Synthesis of Ruthenium(II) Complexes Containing Tridentate Triamine (′N ͡N ͡N′) and Bidentate Diamine Ligands (N ͡N′): as Catalysts for Transfer Hydrogenation of Ketones
A series of neutral and cationic Ru(II) complexes (1–10), bearing pyridine-based tridentate (′N ͡N ͡N′), pyridine-based bidentate (N ͡N′), and mixed ′N ͡N ͡N′ + N ͡N′ ligands, were synthesized by starting from [RuCl2(DMSO)4] and [RuCl2(p-cymene)]2 precursors. Solid-state structures of mixed-ligand c...
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Veröffentlicht in: | Organometallics 2011-08, Vol.30 (15), p.4165-4173 |
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creator | Günnaz, Salih Özdemir, Namık Dayan, Serkan Dayan, Osman Çetinkaya, Bekir |
description | A series of neutral and cationic Ru(II) complexes (1–10), bearing pyridine-based tridentate (′N ͡N ͡N′), pyridine-based bidentate (N ͡N′), and mixed ′N ͡N ͡N′ + N ͡N′ ligands, were synthesized by starting from [RuCl2(DMSO)4] and [RuCl2(p-cymene)]2 precursors. Solid-state structures of mixed-ligand complexes 9 and 10 were determined by single-crystal X-ray diffraction. Both complexes are unusual in that N ͡N′ ligands were spontaneously oxidized in air under base-free conditions to give imine-amine bidentate ligands upon replacement of p-cymene by meridional ′N ͡N ͡N′. The complexes 1–10 were screened for transfer hydrogenation (TH) of aryl ketones with 2-propanol. The highest catalytic activity was obtained with the complexes containing tridentate ′N ͡N ͡N′ and 7, which contain nonsulfonated 2-(aminomethyl)pyridine. However, for complexes 6 a–c , containing p-cymene (a facial tridentate ligand), a slower reaction rate was observed. |
doi_str_mv | 10.1021/om200470p |
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Solid-state structures of mixed-ligand complexes 9 and 10 were determined by single-crystal X-ray diffraction. Both complexes are unusual in that N ͡N′ ligands were spontaneously oxidized in air under base-free conditions to give imine-amine bidentate ligands upon replacement of p-cymene by meridional ′N ͡N ͡N′. The complexes 1–10 were screened for transfer hydrogenation (TH) of aryl ketones with 2-propanol. The highest catalytic activity was obtained with the complexes containing tridentate ′N ͡N ͡N′ and 7, which contain nonsulfonated 2-(aminomethyl)pyridine. However, for complexes 6 a–c , containing p-cymene (a facial tridentate ligand), a slower reaction rate was observed.</description><identifier>ISSN: 0276-7333</identifier><identifier>EISSN: 1520-6041</identifier><identifier>DOI: 10.1021/om200470p</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Organometallics, 2011-08, Vol.30 (15), p.4165-4173</ispartof><rights>Copyright © 2011 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a240t-595c32ae75af07e22403439eba4c083239d184ad218c6f3e63a1daa1ce07bd623</citedby><cites>FETCH-LOGICAL-a240t-595c32ae75af07e22403439eba4c083239d184ad218c6f3e63a1daa1ce07bd623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/om200470p$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/om200470p$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids></links><search><creatorcontrib>Günnaz, Salih</creatorcontrib><creatorcontrib>Özdemir, Namık</creatorcontrib><creatorcontrib>Dayan, Serkan</creatorcontrib><creatorcontrib>Dayan, Osman</creatorcontrib><creatorcontrib>Çetinkaya, Bekir</creatorcontrib><title>Synthesis of Ruthenium(II) Complexes Containing Tridentate Triamine (′N ͡N ͡N′) and Bidentate Diamine Ligands (N ͡N′): as Catalysts for Transfer Hydrogenation of Ketones</title><title>Organometallics</title><addtitle>Organometallics</addtitle><description>A series of neutral and cationic Ru(II) complexes (1–10), bearing pyridine-based tridentate (′N ͡N ͡N′), pyridine-based bidentate (N ͡N′), and mixed ′N ͡N ͡N′ + N ͡N′ ligands, were synthesized by starting from [RuCl2(DMSO)4] and [RuCl2(p-cymene)]2 precursors. Solid-state structures of mixed-ligand complexes 9 and 10 were determined by single-crystal X-ray diffraction. Both complexes are unusual in that N ͡N′ ligands were spontaneously oxidized in air under base-free conditions to give imine-amine bidentate ligands upon replacement of p-cymene by meridional ′N ͡N ͡N′. The complexes 1–10 were screened for transfer hydrogenation (TH) of aryl ketones with 2-propanol. The highest catalytic activity was obtained with the complexes containing tridentate ′N ͡N ͡N′ and 7, which contain nonsulfonated 2-(aminomethyl)pyridine. 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Solid-state structures of mixed-ligand complexes 9 and 10 were determined by single-crystal X-ray diffraction. Both complexes are unusual in that N ͡N′ ligands were spontaneously oxidized in air under base-free conditions to give imine-amine bidentate ligands upon replacement of p-cymene by meridional ′N ͡N ͡N′. The complexes 1–10 were screened for transfer hydrogenation (TH) of aryl ketones with 2-propanol. The highest catalytic activity was obtained with the complexes containing tridentate ′N ͡N ͡N′ and 7, which contain nonsulfonated 2-(aminomethyl)pyridine. However, for complexes 6 a–c , containing p-cymene (a facial tridentate ligand), a slower reaction rate was observed.</abstract><pub>American Chemical Society</pub><doi>10.1021/om200470p</doi><tpages>9</tpages></addata></record> |
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title | Synthesis of Ruthenium(II) Complexes Containing Tridentate Triamine (′N ͡N ͡N′) and Bidentate Diamine Ligands (N ͡N′): as Catalysts for Transfer Hydrogenation of Ketones |
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