| Project/Area Number |
11309003
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
広領域
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| Research Institution | The University of Tokyo |
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Principal Investigator |
NISHIHARA Hiroshi The University of Tokyo, Graduate School of Science, Professor, 大学院・理学系研究科, 教授 (70156090)
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| Co-Investigator(Kenkyū-buntansha) |
KURIHARA Masato The University of Tokyo, Graduate School of Science, Assistant, 大学院・理学系研究科, 助手 (50292826)
KUBO Kenya The University of Tokyo, Graduate School of Science, Assistant, 大学院・理学系研究科, 助手 (60214988)
水谷 淳 東京大学, 大学院・理学系研究科, 助手 (00308256)
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| Project Period (FY) |
1999 – 2001
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| Project Status |
Completed (Fiscal Year 2001)
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| Budget Amount *help |
¥30,760,000 (Direct Cost: ¥29,800,000、Indirect Cost: ¥960,000)
Fiscal Year 2001: ¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2000: ¥8,400,000 (Direct Cost: ¥8,400,000)
Fiscal Year 1999: ¥18,200,000 (Direct Cost: ¥18,200,000)
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| Keywords | metal nanoparticles / azo-coningated comolexes / photochromic complexes / donor-acceptor interaction / quinone / ferrocene / redox / intramolecular electron transfer / 錯体 / 共役 / 高次構造 / オリゴマー / フラスター / ポリマー / クラスター |
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| Research Abstract |
To construct new multi-dimensional functional molecular systems by utilizing complex reactions of transition metal complexes has been investigated in this research project. The molecular systems that have been focused are 1) azo-conjugated metal complexes with photo-functions, 2) donor-acceptor conjugated complexes with an ability of proton-coupled intramolecular electron-transfer reactions, and 3) metal nanoparticles modified with redox- and photo-functional complexes. The summary of the results is as follows.
The trans-to-cis isomerization of azoferrocene proceeds not only by the photoexcitation of the π-π^* transition band but also by photoexcitation of the MLCT (d-π^* transition) band. The trans/cis ratio of the azobenzene-attached bipyridine ligands in their cobalt complex is reversibly altered by a combination of photoirradiation with a single UV light source and the reversible redox change between Co(II) and Co(III). A newly synthesized Ni, Pd and Pt tolylazophenylenedithiolato c
… More
omplexes 2-4 show reversible trans-to-cis photoisomerization, proto-chromism, and novel proton-coupled cis-to-trans isomerization.
The protonation to carbonyl groups of the anthraquinone moiety in 1 -ferrocenylethynylanthraquinone causes intramolecular electron transfer leading to a novel structural change into a η^6-fulvene-cumulene Fe(II) complex. A 2:1 donor-acceptor complex, l,5-bis(ferrocenylethynyl)anthraquinone undergoes a two-step proton response, and the doubly protonated species involves a η^6-fulvene-Fe(II) complex-cumulene structure, and a novel spin-separated form of a ferrocenium (Fe(III)) ion and a semiquinone radical in the solution. Furthermore, the complex is in a thermal equilibrium between the valence tautomers of a donor-acceptor system in the solid state.
Synthesis and electrochemical deposition behavior of biferrocene and anthraquinone derivative-modified Au and Pd clusters have been investigated. It is also possible to fabricate hetero structures by alternative electrodeposition of Bfc-modified gold and palladium nanoparticles. Less
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