Calix[4]arene supported group 5 imido complexes
Calix[4]arene supported group 5 imido complexes
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杯[4]芳烃支持的第 5 族酰亚胺配合物
DOI:
10.1016/j.ica.2006.06.029
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发表时间:
2006
影响因子:
2.8
通讯作者:
U. Radius
中科院分区:
文献类型:
--
作者:
S. Dürr;B. Bechlars;U. Radius
The reaction of imidoyl chlorides [V(NR)Cl3] (R=Ph 1, Tol 2, tBu 3) and calix[4]arene methyl ether H3Mecalix unexpectedly leads to the formation of the structurally characterized vanadium (IV) complex [VCl(Mecalix)] (4). Calix[4]arene methyl ether stabilized imido complexes of the type [V(NR)(Mecalix)] (R=Ph 7, Tol 8, tBu 9) were afforded from the reaction of [V(NR)Cl3] (R=Ph 1, Tol 2, tBu 3) and the tris(lithium) or tris(sodium) salt of the calix[4]arene ether. The lithium salt [{Li3(Mecalix)}2] (5) is a dimer in the solid state, in which two monomeric trianions are bridged by lithium cations. Imido complexes [M(NR)(Mecalix)] (M=Nb: R=tBu, 12, R=Tol 13, R=Mes 14, R=Dipp 15; M=Ta: R=tBu 16, R=Tol 17) (Tol=4-C6H4Me, Mes=2,6-C6H3Me2; Dipp=2,6-C6H3iPr2) have been prepared from structurally characterized [NbCl2(Mecalix)] (10) and previously known [TaCl2(Mecalix)] (11) via reaction with two equivalents of the appropriately metallated (Li, K) primary amine. The molecular structures of 13 and 15 confirm the mononuclear nature of these complexes.