Luminescent cis-Bis(bipyridyl)ruthenium(II) Complexes with 1,2-Azolylamidino Ligands: Photophysical, Electrochemical Studies, and Photocatalytic Oxidation of Thioethers

New 1,2-azolylamidino complexes cis-[Ru­(bipy)2(NHC­(R)­az*-κ2 N,N)]­(OTf)2 (R = Me, Ph; az* = pz, indz, dmpz) are synthesized via chloride abstraction after a subsequent base-catalyzed coupling of a nitrile with the previously coordinated 1,2-azole. The synthetic procedure allows the easy obtainme...

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Veröffentlicht in:Inorganic chemistry 2021-05, Vol.60 (10), p.7008-7022
Hauptverfasser: Cuéllar, Elena, Diez-Varga, Alberto, Torroba, Tomás, Domingo-Legarda, Pablo, Alemán, José, Cabrera, Silvia, Martín-Alvarez, Jose M, Miguel, Daniel, Villafañe, Fernando
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container_end_page 7022
container_issue 10
container_start_page 7008
container_title Inorganic chemistry
container_volume 60
creator Cuéllar, Elena
Diez-Varga, Alberto
Torroba, Tomás
Domingo-Legarda, Pablo
Alemán, José
Cabrera, Silvia
Martín-Alvarez, Jose M
Miguel, Daniel
Villafañe, Fernando
description New 1,2-azolylamidino complexes cis-[Ru­(bipy)2(NHC­(R)­az*-κ2 N,N)]­(OTf)2 (R = Me, Ph; az* = pz, indz, dmpz) are synthesized via chloride abstraction after a subsequent base-catalyzed coupling of a nitrile with the previously coordinated 1,2-azole. The synthetic procedure allows the easy obtainment of complexes having different electronic and steric 1,2-azoylamidino ligands. All of the compounds have been characterized by 1H, 13C, and 15N NMR and IR spectroscopy and by monocrystal X-ray diffraction. Photophysical studies support their phosphorescence, whereas their electrochemistry reveals reversible RuII/RuIII oxidations between +1.13 and +1.25 V (vs SCE). The complexes have been successfully used as catalysts in the photooxidation of different thioethers, the complex cis-[Ru­(bipy)2(NHC­(Me)­dmpz-κ2 N,N)]2+ showing better catalytic performance in comparison to that of [Ru­(bipy)3]2+. Moreover, the significant catalytic performance of the dimethylpyrazolylamidino complex is applied to the preparation of the drug modafinil, which is obtained using ambient oxygen as an oxidant. Finally, mechanistic assays suggest that the oxidation reaction follows a photoredox route via oxygen radical anion formation.
doi_str_mv 10.1021/acs.inorgchem.0c03389
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The synthetic procedure allows the easy obtainment of complexes having different electronic and steric 1,2-azoylamidino ligands. All of the compounds have been characterized by 1H, 13C, and 15N NMR and IR spectroscopy and by monocrystal X-ray diffraction. Photophysical studies support their phosphorescence, whereas their electrochemistry reveals reversible RuII/RuIII oxidations between +1.13 and +1.25 V (vs SCE). The complexes have been successfully used as catalysts in the photooxidation of different thioethers, the complex cis-[Ru­(bipy)2(NHC­(Me)­dmpz-κ2 N,N)]2+ showing better catalytic performance in comparison to that of [Ru­(bipy)3]2+. Moreover, the significant catalytic performance of the dimethylpyrazolylamidino complex is applied to the preparation of the drug modafinil, which is obtained using ambient oxygen as an oxidant. 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Chem</addtitle><description>New 1,2-azolylamidino complexes cis-[Ru­(bipy)2(NHC­(R)­az*-κ2 N,N)]­(OTf)2 (R = Me, Ph; az* = pz, indz, dmpz) are synthesized via chloride abstraction after a subsequent base-catalyzed coupling of a nitrile with the previously coordinated 1,2-azole. The synthetic procedure allows the easy obtainment of complexes having different electronic and steric 1,2-azoylamidino ligands. All of the compounds have been characterized by 1H, 13C, and 15N NMR and IR spectroscopy and by monocrystal X-ray diffraction. Photophysical studies support their phosphorescence, whereas their electrochemistry reveals reversible RuII/RuIII oxidations between +1.13 and +1.25 V (vs SCE). The complexes have been successfully used as catalysts in the photooxidation of different thioethers, the complex cis-[Ru­(bipy)2(NHC­(Me)­dmpz-κ2 N,N)]2+ showing better catalytic performance in comparison to that of [Ru­(bipy)3]2+. 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Chem</addtitle><date>2021-05-17</date><risdate>2021</risdate><volume>60</volume><issue>10</issue><spage>7008</spage><epage>7022</epage><pages>7008-7022</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>New 1,2-azolylamidino complexes cis-[Ru­(bipy)2(NHC­(R)­az*-κ2 N,N)]­(OTf)2 (R = Me, Ph; az* = pz, indz, dmpz) are synthesized via chloride abstraction after a subsequent base-catalyzed coupling of a nitrile with the previously coordinated 1,2-azole. The synthetic procedure allows the easy obtainment of complexes having different electronic and steric 1,2-azoylamidino ligands. All of the compounds have been characterized by 1H, 13C, and 15N NMR and IR spectroscopy and by monocrystal X-ray diffraction. Photophysical studies support their phosphorescence, whereas their electrochemistry reveals reversible RuII/RuIII oxidations between +1.13 and +1.25 V (vs SCE). The complexes have been successfully used as catalysts in the photooxidation of different thioethers, the complex cis-[Ru­(bipy)2(NHC­(Me)­dmpz-κ2 N,N)]2+ showing better catalytic performance in comparison to that of [Ru­(bipy)3]2+. Moreover, the significant catalytic performance of the dimethylpyrazolylamidino complex is applied to the preparation of the drug modafinil, which is obtained using ambient oxygen as an oxidant. 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