Studies on the Multi-responsible Molecular Systems Involving Visible Light Switching Using Radical Ions

利用自由基离子进行可见光切换的多响应分子系统的研究

基本信息

  • 批准号:
    09450319
  • 负责人:
  • 金额:
    $ 1.98万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 财政年份:
    1997
  • 资助国家:
    日本
  • 起止时间:
    1997 至 1999
  • 项目状态:
    已结题

项目摘要

Radical ions have sharp and intense absorption bands in the visible wavelength range which depend on the structure and substituents of the radical ions. Therefore, it is suggested that radical ions can be excited by diode lasers, that undestructed reading of memory can be essentially performed with high sensitivity, and that triple memory of a molecule can be done with three independent characters of the neutral molecule and radical cation and anion of the molecule. Radical ions are used as starting material for developing of a new multiple-photoresponsible molecular system on the basis of their visile light switching characters. Since radical ions are well known to be generated from radiation reactions and are stable in the μs time scale in solution at room temperature, this study was carried out with a pulse radiolysis-laser flash photolysis combined method which is constructed at ISIR, Osaka University. Photoresponsiblity was examined through one-way photoisomerization of cis-stilbe … More ne radical cation to trans-stilbene radical cation, intermolecular electron transfer from pyrene radical anion in the photoexcited state to an electron acceptor such as bipheny1, and multiple-isomerizations of 1, 4-dipheny1-1, 3-butadiene radical cation and 1, 6-dipheny1-1, 3, 5-hexatriene radical cation. On the basis of experimental results, a new idea of multiple memory involving a neutral mlecule and the radical ions is proposed and possibility of photon-mode memory with high density is suggested by reversible reactions of radical ions. Since photoresponsible reactions of radical ions are performed in an appropriate time range after irradiation of an electron pulse, they are established to be electron-pulse gated photoresponsible reactions. Moreover, various types of molecules are synthesized to be suitable for the multi-responsible molecular systems involving visible light switching using radical ions. Radical ions of the synthetic molecular systems were used to develop new photoresponsible functional materials with high reliability and high speed from visible light as the information source. Less
自由基离子在可见光波长范围内具有尖锐而强烈的吸收带,这取决于自由基离子的结构和取代基。因此,提出了半导体激光器可以激发自由基离子,本质上可以高灵敏度地无损地读取记忆,分子的三重记忆可以通过分子的中性分子和自由基正负离子三个独立的性质来完成。基于自由基离子的光开关特性,我们以自由基离子为原料,开发了一种新型的多光响应型分子体系。由于自由基离子是由辐射反应产生的,并且在室温下在溶液中稳定在μ-S时间尺度内,本研究采用大阪大学ISIR建立的脉冲辐解-激光闪光光解相结合的方法进行。通过顺式仍然存在的…的单向光异构化检测光响应性更多的Ne自由基阳离子转移到反式二苯乙烯自由基阳离子,分子间电子从光激发态的Py自由基阴离子转移到电子受体如联苯1,以及1,4-二苯基-1,3-丁二烯自由基阳离子和1,6-二苯基-1,3,5-己三烯自由基阳离子的多重异构化。根据实验结果,提出了中性分子和自由基离子多重记忆的新概念,并提出了通过自由基离子的可逆反应实现高密度光子模式记忆的可能性。由于自由基离子的光响应反应是在电子脉冲照射后的适当时间范围内进行的,因此被确定为电子脉冲选通的光响应反应。此外,还合成了各种类型的分子,以适用于利用自由基离子进行可见光开关的多责任分子体系。利用合成分子体系中的自由基离子,以可见光为信息源,研制出高可靠性、高速度的新型光响应性功能材料。较少

项目成果

期刊论文数量(0)
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Tetsuro Majima: "Decomposition of cyclopentadienyltricarbonylmanganse in highly vibrational excited states"J. Organomet. Chem.. 574・1. 155-162 (1999)
Tetsuro Majima:“高振动激发态下环戊二烯基三羰基锰的分解”J. Organomet.. 155-162 (1999)。
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    0
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Mitsunobu Nakamura, the late Reizo Dohno, and Tetsuro Majima: "Binaphthyl formation from the radical cation of tri-1-naphthyl phosphate and their related compounds in photoinduced electron transfer reactions"J. Org. Chem. 63・18. 6258-6265 (1998)
Mitsunobu Nakamura、已故的 Reizo Dohno 和 Tetsuro Majima:“光诱导电子转移反应中三-1-萘基磷酸酯及其相关化合物的联萘基形成”J. 63・18。 1998)
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    0
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Akito Ishida and Tetsuro Majima: "Surface Plasmon Enhanced Fluorescence Spectroscopy towards Observation of Molecular Exchange in a Self-Assembly Monolayer"Chem. Commun. 1999. 1299-1300 (1999)
Akito Ishida 和 Tetsuro Majima:“表面等离激元增强荧光光谱用于观察自组装单层中的分子交换”Chem。
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    0
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Akito Ishida and Tetsuro Majima: "Surface Plasmon Enhanced Fluorescence Measurement on Flat and Constructed Gold Surfaces"Analyst. (in press). (2000)
Akito Ishida 和 Tetsuro Majima:“平面和构造金表面上的表面等离激元增强荧光测量”分析师。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Kyoko Sugita: "^<18>O-Selective Infrared Multiple Photon Decomposition of Natural and ^<18>O-Enriched Diidopropyl Ethers" J.Phys Chem.A. (印刷中). (1999)
Kyoko Sugita:“^ 18 O-选择性红外多光子分解天然和^ 18 O-富集二氨基丙醚”J.Phys Chem.A(出版中)。
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    0
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MAJIMA Tetsuro其他文献

MAJIMA Tetsuro的其他文献

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{{ truncateString('MAJIMA Tetsuro', 18)}}的其他基金

Single-molecule chemistry of nanocatalysis for light energy conversion
光能转换纳米催化的单分子化学
  • 批准号:
    25220806
  • 财政年份:
    2013
  • 资助金额:
    $ 1.98万
  • 项目类别:
    Grant-in-Aid for Scientific Research (S)
Higher Excited State Chemistry Towards Molecular Device, Environmental Chemistry, and Nano- and Biotechnologies
分子器件、环境化学以及纳米和生物技术的更高激发态化学
  • 批准号:
    22245022
  • 财政年份:
    2010
  • 资助金额:
    $ 1.98万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Fundamental Science and Technology of Photofunctional Interfaces
光功能界面基础科学与技术
  • 批准号:
    14050055
  • 财政年份:
    2001
  • 资助金额:
    $ 1.98万
  • 项目类别:
    Grant-in-Aid for Scientific Research on Priority Areas
Molecular devices by functionalization of modified DNA
通过修饰 DNA 功能化的分子装置
  • 批准号:
    13305058
  • 财政年份:
    2001
  • 资助金额:
    $ 1.98万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Photochemistry of radical ions with irradiation of electron and laser pulses
电子和激光脉冲照射下自由基离子的光化学
  • 批准号:
    07455341
  • 财政年份:
    1995
  • 资助金额:
    $ 1.98万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)

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