Two New Supramolecular Compounds that Involve Trans-1,2-bis(4-pyridyl)ethylene (bpe), Barbituric Acid and Fe(II) ions

H. Garcia, R. Diniz, L. C. Oliveira
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引用次数: 2

Abstract

In this study, the synthesis, spectroscopic properties (infrared and Raman) and crystal structures of two new compounds named (H2bpe)B2 . 2H2O (1) and (Fe(bpe)(H2O)4)B2·4H2O (2) have been reported, where bpe is trans-1,2- bis(4-pyridil)-ethylene, H2bpe is protonated bpe and B - is the barbiturate anion. For both complexes, we observed the presence of supramolecular interactions, such as electrostatic, hydrogen bonding and � -stacking interactions. Compound 1 crystallised in a triclinic system with the space group P-1, which was generated by cationic and anionic units formed by protonated bpe, the barbiturate anion and water molecules. These molecules interacted through weak intermolecular inter- actions and were responsible for the crystalline stability of the synthesised compounds. For compound 2, an orthorhombic crystal system was observed with a Pbcn space group. In this crystal, the metallic site adopted a distorted octahedral ge- ometry that was coordinated by two pyridine nitrogen atoms and four oxygen atoms from coordinated water molecules. The three-dimensional arrangement of the structure consisted of one covalent one-dimensional linear cationic (Fe(bpe)(H2O)4) 2+ chain, which interacts by forming hydrogen-bonding, � -stacking and electrostatic interactions with bar- biturate anions and water molecules that were trapped in the crystal. The vibrational spectra of the two compounds were very similar despite the different crystalline arrangements that were adopted by the two structures. In the infrared spectra, two intense bands at 1684 and 1630 cm -1 were observed and assigned to the CO stretching ( CO) of the barbiturate anion and  C=C of the bpe ligand, respectively. In the Raman spectra of the compounds, the most important bands were attrib- uted to the bpe ligand at 1629 and 1006 cm -1 , which were assigned to the  C=C and  ring, respectively. The presence of the barbiturate anion was confirmed by the presence of a band of low intensity located at 680 cm -1 and was assigned as the
涉及反式-1,2-双(4-吡啶基)乙烯(bpe)、巴比妥酸和铁(II)离子的两种新的超分子化合物
本文研究了两种新化合物(H2bpe)B2的合成、光谱性质(红外和拉曼光谱)和晶体结构。已经报道了2H2O(1)和(Fe(bpe)(H2O)4)B2·4H2O(2),其中bpe是反式-1,2-双(4-吡啶)-乙烯,H2bpe是质子化的bpe, B -是巴比妥酸盐阴离子。对于这两种配合物,我们观察到超分子相互作用的存在,如静电、氢键和堆叠相互作用。化合物1结晶于具有空间基P-1的三斜体系中,该体系是由质子化bpe、巴比妥酸盐阴离子和水分子形成的正离子和阴离子单元生成的。这些分子通过弱分子间相互作用相互作用,并负责合成化合物的结晶稳定性。对于化合物2,观察到一个具有Pbcn空间群的正交晶系。在该晶体中,金属位采用畸变八面体几何结构,由两个吡啶氮原子和来自配位水分子的四个氧原子配位。该结构的三维排列由一个共价的一维线性阳离子(Fe(bpe)(H2O)4) 2+链组成,该链通过与被捕获在晶体中的棒-双酸盐阴离子和水分子形成氢键、堆叠和静电相互作用。两种化合物的振动谱非常相似,尽管这两种结构采用了不同的晶体排列。红外光谱在1684和1630 cm -1处观察到两个强波段,分别属于巴比妥酸盐阴离子的CO拉伸(CO)和bpe配体的C=C。在化合物的拉曼光谱中,最重要的波段归属于bpe配体在1629和1006 cm -1处,分别归属于C=C和环。巴比妥酸盐阴离子的存在通过位于680 cm -1的低强度波段的存在得到证实,并被指定为
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