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Published on: July 27, 2022
Acceptor (CF3)PCPH pincer reactivity with (PPh3)3Ir(CO)H
Jeramie J Adams1, Navamoney Arulsamy, Dean M Roddick
1Department of Chemistry, University of Wyoming, Box 3838, Laramie, Wyoming 82071, USA.
New iridium complexes with electron-withdrawing pincer ligands were synthesized. These complexes exhibit varying structures and catalytic activity in decarbonylation reactions, offering insights into organometallic chemistry.
Area of Science:
- Organometallic Chemistry
- Coordination Chemistry
- Catalysis
Background:
- Pincer ligands are crucial in stabilizing metal complexes.
- Electron-withdrawing groups on ligands can tune reactivity.
- Iridium complexes are known for catalytic applications.
Purpose of the Study:
- To synthesize and characterize novel iridium complexes with a specific electron-withdrawing pincer ligand.
- To investigate the structural diversity of these complexes under different reaction conditions.
- To evaluate the catalytic potential of the synthesized iridium complexes.
Main Methods:
- Synthesis of iridium(I) and iridium(III) complexes using (PPh3)3Ir(CO)H and the pincer ligand (1,3-C6H4(CH2P(CF3)2)2) ((CF3)PCPH).
- Characterization of complexes through varying stoichiometry, reaction conditions (ambient vs. high temperature), and presence of MeI.
- Investigation of catalytic activity for decarbonylation reactions.
Main Results:
- Formation of mono-bridged, doubly-bridged, and tetrameric oligomeric iridium complexes under different conditions.
- Synthesis of a 5-coordinate Ir(I) complex ((CF3)PCP)Ir(CO)(PPh3) at higher temperatures.
- The Ir(I) complex demonstrated mild catalytic activity in the decarbonylation of 2-naphthaldehyde.
Conclusions:
- The electron-withdrawing pincer ligand ((CF3)PCPH) can form diverse iridium complexes with varying nuclearities.
- Reaction conditions significantly influence the structure of the resulting iridium complexes.
- The synthesized Ir(I) complex shows potential as a catalyst in organic transformations.
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