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Control reactions were performed (a) without oxygen and (b) without copper(II) complex. While the oxidation was completely inhibited in a sealed cuvette containing degassed, nitrogen-purged methanol, slow spontaneous oxidation of 3,5-DTBC to 3,5-DTBQ was observed in the presence of oxygen. The rate constant was determined from spectral data collected over a 1 h period.
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Control reactions were performed (a) without oxygen and (b) without copper(II) complex. While the oxidation was completely inhibited in a sealed cuvette containing degassed, nitrogen-purged methanol, slow spontaneous oxidation of 3,5-DTBC to 3,5-DTBQ was observed in the presence of oxygen. The rate constant was determined from spectral data collected over a 1 h period.
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38749083731
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Typical procedure for emulsion polymerization: Poly(acrylate) beads were prepared by mixing of 3 g of butyl acrylate and 3 g of styrene in 500 mg of decane with 48 mL of water containing 144 mg of sodium dodecyl sulfate (SDS). Ligand 2 (144 mg, 0.26 mmol) dissolved in 1 g of DMSO was then added and the resulting mixture was stirred vigourously for 1 h followed by sonication for 2 min. The polymerization was initiated by addition of aqueous potassium peroxysulfate at 72 °C and allowed to proceed for 3 h. The polymer particles obtained were purified by ultracentrifugation using micropore filters with a 10 000 MW cutoff. A sample aliquot of the aqueous polymer solution was dried for elemental analysis.
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Typical procedure for emulsion polymerization: Poly(acrylate) beads were prepared by mixing of 3 g of butyl acrylate and 3 g of styrene in 500 mg of decane with 48 mL of water containing 144 mg of sodium dodecyl sulfate (SDS). Ligand 2 (144 mg, 0.26 mmol) dissolved in 1 g of DMSO was then added and the resulting mixture was stirred vigourously for 1 h followed by sonication for 2 min. The polymerization was initiated by addition of aqueous potassium peroxysulfate at 72 °C and allowed to proceed for 3 h. The polymer particles obtained were purified by ultracentrifugation using micropore filters with a 10 000 MW cutoff. A sample aliquot of the aqueous polymer solution was dried for elemental analysis.
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The kinetic experiments were conducted after addition of appropriate amounts of aqueous copper(II) acetate solution to prepare a 0.09 mM aqueous catalyst stock solution that was subsequently diluted into methanol to yield a final 1.5 μM concentration of catalyst pol3a.
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The kinetic experiments were conducted after addition of appropriate amounts of aqueous copper(II) acetate solution to prepare a 0.09 mM aqueous catalyst stock solution that was subsequently diluted into methanol to yield a final 1.5 μM concentration of catalyst pol3a.
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