2010
DOI: 10.1134/s0023158410010180
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Problems of distinguishing the homogeneous and heterogeneous mechanisms of the Suzuki reaction

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Cited by 3 publications
(3 citation statements)
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“…Further support for the direct role of a heterogeneous active phase emerged in a recent kinetic investigation, wherein ultracentrifugation revealed Suzuki coupling of bromobenzene and phenylboronic acid in EtOH-H 2 O (mediated by NaOH at 22 • C) arose solely from nanosized Pd clusters. 42 Perhaps the most compelling evidence for surface-driven Suzuki coupling derives from an elegant experiment in which Davis and co-workers effected spatially controlled Suzuki and Heck crosscouplings of surface tethered aryl halides and styrene respectively via a PdNP coated AFM probe; such highly localised reaction is unexpected if coupling were indeed mediated via mobile, solubilised Pd species freely diffusing throughout the solvent media.…”
Section: Introductionmentioning
confidence: 99%
“…Further support for the direct role of a heterogeneous active phase emerged in a recent kinetic investigation, wherein ultracentrifugation revealed Suzuki coupling of bromobenzene and phenylboronic acid in EtOH-H 2 O (mediated by NaOH at 22 • C) arose solely from nanosized Pd clusters. 42 Perhaps the most compelling evidence for surface-driven Suzuki coupling derives from an elegant experiment in which Davis and co-workers effected spatially controlled Suzuki and Heck crosscouplings of surface tethered aryl halides and styrene respectively via a PdNP coated AFM probe; such highly localised reaction is unexpected if coupling were indeed mediated via mobile, solubilised Pd species freely diffusing throughout the solvent media.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, it is possible to conduct the above equifinal processes on catalymetric chips with platinum enthrakometers under conditions of specific acceleration by the microwave field. Reactions of the latter type may, in part, be described as autocatalytic, as the agglomeration mechanisms of the metal-catalyst involved in the remetallation (e.g., Pd), are autocatalytic and indifferent to the introduction of the additional amounts of catalyst (therefore there is no need to replace the enthrakometer) [183][184][185].…”
Section: Microwave Acceleration Of Chemical Reactions and Microwave Catalysismentioning
confidence: 99%
“…This is mainly because the Pd ion complex formed by the oxidative addition reaction between BrPy and PdCl 2 increased the reactivity toward phenylboronic acid efficiently. 31,32 For Cu and Ni ion catalysts, it is difficult to generate the highly active reaction substance with BrPy for the subsequent reaction with phenylboronic acid. Based on the above facts, operando SERS plays an important role in the search of catalysts with high activities.…”
mentioning
confidence: 99%