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利用振动和电子光谱研究甲酰胺/氯化镍体系中不同配合物的结构。

Using vibrational and electronic spectroscopies to investigate different complexes in the formamide/nickel chloride system.

机构信息

Departamento de Química, Instituto de Ciências Exatas, Universidade Federal Rural do Rio de Janeiro, Rodovia BR 465/Km 7, Seropédica, RJ 23890-000, Brazil.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2012 Apr;89:259-63. doi: 10.1016/j.saa.2011.12.016. Epub 2011 Dec 20.

Abstract

Raman, IR and UV-vis-NIR experiments of formamide (FA) and nickel chloride solutions at different compositions were carried out. The quantitative Raman study at the νCN region shows that 5 FA molecules are coordinated to Ni (II) and the sixth position of the octahedron is occupied by one chloride, with preferential formation of [Ni(FA)5Cl]Cl in concentrations near 0.1 mol kg(-1). In higher concentrations the [Ni(FA)4Cl2] complex becomes the most abundant. The downshift of the νCO mode of FA was evidenced by the appearance of a new band at 1640 cm(-1) in the IR spectra of the most concentrated salt solutions. Also, the downshift of the δOCN mode combined with the upshift of the νCN vibration have allowed us realize that Ni (II) is coordinated by the O atom of FA. The d orbital splitting (Δo) has been directly determined from the electronic spectrum of the [Ni(FA)6]Cl2 complex and FA has been included in the spectrochemical series.

摘要

进行了甲酰胺(FA)和氯化镍溶液在不同组成下的拉曼、红外和紫外-可见-近红外实验。νCN 区域的定量拉曼研究表明,5 个 FA 分子与 Ni(II)配位,八面体的第六个位置被一个氯离子占据,在接近 0.1 mol kg(-1)的浓度下优先形成 [Ni(FA)5Cl]Cl。在更高的浓度下,[Ni(FA)4Cl2] 配合物成为最丰富的。FA 的 νCO 模式的下移通过在最浓盐溶液的红外光谱中在 1640 cm(-1)处出现新的带得到证明。此外,δOCN 模式的下移与 νCN 振动的上移相结合,使我们意识到 Ni(II)与 FA 的 O 原子配位。d 轨道分裂(Δo)已直接从 [Ni(FA)6]Cl2 配合物的电子光谱中确定,并且 FA 已被包含在光谱化学序列中。

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