Benzoato and Thiobenzoato Ligands in the Synthesis of Dinuclear Palladium(III) and -(II) Compounds: Stability and Catalytic Applications

• Published in: European journal of inorganic chemistry 2015-06, Vol.2015 (17), p.2822-2832
• Main Authors: Estevan, Francisco, Ibáñez, Susana, Ofori, Albert, Hirva, Pipsa, Sanaú, Mercedes, Úbeda, Ma Angeles
• Format: Article
• Language: English
• Subjects: Catalysis; Catalysts; Conversion; Density functional calculations; Electrochemistry; Homogeneous catalysis; Indoles; Ligands; Mathematical analysis; NMR spectroscopy; Palladium; S ligands; Stability; Structure elucidation
• ISSN: 1434-1948; 1099-0682
• DOI: 10.1002/ejic.201500324

New palladium(III) compounds of formula Pd2[(C6H4)PPh2]2[OXC(C6H5)]2Cl2 [3a (X = O); 3b (X = S)] were obtained by the oxidation of the analogous palladium(II) ones with PhICl2 and were characterized by 31P, 1H, and 13C NMR spectroscopy at 223 K. Compound 3a was also structurally characterized by single‐crystal X‐ray diffraction methods, which revealed a Pd–Pd distance of 2.5212(10) Å. DFT calculations were conducted to study the stability of all of these new palladium(III) and ‐(II) compounds with focus on the influence of the O↔S substitution of the donor atom in the ligand. The palladium(II) compounds Pd2[(C6H4)PPh2]2[OXC(C6H5)]2 [2a (X = O), 2b (X = S)] were also tested as precatalyst in two reactions: (1) the acetoxylation of 2‐phenylpyridine and (2) the room‐temperature 2‐phenylation of indoles. Compound 2b is a better precatalyst than 2a in the first reaction (4 h; isolated yield, 67.5 vs. 50.4 %). In the second catalytic reaction, isolated yields of 97 (10 h, substrate: 1‐methylindole) and 99 % (24 h, substrate: indole) were obtained with 2a as the precatalyst, whereas 2b gave low or no conversion. Dinuclear palladium(III) and ‐(II) compounds with benzoato and thiobenzoato ligands are synthesized. DFT calculations are performed to study the stability of these compounds and the influence of the O↔S substitution of the donor atom. The catalytic activity of the palladium(II) complexes is also tested in the acetoxylation of 2‐phenylpyridine and the room‐temperature 2‐phenylation of indoles.