Dendrimeric Organotelluride Catalysts for the Activation of Hydrogen Peroxide. Improved Catalytic Activity through Statistical and Stereoelectronic Effects
Dendrimeric polyorganotellurides are prepared in high yield using propyloxy spacers to connect the organotelluride groups to the core molecules. The polyorganotellurides catalyze the oxidation of thiophenol with hydrogen peroxide to give diphenyl disulfide in homogeneous solutions (5% CH2Cl2/MeOH or...
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Published in | Organometallics Vol. 22; no. 14; pp. 2883 - 2890 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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WASHINGTON
American Chemical Society
07.07.2003
Amer Chemical Soc |
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Abstract | Dendrimeric polyorganotellurides are prepared in high yield using propyloxy spacers to connect the organotelluride groups to the core molecules. The polyorganotellurides catalyze the oxidation of thiophenol with hydrogen peroxide to give diphenyl disulfide in homogeneous solutions (5% CH2Cl2/MeOH or 46% CH2Cl2/MeOH). The polyorganotellurides with two, three, four, and six catalytic groups show roughly statistical increases for the number of catalytic groups relative to the corresponding monotellurides. Catalysts containing [4-(dimethylamino)phenyl]telluro groups and n-hexyltelluro groups are oxidized more rapidly by hydrogen peroxide and also show greater catalytic activity than the corresponding catalysts containing phenyltelluro groups. A combination of statistical effects and stereoelectronic effects give a 26-fold increase in catalytic activity from 1-phenoxy-3-(phenyltelluro)propane (23a; ν0 = 12 μM min-1) to dendrimer 22c with six n-hexyltelluro groups (ν0 = 312 μM min-1) for the oxidation of 1.0 × 10-3 M PhSH with 3.75 × 10-3 M H2O2 in the presence of 1.0 × 10-5 M catalyst. The rate of appearance of PhSSPh, with a molar extinction coefficient, ε, of 1.24 × 10-3 L mol-1 cm-1 at 305 nm, was monitored at 305 nm. |
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AbstractList | Dendrimeric polyorganotellurides are prepared in high yield using propyloxy spacers to connect the organotelluride groups to the core molecules. The polyorganotellurides catalyze the oxidation of thiophenol with hydrogen peroxide to give diphenyl disulfide in homogeneous solutions (5% CH2Cl2/MeOH or 46% CH2Cl2/MeOH). The polyorganotellurides with two, three, four, and six catalytic groups show roughly statistical increases for the number of catalytic groups relative to the corresponding monotellurides. Catalysts containing [4-(dimethylamino)-phenyl]telluro groups and n-hexyltelluro groups are oxidized more rapidly by hydrogen peroxide and also show greater catalytic activity than the corresponding catalysts containing phenyltelluro groups. A combination of statistical effects and stereoelectronic effects give a 26-fold increase in catalytic activity from 1-phenoxy-3-(phenyltelluro)propane (23a; nu(0) = 12 muM min(-1)) to dendrimer 22c with six n-hexyltelluro groups (nu(0) = 312 muM min(-1)) for the oxidation of 1.0 x 10(-3) M PhSH with 3.75 x 10(-3) M H2O2 in the presence of 1.0 x 10(-5) M catalyst. The rate of appearance of PhSSPh, with a molar extinction coefficient, epsilon, of 1.24 x 10(-3) L mol(-1) cm(-1) at 305 nm, was monitored at 305 nm. Dendrimeric polyorganotellurides are prepared in high yield using propyloxy spacers to connect the organotelluride groups to the core molecules. The polyorganotellurides catalyze the oxidation of thiophenol with hydrogen peroxide to give diphenyl disulfide in homogeneous solutions (5% CH2Cl2/MeOH or 46% CH2Cl2/MeOH). The polyorganotellurides with two, three, four, and six catalytic groups show roughly statistical increases for the number of catalytic groups relative to the corresponding monotellurides. Catalysts containing [4-(dimethylamino)phenyl]telluro groups and n-hexyltelluro groups are oxidized more rapidly by hydrogen peroxide and also show greater catalytic activity than the corresponding catalysts containing phenyltelluro groups. A combination of statistical effects and stereoelectronic effects give a 26-fold increase in catalytic activity from 1-phenoxy-3-(phenyltelluro)propane (23a; ν0 = 12 μM min-1) to dendrimer 22c with six n-hexyltelluro groups (ν0 = 312 μM min-1) for the oxidation of 1.0 × 10-3 M PhSH with 3.75 × 10-3 M H2O2 in the presence of 1.0 × 10-5 M catalyst. The rate of appearance of PhSSPh, with a molar extinction coefficient, ε, of 1.24 × 10-3 L mol-1 cm-1 at 305 nm, was monitored at 305 nm. |
Author | You, Youngjae Ahsan, Khalid Wojciechowski, Amy L Drake, Michael D Detty, Michael R Higgs, Donald E Tse, Brian N Bateman, Margaret A |
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CitedBy_id | crossref_primary_10_1002_ejic_201001111 crossref_primary_10_1039_b616288f crossref_primary_10_1021_om2001553 crossref_primary_10_1002_chem_200500556 crossref_primary_10_1021_ja505648x crossref_primary_10_1021_ic402485d crossref_primary_10_1021_ma052268m crossref_primary_10_1021_om049722f crossref_primary_10_1039_c2cs35030k crossref_primary_10_1039_D4OB00552J crossref_primary_10_1021_jacsau_2c00193 crossref_primary_10_1080_10426500801900915 crossref_primary_10_1021_om500883f crossref_primary_10_1039_B311782K crossref_primary_10_1560_IJC_49_1_109 crossref_primary_10_3762_bjoc_20_112 crossref_primary_10_1590_S0001_37652009000300006 crossref_primary_10_1002_ejic_200900682 crossref_primary_10_1016_j_abb_2017_08_002 |
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Keywords | ANTIOXIDANT ACTIVITY OXIDATION THIOL PEROXIDASE GLUTATHIONE SPHERICAL SUPRAMOLECULAR DENDRIMERS CONVERGENT APPROACH HIGHLY ENANTIOSELECTIVE EPOXIDATION TELLURIDES GENERATION DIBROMIDES |
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Snippet | Dendrimeric polyorganotellurides are prepared in high yield using propyloxy spacers to connect the organotelluride groups to the core molecules. The... |
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SubjectTerms | Chemistry Chemistry, Inorganic & Nuclear Chemistry, Organic Physical Sciences Science & Technology |
Title | Dendrimeric Organotelluride Catalysts for the Activation of Hydrogen Peroxide. Improved Catalytic Activity through Statistical and Stereoelectronic Effects |
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