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双N-稠合六卟啉:一种新型的在核心部位能络合双金属的芳香性扩展卟啉。

Doubly N-confused hexaphyrin: a novel aromatic expanded porphyrin that complexes bis-metals in the core.

作者信息

Srinivasan Alagar, Ishizuka Tomoya, Osuka Atsuhiro, Furuta Hiroyuki

机构信息

Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.

出版信息

J Am Chem Soc. 2003 Jan 29;125(4):878-9. doi: 10.1021/ja029018v.

Abstract

Meso-hexakis(pentafluorophenyl)-substituted doubly N-confused hexaphyrins and their metal complexes were synthesized for the first time, and the structures were elucidated by X-ray single-crystal analyses. The free base form of oxidized hexaphyrin (5) had two preorganized N3O pockets in the macrocyclic core, where a hydrogen-bonding network was formed to keep the molecule planar (the mean plane deviation is 0.054 A). The formation of a planar bis-Cu(II) complex was confirmed by UV/vis, magnetic susceptibility measurements, and X-ray crystallography. The bis-Ni(II) complex (7), on the other hand, was distored from planarity, but it changed to the planar structure upon solvent (acetonitrile) coordination as judged by the observation of a sharp Soret-like band in absorption spectra and the X-ray structures of the complexes.

摘要

首次合成了中六(五氟苯基)取代的双N-稠合六卟啉及其金属配合物,并通过X射线单晶分析阐明了其结构。氧化六卟啉(5)的游离碱形式在大环核心中有两个预组织的N3O口袋,在那里形成了氢键网络以保持分子平面(平均平面偏差为0.054 Å)。通过紫外可见光谱、磁化率测量和X射线晶体学证实了平面双铜(II)配合物的形成。另一方面,双镍(II)配合物(7)偏离平面,但根据吸收光谱中尖锐的类Soret带的观察以及配合物的X射线结构判断,它在溶剂(乙腈)配位时转变为平面结构。

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