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基于锌(II)的金属有机配位聚合物对三价金属离子(铝、铁和铬)的响应:光谱法研究

Response of a Zn(II)-based metal-organic coordination polymer towards trivalent metal ions (Al, Fe and Cr) probed by spectroscopic methods.

作者信息

Daga Pooja, Manna Priyanka, Majee Prakash, Singha Debal Kanti, Hui Sayani, Ghosh Ananta Kumar, Mahata Partha, Mondal Sudip Kumar

机构信息

Department of Chemistry, Siksha-Bhavana, Visva-Bharati University, Santiniketan-731235, West Bengal, India.

Department of Chemistry, Jadavpur University, Jadavpur, Kolkata-700 032, West Bengal, India.

出版信息

Dalton Trans. 2021 Jun 1;50(21):7388-7399. doi: 10.1039/d1dt00729g.

Abstract

A new zinc-based two-dimensional coordination polymer, [Zn(5-AIP)(Ald-4)]·H2O (5-AIP = 5-amino isophthalate, Ald-4 = aldrithiol-4), 1, has been synthesized at room temperature by the layer diffusion technique. Single-crystal X-ray diffraction analysis of 1 showed a two-dimensional bilayer structure. An aqueous suspension of 1 upon excitation at 300 nm displayed an intense blue emission at 403 nm. The luminescence spectra were interestingly responsive and selective to Al3+, Cr3+ and Fe3+ ions even in the presence of other interfering ions. The calculated detection limits for Al3+, Cr3+ and Fe3+ were 0.35 μM ([triple bond, length as m-dash]8.43 ppb), 0.46 μM ([triple bond, length as m-dash]22.6 ppb) and 0.30 μM ([triple bond, length as m-dash]15.85 ppb), respectively. Notably, with the cumulative addition of Al3+ ions, the luminescence intensity at 403 nm decreased steadily with a gradual red shift up to 427 nm. Afterward, this red shifted peak showed a turn-on effect upon further addition of Al3+ ions. On the other hand, for Cr3+ and Fe3+ ions, there was only drastic luminescence quenching and a large red shift up to 434 nm. This indicated the formation of a complex between 1 and these metal ions, which was also supported by the UV-Visible absorption spectra of 1 that showed the appearance of a new band at 280 nm in the presence of these three metal ions. The FTIR spectra revealed that these ions interacted with the carboxylate oxygen atom of 5-AIP and the nitrogen atom of the Ald-4 ligand in the structure. The luminescence lifetime decay analysis manifested that a charge-transfer type complex was formed between 1 and Cr3+ and Fe3+ ions that resulted in huge luminescence quenching due to the efficient charge transfer involving the vacant d-orbitals, whereas for Al3+ ions having no vacant d-orbital, turn-on of luminescence occurred because of the increased rigidity of 1 upon complexation.

摘要

一种新型的锌基二维配位聚合物[Zn(5-AIP)(Ald-4)]·H₂O(5-AIP = 5-氨基间苯二甲酸,Ald-4 = 4-醛基硫醇),即化合物1,已通过层扩散技术在室温下合成。对化合物1进行的单晶X射线衍射分析表明其具有二维双层结构。化合物1的水悬浮液在300 nm激发下于403 nm处呈现出强烈的蓝色发射。有趣的是,即使存在其他干扰离子,其发光光谱对Al³⁺、Cr³⁺和Fe³⁺离子仍具有响应性和选择性。计算得出Al³⁺、Cr³⁺和Fe³⁺的检测限分别为0.35 μM(相当于8.43 ppb)、0.46 μM(相当于22.6 ppb)和0.30 μM(相当于15.85 ppb)。值得注意的是,随着Al³⁺离子的累积添加,403 nm处的发光强度稳步下降,同时逐渐发生红移,直至427 nm。此后,该红移峰在进一步添加Al³⁺离子时出现开启效应。另一方面,对于Cr³⁺和Fe³⁺离子,仅出现剧烈的发光猝灭以及高达434 nm的大幅红移。这表明化合物1与这些金属离子之间形成了配合物,这也得到了化合物1的紫外可见吸收光谱的支持,该光谱显示在这三种金属离子存在下在280 nm处出现了一个新的吸收带。傅里叶变换红外光谱表明这些离子与结构中5-AIP的羧酸根氧原子以及Ald-4配体的氮原子相互作用。发光寿命衰减分析表明,化合物1与Cr³⁺和Fe³⁺离子之间形成了电荷转移型配合物,由于涉及空d轨道的有效电荷转移导致了巨大的发光猝灭,而对于没有空d轨道的Al³⁺离子,由于配合后化合物1的刚性增加而发生发光开启。

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