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Synthesis and Characterization of Ir(H)(CO)(PEt 3 }) 2 (η 2 -C 60 )
The title complex, Ir(H)(CO)(PEt3)2(h2-C60) (2), has been prepared by the reaction of excess C60 (4 equiv) with a tetrairidium complex Ir4(CO)8(PEt3)4 (1) in refluxing chlorobenzene in 40% yield as green crystals. Compound 2 has been characterized by cyclic voltammetry (CV), spectroscopic methods (m...
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Published in: | Bulletin of the Korean Chemical Society 2007, 28(11), , pp.1958-1962 |
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container_end_page | 1962 |
container_issue | 11 |
container_start_page | 1958 |
container_title | Bulletin of the Korean Chemical Society |
container_volume | 28 |
creator | Chang Yeon Lee Gaehang Lee Hongkyu Kang 박보근 Joon T. Park |
description | The title complex, Ir(H)(CO)(PEt3)2(h2-C60) (2), has been prepared by the reaction of excess C60 (4 equiv) with a tetrairidium complex Ir4(CO)8(PEt3)4 (1) in refluxing chlorobenzene in 40% yield as green crystals. Compound 2 has been characterized by cyclic voltammetry (CV), spectroscopic methods (mass, IR, 1H and 31P NMR), and a single crystal X-ray diffraction study. The molecular structure reveals that the iridium atom of 2 is coordinated by two axial ligands of a hydrogen atom and a carbonyl group, and three equatorial ligands of two phosphorus atoms and an h2-C60 moiety. The CV study exhibits three reversible one-electron redox waves for the successive reductions of 2, together with additional four redox waves due to free C60 reductions, which was formed by decomposition of 2 in the reduced states. The three reversible redox waves of 2 are shifted to more negative potentials by ca. 270 mV compared to free C60, reflecting both metal-to-C60 p-back-donation and the electron-donating nature of the two phosphorus ligands. KCI Citation Count: 2 |
doi_str_mv | 10.5012/bkcs.2007.28.11.1958 |
format | article |
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Park</creator><creatorcontrib>Chang Yeon Lee ; Gaehang Lee ; Hongkyu Kang ; 박보근 ; Joon T. Park</creatorcontrib><description>The title complex, Ir(H)(CO)(PEt3)2(h2-C60) (2), has been prepared by the reaction of excess C60 (4 equiv) with a tetrairidium complex Ir4(CO)8(PEt3)4 (1) in refluxing chlorobenzene in 40% yield as green crystals. Compound 2 has been characterized by cyclic voltammetry (CV), spectroscopic methods (mass, IR, 1H and 31P NMR), and a single crystal X-ray diffraction study. The molecular structure reveals that the iridium atom of 2 is coordinated by two axial ligands of a hydrogen atom and a carbonyl group, and three equatorial ligands of two phosphorus atoms and an h2-C60 moiety. The CV study exhibits three reversible one-electron redox waves for the successive reductions of 2, together with additional four redox waves due to free C60 reductions, which was formed by decomposition of 2 in the reduced states. The three reversible redox waves of 2 are shifted to more negative potentials by ca. 270 mV compared to free C60, reflecting both metal-to-C60 p-back-donation and the electron-donating nature of the two phosphorus ligands. 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Park</creatorcontrib><title>Synthesis and Characterization of Ir(H)(CO)(PEt 3 }) 2 (η 2 -C 60 )</title><title>Bulletin of the Korean Chemical Society</title><description>The title complex, Ir(H)(CO)(PEt3)2(h2-C60) (2), has been prepared by the reaction of excess C60 (4 equiv) with a tetrairidium complex Ir4(CO)8(PEt3)4 (1) in refluxing chlorobenzene in 40% yield as green crystals. Compound 2 has been characterized by cyclic voltammetry (CV), spectroscopic methods (mass, IR, 1H and 31P NMR), and a single crystal X-ray diffraction study. The molecular structure reveals that the iridium atom of 2 is coordinated by two axial ligands of a hydrogen atom and a carbonyl group, and three equatorial ligands of two phosphorus atoms and an h2-C60 moiety. The CV study exhibits three reversible one-electron redox waves for the successive reductions of 2, together with additional four redox waves due to free C60 reductions, which was formed by decomposition of 2 in the reduced states. The three reversible redox waves of 2 are shifted to more negative potentials by ca. 270 mV compared to free C60, reflecting both metal-to-C60 p-back-donation and the electron-donating nature of the two phosphorus ligands. 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Park</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Characterization of Ir(H)(CO)(PEt 3 }) 2 (η 2 -C 60 )</atitle><jtitle>Bulletin of the Korean Chemical Society</jtitle><date>2007-11-20</date><risdate>2007</risdate><volume>28</volume><issue>11</issue><spage>1958</spage><epage>1962</epage><pages>1958-1962</pages><issn>0253-2964</issn><eissn>1229-5949</eissn><abstract>The title complex, Ir(H)(CO)(PEt3)2(h2-C60) (2), has been prepared by the reaction of excess C60 (4 equiv) with a tetrairidium complex Ir4(CO)8(PEt3)4 (1) in refluxing chlorobenzene in 40% yield as green crystals. Compound 2 has been characterized by cyclic voltammetry (CV), spectroscopic methods (mass, IR, 1H and 31P NMR), and a single crystal X-ray diffraction study. The molecular structure reveals that the iridium atom of 2 is coordinated by two axial ligands of a hydrogen atom and a carbonyl group, and three equatorial ligands of two phosphorus atoms and an h2-C60 moiety. The CV study exhibits three reversible one-electron redox waves for the successive reductions of 2, together with additional four redox waves due to free C60 reductions, which was formed by decomposition of 2 in the reduced states. The three reversible redox waves of 2 are shifted to more negative potentials by ca. 270 mV compared to free C60, reflecting both metal-to-C60 p-back-donation and the electron-donating nature of the two phosphorus ligands. KCI Citation Count: 2</abstract><pub>대한화학회</pub><doi>10.5012/bkcs.2007.28.11.1958</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | Full-Text Journals in Chemistry (Open access) |
subjects | 화학 |
title | Synthesis and Characterization of Ir(H)(CO)(PEt 3 }) 2 (η 2 -C 60 ) |
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