4.8 Article

Oxygen reduction reactivity of cobalt(II) hangman porphyrins

期刊

CHEMICAL SCIENCE
卷 1, 期 3, 页码 411-414

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0sc00281j

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资金

  1. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the U.S. Department of Energy [DE-FG02-05ER15745]
  2. National Science Foundation [DMR 0819762]
  3. Fannie and John Hertz Foundation
  4. Direct For Mathematical & Physical Scien
  5. Division Of Materials Research [GRANTS:13714308] Funding Source: National Science Foundation
  6. Division Of Materials Research
  7. Direct For Mathematical & Physical Scien [0819762] Funding Source: National Science Foundation

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Cobalt(II) hangman porphyrins are delivered from easily available starting materials, in two steps, in good yields, and with abbreviated reaction times. Selected compounds from a library of Co(II) hangman porphyrins immobilized on multiwall carbon nanotubes establish that the four-electron four-proton catalytic reduction of oxygen to water in aqueous solution can be achieved at the single cobalt center of the hangman platform. Reaction trends within the library reveal that the selective reduction of O(2) to H(2)O occurs at electron deficient hangman porphyrin platforms possessing a distal group that is capable of proton transfer.

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