Central vs. peripheral Ag(i) coordination in NS3-open chain and cage ligands

J. Baumeister, R. Alberto, K. Ortner, B. Spingler, P. Schubiger, T. Kaden
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引用次数: 25

Abstract

A series of NS3-open chain and cage ligands were synthesised and their complexation behaviour towards Ag(I) and Cu(I) studied. Crystal structures show that all open chain ligands form complexes in which the four donor atoms of the ligands coordinate the metal ions in a trigonal pyramidal geometry. For the NS3-cages, however, the ions are not in the centre of the cage, but show peripheral coordination resulting in polymeric crystal structures. The new NS3-aromatic cage ligand 18 binds Ag(I) peripherally giving a polymeric structure in the solid state and fluxional behaviour in solution. NMR evidence for equally populated central and peripheral coordination sites is coherent with results from DFT calculations.
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ns3开链和笼形配体中Ag(i)的中心与外周配位
合成了一系列ns3开链和笼形配体,研究了它们对Ag(I)和Cu(I)的络合行为。晶体结构表明,所有开链配体都形成配合物,其中配体的四个给体原子以三角锥体几何形式配位金属离子。而对于ns3笼,离子不在笼的中心,而是呈现外围配位,从而形成聚合物晶体结构。新型ns3 -芳香族笼形配体18与Ag(I)外周结合,在固态下具有聚合物结构,在溶液中具有流动行为。核磁共振证据表明,中心和外围配位点分布均匀,与DFT计算结果一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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