Daga Pooja, Manna Priyanka, Majee Prakash, Singha Debal Kanti, Hui Sayani, Ghosh Ananta Kumar, Mahata Partha, Mondal Sudip Kumar
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.
Dalton Trans. 2021 Jun 1;50(21):7388-7399. doi: 10.1039/d1dt00729g.
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.
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。