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通过配位链构建的金属氢键有机框架用于磁性和质子传导双功能

Metalo Hydrogen-Bonded Organic Frameworks Constructed by Coordinated Chains for Magnetic and Proton-Conductive Bifunctionality.

作者信息

Dong Jing, Huang Long, Shi Le, Yang Jiong, Wan Yi, Shao Dong

机构信息

Hubei Key Laboratory of Processing and Application of Catalytic Materials, College of Chemistry and Chemical Engineering, Huanggang Normal University, Huanggang 438000, China.

State Key Laboratory of Chemical Engineering, Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou 310027, China.

出版信息

Inorg Chem. 2024 Sep 23;63(38):17478-17487. doi: 10.1021/acs.inorgchem.4c01847. Epub 2024 Sep 4.

Abstract

Metalo hydrogen-bonded organic frameworks (MHOFs) have received growing interest in designing crystalline functional materials. However, reports on bifunctional MHOFs showing magnetic and proton-conductive properties are extremely limited and their design is challenging. Herein, we investigated the magnetic and proton-conductive properties of two sulfonated and , {M(HO)(abs)} (M = Co and Mn, Habs = 4-aminoazobenzene-4'-sulfonic anion), constructed by coordination chains. The supramolecular frameworks sustained by H bonds between -SO and coordinated water show directional ladder-type H bonds with hydrophilic nanochannels, leading to high proton conduction with exceptionally high conductivity around 10 S cm at 100 °C under 97% relative humidity. In particular, the maximum σ value of , 2.11 × 10 S cm, recorded the highest value among the reported proton-conducting materials showing slow magnetic relaxation. Meanwhile, the molecular structure of organosulfonate enables the magnetic isolation of high-spin Co and Mn centers in the frameworks. Magnetic measurements indicated that the MHOFs show field-induced single-ion magnet (SIM) properties, making these compounds rare magnetic-proton-conductive MHOFs. The work provides not only two unique MHOFs with SIM behavior and high proton conduction performance but also avenues for designing stable bifunctional MHOFs via a coordination chain approach.

摘要

金属氢键有机框架(MHOFs)在设计晶体功能材料方面越来越受到关注。然而,关于具有磁性和质子传导特性的双功能MHOFs的报道极为有限,其设计也具有挑战性。在此,我们研究了两种由配位链构建的磺化{M(HO)(abs)}(M = Co和Mn,Habs = 4-氨基偶氮苯-4'-磺酸阴离子)的磁性和质子传导特性。由-SO与配位水之间的氢键维持的超分子框架显示出与亲水性纳米通道的定向梯型氢键,导致在97%相对湿度下100°C时具有约10 S cm的极高电导率,从而实现高质子传导。特别是,的最大σ值为2.11×10 S cm,在已报道的显示缓慢磁弛豫的质子传导材料中记录了最高值。同时,有机磺酸盐的分子结构使框架中的高自旋Co和Mn中心实现磁隔离。磁性测量表明,MHOFs显示出场诱导单离子磁体(SIM)特性,使这些化合物成为罕见的磁性-质子传导MHOFs。这项工作不仅提供了两种具有SIM行为和高质子传导性能的独特MHOFs,还为通过配位链方法设计稳定的双功能MHOFs提供了途径。

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