2009
DOI: 10.1016/j.jorganchem.2009.03.021
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Bis(imino)pyridine palladium(II) complexes: Synthesis, structure and catalytic activity

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Cited by 34 publications
(16 citation statements)
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“…The Pd1-O1 (1.969 Å) bond length is slightly shorter than that found in the related bis(phenoxyketimine) palladium complex (1.985 Å) [8] and schiff bases of 1-hydroxy-2-acetonaphthone palladium complexes (1.973-2.061 Å) [9]. The Pd1-N1 (2.019 Å) bond length is comparable to that in schiff bases of 1-hydroxy-2-acetonaphthone palladium complexes (2.010-2.019 Å), and is shorter than that in bis(phenoxyketimine) palladium complex (2.033 Å) and bis(imino)pyridine palladium complexes (2.04-2.06 Å) [10]. The angles of N1-Pd1-O1, N1-Pd1-Cl1, O1-Pd1-Cl2 and Cl1-Pd1-Cl2 are 91.03 (11), 94.28 (8) (Table 1).…”
Section: Oh O Rmentioning
confidence: 83%
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“…The Pd1-O1 (1.969 Å) bond length is slightly shorter than that found in the related bis(phenoxyketimine) palladium complex (1.985 Å) [8] and schiff bases of 1-hydroxy-2-acetonaphthone palladium complexes (1.973-2.061 Å) [9]. The Pd1-N1 (2.019 Å) bond length is comparable to that in schiff bases of 1-hydroxy-2-acetonaphthone palladium complexes (2.010-2.019 Å), and is shorter than that in bis(phenoxyketimine) palladium complex (2.033 Å) and bis(imino)pyridine palladium complexes (2.04-2.06 Å) [10]. The angles of N1-Pd1-O1, N1-Pd1-Cl1, O1-Pd1-Cl2 and Cl1-Pd1-Cl2 are 91.03 (11), 94.28 (8) (Table 1).…”
Section: Oh O Rmentioning
confidence: 83%
“…Similarly, several bases were employed in Suzuki reactions (entries 6-9), K 2 CO 3 proving superior (entry 6). Further studies indicated that the catalytic activity could be reduced with lowering the reaction temperature (entries [10][11][12].…”
Section: Oh O Rmentioning
confidence: 99%
“…Recently, Scheuermann and co-workers developed a palladium nanoparticle catalyst on graphite oxide, which showed excellent catalytic activity in the Suzuki reaction of 4-bromo-1,2-difluorobenzene with arylboronic acids [49]. However, the coupling reaction of 3,4-difluorophenylboronic acid with aryl bromide is rarely reported [23,24]. Therefore, the Suzuki reaction of 3,4-difluorophenylboronic acid was also investigated in this thermoregulated system.…”
Section: Scope and Limitations Of Substratesmentioning
confidence: 99%
“…However, this method is limited in applications due to harsh reaction conditions and low product yield. Recently, the synthesis of TFT-LCDs in organic solvent via path II was emerged [23,24]. However, to the best of our knowledge, there is no previous report of the efficient synthesis of fluorinated liquid crystals using the commercially available arylboronic acids in water.…”
Section: Application In Synthesis Of Fluorinated Liquid Crystalsmentioning
confidence: 99%
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