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Synthesis and crystal structure of the coordination compound of pyridoxine with manganese sulfate

机译:吡ido醇与硫酸锰配位化合物的合成及晶体结构

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The reaction of pyridoxine with manganese sulfate in an aqueous solution gave the coordination compound MnSO _4 · 2C _8H _(11)O _3N · 2H _2O (I). The structure of I was determined from single-crystal X-ray diffraction data. In the centrosymmetric complex (sp. gr. P1?, Z=1), the Mn atom is coordinatedby two pyridoxine molecules and two water molecules, thus adopting an octahedral coordination. The sulfate anion is also at a center of symmetry and, consequently, is disordered. The pyridoxine molecules are coordinated to the metal atom through the oxygen atoms of the deprotonated hydroxyl group and the CH _2OH group that retains the hydrogen atom. The nitrogen atom is protonated in such a way that the heterocycle assumes a pyridinium character. The crystal structure also contains six water molecules of crystallization. A thermogravimetric study showed that the decomposition of I occurs in several successive steps, such as dehydration, the combustion of organic ligands, and the formation of an inorganic residue.
机译:吡ido醇与硫酸锰在水溶液中的反应得到配位化合物MnSO _4·2C _8H _(11)O _3N·2H _2O(I)。从单晶X射线衍射数据确定I的结构。在中心对称络合物(sp.gr.P1α,Z = 1)中,Mn原子由两个吡ido醇分子和两个水分子配位,因此采用八面体配位。硫酸根阴离子也处于对称中心,因此是无序的。吡ido醇分子通过去质子化羟基的氧原子和保留氢原子的CH _2OH与金属原子配位。氮原子被质子化,使得杂环具有吡啶鎓特性。晶体结构还包含六个结晶水分子。热重研究表明,I的分解发生在几个连续的步骤中,例如脱水,有机配体的燃烧以及无机残基的形成。

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