双(2-甲氧基-6-((Z)-(对甲基)苯氧基)钯的晶体结构

IF 0.1 Q4 CRYSTALLOGRAPHY
K. Kassim, Muhammad Ashraf Mohd Kahar, B. Yamin, Mohd Abdul Fatah Abdul Manan, M. Yusof
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引用次数: 0

摘要

希夫碱配合物由于其结构基础和理论认识,在催化剂、1-3生物医学和材料应用等方面得到了不断的研究。Pd(II)席夫碱配合物具有高选择性和可调节配体环境的活性等显著特性根据前人的研究合成了配合物C30H28N2O4Pd,并进行了轻微的修饰。将0.2mmol (Z)-2-甲氧基-6-(对甲苯)甲基)苯酚加入到0.1 mmol (II)乙酸钯(5 mL乙醇)的搅拌溶液中。溶液回流6小时,冷却至室温。沉淀物被过滤掉,然后风干。该产品在乙醇:氯仿(1:1)中通过慢蒸发法重结晶,得到橙色晶体。收益率62.0%;m.p 558 - 561分析的C30H28N2O4Pd: C, 61.8;H, 4.4;N, 10.3%;发现:C, 61.6;H, 4.5;N, 10.7%。在Perkin Elmer spectrum One FTIR光谱仪上以KBr圆盘的形式获得了450 ~ 4000 cm-1的红外光谱。1596、1327、1258、1542、580和449 cm-1处的峰分别归属于ν(C=N)、ν(C - N)、ν(C - o)、ν(C=C芳香)、ν(Pd-O)和ν(Pd-N)。所获得的红外数据与先前报道的一项研究几乎相似在Jeol 400 MHz谱仪上以CDCl3溶液获得了核磁共振谱。观察到的1H NMR化学位移δ为(ppm): 2.42 (s, 3H, CH3), 3.36 (s, 3H, OCH3), 6.39 - 7.29 (m, 7H,芳香族,JHH = 1 - 3和6 - 9 Hz), 7.66 (s, 1H, HC=N)。偶联常数表明存在间位和邻位芳香质子。晶体和结构细化数据总结于表1,选择的键距和角度见表2。将H原子按几何位置放置,使其附着在母体C原子上,其C - H = 0.95 ~ 0.98 Å, Uiso(H) = 1.2(甲基为1.5)乘以Ueq(C)。图1为化学结构图,图2为标题化合物的ORTEP结构。在这个中心对称配合物中,两个配体彼此对称相关,并且具有相同的键角和距离。配体通过ONNO原子与金属中心配位,形成一个方形平面配合物,在金属中心周围形成两个六元环。2019©日本分析化学学会
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Crystal Structure of Bis(2-methoxy-6-((Z)-(p-tolylimino)methyl)phenoxy)palladium
Schiff-base complexes are being continuously studied concerning catalyst,1–3 biomedical4,5 and material applications for their structural fundamental and theoretical understanding. Pd(II) Schiff-base complexes have remarkable properties, such as high selectivity and activity by manipulating the ligand environment.6 The complex C30H28N2O4Pd was synthesized according to previous studies7 with slight modification. A 0.2mmol (Z)-2-methoxy-6-((p-tolylimino)methyl)phenol was added to a stirred solution of 0.1 mmol of palladium(II) acetate in 5 mL of ethanol. The solution was refluxed for 6 h, and cooled to the room temperature. The precipitate was filtered off and air-dried. The product was recrystallized in ethanol:chloroform (1:1) through a slow evaporation method to produce an orange crystal. Yield, 62.0%; m.p. 558 – 561 K. Anal. Calc. for C30H28N2O4Pd: C, 61.8; H, 4.4; N, 10.3%; Found: C, 61.6; H, 4.5; N, 10.7%. The IR spectrum was obtained as a KBr disc on a Perkin Elmer Spectrum One FTIR Spectrometer from 450 – 4000 cm–1. The peaks at 1596, 1327, 1258, 1542, 580 and 449 cm–1 were assigned to ν(C=N), ν(C–N), ν(C–O), ν(C=C aromatic), ν(Pd–O) and ν(Pd–N), respectively. The infrared data obtained are nearly similar based on a previous study reported.8 The NMR spectrum was obtained as a CDCl3 solution on Jeol 400 MHz spectrometer. The 1H NMR chemical shifts, δ, observed are (ppm): 2.42 (s, 3H, CH3), 3.36 (s, 3H, OCH3), 6.39 – 7.29 (m, 7H, aromatic, JHH = 1 – 3 and 6 – 9 Hz), 7.66 (s, 1H, HC=N). The coupling constant indicates the presence of meta and ortho aromatic protons. The crystal and structure-refinement data are summarized in Table 1 and selected bond distances and angles in Table 2. H atoms were positioned geometrically and allowed to ride on the parent C atom, with C–H = 0.95 – 0.98 Å, and with Uiso(H) = 1.2 (1.5 for methyl groups) times Ueq(C). Figure 1 represents the chemical diagram whereas Fig. 2 shows the ORTEP structure of the title compound. In this centrosymmetric complex, the two ligands are symmetrically related to each other and have the same bond angles and distances. The ligand was coordinated to the metal center through ONNO atoms, forming a square-planar complex, yielding two six-membered rings surrounding the metal center. 2019 © The Japan Society for Analytical Chemistry
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CiteScore
0.60
自引率
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