Pengkompleksan 5,5,7,12,12,14-heksametil-1,4,8,11-tetraazasiklo tetraazadeka-7,14-dienium diperklorat dengan kuprum(II) asetat monohidrat dalam cecair ionik

N. M. Ali, N. Zaid, Nurul Huda Abd Karim, B. M. Yamin, Nur Hasyareeda Hassan
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Abstract

In the previous study, 5,5,7,12,12,14–hexamethyl–1,4,8,11–tetraazacyclotetradeca–7,14–dienium diperchlorate, [Me6C10H16N4](ClO4)2 formed complex of C16H34N4OCu(ClO4)2 and C16H32N4Cu(ClO4)2 when reacted with copper(II) acetate monohydrate in acetonitrile and aqueous solutions, respectively. However, when the same reaction carried out in 1–butyl–3– methylimidazolium hexafluorophosphate ionic liquid, [Bmim][PF6], disproportionation took place to give bis(ethylenediamine) bis(perchlorato-O) copper(II) complex, C4H16N4Cu(ClO4)2. X-ray study showed that the central copper atom was coordinated to two ethylenediamine ligands and two oxygen atoms of perchlorate ions in a distorted octahedral environment. Thermogravimetric Analysis (TGA) study showed the complex decomposition in one spontaneous mass loss at 260 oC due to the explosive nature of the perchlorate.
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在之前的研究中,5,5,7,12,12,14 -六亚甲基- 1,4,8,11 -四氮杂环十四十四- 7,14 -二高氯酸二烯,[Me6C10H16N4](ClO4)2分别在乙腈和水溶液中与(II)乙酸铜反应形成C16H34N4OCu(ClO4)2和C16H32N4Cu(ClO4)2络合物。然而,当同样的反应在1 -丁基- 3 -甲基咪唑六氟磷酸离子液体[Bmim][PF6]中进行时,歧化反应产生了双(乙二胺)双(高氯酸盐- o)铜(II)络合物C4H16N4Cu(ClO4)2。x射线研究表明,在畸变八面体环境中,中心铜原子与两个乙二胺配体和两个高氯酸盐氧原子配位。热重分析(TGA)研究表明,由于高氯酸盐的爆炸性,在260℃时复合分解为一次自发质量损失。
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