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Photochemical and photophysical investigations of newly designed supramolecular structures composed of quantum dots and nitric oxide donors.

机译:新设计的由量子点和一氧化氮供体组成的超分子结构的光化学和光物理研究。

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摘要

Nitric oxide (NO), a ubiquitous messenger molecule in mammalian physiology, is also known to act as a potent gamma-radiation sensitizer. For this reason, there is considerable interest in the development of thermally stable compounds capable of controllably releasing NO. Such compounds could see broad application for the enhancement of existing cancer treatment strategies. In this context, photochemically activated NO precursors are attractive given the opportunity to control the location and timing of the signal leading to release of NO. With this in mind, the work described here exploits the extraordinary light absorbing capabilities of semiconductor quantum dots (QDs) both in the single photon excitation (SPE) and two photon excitation (TPE) regimes and demonstrates their potential applicability as photosensitizers for NO releasing prodrugs.; In this dissertation, new supramolecular structures will be described that are composed of chromium(III) complexes of cyclam (cyclam = 1,4,8,11-tetraazacyclotetradecane) both covalently bound to and electrostatically assembled on the surface of water soluble CdSe/ZnS QDs. Previous studies on the nitrito (ONO) derivatives of the chromium cyclam complexes indicated that they are photo-labile towards release of NO with quantum yields as high as 50%. However, these complexes lack absorption at long wavelengths (>600 run) where biological tissue penetration is enhanced. Investigations of the electrostatic assemblies in aqueous solution demonstrate that the Cr(III) complexes quench the QD photoluminescence (PL) obtained via either SPE (366-546 nm) or TPE (800 nm) excitation in a concentration dependent manner. Furthermore, in the electrostatic assemblies containing the dinitrito trans-Cr(cyclam)(ONO) 2+ cation and CdSe/ZnS QDs, photolysis of the assembly results in enhanced photochemical NO release (up to 50 fold more) as compared to the Cr(III) complexes alone. The photophysical and photochemical properties of these QD/chromium(III) cyclam structures are the subjects of this dissertation.
机译:一氧化氮(NO)是哺乳动物生理中无处不在的信使分子,也被称为有效的伽马辐射敏化剂。因此,人们对开发能够可控地释放NO的热稳定化合物非常感兴趣。此类化合物可广泛应用于增强现有癌症治疗策略。在这种情况下,光化学活化的NO前驱物很有吸引力,因为有机会控制导致NO释放的信号的位置和时间。考虑到这一点,此处描述的工作在单光子激发(SPE)和两种光子激发(TPE)方案中都利用了半导体量子点(QD)的非凡光吸收能力,并证明了它们作为光敏剂用于NO释放前药的潜在适用性。 。;在这篇论文中,将描述新的超分子结构,该结构由共价键合并静电组装在水溶性CdSe / ZnS表面上的Cyclam的铬(III)配合物(cyclam = 1,4,8,11-四氮杂环十四烷)组成QD。先前对铬环蛋白络合物的亚硝基(ONO)衍生物的研究表明,它们对释放NO具有光不稳定的作用,量子产率高达50%。但是,这些复合物在长波长(> 600纳米)处缺乏吸收,从而增强了生物组织的渗透性。对水溶液中静电组件的研究表明,Cr(III)配合物可抑制SD(366-546 nm)或TPE(800 nm)激发以浓度依赖的方式获得的QD光致发光(PL)。此外,在包含dinitrito反式Cr(cyclam)(ONO)2+阳离子和CdSe / ZnS QD的静电组件中,组件的光解导致与Cr(相比,光化学NO释放增强(多达50倍) III)单独的复合物。这些QD /铬(III)Cyclam结构的光物理和光化学性质是本论文的主题。

著录项

  • 作者

    Neuman, Daniel.;

  • 作者单位

    University of California, Santa Barbara.;

  • 授予单位 University of California, Santa Barbara.;
  • 学科 Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 202 p.
  • 总页数 202
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 无机化学;
  • 关键词

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