Matussek Julia, Herbst-Irmer Regine, Objartel Ina, Stalke Dietmar
Institut für Anorganische Chemie der Georg-August-Universität Göttingen, Tammannstr. 4, 37077 Göttingen, Germany.
Dalton Trans. 2014 Nov 14;43(42):15944-9. doi: 10.1039/c4dt01995d.
Three novel metal complexes [(acac)2Cu2(NtBu)4S] (), [Li(thf)4]2[I4Cd2(NtBu)4S] () and [(thf)2Li{(SiMe3)2N}Zn(NtBu)4S] () are prepared from the intended transmetalation of the dilithium complex of N,N',N'',N'''-tetrakis(tert-butyl)tetraimidosulfate [(thf)4Li2(NtBu)4S] (). The two lithium cations are replaced by either the cationic (acac)Cu(ii) moiety, the neutral I2Cd(ii) residue or only a single lithium cation is substituted by the cationic (Me3Si)2NZn(ii) fragment. The complexes show two main results: first the S(NtBu)4(2-) tetrahedron can serve as a ligand to transition metals from the soft Cu(ii) to the harder Zn(ii) at opposite sides and second the S-N bond distances vary only marginally in response to the various metals and the four distances constantly sum up to 6.38(2) Å. Hence the electropositive sulfur atom responds by internal shift to the metal-polarized negative charge at the outside of the S(NR)4(2-) tetrahedron.
通过N,N',N'',N'''-四(叔丁基)四亚氨基硫酸二锂配合物[(thf)4Li2(NtBu)4S]的预期金属转移反应,制备了三种新型金属配合物[(acac)2Cu2(NtBu)4S]()、[Li(thf)4]2[I4Cd2(NtBu)4S]()和[(thf)2Li{(SiMe3)2N}Zn(NtBu)4S]()。两个锂阳离子被阳离子性的(acac)Cu(ii)部分、中性的I2Cd(ii)残基取代,或者只有一个锂阳离子被阳离子性的(Me3Si)2NZn(ii)片段取代。这些配合物显示出两个主要结果:第一,S(NtBu)4(2-)四面体可以作为配体,在相对的两侧与从软的Cu(ii)到较硬的Zn(ii)的过渡金属配位;第二,S-N键距仅随各种金属略有变化,且四个键距总和恒定为6.38(2) Å。因此,电正性的硫原子通过内部位移对S(NR)4(2-)四面体外部的金属极化负电荷作出响应。