Abstract:
The bis(carbazolide) complex of SmII, Sm[3,6-But2-1,8-(Me3SiC≡C)2Carb]2, was synthesized by the transamination reaction of Sm[N(SiMe3)2]2(THF)2 with two molar equivalents of carbazole 3,6-But2-1,8 (Me3SiC≡C)2CarbH. A similar reaction of the less sterically demanding carbazole 3,6-But2-1,8-(PhC≡C)2CarbH is accompanied by the oxidation of SmII to SmIII and lead to the formation of bis(carbazolide) amido complex [3,6-But2-1,8-(PhC≡C)2Carb]2Sm[N(SiMe3)2]. For both Sm complexes, η2-interactions with C≡C bonds, which are unconventional for LnII and LnIII metals, were experimentally confirmed by single-crystal X-ray diffraction, IR and Raman spectroscopy along with QTAIM analysis.
Citation:
H. Zakaria, D. M. Lyubov, R. R. Aysin, Yu. V. Nelyubina, S. S. Bukalov, A. A. Trifonov, “η2-Acetylene SmII and SmIII complexes: mirage or reality?”, Mendeleev Commun., 35:3 (2025), 310–313