Di Santo Alejandro, Pérez Hiram, Echeverría Gustavo A, Piro Oscar E, Iglesias Rodrigo A, Carbonio Raúl E, Ben Altabef Aida, Gil Diego M
INQUINOA (CONICET-UNT). Instituto de Química Física. Facultad de Bioquímica, Química y Farmacia, Universidad Nacional de Tucumán San Lorenzo 456 T4000CAN San Miguel de Tucumán Argentina
Departamento de Química General e Inorgánica, Facultad de Química, Universidad de La Habana Habana 10400 Cuba
RSC Adv. 2018 Jun 29;8(42):23891-23902. doi: 10.1039/c8ra04452j. eCollection 2018 Jun 27.
Four new thiocyanate-Zn(ii) and -Cd(ii) complexes with 1-methylimidazole (1-MeIm) and 2-methylimidazole (2-MeIm), namely, Zn(1-MeIm)(SCN) (1), Zn(2-MeIm)(SCN) (2), Cd(1-MeIm)(SCN) (3) and polymeric [Cd(2-MeIm)(SCN)] (4), have been synthesized and characterized by IR, Raman and UV-Vis spectroscopy. The thermal behavior for all complexes was evaluated by thermo-gravimetric analysis and differential thermal analysis. The crystal structures of complexes 1-4 were solved by single-crystal X-ray diffraction methods. A study of intermolecular interactions in the solid state compounds revealed that molecules are linked by weak N-H⋯S and C-H⋯S hydrogen bonds and also by C-H⋯π interaction in the case of structures 2-4, which are responsible for the formation and stability of the molecular assemblies. Hirshfeld surfaces and 2D-fingerprint plots allowed us to visualize the intermolecular contacts and their relative contributions to the total surface for each compound. A comparative analysis against similar halogen-bonded complexes was carried out to investigate the tendency of inter-molecular interactions to form contacts in crystals by using the enrichment ratio descriptor. The emission spectra of the free imidazole derivatives and their Zn(ii) and Cd(ii) complexes were recorded in acetonitrile solutions. The emissions observed in the spectra of complexes were ascribed to the intra-ligand transitions and ligand-to-metal charge transfer and we have observed an interesting correlation between the fluorescence intensities and C-H⋯π interactions.
合成了四种新的硫氰酸根 - 锌(II)和 - 镉(II)与1 - 甲基咪唑(1 - MeIm)和2 - 甲基咪唑(2 - MeIm)的配合物,即Zn(1 - MeIm)(SCN) (1)、Zn(2 - MeIm)(SCN) (2)、Cd(1 - MeIm)(SCN) (3)和聚合物[Cd(2 - MeIm)(SCN)] (4),并通过红外光谱、拉曼光谱和紫外 - 可见光谱对其进行了表征。通过热重分析和差示热分析评估了所有配合物的热行为。配合物1 - 4的晶体结构通过单晶X射线衍射方法解析。对固态化合物中分子间相互作用的研究表明,分子通过弱的N - H⋯S和C - H⋯S氢键相连,在结构2 - 4的情况下还通过C - H⋯π相互作用相连,这些相互作用负责分子聚集体的形成和稳定性。Hirshfeld表面和二维指纹图谱使我们能够可视化分子间的接触及其对每种化合物总表面的相对贡献。通过使用富集比描述符,对类似的卤键配合物进行了对比分析,以研究分子间相互作用在晶体中形成接触的趋势。在乙腈溶液中记录了游离咪唑衍生物及其锌(II)和镉(II)配合物的发射光谱。配合物光谱中观察到的发射归因于配体内跃迁和配体到金属的电荷转移,并且我们观察到荧光强度与C - H⋯π相互作用之间存在有趣的相关性。