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基于发射噻吩基咪唑配体的线性 Mn 节点 MOF 的磁性和发光性。

Magnetism and Luminescence of a MOF with Linear Mn Nodes Derived from an Emissive Terthiophene-Based Imidazole Linker.

机构信息

Department of Chemistry, The University of Texas at Austin, 105 E. 24th Street, Stop A5300, Austin, TX 78712-1224, USA.

出版信息

Molecules. 2021 Jul 15;26(14):4286. doi: 10.3390/molecules26144286.

DOI:10.3390/molecules26144286
PMID:34299563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8305848/
Abstract

A new terthiophene-based imidazole luminophore 5,5'-(1-thieno[3,4-d]imidazole-4,6-diyl)bis(thiophene-2-carboxylic acid) (TIBTCH, ) was synthesized in one step from previously reported 4,6-di(thiophen-2-yl)-1-thieno[3,4-d]imidazole (DTTI, ), and their photophysical properties were studied and compared accordingly. Under solvothermal conditions, reacting with Mn(OAc) yielded a new three-dimensional metal-organic framework (MOF, ) which was structurally defined by single-crystal X-ray diffraction. In , all Mn(II) ions octahedrally bind to carboxylate- atoms to form a linear Mn secondary building unit (SBU) that contains three distinct coordination modes. Importantly, exhibits dual functional properties of ligand-based emission and metal-based magnetic behaviors.

摘要

一种新的基于噻吩并[3,4-d]咪唑的咪唑发光体 5,5'-(1-噻吩并[3,4-d]咪唑-4,6-二基)双(噻吩-2-羧酸)(TIBTCH,)由先前报道的 4,6-二(噻吩-2-基)-1-噻吩并[3,4-d]咪唑(DTTI,)一步合成,并相应地研究和比较了它们的光物理性质。在溶剂热条件下,与 Mn(OAc)反应生成了一种新的三维金属-有机骨架(MOF,),其结构由单晶 X 射线衍射确定。在中,所有 Mn(II)离子以八面体形式与羧酸根原子配位,形成包含三种不同配位模式的线性 Mn 次级构筑单元(SBU)。重要的是,表现出配体基发射和金属基磁行为的双重功能特性。

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