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Mechanistic Studies on Ni(dppe)CI_2-Catalyzed Chain-Growth Polymerizations: Evidence for Rate-Determining Reductive Elimination

机译:Ni(dppe)Cl_2催化的链增长聚合机理的研究:速率确定还原消除的证据。

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摘要

The mechanisms for Ni(dppe)Cl_2-catalyzed chain-growth polymerization of 4-bromo-2,5-bis-(hexyloxy)phenylmagnesium chloride and 5-bromo-4-hexylthiophen-2-ylmagnesium chloride were investigated. Rate studies utilizing IR spectroscopy and gas chromatography revealed that both polymerizations exhibit a first-order dependence on the catalyst concentration but a zeroth-order dependence on the monomer concentration. ~(31)P NMR spectroscopic studies of the reactive organometallic intermediates suggest that the resting states are unsymmetrical Ni~(II)-biaryl and Ni~(II)-bithiophene complexes. In combination, the data implicate reductive elimination as the rate-determining step for both monomers. Additionally, LiCI was found to have no effect on the rate-determining step or molecular weight distribution in the arene polymerization.
机译:研究了Ni(dppe)Cl_2催化4-溴-2,5-双-(己氧基)苯基氯化镁和5-溴-4-己基噻吩-2-基氯化镁链增长聚合的机理。利用红外光谱和气相色谱的速率研究表明,两种聚合反应均显示出对催化剂浓度的一级依赖性,但对单体浓度的显示为零级依赖性。反应性有机金属中间体的〜(31)P NMR光谱研究表明,静止态为不对称的Ni〜(II)-联芳基和Ni〜(II)-联噻吩配合物。结合起来,数据暗示着还原消除是两种单体的速率确定步骤。另外,发现LiCl对芳烃聚合中的速率确定步骤或分子量分布没有影响。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2009年第45期|16573-16579|共7页
  • 作者

    Erica L. Lanni; Anne J. McNeil;

  • 作者单位

    Department of Chemistry and Macromolecular Science and Engineering Program, University of Michigan, 930 North University Avenue, Ann Arbor, Michigan 48109-1055;

    Department of Chemistry and Macromolecular Science and Engineering Program, University of Michigan, 930 North University Avenue, Ann Arbor, Michigan 48109-1055;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:17:29

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