Ligand‐Free Pd‐Catalyzed Direct C‐H Arylation of Polyfluoroarenes with Aryl Iodides under Ambient Air Conditions

We report the synergistic use of Pd(OAc)₂ and Ag₂O for the direct C-H arylation of polyfluoroarenes with aryl iodides in DMF as the solvent. This method is straightforward, can be conducted in air, and does not require additional ligands, yielding fluorinated unsymmetrical biaryl products in up to 99 %. Experimental studies and DFT calculations suggest that the formation of [(DMF)<sub>2</sub>Pd<sup>II</sup>(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>] in DMF as a coordinating solvent does not inhibit the reaction, as the Pd complex reacts with aryl iodides by oxidative addition upon dissociation of a single DMF ligand to form [(DMF)Pd<sup>IV</sup>(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>(Ar)(I)] before the desired arylation product is released. This contrasts with our previous report on the nucleophilic coupling between C₆F₅H and aryl-Bpin, in which the formation of [(DMF)₂Pd<sup>II</sup>(C₆F₅)₂] was found to halt the reaction.

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Publication Details

Journal
Chemistry - An Asian Journal
Published
2025-03-13
DOI
https://doi.org/10.1002/asia.202500073
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
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article
Field-Weighted Citation Impact
0.94
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article

Ligand‐Free Pd‐Catalyzed Direct C‐H Arylation of Polyfluoroarenes with Aryl Iodides under Ambient Air Conditions

Muhammad Rafif Ramadhan, Yudha P. Budiman, Todd B. Marder, Solihudin Solihudin et al.
1 citations
Chemistry - An Asian Journal
Catalytic C–H Functionalization Methods
0.94
article

Ligand‐Free Pd‐Catalyzed Direct C‐H Arylation of Polyfluoroarenes with Aryl Iodides under Ambient Air Conditions

Muhammad Rafif Ramadhan, Yudha P. Budiman, Todd B. Marder, Solihudin Solihudin, Yusi Deawati, Udo Radius, Tri Mayanti, Miftahussurur Hamidi Putra, Raiza Hannifah, Pambudi Tasripin
article en
1 citations

Abstract

We report the synergistic use of Pd(OAc)₂ and Ag₂O for the direct C-H arylation of polyfluoroarenes with aryl iodides in DMF as the solvent. This method is straightforward, can be conducted in air, and does not require additional ligands, yielding fluorinated unsymmetrical biaryl products in up to 99 %. Experimental studies and DFT calculations suggest that the formation of [(DMF)<sub>2</sub>Pd<sup>II</sup>(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>] in DMF as a coordinating solvent does not inhibit the reaction, as the Pd complex reacts with aryl iodides by oxidative addition upon dissociation of a single DMF ligand to form [(DMF)Pd<sup>IV</sup>(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>(Ar)(I)] before the desired arylation product is released. This contrasts with our previous report on the nucleophilic coupling between C₆F₅H and aryl-Bpin, in which the formation of [(DMF)₂Pd<sup>II</sup>(C₆F₅)₂] was found to halt the reaction.

Chemistry - An Asian JournalVol. 20(10)
Universität Ulm (DE), University of Würzburg (DE), Padjadjaran University (ID)
Clean water and sanitation
Openalex Percentile: Top 28%
Catalytic C–H Functionalization Methods
0.94
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Ligand‐Free Pd‐Catalyzed Direct C‐H Arylation of Polyfluoroarenes with Aryl Iodides under Ambient Air Conditions — Muhammad Rafif Ramadhan, Yudha P. Budiman, et al. · Chemistry - An Asian Journal (2025) | TGRS Research Map | TGRS