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通过锰金属纳米粒子方法制备的半导体锰-联吡啶配位聚合物

Semiconducting Manganese-Bipyridyl Coordination Polymer via a Manganese-Metal-Nanoparticle Approach.

作者信息

Reiß Andreas, Göttlicher Jörg, Vitova Tonya, Feldmann Claus

机构信息

Institute for Inorganic Chemistry, Karlsruhe Institute of Technology (KIT) Engesserstrasse 15, D-76131 Karlsruhe, Germany.

Institute for Photon Science and Synchrotron Radiation, Karlsruhe Institute of Technology (KIT), D-76021 Karlsruhe, Germany.

出版信息

Inorg Chem. 2025 May 19;64(19):9469-9476. doi: 10.1021/acs.inorgchem.5c00080. Epub 2025 May 4.

Abstract

The coordination polymer [NaMn(4,4'-bipy)(2,2'-bipy)] is prepared by a novel redox approach using Mn(0) nanoparticles (2.4 ± 0.3 nm in size) as the starting material. The Mn(0) nanoparticles are then reacted with 2,2'-bipyridine (2,2'-bipy) and 4,4'-bipyridine (4,4'-bipy) in toluene at 80 °C. The title compound is composed of [Mn(2,2'-bipy)(4,4'-bipy)] chains and double-stranded [Na(2,2'-bipy)(4,4'-bipy)] chains forming an interpenetrating coordination network with five noncharged bipy ligands and six anionic [bipy] ligands. Such composition and coordination with bipy as sole ligand and anion are observed for the first time. Structure and composition are validated by X-ray diffraction based on single crystals and powders, XANES spectroscopy, infrared spectroscopy, and elemental analysis. Optical spectroscopy of the black-red, shiny metallic crystals shows absorption below 350 nm with a band gap <1.5 eV. Power-voltage curves indicate semiconducting behavior with a positive temperature gradient and silicon-like conductivity (3 × 10 S/m, 25 °C). In sum, the redox approach using Mn(0) nanoparticles allows for preparation of a Mn-coordinated interpenetrating network with 2,2'-bipy and 4,4'-bipy as sole ligands and semiconducting properties. The redox approach generally offers the option to realize further bipyridyl networks with other metals and semiconducting or metallic properties.

摘要

配位聚合物[NaMn(4,4'-联吡啶)(2,2'-联吡啶)]是通过一种新颖的氧化还原方法制备的,该方法使用尺寸为2.4±0.3 nm的Mn(0)纳米颗粒作为起始原料。然后将Mn(0)纳米颗粒与2,2'-联吡啶(2,2'-bipy)和4,4'-联吡啶(4,4'-bipy)在80℃的甲苯中反应。标题化合物由[Mn(2,2'-联吡啶)(4,4'-联吡啶)]链和双链[Na(2,2'-联吡啶)(4,4'-联吡啶)]链组成,形成一个具有五个不带电荷的联吡啶配体和六个阴离子[联吡啶]配体的互穿配位网络。首次观察到这种以联吡啶作为唯一配体和阴离子的组成和配位情况。通过基于单晶和粉末的X射线衍射、XANES光谱、红外光谱和元素分析对结构和组成进行了验证。对黑红色有光泽的金属晶体进行光谱分析,结果表明其在350 nm以下有吸收,带隙<1.5 eV。功率-电压曲线表明其具有半导体行为,具有正温度梯度和类似硅的电导率(3×10 S/m,25℃)。总之,使用Mn(0)纳米颗粒的氧化还原方法能够制备以2,2'-联吡啶和4,4'-联吡啶作为唯一配体且具有半导体性质的锰配位互穿网络。氧化还原方法通常提供了实现具有其他金属以及半导体或金属性质的进一步联吡啶网络的选择。

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