Taghizadeh L, Montazerozohori M, Masoudiasl A, Joohari S, White J M
Department of Chemistry, Yasouj University, Yasouj 7591874831, Iran.
Department of Chemistry, Yasouj University, Yasouj 7591874831, Iran.
Mater Sci Eng C Mater Biol Appl. 2017 Aug 1;77:229-244. doi: 10.1016/j.msec.2017.03.150. Epub 2017 Mar 21.
A new bidentate Schiff base ligand named as N,N'-bis((E)-3-phenylallylidene)butane-1,4-diamine (L) and three its zinc halide complexes were synthesized and characterized by FT-IR, H NMR, C NMR and UV-Vis spectroscopy. The crystal structure of zinc bromide and iodide complexes were characterized using single crystal X-ray diffraction. The two structures are isomorphous, crystallizing in the monoclinic crystal system with space group C2/c with closely similar unit cell dimensions. In these complexes, the Zn(II) ion is in the center of a distorted tetrahedral environment completed by two iminic nitrogen atoms of Schiff base ligand and two halide anions. The analysis of crystal structures shows that intermolecular interactions such as CH⋯halogen, π⋯π and CH⋯π interactions have effective role in stabilization of complexes structure. Intermolecular interactions were more analyzed using 3D Hirshfeld surface analysis and corresponding 2D fingerprint plots. Furthermore, structural optimization by DFT calculations at the B3LYP/LANL2DZ level have been performed and then compared with the experimental data. Time-dependent density functional theory (TDDFT) has been also used to calculate the electronic transitions of molecules at B3LYP/LANL2DZ level using the optimized ground-state geometries. NBO analysis was applied for investigation of intra and inter-molecular bonding and conjugative interaction in molecular systems. Schiff base ligand and their zinc complexes have been screened for their antibacterial and antifungal activities by disc diffusion method. Thermal behaviors of all compounds were studied by TG/DTG analysis data. Also, nanostructures of zinc complexes were synthesized by sonochemical method and characterized by FT-IR spectroscopy, X-ray diffraction (XRD) and scanning electron microscopy (SEM). ZnO nanoparticles were simply prepared by calcination of zinc iodide complex as new precursor at 600°C.
合成了一种名为N,N'-双((E)-3-苯基亚烯丙基)丁烷-1,4-二胺(L)的新型双齿席夫碱配体及其三种卤化锌配合物,并通过傅里叶变换红外光谱(FT-IR)、氢核磁共振(H NMR)、碳核磁共振(C NMR)和紫外可见光谱对其进行了表征。利用单晶X射线衍射对溴化锌和碘化锌配合物的晶体结构进行了表征。这两种结构是同构的,在单斜晶体系统中结晶,空间群为C2/c,晶胞尺寸非常相似。在这些配合物中,Zn(II)离子处于由席夫碱配体的两个亚胺氮原子和两个卤离子完成的扭曲四面体环境的中心。晶体结构分析表明,分子间相互作用如CH⋯卤素、π⋯π和CH⋯π相互作用在配合物结构的稳定中起有效作用。使用三维赫什菲尔德表面分析和相应的二维指纹图谱对分子间相互作用进行了更深入的分析。此外,在B3LYP/LANL2DZ水平上通过密度泛函理论(DFT)计算进行了结构优化,然后与实验数据进行了比较。还使用含时密度泛函理论(TDDFT)在B3LYP/LANL2DZ水平上利用优化的基态几何结构计算了分子的电子跃迁。应用自然键轨道(NBO)分析研究了分子体系中的分子内和分子间键合及共轭相互作用。通过纸片扩散法筛选了席夫碱配体及其锌配合物的抗菌和抗真菌活性。通过热重/微商热重(TG/DTG)分析数据研究了所有化合物的热行为。此外,通过声化学方法合成了锌配合物的纳米结构,并通过傅里叶变换红外光谱(FT-IR)、X射线衍射(XRD)和扫描电子显微镜(SEM)对其进行了表征。通过在600°C下煅烧新型前驱体碘化锌配合物简单制备了氧化锌纳米颗粒。