| Project/Area Number |
16074215
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| Research Category |
Grant-in-Aid for Scientific Research on Priority Areas
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| Allocation Type | Single-year Grants |
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| Review Section |
Science and Engineering
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| Research Institution | Chuo University |
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Principal Investigator |
HAGA Masa-aki Chuo University, Department of Applied Chemistry, Professor (70115723)
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| Co-Investigator(Kenkyū-buntansha) |
KOBAYASHI Katsuaki Chuo University, Department of Applied Chemistry, Assistant Professor (30433874)
豊 智奈 中央大学, 理工学部, 助手 (00365884)
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| Project Period (FY) |
2004 – 2007
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| Project Status |
Completed (Fiscal Year 2007)
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| Budget Amount *help |
¥11,600,000 (Direct Cost: ¥11,600,000)
Fiscal Year 2007: ¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2006: ¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2005: ¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2004: ¥2,300,000 (Direct Cost: ¥2,300,000)
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| Keywords | surface coordination conplex / Molecular electronics / Photoelectronic Properties / Self assembly / Multilayer film / DNA nanowire / Memory effect / DNAワイヤ / 自己組織化膜 / コンビナトリアル化学 / 分子アレイ / 分子ナノテクノロジー / DNA / ルテニウム錯体 / ナノワイヤ / ホスホン酸基 / インターカレーター |
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| Research Abstract |
The bottom-up assembly of functional nanoscale architecture from molecular components at the surface has attracted much interest in the advancement of nanotechnology. Particularly, the chemistry of surface modification by self-assembled monolayers (SAM) and layer-by-layer (LbL) growth of multilayers is highly promising to construct two-dimensional (2D) and three-dimensional (3D) chemical systems on surfaces. To attain this aim, we have undertaken two synthetic approaches based on surface coordination chemistry; i.e., (1) fabrication and functions of multilayers based on redox-active metal complexes on surface, introducing, and (2) DNA nanowiring between two gold terminals on Au/Si02 patterned surface.
Novel molecular units with tetrapod or hexapod phosphonate anchoring groups(XP) have been synthesized in order to keep the molecular orientation on the surface. Mono- and dinuclear Ru complexes, [Ru(XP) (btpb)] and 〔[Ru2(XP)2] (btpb)〕, have been immobilized on an ITO electrode. The vertical molecular orientation was supported by AFM measurements. The direction of photocurrent was altered by the direction of applied potential pulse; i.e., the positive potential pulse (0 V -+1 V - 0 V) revealed a cathodic transient photocurrent, however the negative potential pulse (0 V - -1 V - 0 V) gave an anodic current. These responses fulfill a fundamental requirement for molecular memory functionality. Nanowiring of λ-DNA molecules on the micrometer-sized Au/Si02 patterned silicon substrate was also studied.
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