2012
DOI: 10.1016/j.ccr.2012.04.003
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Stereochemical and structural characteristics of single- and double-site Pd(II)–N-heterocyclic carbene complexes: Promising catalysts in organic syntheses ranging from CC coupling to olefin polymerizations

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Cited by 165 publications
(55 citation statements)
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“…According to the results as mentioned in Table 3, Pd4 like Pd5 exhibited excellent conversion (93%) and high ToF value (Run 14, Table 3). In contrast, PdCl 2 and Pd(OAc) 2 showed only 22% and 41% conversion, respectively, albeit at higher catalyst loading, illustrating the role of the ligand in the catalytic efficiency (Runs 15 and 16, Table 3). Complexes Pd4 and Pd5 have additional methyl groups on the para-position, which showed a detrimental effect that led to a slightly lower conversion rate as compared to analogous complexes [48].…”
Section: Heck Coupling Reactionmentioning
confidence: 93%
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“…According to the results as mentioned in Table 3, Pd4 like Pd5 exhibited excellent conversion (93%) and high ToF value (Run 14, Table 3). In contrast, PdCl 2 and Pd(OAc) 2 showed only 22% and 41% conversion, respectively, albeit at higher catalyst loading, illustrating the role of the ligand in the catalytic efficiency (Runs 15 and 16, Table 3). Complexes Pd4 and Pd5 have additional methyl groups on the para-position, which showed a detrimental effect that led to a slightly lower conversion rate as compared to analogous complexes [48].…”
Section: Heck Coupling Reactionmentioning
confidence: 93%
“…The abundant chemistry of palladium-based complex catalysts has attracted considerable attention, particularly in the field of C-C bond formation, C-H functionalization, hydrocarbon oxidation, as well as radical insertion and addition reaction in polymerization, indicating that palladium is one of the most catalytically versatile transition metals [1][2][3].…”
Section: Introductionmentioning
confidence: 99%
“…According to the 13 C NMR spectrum, the diagnostic Pd-NC N (3a-c) resonances appeared as singlets between δ 174.1 and 174.3 ppm. 13 C chemical shifts provide a useful diagnostic tool for this type of metal carbene complexes.…”
Section: Preparation Of Palladacyclic Complexes (3a-c)mentioning
confidence: 99%
“…In addition, NHC ligated palladacycles were investigated for their catalytic activity for Suzuki-Miyaura coupling of organic halides with phenylboronic acid. All complexes were fully characterized by 1 H NMR, 13 C NMR, and elemental analysis.…”
Section: 12mentioning
confidence: 99%
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