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铈与苯并恶嗪二聚体的异核单核配合物中氧化配位的晶体学和光谱学研究。

Crystallographic and Spectroscopic Investigations on Oxidative Coordination in the Heteroleptic Mononuclear Complex of Cerium and Benzoxazine Dimer.

机构信息

Department of Materials Engineering, Faculty of Engineering, Kasetsart University, Ladyao, Chatuchak, Bangkok 10900, Thailand.

School of Chemistry, Institute of Science, Suranaree University of Technology, 111 University Avenue, Suranaree, Muang, Nakhon Ratchasima 30000, Thailand.

出版信息

Molecules. 2021 Sep 6;26(17):5410. doi: 10.3390/molecules26175410.

Abstract

Among lanthanide-based compounds, cerium compounds exhibit a significant role in a variety of research fields due to their distinct tetravalency, high economic feasibility, and high stability of Ce(IV) complexes. Herein, a systematic investigation of crystallographic information, chemical properties, and mechanistic formation of the novel Ce(IV) complex synthesized from cerium(III) nitrate hexahydrate and 2,2'-(methylazanediyl)bis(methylene)bis(4-methylphenol) (MMD) ligand has been explored. According to the analysis of the crystallographic information, the obtained complex crystal consists of the Ce(IV) center coordinated with two nitrate ligands and two bidentate coordinated (-protonated and O,O-deprotonated) MMD ligands. The fingerprint plots and the Hirshfeld surface analyses suggest that the C-H⋯O and C-H⋯π interactions significantly contribute to the crystal packing. The C-H⋯O and C-H⋯π contacts link the molecules into infinite molecular chains propagating along the [100] and [010] directions. Synchrotron powder X-ray diffraction (XRD) and X-ray absorption spectroscopy (XAS) techniques have been employed to gain an understanding of the oxidative complexation of Ce(IV)-MMD complex in detail. This finding would provide the possibility to systematically control the synthetic parameters and wisely design the precursor components in order to achieve the desired properties of novel materials for specific applications.

摘要

在镧系化合物中,由于铈的四价、高经济可行性和 Ce(IV)配合物的高稳定性,铈化合物在各种研究领域中表现出重要作用。本文系统研究了由硝酸铈六水合物和 2,2'-(甲基亚氨基)双(亚甲基)双(4-甲基苯酚)(MMD)配体合成的新型 Ce(IV)配合物的晶体学信息、化学性质和形成机理。根据晶体学信息的分析,所得配合物晶体由 Ce(IV)中心与两个硝酸根配体和两个双齿配位(-质子化和 O,O-去质子化)MMD 配体配位。指纹图谱和 Hirshfeld 表面分析表明,C-H⋯O 和 C-H⋯π 相互作用对晶体堆积有重要贡献。C-H⋯O 和 C-H⋯π 接触将分子连接成沿[100]和[010]方向延伸的无限分子链。同步辐射粉末 X 射线衍射(XRD)和 X 射线吸收光谱(XAS)技术被用于详细了解 Ce(IV)-MMD 配合物的氧化络合。这一发现为系统地控制合成参数和明智地设计前体成分提供了可能性,以便为特定应用实现新型材料的所需性质。

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