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Syntheses and Properties of Palladium Complexes Containing Phosphorus−Nitrogen−Phosphorus Ligands with a Tunable Hemilabile Site
A series of phosphorus−nitrogen−phosphorus (PNP) ligands of the type R−N(CH2CH2PPh2)2 (R = C(O)(C6H4OMe-p), t Bu, Ph, C6H4OMe-p) have been prepared. Their coordination chemistry to palladium(II) and palladium(0) complexes was examined using a combination of X-ray crystallography, NMR, and electroch...
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Published in: | Organometallics 1999-05, Vol.18 (10), p.1887-1896 |
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container_end_page | 1896 |
container_issue | 10 |
container_start_page | 1887 |
container_title | Organometallics |
container_volume | 18 |
creator | Hii, King Kuok (Mimi) Thornton-Pett, Mark Jutand, Anny Tooze, Robert P |
description | A series of phosphorus−nitrogen−phosphorus (PNP) ligands of the type R−N(CH2CH2PPh2)2 (R = C(O)(C6H4OMe-p), t Bu, Ph, C6H4OMe-p) have been prepared. Their coordination chemistry to palladium(II) and palladium(0) complexes was examined using a combination of X-ray crystallography, NMR, and electrochemical techniques. The palladium(0) complexes undergo reactions with aryl iodides to give the palladium(II) complexes [Pd(Ar){R−N(CH2CH2PPh2)2}]+I-, where the rate of oxidative addition was found to be dependent on the nature of the aryl group, as well as the substitution on nitrogen. |
doi_str_mv | 10.1021/om980978t |
format | article |
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Their coordination chemistry to palladium(II) and palladium(0) complexes was examined using a combination of X-ray crystallography, NMR, and electrochemical techniques. The palladium(0) complexes undergo reactions with aryl iodides to give the palladium(II) complexes [Pd(Ar){R−N(CH2CH2PPh2)2}]+I-, where the rate of oxidative addition was found to be dependent on the nature of the aryl group, as well as the substitution on nitrogen.</description><identifier>ISSN: 0276-7333</identifier><identifier>EISSN: 1520-6041</identifier><identifier>DOI: 10.1021/om980978t</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Organometallics, 1999-05, Vol.18 (10), p.1887-1896</ispartof><rights>Copyright © 1999 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a295t-98ed9443547d4ea0016538326920647ee25066c5c2f7698725cdeba9309675783</citedby><cites>FETCH-LOGICAL-a295t-98ed9443547d4ea0016538326920647ee25066c5c2f7698725cdeba9309675783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Hii, King Kuok (Mimi)</creatorcontrib><creatorcontrib>Thornton-Pett, Mark</creatorcontrib><creatorcontrib>Jutand, Anny</creatorcontrib><creatorcontrib>Tooze, Robert P</creatorcontrib><title>Syntheses and Properties of Palladium Complexes Containing Phosphorus−Nitrogen−Phosphorus Ligands with a Tunable Hemilabile Site</title><title>Organometallics</title><addtitle>Organometallics</addtitle><description>A series of phosphorus−nitrogen−phosphorus (PNP) ligands of the type R−N(CH2CH2PPh2)2 (R = C(O)(C6H4OMe-p), t Bu, Ph, C6H4OMe-p) have been prepared. Their coordination chemistry to palladium(II) and palladium(0) complexes was examined using a combination of X-ray crystallography, NMR, and electrochemical techniques. 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Their coordination chemistry to palladium(II) and palladium(0) complexes was examined using a combination of X-ray crystallography, NMR, and electrochemical techniques. The palladium(0) complexes undergo reactions with aryl iodides to give the palladium(II) complexes [Pd(Ar){R−N(CH2CH2PPh2)2}]+I-, where the rate of oxidative addition was found to be dependent on the nature of the aryl group, as well as the substitution on nitrogen.</abstract><pub>American Chemical Society</pub><doi>10.1021/om980978t</doi><tpages>10</tpages></addata></record> |
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title | Syntheses and Properties of Palladium Complexes Containing Phosphorus−Nitrogen−Phosphorus Ligands with a Tunable Hemilabile Site |
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