AL) and cyclic (>CL) aza-bridged ligands incorporating 2,2-pipryidine subunits is described. 1H-NMR and IR spectral data support t'/> Synthesis and Characterization of Acyclic and Cyclic Aza-bridged Ligands Incorporating 22-Bipyridine Subunits and Their Complexes With Copper(II) Cobalt(II) and Nickel(II)
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Synthesis and Characterization of Acyclic and Cyclic Aza-bridged Ligands Incorporating 22-Bipyridine Subunits and Their Complexes With Copper(II) Cobalt(II) and Nickel(II)

机译:含22-联吡啶亚基及其与铜(II)钴(II)和镍(II)的配合物的无环环状氮杂桥联配体的合成与表征

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摘要

The synthesis of a series of N,N'-disubstituted acyclic (>AL) and cyclic (>CL) aza-bridged ligands incorporating 2,2-pipryidine subunits is described. 1H-NMR and IR spectral data support the proposed ligand structures. Dynamic 1H-NMR studies on diurea and diamide derivatives point to the presence of slowly interconverting conformers on the 1H-NMR time-scale, owing to N−H···N hydrogen bonding and/or a restricted rotation around the amide bonds. The ligands synthesized form 1:1 complexes with divalent transition metal ions. Upon complexation, bis-ester derivatives >AL5 and >CL5 undergo a metal-induced hydrolysis of the ester groups to carboxyl functions, which act as additional binding sites for the metal ion, as well as hydrogen-bonding donor-acceptor binding site to produce dimeric complexes.
机译:描述了一系列N,N'-二取代的无环(> AL )和环状(> CL )氮杂桥联配体,其中包含2,2-吡啶基亚基。 1 H-NMR和红外光谱数据支持所提出的配体结构。对双脲和二酰胺衍生物的动态 1 H-NMR研究表明,由于NH··,在 1 H-NMR时标上存在缓慢互变的构象异构体·N氢键和/或绕酰胺键的受限旋转。合成的配体与二价过渡金属离子形成1:1配合物。络合后,双酯衍生物> AL5 和> CL5 经历金属诱导的酯基水解为羧基官能团,后者充当金属离子的附加结合位点,以及氢键结合的供体-受体结合位点以产生二聚体复合物。

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