| Project/Area Number |
13555250
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 展開研究 |
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| Research Field |
Synthetic chemistry
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| Research Institution | Tohoku University |
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Principal Investigator |
INOUE Yoshio Tohoku University, Graduate School of Engineering, Professor, 大学院・工学研究科, 教授 (50005518)
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| Co-Investigator(Kenkyū-buntansha) |
KITA Hiroshi Konica Minolta Japan, Technology Center, Chief Investigator, 材料技術研究所, 主任研究員
OI Shuichi Tohoku University, Graduate School of Engineering, Associate Professor, 大学院・工学研究科, 助教授 (00241547)
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| Project Period (FY) |
2001 – 2004
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| Project Status |
Completed (Fiscal Year 2004)
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| Budget Amount *help |
¥13,400,000 (Direct Cost: ¥13,400,000)
Fiscal Year 2004: ¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 2003: ¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 2002: ¥1,800,000 (Direct Cost: ¥1,800,000)
Fiscal Year 2001: ¥7,700,000 (Direct Cost: ¥7,700,000)
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| Keywords | direct arylation / ruthenium complex / aryl halide / organic EL device / phosphorescence luminescence / electron transporting material / C-H結合活性化 / アゾベンゼン / アリールカップリング / アルケニルピリジン / ロジウム錯体 / アリール化 / イミダゾリン / フェノール / 遷移金属錯体 / ポリアリール |
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| Research Abstract |
1.We observed that direct arylation of the ortho position in the benzene ring of 2-phenylpyridine took place when 2-phenylpyridine and aryl halides were reacted in the presence of a ruthenium complex catalyst and base. After intensive works, the best conditions were established for this important reaction as follows : Ruthenium complex catalysts coordinating tertiary phosphine, above all, [η^6-C_6H_6RuCl_2]_2-4PPh_3 showed the best performance in activity. The employment of potassium carbonate as base, N-methyl pyrrolidine as solvent, 120℃ as reaction temperature, 20-40 h as reaction time were found to be the best reaction conditions.
2.Pyridyl group is inevitable for the reaction to occur as the directing group which facilitates the ortho directing reaction by coordinating the ruthenium center. However pyridyl group is hard to be converted into another functional group. Development of easily convertible directing group seems essential. We exploited imino and oxazoyl group as the directing group for the direct ortho arylation of the aromatic ring. These groups can easily be converted into other functional groups : Imino group can be converted into ketone, aldehyde, alcohol, amine, and oxazole group can be converted into carboxylic acid, ester, and amide.
3.Then we prepared several nitrogen-containing polyaryl compounds utilizing above reaction method, and investigated the utility of these compounds as organic EL device. They were found to be good electron transporting material and also good ligand for iridium and platinum complexes with efficient phosphorescence luminescence.
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