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PREPARATIVE STUDIES ON THE FUNCTIONALIZED NEW ORGANOMETALLIC COMPOUNDS FURNISHED WITH THE pi-CONJUGATE SYSTEM

PREPARATIVE STUDIES ON THE FUNCTIONALIZED NEW ORGANOMETALLIC COMPOUNDS FURNISHED WITH THE pi-CONJUGATE SYSTEM
π-共轭体系功能化新型有机金属化合物的制备研究
批准号:
07455354
负责人:
ITO Takashi
金额:
$4.93万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1997

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中文摘要
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英文摘要
Coordination of such ligand that possesses pi-conjugate system onto the transition metal center may possibly provide the organo-transition metal complexes with a long distance charge separation through the molecule. In addition, this is facilitated with the characteristics of the transition metal to adopt a wide variety of the oxidation states. Introduction of the elctron-withdrawing or-donating substituent on the far end of the chain of the conjugated system connected to the transition metal center may cause the electron to flow by the resonance effect either from or to the metal center, resulting in promotion or descent of the valency state of the metal. In the present research project, we intended to design and synthesize these sorts of complexes, which are usually hard to be prepared, by utilizing vairous sophisticated preparation techniques accumulated through long years of our research experiences on the preparation and reactions of the new complexes of the group 6 elements such as molybdenum and tungsten. The preparation of some new organometallic complexes which possess the ligand incorporating the pi-conjugate system in the molecule was thus achieved and the resulting complexes were characterized by IR and NMR spectroscopies as well as through X-ray crystallographic studies. The new complexes prepared and examined in the present research project are categorized into three groups a follows :1. The hydrido complexes of molybdenum and tungsten with diphosphine ligand which contain(1) 4-substituted phthalimide moiety and (2) 4-substituted catecholato ligand.2. The cationic molybdenocene derivatives coordinated with p-substituted phenoxo ligand3. The ferrocenyl derivatives bearing both of conjugated electron donatign substituents such as methylbenzodithiolato moiety or amino group in one cp ring and elctron accepting substituents such as p-nitrophenylethenyl group or formyl group in another cp ring.
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D.-Y.Zhou: "Novel concurrent Formation of Mo-Si and Si-C Bonds by the Reaction between [MoH_4(Ph_2PCH_2CH_2PPh_2)_2] and PhSiH_3" Chem.Lett.(10). 1017-1018 (1997)
D.-Y.Zhou:“通过[MoH_4(Ph_2PCH_2CH_2PPh_2)_2]和PhSiH_3之间的反应同时形成Mo-Si和Si-C键”Chem.Lett.(10)。
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J.-G.Ren: "Synthesis, Structures, and Reactioins of Di-mu-hydroxo Dinuclear Complexes of Tungsten (IV) and Molybdenum (IV)" Organometallics. 15 (2). 852-859 (1996)
J.-G.Ren:“钨 (IV) 和钼 (IV) 的二-mu-羟基双核配合物的合成、结构和反应”有机金属。
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T.Ito: "Synthesis and Some Reactions of Molybdenocene Derivatives Coordinated with the Chiral Carboxylato Ligand" Bull.Chem.Soc.Jpn.69 (2). 417-423 (1996)
T.Ito:“与手性羧化配体配合的二茂钼衍生物的合成和一些反应”Bull.Chem.Soc.Jpn.69 (2)。
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