含7-氮杂吲哚功能的内球氢键配体:结构和光物理研究

IF 1 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY
Alec Coles, Oskar Wood, Chris Hawes
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引用次数: 0

摘要

本文报道了三种新型7-叠氮吲哚配体的合成、结构分析和光谱表征,以及一种新型的7-叠氮吲哚衍生配位聚合物,目的是鉴定含有内球氢键给体官能团的新型桥接配体。结构表征表明,7-氮杂酚在腙类和亚胺类1和2中的氢键施主能力明显强于胺类3,而它们的氢键受体能力则相反。这些发现反映在荧光光谱结果中,显示双峰发射,与质子转移相关的多发射物种的特征,只在胺类中明显,而在酸性更强的亚胺中不明显。腙配体1的聚合铜(II)配合物显示出预期的球内氢键,其供体强度与在自由配体中观察到的相似,这导致配位球的其余部分变形。这些结果表明,7-氮杂吲哚官能团作为配位聚合物和其他多核组合中的配体的构建块具有未开发的多功能性,具有通过氢键稳定和有趣的光物理性质的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ligands containing 7-azaindole functionality for inner-sphere hydrogen bonding: structural and photophysical investigations
The synthesis, structural analysis and spectroscopic characterisation of three new 7-azaindole ligands is reported, alongside a novel 7-azaindole derived coordination polymer, with the aim of identifying new bridging ligands containing inner-sphere hydrogen bond donor functionality. Structural characterisation shows that the 7-azaindole hydrogen bond donor ability is significantly stronger in the hydrazone and imine species 1 and 2 compared to the amine 3, with the opposite trend evident in their hydrogen bond acceptor character. These findings are mirrored by the fluorescence spectroscopy results which show bimodal emission, characteristic of multiple emissive species related by proton transfer, is only evident in the amine species and not the more acidic imines. The polymeric copper(II) complex of the hydrazone ligand 1 shows the anticipated inner-sphere hydrogen bonding with a similar donor strength to that observed in the free ligand, which leads to deformation in the remainder of the coordination sphere. These results show the untapped versatility of the 7-azaindole functional group as a building block for ligands in coordination polymers and other multinuclear assemblies, with the potential for both stabilisation through hydrogen bonding and interesting photophysical properties.
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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
76
审稿时长
1 months
期刊介绍: The Journal of the Serbian Chemical Society -JSCS (formerly Glasnik Hemijskog društva Beograd) publishes articles original papers that have not been published previously, from the fields of fundamental and applied chemistry: Theoretical Chemistry, Organic Chemistry, Biochemistry and Biotechnology, Food Chemistry, Technology and Engineering, Inorganic Chemistry, Polymers, Analytical Chemistry, Physical Chemistry, Spectroscopy, Electrochemistry, Thermodynamics, Chemical Engineering, Textile Engineering, Materials, Ceramics, Metallurgy, Geochemistry, Environmental Chemistry, History of and Education in Chemistry.
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