Abstract
Two-coordinate dialkylsilylene-coinage metal complexes 3+·TPFPB-(Cu) and 4+·TPFPB-(Ag) were synthesized as the first dialkylsilylene-copper complex and the first silylene-silver complex, respectively, by the reaction of dialkylsilylene 1 with the corresponding metal borate. X-ray analys is showed that both the complexes adopted a linear structure with two perpendicular dialkylsilylene units. Theoretical study indicated that weak π back-donation of the copper and silver complexes compared to that of the corresponding isoelectronic neutral palladium complex would be due to low-lying d orbitals of Cu+and Ag+centers and responsible for the linear structures.
Original language | English |
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Article number | CL-140651 |
Pages (from-to) | 1665-1667 |
Number of pages | 3 |
Journal | Chemistry Letters |
Volume | 43 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2014 |