Linear bilateral extended 2,2′:6′,2"-terpyridine ligands, their coordination complexes and heterometallic supramolecular networks

被引:20
作者
Veliks, Janis [1 ]
Tseng, Jui-Chang [2 ]
Arias, Karla I. [1 ]
Weisshar, Florian [1 ]
Linden, Anthony [1 ]
Siegel, Jay S. [1 ,3 ]
机构
[1] Univ Zurich, Dept Chem, CH-8057 Zurich, Switzerland
[2] Chaoyang Univ Technol, Dept Appl Chem, Taichung 41349, Taiwan
[3] Tianjin Univ, Sch Pharmaceut Sci & Technol, Tianjin 300072, Peoples R China
基金
瑞士国家科学基金会;
关键词
PALLADIUM-CATALYZED REACTION; METAL-ORGANIC FRAMEWORKS; ORGANOMETALLIC COMPOUNDS; SELECTIVE SYNTHESIS; CRYSTAL-STRUCTURES; CONVENIENT METHOD; DESIGN; TERPYRIDINE; ACETONITRILE; BIPYRIDINE;
D O I
10.1039/c4sc01025f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Octahedral metal complexes of tridentate 2,2':6',2"-terpyridine (terpy) fused with five-membered furan rings mimic the topology of tetrahedral metal complexes of bidentate 5,5'-functionalized 2,2'-bipyridine (bipy). Herein, we report the robust synthesis of 2,6-bis(2-substituted-furo[2,3-c]pyridine-5-yl)pyridine based ligands to access a series of linear bilateral extended terpy derivatives. This molecular design of alternating five-and six-membered rings has been applied to extend the applicability of terpy as a building block in supramolecular chemistry. The complexation of 2,6-bis(2-substituted-furo[2,3-c] pyridine-5-yl) pyridine derivatives with metal ions preferring octahedral geometry (Fe2+, Ru2+, and Zn2+) gives molecular "crossings" and "corners". Such design elements, functionalized with 4-pyridyl groups, allowed the construction of 3D and 2D heterometallic supramolecular networks containing Fe2+, Ag+ or Fe2+, Cu+ metal centers.
引用
收藏
页码:4317 / 4327
页数:11
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