Głuchowska Halina, Łyszczek Renata, Mazur Liliana, Kirillov Alexander M
Department of General and Coordination Chemistry and Crystallography, Faculty of Chemistry, Institute of Chemical Sciences, Maria Curie-Skłodowska University in Lublin, M.C. Skłodowskiej Sq. 2, 20-031 Lublin, Poland.
Centro de Química Estrutural, Departamento de Engenharia Química, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisbon, Portugal.
Materials (Basel). 2021 Jun 25;14(13):3545. doi: 10.3390/ma14133545.
Two coordination polymers, [Co(µ-L)(HO)] () and [Ni(µ-L)(HO)] (), were solvothermally assembled from the corresponding metal(II) chlorides and biphenyl-4,4-dioxydiacetic acid (HL) as a flexible dicarboxylate linker. The cobalt(II) compound featured a layer-pillared 3D metal-organic network with a cds topology, while the nickel(II) derivative represented a linear chain 1D coordination polymer with a 2C1 topology. The µ and µ-L linkers exhibited different denticity and coordination modes in the synthesized compounds, thus contributing to their structural diversity. The dimensionality of and had an influence on their thermal stability and decomposition processes, which were investigated in detail by TG-DSC and TG-FTIR methods. Thermal decomposition products of coordination polymers were also analyzed by PXRD, confirming the formation of CoO/CoO and NiO as final materials. The obtained compounds broaden a family of coordination polymers assembled from flexible dicarboxylate linkers.
两种配位聚合物,[Co(µ-L)(H₂O)] ()和 [Ni(µ-L)(H₂O)] (),通过溶剂热法由相应的金属(II)氯化物和联苯-4,4-二氧二乙酸(HL)作为柔性二羧酸连接体组装而成。钴(II)化合物 具有层柱状的三维金属有机网络,拓扑结构为cds,而镍(II)衍生物 代表具有2C1拓扑结构的线性链一维配位聚合物。µ 和 µ-L 连接体在合成的化合物中表现出不同的配位数和配位模式,从而导致了它们结构的多样性。 和 的维度对它们的热稳定性和分解过程有影响,通过TG-DSC和TG-FTIR方法对其进行了详细研究。配位聚合物的热分解产物也通过PXRD进行了分析,证实最终形成了CoO/Co₃O₄和NiO。所得到的化合物扩展了由柔性二羧酸连接体组装而成的配位聚合物家族。