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Photochemistry and photophysics of 1-naphthyl acylates in polyethylene films.

机译:聚乙烯薄膜中1-萘基酰化物的光化学和光物理性质。

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摘要

This thesis describes the use of polyethylenes as reaction media for conducting the photo-Fries rearrangements of 1-naphthyl acylates. The photo-Fries rearrangements of three 1-naphthyl acylates have been investigated in three unstretched and stretched polyethylene films and in isotropic solutions. The influence of variables such as the size and position of the acyl groups on the naphthyl rings, the degree of film crystallinity, film free volume, and the unstretched/stretched state of the films on the rearrangements has been explored. The crystal structure of 2-naphthyl acetate was determined and compared with that of 1-naphthyl acetate. Their electric dipole moments were evaluated by both theoretical and experimental methods, and were applied to interpret their polarized spectroscopies. The polarized spectroscopy of both 1- and 2-naphthyl acylates in unstretched/stretched polyethylene films supports the idea that stretching reduces free volume and increases the order of guest molecules. The degree of order increases with the length of acyl groups for 1-naphthyl acylates, but 2-naphthyl myristate is less ordered than the 1-naphthyl acylates.; Higher viscosity or lower temperature “hardens” reaction cavity walls and confines more the movement of guest species, thus enhancing the selectivity of photo-Fries rearrangements of 1-naphthyl acylates.; The selectivity of the photo-Fries rearrangements of 1-naphthyl acylates is larger in PE films than in isotropic solutions, and increased with the size of the aryl group, crystallinity of film, and upon film stretching. Long alkyl chains on naphthyl myristates not only affect the shape anisotropy of their cavities but also induce large van der Waals interactions with the cavity walls. Film stretching enforces the templating effect of the cavities and strengthens the van der Waals attractions between the guest molecules and polymer chains that constitute the cavity walls in the case of naphthyl myristates.
机译:本论文描述了使用聚乙烯作为反应介质进行1-萘基酰化物的光-弗里斯重排。已经研究了三种未拉伸和拉伸的聚乙烯薄膜以及各向同性溶液中三种1-萘基酰化物的光-弗里斯重排。已经探索了诸如萘基上的酰基的大小和位置,膜的结晶度,膜的自由体积以及膜在重排上的未拉伸/拉伸状态等变量的影响。测定乙酸2-萘酯的晶体结构,并将其与乙酸1-萘酯的晶体结构进行比较。通过理论和实验方法对它们的电偶极矩进行了评估,并将其用于解释其极化光谱。未拉伸/拉伸的聚乙烯薄膜中的1-和2-萘基酰化物的偏振光谱支持这样的想法,即拉伸可减少自由体积并增加客体分子的顺序。 1-萘基酰化物的有序度随酰基长度的增加而增加,但是肉豆蔻酸2-萘酯比1-萘基酰化物的有序度低。较高的粘度或较低的温度“硬化”了反应腔壁,并限制了客体的更多运动,从而提高了1-萘基酰化物的光-弗里斯重排的选择性。在PE膜中,1-萘基酰化产物的光-弗里斯重排的选择性比在各向同性溶液中要大,并随芳基基团的大小,膜的结晶度和膜的拉伸而增加。十四烷基肉豆蔻酸酯上的长烷基链不仅影响其空腔的形状各向异性,而且还引起与空腔壁的大范德华相互作用。薄膜拉伸增强了空腔的模板效应,并增强了肉豆蔻酸萘酯的客体分子与构成空腔壁的聚合物链之间的范德华力吸引力。

著录项

  • 作者

    Wang, Xiaochun.;

  • 作者单位

    Georgetown University.;

  • 授予单位 Georgetown University.;
  • 学科 Chemistry Organic.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 243 p.
  • 总页数 243
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

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