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2,2-双(羟甲基)丙酸铜(II)与六亚甲基四胺的配位化合物:从单核配合物到一维配位聚合物

Copper(II) 2,2-Bis(Hydroxymethyl)Propionate Coordination Compounds with Hexamethylenetetramine: From Mononuclear Complex to One-Dimensional Coordination Polymer.

作者信息

Rauf Sadaf, Trzesowska-Kruszynska Agata, Sierański Tomasz, Świątkowski Marcin

机构信息

Institute of General and Ecological Chemistry, Lodz University of Technology, Zeromskiego 116, 90-924 Lodz, Poland.

出版信息

Molecules. 2021 Jun 2;26(11):3358. doi: 10.3390/molecules26113358.

DOI:10.3390/molecules26113358
PMID:34199524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8199667/
Abstract

Three new copper coordination compounds derived from 2,2-bis(hydroxymethyl)propionic acid (dmpa) and hexamethylenetetramine (hmta) were obtained and their crystal structures were determined. The stoichiometry of the reagents applied in the syntheses reflects the metal to ligand molar ratio in the formed solid products. Due to the multiple coordination modes of the used ligands, wide structural diversity was achieved among synthesized compounds, i.e., mononuclear [Cu(dmp)(hmta)(HO)] (1), dinuclear [Cu(dmp)(hmta)] (2), and 1D coordination polymer [Cu(dmp)(hmta)] (3). Their supramolecular structures are governed by O-H•••O and O-H•••N hydrogen bonds. The compounds were characterized in terms of absorption (UV-Vis and IR) and thermal properties. The relationships between structural features and properties were discussed in detail. Owing to discrepancies in the coordination mode of a dmp ligand, bidentate chelating in 1, and bidentate bridging in 2 and 3, there is a noticeable change in the position of the bands corresponding to the stretching vibrations of the carboxylate group in the IR spectra. The differences in the structures of the compounds are also reflected in the nature and position of the UV-Vis absorption maxima, which are located at lower wavelengths for 1.

摘要

得到了三种由2,2 - 二(羟甲基)丙酸(dmpa)和六亚甲基四胺(hmta)衍生的新型铜配位化合物,并测定了它们的晶体结构。合成中所用试剂的化学计量比反映了所形成固体产物中金属与配体的摩尔比。由于所用配体的多种配位模式,在合成的化合物中实现了广泛的结构多样性,即单核[Cu(dmp)(hmta)(HO)] (1)、双核[Cu(dmp)(hmta)] (2)和一维配位聚合物[Cu(dmp)(hmta)] (3)。它们的超分子结构由O - H•••O和O - H•••N氢键控制。对这些化合物进行了吸收(紫外 - 可见和红外)和热性质方面的表征。详细讨论了结构特征与性质之间的关系。由于dmp配体配位模式的差异,在1中为双齿螯合,在2和3中为双齿桥联,红外光谱中对应羧酸盐基团伸缩振动的谱带位置有明显变化。化合物结构的差异也反映在紫外 - 可见吸收最大值的性质和位置上,1的紫外 - 可见吸收最大值位于较低波长处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2434/8199667/5242b94a24b5/molecules-26-03358-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2434/8199667/731cfa4f802c/molecules-26-03358-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2434/8199667/37cc4d0f1ab3/molecules-26-03358-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2434/8199667/5242b94a24b5/molecules-26-03358-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2434/8199667/731cfa4f802c/molecules-26-03358-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2434/8199667/37cc4d0f1ab3/molecules-26-03358-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2434/8199667/5242b94a24b5/molecules-26-03358-g003.jpg

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