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Heterogeneous catalase-like activity of gold(i)–cobalt(iii) metallosupramolecular ionic crystals
Unique heterogeneous catalase-like activity was observed for metallosupramolecular ionic crystals [Au(I) (4)Co(III) (2)(dppe)(2)(d-pen)(4)]X(n) ([1]X(n); dppe = 1,2-bis(diphenylphosphino)ethane; d-pen = d-penicillaminate; X(n) = (Cl(–))(2), (ClO(4) (–))(2), (NO(3) (–))(2) or SO(4) (2–)) consisting o...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433492/ https://www.ncbi.nlm.nih.gov/pubmed/28553503 http://dx.doi.org/10.1039/c6sc04993a |
Sumario: | Unique heterogeneous catalase-like activity was observed for metallosupramolecular ionic crystals [Au(I) (4)Co(III) (2)(dppe)(2)(d-pen)(4)]X(n) ([1]X(n); dppe = 1,2-bis(diphenylphosphino)ethane; d-pen = d-penicillaminate; X(n) = (Cl(–))(2), (ClO(4) (–))(2), (NO(3) (–))(2) or SO(4) (2–)) consisting of Au(I) (4)Co(III) (2) complex cations, [1](2+), and inorganic anions, X(–) or X(2–). Treatment of the ionic crystals with an aqueous H(2)O(2) solution led to considerable O(2) evolution with a high turnover frequency of 1.4 × 10(5) h(–1) for the heterogeneous cobalt complexes, which was dependent on their size and shape as well as the arrangement of cationic and anionic species. These dependencies were rationalized by the presence of cobalt(ii) centers on the crystal surface and their efficient exposure on the (111) plane rather than the (100) plane based on morphological and theoretical studies. |
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