Solution Synthesis,Structure, and CO2 Reduction Reactivity of a Scandium(II) Complex, {Sc[N(SiMe3)2]3}− |
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Abstract: | The first crystallographically characterizable complex of Sc2+, [Sc(NR2)3]− (R=SiMe3), has been obtained by LnA3/M reactions (Ln=rare earth metal; A=anionic ligand; M=alkali metal) involving reduction of Sc(NR2)3 with K in the presence of 2.2.2‐cryptand (crypt) and 18‐crown‐6 (18‐c‐6) and with Cs in the presence of crypt. Dark maroon [K(crypt)]+, [K(18‐c‐6)]+, and [Cs(crypt)]+ salts of the [Sc(NR2)3]− anion are formed, respectively. The formation of this oxidation state of Sc is also indicated by the eight‐line EPR spectra arising from the I =7/2 45Sc nucleus. The Sc(NR2)3 reduction differs from Ln(NR2)3 reactions (Ln=Y and lanthanides) in that it occurs under N2 without formation of isolable reduced dinitrogen species. [K(18‐c‐6)][Sc(NR2)3] reacts with CO2 to produce an oxalate complex, {K2(18‐c‐6)3}{[(R2N)3Sc]2(μ‐C2O4‐κ 1O:κ 1O′′)}, and a CO2− radical anion complex, [(R2N)3Sc(μ‐OCO‐κ 1O:κ 1O′)K(18‐c‐6)]n . |
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Keywords: | carbon dioxide low-valent metals rare earths reduction scandium |
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