首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Synthesis and spectral characterization of ternary complexes of oxovanadium(IV) containing some acid hydrazones and 2,2 '-bipyridine
【24h】

Synthesis and spectral characterization of ternary complexes of oxovanadium(IV) containing some acid hydrazones and 2,2 '-bipyridine

机译:含某些酸和2,2'-联吡啶的氧钒(IV)三元配合物的合成及光谱表征

获取原文
获取原文并翻译 | 示例
           

摘要

An interesting series of heterocyclic base adducts of oxovanadium(IV) complexes have been synthesized by the reaction of vanadium(IV) oxide acetylacetonate with some hydrazones (H2L) in the presence of a heterocyclic base 2,2'-bipyridine. The compounds were characterized by analytical and different physico-chemical techniques like IR, electron paramagnetic resonance (EPR) and UV-Vis spectral studies and magnetic studies. The EPR spectra indicate that the free electron is in the d(xy) orbital. The coordination geometry around oxovanadium(IV) in all complexes is octahedral, with one dibasic tridentate ligand L2-, and one bidentate heterocyclic base. The IR spectra suggest that coordination takes place through azomethine nitrogen and enolate oxygen from the hydrazide moiety and phenolate oxygen. The pyridyl nitrogens of the hydrazones, H2L2 and H2L4 are not involved in the coordination. The molar conductivities show that all the complexes are non-electrolytes. All electronic transitions were assigned. All the compounds are paramagnetic. EPR studies of all compounds suggest axial symmetry. The calculated bonding parameters indicate that in-plane sigma bonding is more covalent than in-plane pi bonding. (C) 2004 Elsevier B.V. All rights reserved.
机译:氧钒(IV)配合物的一系列有趣的杂环碱加合物已通过在杂环碱2,2'-联吡啶的存在下,使氧化钒(IV)乙酰丙酮化物与某些(H2L)反应而合成。通过分析和不同的物理化学技术(例如IR,电子顺磁共振(EPR)和UV-Vis光谱研究和磁性研究)对化合物进行表征。 EPR光谱表明自由电子在d(xy)轨道中。在所有配合物中,氧钒(IV)周围的配位几何是八面体,具有一个二元三齿配体L2-和一个二齿杂环基。红外光谱表明配位反应是通过甲亚胺氮和酰肼部分的烯醇氧和酚盐的氧发生的。 ,H2L2和H2L4的吡啶基氮原子不参与配位。摩尔电导率表明所有配合物均为非电解质。分配了所有电子转换。所有化合物都是顺磁性的。所有化合物的EPR研究表明轴向对称。计算出的键合参数表明,面内sigma键合比面内pi键更共价。 (C)2004 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号