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Small molecule activation with divalent samarium triflate: a synergistic effort to cleave O2
Author(s) -
Mathieu Xémard,
Marie Cordier≈,
Elisa Louyriac,
Laurent Maron,
Carine Clavaguéra,
Grégory Nocton
Publication year - 2018
Publication title -
dalton transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.98
H-Index - 184
eISSN - 1477-9234
pISSN - 1477-9226
DOI - 10.1039/c8dt02196a
Subject(s) - samarium , trifluoromethanesulfonate , divalent , chemistry , lanthanide , cleave , molecule , carbonate , medicinal chemistry , polymer chemistry , inorganic chemistry , catalysis , organic chemistry , enzyme , ion
The divalent samarium triflate salt does not react with CO2 or water, but does react with traces of O2 or N2O to form a tetrameric bis-oxo samarium motif. The reaction with O2 is a 4e- reductive cleavage where the electrons are coming from four different samarium centers. This highlights a rare synergistic effect for cleaving O2, which has no precedent in divalent lanthanide complexes. Additionally, the addition of CO2 to the tetrameric bis-oxo intermediate leads to the formation of a tetrameric bis-carbonate samarium triflate. Thus, the concomitant reaction of CO2 with traces of O2 leads to the same bis-carbonate tetrameric assembly.

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