“…Published results of the use of thiosemicarbazone complexes as described above for Cheteroatom coupling reactions are summarised in Table 4. Apart from the above C-N coupling reactions, there has also been one report by Suganthy et al of C-O coupling catalysed by a thiosemicarbazone complex [146]. Thus the coupling of p-cresol with a number of aryl halides containing electron-withdrawing or electron-donating groups could be effected, with moderate to very good yields, in DMF at 80 • C after 12 h in an inert atmosphere using a 1 mol% loading of the catalyst [PdCl(PPh 3 )L] (42), where L is the bidentate N,S-chelating ligand derived from the deprotonation of 3-methyl-thiophene-2-carboxaldehyde thiosemicarbazone (Figure 7).…”
Catalysis of cross-coupling reactions under phosphane-free conditions represents an important ongoing challenge. Although transition metal complexes based on the thiosemicarbazone unit have been known for a very long time, their use in homogeneous catalysis has been studied only relatively recently. In particular, reports of cross-coupling catalytic reactions with such complexes have appeared only in the last 15 years. This review provides a survey of the research in this area and a discussion of the prospects for future developments.
“…Published results of the use of thiosemicarbazone complexes as described above for Cheteroatom coupling reactions are summarised in Table 4. Apart from the above C-N coupling reactions, there has also been one report by Suganthy et al of C-O coupling catalysed by a thiosemicarbazone complex [146]. Thus the coupling of p-cresol with a number of aryl halides containing electron-withdrawing or electron-donating groups could be effected, with moderate to very good yields, in DMF at 80 • C after 12 h in an inert atmosphere using a 1 mol% loading of the catalyst [PdCl(PPh 3 )L] (42), where L is the bidentate N,S-chelating ligand derived from the deprotonation of 3-methyl-thiophene-2-carboxaldehyde thiosemicarbazone (Figure 7).…”
Catalysis of cross-coupling reactions under phosphane-free conditions represents an important ongoing challenge. Although transition metal complexes based on the thiosemicarbazone unit have been known for a very long time, their use in homogeneous catalysis has been studied only relatively recently. In particular, reports of cross-coupling catalytic reactions with such complexes have appeared only in the last 15 years. This review provides a survey of the research in this area and a discussion of the prospects for future developments.
“…Published results of the use of thiosemicarbazone complexes as described above for Cheteroatom coupling reactions are summarised in Table 4. Apart from the above C-N coupling reactions, there has also been one report by Suganthy et al of C-O coupling catalysed by a thiosemicarbazone complex [146]. Thus the coupling of p-cresol with a number of aryl halides containing electron-withdrawing or electron-donating groups could be effected, with moderate to very good yields, in DMF at 80 • C after 12 h in an inert atmosphere using a 1 mol% loading of the catalyst [PdCl(PPh 3 )L] (42), where L is the bidentate N,S-chelating ligand derived from the deprotonation of 3-methyl-thiophene-2-carboxaldehyde thiosemicarbazone (Figure 7).…”
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“…These have aroused great interest due to their wide range of applications. Their biological activity depends on the parent aldehyde or ketone [1][2][3]; also, palladium (II) complexes have proved to be useful as catalysts in cross coupling reactions like the Heck and Suzuki-Miyaura cross-coupling reaction [4][5][6][7].…”
Herein we report the design, synthesis and characterization of a series of phenylboronic cyclometallated derivatives bearing different phosphines. The compounds were prepared by reaction of cyclometallated species with different phosphine ligands and they were characterized by IR, 1 H and 31 P NMR spectroscopy.
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