Synthesis of acyclic tetrakis- and pentakis(N2O2) ligands for single-helical heterometallic complexes with a greater number of winding turns

被引:40
作者
Akine, Shigehisa [1 ]
Matsumoto, Takashi [1 ]
Sairenji, Shiho [1 ]
Nabeshima, Tatsuya [1 ]
机构
[1] Univ Tsukuba, Grad Sch Pure & Appl Sci, Tsukuba, Ibaraki 3058571, Japan
关键词
helical structure; foldamer; metal complex; oxime; chelate ligand; SITE-SELECTIVE TRANSMETALATION; COBALT(II) COMPLEX; ABIOTIC METALLOFOLDAMERS; TETRAOXIME LIGAND; ABSOLUTE HELICITY; ZINC(II) COMPLEX; INVERSION; TRINUCLEAR; METAL; CHELATE;
D O I
10.1080/10610278.2010.514906
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Acyclic oligooxime ligands (H8L4 and H10L5) that have four or five N2O2 coordinating moieties (salamo moieties) were synthesised in order to obtain single-helical metal complexes with a greater number of winding turns. When the complexation of the tetrakis (salamo) ligand H8L4 with zinc(II) took place, a complicated mixture of zinc(II) complexes was formed. However, the mixture was converted to a discrete pentanuclear complex in the presence of a guest ion with a suitable size (La3+, Ba2+), which was evidenced by the well-resolved sharp 1H NMR spectra and the mass spectra. Other ions with a smaller size (Lu3+, Ca2+) did not lead to such a discrete species. The 1H NMR spectral feature of the pentanuclear complex [L4Zn4La(OAc)3] is consistent with the single-helical structure in which the nth benzene ring approximately lies on the (n+3)th benzene ring.
引用
收藏
页码:106 / 112
页数:7
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