Transfer Hydrogenation to Bicarbonate Salts and CO2 Catalyzed by IrCp*‐Oxyquinolinate Complexes.

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Title: Transfer Hydrogenation to Bicarbonate Salts and CO2 Catalyzed by IrCp*‐Oxyquinolinate Complexes.
Authors: Gutiérrez, Kevin1 (AUTHOR), Torres, Alejandro1 (AUTHOR), Aleman, José2,3 (AUTHOR) jose.aleman@uam.es, Collado, Alba1,3 (AUTHOR) alba.collado@uam.es
Source: ChemCatChem. 7/8/2025, Vol. 17 Issue 13, p1-7. 7p.
Subjects: Transfer hydrogenation, Atmospheric carbon dioxide, Catalytic activity, Metal complexes, Carbon dioxide reduction, Sodium bicarbonate, Iridium catalysts, Formic acid
Abstract: CO2 functionalization to afford beneficial products is one of the current scientific greatest challenges. Amongst all the possible transformations, the synthesis of formic acid from CO2 is of high interest due to the enormous industrial production of this chemical. Particularly interesting is the obtention of formic acid via transfer hydrogenation (TH) of CO2, allowing milder reaction conditions and eliminating the need to employ a hazardous gas as H2. Iridium catalysts promoted TH reactions have been widely studied; however, examples of TH to CO2 are very scarce. In our search for the development of new and more efficient catalysts, we have studied the ability of [IrCp*(QO)X] complexes (QO = 8‐oxyquinolinate) to promote TH to bicarbonate salts and CO2 to obtain formate salts. The study shows a crucial ligand effect, obtaining the best results when [IrCp*(5,7‐Me,Me‐QO)Cl] was employed. Under optimized conditions, TON values up to 135 and 60 were obtained for TH to bicarbonate salts, and CO2, respectively. Remarkably, [IrCp*(5,7‐Me,Me‐QO)Cl] is able to trap and transform atmospheric CO2 into formate salts. [ABSTRACT FROM AUTHOR]
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  Data: Transfer Hydrogenation to Bicarbonate Salts and CO<subscript>2</subscript> Catalyzed by IrCp*‐Oxyquinolinate Complexes.
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  Data: <searchLink fieldCode="AR" term="%22Gutiérrez%2C+Kevin%22">Gutiérrez, Kevin</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Torres%2C+Alejandro%22">Torres, Alejandro</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Aleman%2C+José%22">Aleman, José</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<i> jose.aleman@uam.es</i><br /><searchLink fieldCode="AR" term="%22Collado%2C+Alba%22">Collado, Alba</searchLink><relatesTo>1,3</relatesTo> (AUTHOR)<i> alba.collado@uam.es</i>
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  Data: <searchLink fieldCode="JN" term="%22ChemCatChem%22">ChemCatChem</searchLink>. 7/8/2025, Vol. 17 Issue 13, p1-7. 7p.
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  Data: <searchLink fieldCode="DE" term="%22Transfer+hydrogenation%22">Transfer hydrogenation</searchLink><br /><searchLink fieldCode="DE" term="%22Atmospheric+carbon+dioxide%22">Atmospheric carbon dioxide</searchLink><br /><searchLink fieldCode="DE" term="%22Catalytic+activity%22">Catalytic activity</searchLink><br /><searchLink fieldCode="DE" term="%22Metal+complexes%22">Metal complexes</searchLink><br /><searchLink fieldCode="DE" term="%22Carbon+dioxide+reduction%22">Carbon dioxide reduction</searchLink><br /><searchLink fieldCode="DE" term="%22Sodium+bicarbonate%22">Sodium bicarbonate</searchLink><br /><searchLink fieldCode="DE" term="%22Iridium+catalysts%22">Iridium catalysts</searchLink><br /><searchLink fieldCode="DE" term="%22Formic+acid%22">Formic acid</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: CO2 functionalization to afford beneficial products is one of the current scientific greatest challenges. Amongst all the possible transformations, the synthesis of formic acid from CO2 is of high interest due to the enormous industrial production of this chemical. Particularly interesting is the obtention of formic acid via transfer hydrogenation (TH) of CO2, allowing milder reaction conditions and eliminating the need to employ a hazardous gas as H2. Iridium catalysts promoted TH reactions have been widely studied; however, examples of TH to CO2 are very scarce. In our search for the development of new and more efficient catalysts, we have studied the ability of [IrCp*(QO)X] complexes (QO = 8‐oxyquinolinate) to promote TH to bicarbonate salts and CO2 to obtain formate salts. The study shows a crucial ligand effect, obtaining the best results when [IrCp*(5,7‐Me,Me‐QO)Cl] was employed. Under optimized conditions, TON values up to 135 and 60 were obtained for TH to bicarbonate salts, and CO2, respectively. Remarkably, [IrCp*(5,7‐Me,Me‐QO)Cl] is able to trap and transform atmospheric CO2 into formate salts. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of ChemCatChem is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1002/cctc.202500036
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      – Code: eng
        Text: English
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        PageCount: 7
        StartPage: 1
    Subjects:
      – SubjectFull: Transfer hydrogenation
        Type: general
      – SubjectFull: Atmospheric carbon dioxide
        Type: general
      – SubjectFull: Catalytic activity
        Type: general
      – SubjectFull: Metal complexes
        Type: general
      – SubjectFull: Carbon dioxide reduction
        Type: general
      – SubjectFull: Sodium bicarbonate
        Type: general
      – SubjectFull: Iridium catalysts
        Type: general
      – SubjectFull: Formic acid
        Type: general
    Titles:
      – TitleFull: Transfer Hydrogenation to Bicarbonate Salts and CO2 Catalyzed by IrCp*‐Oxyquinolinate Complexes.
        Type: main
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          Name:
            NameFull: Gutiérrez, Kevin
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            NameFull: Torres, Alejandro
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            NameFull: Aleman, José
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            NameFull: Collado, Alba
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            – D: 08
              M: 07
              Text: 7/8/2025
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              Y: 2025
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