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Functionalised Mn(VI)-nanoparticles: an advanced high-valent magnetic catalyst.
Khamarui, Saikat; Saima, Yasmin; Laha, Radha M; Ghosh, Subhadeep; Maiti, Dilip K.
Afiliação
  • Khamarui S; Department of Chemistry, University of Calcutta, University College of Science, 92 A. P. C. Road, Kolkata-700009, India.
  • Saima Y; Department of Chemistry, University of Calcutta, University College of Science, 92 A. P. C. Road, Kolkata-700009, India.
  • Laha RM; Department of Chemistry, University of Calcutta, University College of Science, 92 A. P. C. Road, Kolkata-700009, India.
  • Ghosh S; Department of Chemistry, University of Calcutta, University College of Science, 92 A. P. C. Road, Kolkata-700009, India.
  • Maiti DK; Department of Chemistry, University of Calcutta, University College of Science, 92 A. P. C. Road, Kolkata-700009, India.
Sci Rep ; 5: 8636, 2015 Mar 02.
Article em En | MEDLINE | ID: mdl-25727767
ABSTRACT
We discover Mn(VI)-nanoparticles (NPs) bearing functional groups, high oxidation state, strong electron affinity, unique redox and paramagnetic nature, which opens up a new avenue to catalysis, magnetism and material application. However, its synthesis is challenging and remains unexplored because of associated serious difficulties. A simple benign synthetic strategy is devised to fabricate the high-valent NPs using mild reducing agent bromide, which transformed Mn(VII) to valuable Mn(VI)-species. The EELS-imaging of individual elements, ESI-MS, XPS and other techniques established its composition as Br(Me3SiO)Mn(VI)O2. It revealed significantly improved magnetic moment (SQUID) with isotropic hyperfine splitting of six line spectrum (EPR). The high-oxidation state and incorporated-ligands of the metals present on the active surface of the NPs led to development of a general catalytic process for oxidative heterodifunctionalisation to C-C triple bond towards formation of a new O-C/N-C/S-C and C-C coupling cum cyclisation to biologically important flavones and their aza- and marcapto-analogues, and valuable enaloxy synthons.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article