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五配位镍(II)卟啉的结构与性质。

Structure and Properties of a Five-Coordinate Nickel(II) Porphyrin.

机构信息

Max Planck Institute for Chemical Energy Conversion , Stiftstrasse 34-36 , 45470 Mülheim an der Ruhr , Germany.

Institute of Inorganic and Analytical Chemistry , Friedrich Schiller University Jena , Humboldtstrasse 8 , 07743 Jena , Germany.

出版信息

Inorg Chem. 2019 Oct 7;58(19):12542-12546. doi: 10.1021/acs.inorgchem.9b00348. Epub 2019 Mar 29.

Abstract

Axial coordination in nickel(II) porphyrins has been thoroughly investigated and is well understood. However, isolated five-coordinate nickel(II) porphyrins are still elusive after 50 years of intense research, even though they play a crucial role as intermediates in enzymes and catalysts. Herein we present the first fully stable, thoroughly characterized five-coordinate nickel(II) porphyrin in solution and in the solid state (crystal structure). The spectroscopic properties indicate pure high-spin behavior ( = 1). There are distinct differences in the NMR, UV-vis, and redox behavior compared to those of high-spin six-coordinate [with two axial ligands, such as NiTPPF·(py)] and low-spin four-coordinate (NiTPPF) nickel(II) porphyrins. The title compound, a strapped nickel(II) porphyrin, allows a direct comparison of four-, five-, and six-coordinate nickel(II) porphyrins, depending on the environment. With this reference in hand, previous results were reevaluated, for example, the switching efficiencies and thermodynamic data of nickel(II) porphyrin-based spin switches in solution.

摘要

镍(II)卟啉的轴向配位已经得到了深入的研究,并且被很好地理解。然而,尽管它们作为酶和催化剂中的中间体起着至关重要的作用,但经过 50 年的深入研究,仍然难以获得孤立的五配位镍(II)卟啉。在此,我们首次在溶液中和固态(晶体结构)中呈现出完全稳定、彻底表征的五配位镍(II)卟啉。光谱性质表明其具有纯高自旋行为( = 1)。与高自旋六配位镍(II)卟啉(具有两个轴向配体,如 NiTPPF·(py)])和低自旋四配位镍(II)卟啉相比,其 NMR、UV-vis 和氧化还原行为存在明显差异。标题化合物是一种 strapped 镍(II)卟啉,可以根据环境直接比较四配位、五配位和六配位镍(II)卟啉。有了这个参考,我们重新评估了以前的结果,例如,基于镍(II)卟啉的自旋开关在溶液中的开关效率和热力学数据。

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