A doubly interpenetrated Cu(II)-based MOF 1 has been synthesized, structurally characterized and exploited as a heterogeneous catalyst for the ipso-hydroxylation of arylboronic acids.
Abstract
A doubly interpe...
Artikel
A Series of Low‐Coordinate Iron Selenido Complexes: Reactivity of a Linear Iron(I) Silylamide towards Selenium
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We examined the reaction of the linear iron(I) silylamide [Fe(N(Dipp)SiMe3)2]– (Dipp=2,6-diisopropylphenyl) with red selenium. This yields a variety of iron (poly)selenides, and observation of an intramolecular C−H bond activation by a putative terminal iron selenide.
Abstract
A variety of different low-coordinate iron selenide complexes is reported. These are obtained by reaction of the linear iron(I) silylamide K{18c6}[Fe(N(Dipp)SiMe3)2] (Dipp=2,6-diisopropylphenyl) with red selenium. Careful adjustment of the reaction conditions results in the formation of unique low-coordinate selenido iron complexes, namely a monoselenide bridged [2Fe−1Se]2+ complex, as well as mononuclear iron per- and triselenides. Further, C−H bond activation of one of the silylamide ligands by a putative terminal iron monoselenide is observed.
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