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首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >Polymerization of ethylene oxide with a calixarene-based precursor: Synthesis of eight-arm poly(ethylene oxide) stars by the core-first methodology
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Polymerization of ethylene oxide with a calixarene-based precursor: Synthesis of eight-arm poly(ethylene oxide) stars by the core-first methodology

机译:环氧乙烷与杯芳烃基前体的聚合:核先法合成八臂聚环氧乙烷星

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Eight-arm poly(ethylene oxide) (PEO) stars were prepared by the core-first method with a newly designed octallydroxylated precursor. This compound was readily obtained in two steps from commercially available tert-butylcalix[8]arene. The choice of the proper solvent of polymerization proved crucial to obtain PEO star materials with a narrow distribution of molar masses. For instance, the use of dimethyl sulfoxide (DMSO) resulted in PEO samples of rather large polydispersities (PDI: 1.3-1.5). In this solvent, the calixarene-based precursor was only sparingly soluble, and an attempt to metalate its eight hydroxyl groups produced insoluble alkoxides. In addition, the presence of a side population of low-molar-mass species attributable to linear chains was detected because of the chain transfer of propagating alkoxides to DMSO. Polymerization experiments carried out in tetrahydrofuran (THF) as solvent afforded better control over the molar masses and PDIs. This was related to the better solubility of the octafunctional calixarene-based precursor in THF and to the small tendency of the alkoxides formed to aggregate in that solvent. Under such conditions, all eight hydroxyl functions efficiently initiated the polymerization of ethylene oxide. In this way, well-defined PEO stars (PDI < 1.2) of tunable molar masses incorporating a calixarene-based core could be obtained, as it was supported by the characterization of the samples by size exclusion chromatography, NMR, and viscometry. (C) 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 1669-1676, 2003. [References: 32]
机译:采用新设计的八烯丙基氧化前体,通过核先法制备了八臂聚环氧乙烷(PEO)星。该化合物很容易分两步从市售叔丁基杯[8]芳烃中获得。事实证明,选择合适的聚合溶剂对于获得摩尔质量分布较窄的PEO星型材料至关重要。例如,使用二甲基亚砜(DMSO)导致PEO样品具有相当大的多分散性(PDI:1.3-1.5)。在这种溶剂中,基于杯芳烃的前体仅微溶于水,并且尝试使其八个羟基金属化会产生不溶性醇盐。另外,由于传播的醇盐向DMSO的链转移,检测到可归因于线性链的低摩尔质量物种的侧群的存在。在四氢呋喃(THF)中进行的聚合实验提供了对摩尔质量和PDI的更好控制。这与基于八官能杯芳烃的前体在THF中的更好溶解度有关,并且与形成的醇盐在该溶剂中聚集的趋势较小有关。在这种条件下,所有八个羟基官能团均有效地引发了环氧乙烷的聚合。通过这种方法,可以得到结合了杯芳烃基核的可调谐摩尔质量的明确定义的PEO星(PDI <1.2),这是通过尺寸排阻色谱,NMR和粘度测定法对样品进行表征而得到支持的。 (C)2003 Wiley Periodicals,Inc. J Polym Sci Part A:Polym Chem 41:1669-1676,2003。[参考:32]

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