Synthesis, Characterization and Crystal Structure of Fe(III) and Ni(II) Complexes with Furan‐2,5‐Dicarbonylbis(N,N‐Diethylthiourea)

IF 1.4 Q3 CHEMISTRY, MULTIDISCIPLINARY
Canh Dinh Le, Minh Tuan Hoang, Hoang Phuc Nguyen, Vân Hà Nguyễn, Chien Thang Pham
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引用次数: 0

Abstract

Abstract Stoichiometric reactions of furan‐2,5‐dicarbonylbis( N , N ‐diethylthiourea) H 2 L with transition metal ions including Fe 3+ and Ni 2+ in MeOH with the presence of an organic base like Et 3 N bring about two metallacyclic complexes. Chemical compositions and structures of such compounds have been investigated by elemental analyses, spectroscopic means such as HRMS, IR, NMR and X‐ray crystallography. The supportive results indicate the formation of dinuclear complexes resulting from the coordination of metal ions with ( S , O )‐chelating aroylthiourea moieties. Particularly, trivalent Fe(III) ions adopt facial octahedral geometry and, thus, form the cryptand‐like tris‐[Fe 2 (L) 3 ] ( 1 ). In contrast, divalent Ni(II) ions with cis square planar coordination spheres produce the metallacrown ether bis‐[Ni 2 (L) 2 ] ( 2 ).
呋喃- 2,5 -二羰基双(N,N -二乙基硫脲)Fe(III)和Ni(II)配合物的合成、表征和晶体结构
摘要呋喃- 2,5 -二羰基双(N, N -二乙基硫脲)h2l与过渡金属离子(Fe 3+和Ni 2+)在MeOH中,在Et 3n等有机碱的存在下进行化学计量反应,生成两个金属环配合物。这些化合物的化学成分和结构已经通过元素分析、光谱分析手段(如HRMS、IR、NMR和X射线晶体学)进行了研究。支持结果表明,金属离子与(S, O)螯合的芳基硫脲基团配位形成双核配合物。特别是,三价铁(III)离子采用面八面体几何形状,从而形成隐式三[fe2 (L) 3](1)。相反,具有顺式方形平面配位球的二价Ni(II)离子产生金属冠醚[Ni 2 (L) 2](2)。
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来源期刊
Vietnam Journal of Chemistry
Vietnam Journal of Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
1.70
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