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由两种不同的氨基吡啶、异硫氰酸酯配体分子和两种不同的过渡金属原子组成的配位化合物的合成、表征及 Hirshfeld 表面分析

Synthesis, characterization, and Hirshfeld surface analysis of coordination compounds composed of two different aminopyridines, isothiocyanate ligand molecules, and two different transition metal atoms.

作者信息

Şahin Zarife Sibel, Kartal Zeki

机构信息

Department of Energy Systems Engineering, Faculty of Engineering and Architecture, Sinop University, Sinop, Turkiye.

Retired Professor of Atomic and Molecular Physics, Kütahya Dumlupınar University, Kütahya, Turkiye.

出版信息

Turk J Chem. 2024 Sep 17;48(5):780-799. doi: 10.55730/1300-0527.3697. eCollection 2024.

Abstract

In this article, we describe the successful synthesis of three coordination compounds formed by the ligands 3-aminopyridine, 4-aminopyridine, and isothiocyanate ion with copper atoms and 4-aminopyridine and isothiocyanate ion with cadmium atoms, and their structural characterizations. The crystal structures of the compounds were determined by single crystal X-ray diffraction. According to that technique, the open formulae of these compounds are [Cu(3-aminopyridine)(NCS)] (), [Cu(4-aminopyridine)(NCS)] (), and [Cd(4-aminopyridine)(NCS)Cl] (). In addition, the suitability of the structures of the compounds was characterized by elemental analysis, thermal analysis, and Fourier transform infrared spectroscopy. The single crystal X-ray diffraction analyses of these coordination compounds showed that the first of these coordination compounds had a 1D crystal structure and the other two had a 3D crystal structure. N-H⋯S, N-H⋯N, N-H⋯Cl, N-H⋯π, and C-H⋯π bonds and their combinations were effective in the formation of the crystal structures of the said coordination compounds. The metal atoms [Cu(II), Cu(II), and Cd(II)] in these coordination compounds were surrounded by various ligand molecules in a square planar, square pyramidal, and octahedral arrangement, respectively. In order to investigate some chemical and structural properties of these coordination compounds, theoretical calculations were performed with the software package Gaussian 03. The highest occupied molecular orbital (HOMO), lowest occupied molecular orbital (LUMO), and natural bond orbital (NBO) values of the coordination compounds were used in these calculations. When the energy gap value between the HOMO and LUMO states of the compounds was examined, it was predicted that compound may have lower kinetic stability, higher chemical activity, and lower semiconductor properties than all the other compounds. According to the Hirshfeld surface analysis of the compounds, C⋯H, S⋯H, H⋯H, and N⋯H interactions are generally seen in the crystal structures of all compounds. In addition, Cd⋯Cl, Cd⋯S, H⋯Cl, and Cl⋯Cl interactions also occur in compound .

摘要

在本文中,我们描述了由配体3 - 氨基吡啶、4 - 氨基吡啶和异硫氰酸根离子与铜原子形成的三种配位化合物以及由4 - 氨基吡啶和异硫氰酸根离子与镉原子形成的配位化合物的成功合成及其结构表征。这些化合物的晶体结构通过单晶X射线衍射确定。根据该技术,这些化合物的开放式为[Cu(3 - 氨基吡啶)(NCS)] ()、[Cu(4 - 氨基吡啶)(NCS)] ()和[Cd(4 - 氨基吡啶)(NCS)Cl] ()。此外,通过元素分析、热分析和傅里叶变换红外光谱对化合物结构的适用性进行了表征。这些配位化合物的单晶X射线衍射分析表明,这些配位化合物中的第一个具有一维晶体结构,另外两个具有三维晶体结构。N - H⋯S、N - H⋯N、N - H⋯Cl、N - H⋯π和C - H⋯π键及其组合对上述配位化合物晶体结构的形成有效。这些配位化合物中的金属原子[Cu(II)、Cu(II)和Cd(II)]分别被各种配体分子以平面正方形、正方锥和八面体排列包围。为了研究这些配位化合物的一些化学和结构性质,使用软件包Gaussian 03进行了理论计算。这些计算中使用了配位化合物的最高占据分子轨道(HOMO)、最低未占据分子轨道(LUMO)和自然键轨道(NBO)值。当检查化合物的HOMO和LUMO态之间的能隙值时,预测化合物 可能比所有其他化合物具有更低的动力学稳定性、更高的化学活性和更低的半导体性质。根据化合物的Hirshfeld表面分析,C⋯H、S⋯H、H⋯H和N⋯H相互作用在所有化合物的晶体结构中普遍可见。此外,化合物 中还存在Cd⋯Cl、Cd⋯S、H⋯Cl和Cl⋯Cl相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1932/11539913/98282d523893/tjc-48-05-780f1.jpg

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