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翻訳と辞書　辞書検索 [ 開発暫定版 ] スポンサード リンク Cyclooctadiene iridium chloride dimer ： ウィキペディア英語版 Cyclooctadiene iridium chloride dimer Cyclooctadiene iridium chloride dimer is an organoiridium compound with the formula Ir2Cl2(C8H12)2, where C8H12 is the diene 1,5-cyclooctadiene. It is an orange solid that is soluble in organic solvents. The complex is used as a precursor to other iridium complexes, some of which are used in homogeneous catalysis.〔J. Hartwig, "Organotransition Metal Chemistry: From Bonding to Catalysis" University Science Books, 2009. ISBN 978-1891389535.〕 The solid is air-stable but its solutions degrades in air. ==Preparation, structure, reactions== The compound is prepared by heating hydrated iridium trichloride and cyclooctadiene in alcohol solvent. In the process, Ir(III) is reduced to Ir(I).〔J. L. Herdé, J. C. Lambert, C. V. Senoff "Cyclooctene and 1,5-Cyclooctadiene Complexes of Iridium(I)" Inorganic Syntheses, 1974, Volume 15, pp. 18–20. 〕 In terms of its molecular structure, the iridium centers are square planar as is typical for a d8 complex. The Ir2Cl2 core is folded with a dihedral angle of 86°. The molecule crystallizes in yellow-orange and red-orange polymorphs; the latter one is more common.〔F. Albert Cotton, Pascual Lahuerta, Mercedes Sanau, Willi Schwotzer "Air oxidation of Ir2(Cl)2(COD)2 revisited. The structures of ()2 (ruby form) and its oxidation product, Ir2Cl2(COD)2(μ2-OH)2(μ2-O)" Inorganica Chimica Acta, 1986 vol. 120, Pages 153–157. 〕〔Tabrizi, D., Manoli, J. M., Dereigne, A., "Etude radiocristallographique de μ-dichloro-bis (π cyclooctadiène-1,5) diiridium: ()2, variété jaune-orange", Journal of the Less Common Metals 1970, vol. 21, pp. 337. 〕 The complex is widely used precursor to other iridium complexes. A notable derivative is Crabtree's catalyst.〔Robert H. Crabtree, Sheila M. Morehouse "[η4-1,5-Cyclooctadiene)(Pyridine)-(Tricyclohexylphosphine)Iridium(I)Hexafluorophosphate" Inorganic Syntheses, 1986, Volume 24, pp. 173–176. 〕 The chloride ligands can also be replaced to give diiridium complexes exhibiting modified reactivity, e.g. Ir2(OCH3)2(C8H12)2. A closely related but still more reactive complex is chlorobis(cyclooctene)iridium dimer. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Cyclooctadiene iridium chloride dimer」の詳細全文を読む スポンサード リンク 翻訳と辞書 : 翻訳のためのインターネットリソース Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.