sequence. (polystyrene-b-polyvinyl-2-pyridine quaternized with ethylbromid).These polyelectrolytic sequences build at the interface a much larger electric potential drop than usual detergents do. It follows that the system keeps far away from the thermodynamic equilibrium. Since adsorption and desorption processes have activation energies of different natures, it turns out that the (,c) curves are quite different in characters if constructed in growing or fallingc values.
Zusammenfassung Kurven, welche die Wasser-Toluol-Grenzflächenspannung als Funktion der Konzentrationc wiedergeben, sind für gewöhnliche Tenside und für Ampholytblock-Copolymere mit einer polyelektrolytartigen Sequenz, völlig verschiedenDie polyelektrolytartige Sequenz bildet an der Grenzfläche einen weitaus größeren elektrischen Potentialsprung als gewöhnliche Tenside. Daraus folgt, daß man dem thermodynamischen Gleichgewicht fern bleibt, und, da Ad- und Desorptionsprozesse unterschiedliche Aktivationsenergien besitzen, sind die (,c) Kurven mit steigenden und fallendenc-Werten völlig verschieden.相似文献
8.
Amphiphilic triblock copolymers of poly(3-hydroxybutyrate)-poly(ethylene glycol)-poly(3-hydroxybutyrate) (PHB-PEG-PHB) were directly synthesized by the ring-opening copolymerization of β-butyrolactone monomer using PEG as macroinitiator. Their structure, thermal properties and crystallization were investigated by 1H NMR, differential scanning calorimetry (DSC) and X-ray diffraction. It was found that both PHB and PEG blocks were miscible. With the increase in the PHB block length, the triblock copolymers became amorphous because amorphous PHB block remarkably depressed the crystallization of the PEG block. Biodegradable nanoparticles with core-shell structure were prepared in aqueous solution from the amphiphilic triblock copolymers, and characterized by 1H NMR, SEM and fluorescence. The hydrophobic PHB segments formed the central solid-like core, and stabilized by the hydrophilic PEG block. The nanoparticle size was close related to the initial concentrations of the nanoparticle dispersions and the compositions of the triblock copolymers. Moreover, the PHB-PEG-PHB nanoparticles also showed good drug loading properties, which suggested that they were very suitable as delivery vehicles for hydrophobic drugs. 相似文献
9.
葡聚糖为载体的双亲型LDL吸附剂吸附动力学研究 总被引:3,自引:0,他引:3
合成了以葡聚为载体,同时具有亲水性磺酸基和疏水性胆固醇两类配基的新型低密度脂蛋白(LDL)吸附剂。通过对LDL纯溶液中吸附等温线的测试,比较了以Dextran G-75为载体的双亲型LDL吸附剂与单一亲水型磺酸基配基,单一疏水型胆固醇基吸附剂吸附量和亲和吸附系数的关系。对双亲型LDL吸附剂的吸附动力学进行了初步研究,在LDL溶液中,亲水型磺酸基,疏水型胆固醇配基,双亲型LDL吸附剂对LDL的吸附曲线基本上符合Langmuir吸附方程,另外通过高离子强度NaCl洗脱实验,测定了双亲型LDL吸附剂上具有的磺酸基与胆固醇两类基在对低密脂蛋白吸附过程中所起的配合效果,为下一步作用力机制研究提供了参考依据。 相似文献
10.
E. Rotureau 《European Polymer Journal》2006,42(5):1086-1092
Amphiphilic polysaccharides have been obtained by hydrophobic modification of a neutral bacterial polysaccharide, dextran. Various amounts and types of aliphatic hydrocarbon groups have been attached to dextran.The solution behaviour of unmodified dextran samples and amphiphilic dextran derivatives is characterized by viscometric measurements. The overall viscosity behaviour of unmodified polysaccharides is described up to C × [η] = 3, using the equation of Fedors [Fedors RF. Polymer 1979;20:225] which involves only a concentration parameter. The latter is shown to depend on the hydrodynamic volume of the macromolecules in solution.The equation of Fedors is shown to conveniently estimate the viscosity behaviour of amphiphilic dextran derivatives up to C × [η] = 1. The interdependence between Fedors parameter and other viscometric characteristics (intrinsic viscosity, Huggins coefficient) is evidenced. These results are extended to the data of other authors. 相似文献