Near-instantaneous chemoselective transfer hydrogenation of aldehydes with visual endpoint reporting and ultrahigh TOF

A bench-stable Ru(II)-<i>para</i>-cymene catalyst bearing proton-responsive ligands enables rapid and chemoselective transfer hydrogenation (TH) of aldehydes under mild, base-free conditions, achieving turnover frequencies (TOFs) up to 166 s<sup>-1</sup> with dual proton and hydride donors. A distinct, reversible green-to-yellow color change allows real-time visual endpoint detection and helps prevent over-reduction. The catalyst remains recyclable over multiple cycles with sustained activity and selectivity, providing a practical, self-indicating platform for efficient transfer hydrogenation in complex synthetic workflows.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc03450g
Citations
2
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
1.07

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article

Near-instantaneous chemoselective transfer hydrogenation of aldehydes with visual endpoint reporting and ultrahigh TOF

Sanjay Pratihar, Manohar Shivaji Padmor
2 citations
Chemical Communications
Asymmetric Hydrogenation and Catalysis
1.07
article

Near-instantaneous chemoselective transfer hydrogenation of aldehydes with visual endpoint reporting and ultrahigh TOF

Sanjay Pratihar, Manohar Shivaji Padmor
article en
2 citations

Abstract

A bench-stable Ru(II)-<i>para</i>-cymene catalyst bearing proton-responsive ligands enables rapid and chemoselective transfer hydrogenation (TH) of aldehydes under mild, base-free conditions, achieving turnover frequencies (TOFs) up to 166 s<sup>-1</sup> with dual proton and hydride donors. A distinct, reversible green-to-yellow color change allows real-time visual endpoint detection and helps prevent over-reduction. The catalyst remains recyclable over multiple cycles with sustained activity and selectivity, providing a practical, self-indicating platform for efficient transfer hydrogenation in complex synthetic workflows.

Chemical CommunicationsVol. 61(69)
Central Salt and Marine Chemicals Research Institute (IN), Academy of Scientific and Innovative Research (IN)
University Grants Committee, Science and Engineering Research Board
Openalex Percentile: Top 22%
Asymmetric Hydrogenation and Catalysis
1.07
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