首页> 外文学位 >Excited-state complex formation of perylene and naphthalimides in solutions and films: New materials for molecular thermometers.
【24h】

Excited-state complex formation of perylene and naphthalimides in solutions and films: New materials for molecular thermometers.

机译:溶液和薄膜中per和萘二甲酰亚胺的激发态络合物形成:分子温度计的新材料。

获取原文
获取原文并翻译 | 示例

摘要

Synthetic polymers that are designed to change their physical or optical properties in response to environmental stimuli have wide-reaching applications in engineering, biological sensing, and medical fields. The fluorescent polymers can be used in the surface temperature measurement, which has broad applications in aerodynamics and engineering. Dually luminescent systems have become a good alternative over current temperature-sensitive paints since the intensity ratio is measured in these systems. An exciplex is a complex between one compound in the excited-state and the other in the ground-state. Generally, the monomer and the exciplex emission are observed at different wavelengths. The fluorescence intensity ratio of the exciplex to the monomer is temperature and structure dependent. The effect of monomer and polymer structure on the temperature-dependent exciplex formation was the main study focus of this work.Exciplex formation between encapsulated perylene and N-isoproprylacryamide (NIPAM) and N,N-dimethylstyrene (NDS) copolymers was studied in films. Poly(N-isoproprylacryamide) (PNIPAM) is among a class of polymers having a well-characterized lower critical solution temperature (LCST) of 31°C in water. Thus, it is of interest to study temperature-dependent exciplex formation in these polymers. The polymer composition was varied by changing the ratio of NIPAM to NDS. Polymer films containing encapsulated perylene were prepared and studied using steady-state fluorescence spectroscopy. The relative population of exciplex to monomer is temperature dependent. The percent variation of the ratiometric intensity per degree centigrade in poly(N,N-diemthylstyrene) (PNDS) film was found to be about 3%/°C.Perylene derivatives with polymerizable function groups were synthesized for the purpose of covalently attaching perylene into the polymer. The intermolecular exciplexes formed between the perylene derivatives and different anilines were studied by measuring the fluorescence decays at specific temperatures. The decays were fitted to the classic Birk's two-state model. The rate constants for exciplex formation and dissociation and the thermodynamics for exciplex formation were obtained from the fits. The activation barriers for exciplex formation and dissociation for the perylene derivatives with N, N-dimethylaniline were found in the range of 3-40 kJ/mol. The polymers with covalently attached perylene and donors showed a less sensitive temperature response than perylene films. The intramolecular excimer formation in bisnaphthalimide was studied using the similar method at different pHs. The excimers formed in bisnaphthalimide were mainly static excimers at low pHs.
机译:旨在响应环境刺激而改变其物理或光学特性的合成聚合物在工程,生物传感和医学领域具有广泛的应用。荧光聚合物可用于表面温度测量,该表面温度在空气动力学和工程领域具有广泛的应用。由于在这些系统中测量了强度比,因此双发光系统已成为当前对温度敏感的涂料的良好替代方案。激基复合物是激发态的一种化合物与基态的另一种化合物之间的复合物。通常,在不同波长下观察到单体和激基复合物发射。激基复合物与单体的荧光强度比取决于温度和结构。单体和聚合物结构对温度依赖性激基复合物形成的影响是本研究的主要研究重点。研究了薄膜中包封的per与N-异丙基丙烯酰胺(NIPAM)和N,N-二甲基苯乙烯(NDS)共聚物之间的激基形成。聚(N-异丙基丙烯酰胺)(PNIPAM)是一类在水中具有良好表征的31℃的较低临界溶液温度(LCST)的聚合物。因此,研究这些聚合物中依赖温度的激基复合物的形成是令人感兴趣的。通过改变NIPAM与NDS的比例来改变聚合物组成。制备包含封装的per的聚合物膜,并使用稳态荧光光谱进行研究。激基复合物与单体的相对种群是温度依赖性的。发现在聚(N,N-二甲基苯乙烯)(PNDS)薄膜中每摄氏度的比例强度的变化百分数为约3%/℃。合成具有可聚合官能团的Per衍生物,以将ylene共价连接到丙烯酸中。聚合物。通过测量特定温度下的荧光衰减,研究了per衍生物与不同苯胺之间形成的分子间激基复合物。衰减符合经典的Birk的二态模型。从拟合中获得激基复合物形成和解离的速率常数以及激基复合物形成的热力学。发现per衍生物与N,N-二甲基苯胺的激基复合物形成和离解的活化势垒为3-40 kJ / mol。与per膜共价连接的聚合物与per和供体共价时,其温度响应灵敏度较低。使用相似的方法在不同的pH下研究了双萘二甲酰亚胺中分子内准分子的形成。双萘二甲酰亚胺中形成的准分子主要是在低pH值下的静态准分子。

著录项

  • 作者

    Zhang, Yu.;

  • 作者单位

    University of Maryland, Baltimore County.;

  • 授予单位 University of Maryland, Baltimore County.;
  • 学科 Chemistry Physical.Engineering Materials Science.Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 184 p.
  • 总页数 184
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号