Rosales-Vázquez Luis D, Valdes-García Josue, Bazany-Rodríguez Iván J, Germán-Acacio Juan M, Martínez-Otero Diego, Vilchis-Néstor Alfredo R, Morales-Luckie Raúl, Sánchez-Mendieta Víctor, Dorazco-González Alejandro
Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, México, 04510, CDMX, México.
Red de Apoyo a la Investigación, Universidad Nacional Autónoma de México-CIC, Instituto Nacional de Ciencias Médicas y Nutrición SZ, C. P.14000, Ciudad de México, México.
Dalton Trans. 2019 Sep 7;48(33):12407-12420. doi: 10.1039/c9dt01861a. Epub 2019 Jul 10.
Sensitive and direct sensing of cyanide in buffered aqueous solutions at pH = 7.0 by three new blue photoluminescent zinc-1,4-cyclohexanedicarboxylato coordination polymers bearing di-alkyl-2,2'-bipyridines has been achieved. Specifically, a Zn-polymer with the general formula: {[Zn(HO)(e,a-cis-1,4-chdc)(4,4'-dtbb)]·7HO}, (1,4-chdc = 1,4-cyclohexanedicarboxylato and 4,4'-dtbb = 4,4'-ditert-butyl-2,2'-bipyridine) has been synthesized in high yield and studied as a luminescent chemosensor for halides, pseudohalides and a series of oxyanions in neutral water. CN ions can be quantitatively detected by this polymer based on complete quenching (λ = 434 nm) in the sub-micromolar concentration range with a pronounced selectivity over common anions such as acetate, bromide and iodide. The quenching response (K = 9.7(±0.2) × 10 M) by the addition of CN was also observed in the presence of typical interfering anions with a very low detection limit of 0.9 μmol L in buffered water at pH = 7.0. On the basis of the crystal structure and solid state CPMAS C-NMR correlation and H NMR, IR-ATR, MS-ESI(+) and SEM-EDS experiments, the optical change is attributed to the efficient release of its corresponding ditert-butyl-bipyridine, with the simultaneous formation of a zinc cyanide complex. The CPMAS C-NMR spectrum of the coordination polymer is consistent with the symmetry of the crystal structure. The use of flexible coordination polymers as fluorescent sensors for fast and selective detection of cyanide ions in pure aqueous solutions has been unexplored until now.
通过三种带有二烷基 - 2,2'-联吡啶的新型蓝色光致发光锌 - 1,4 - 环己烷二羧酸酯配位聚合物,在pH = 7.0的缓冲水溶液中实现了对氰化物的灵敏且直接的传感。具体而言,已高产率合成了通式为{[Zn(HO)(e,a - cis - 1,4 - chdc)(4,4'-dtbb)]·7HO}的锌聚合物(1,4 - chdc = 1,4 - 环己烷二羧酸酯,4,4'-dtbb = 4,4'-二叔丁基 - 2,2'-联吡啶),并将其作为用于中性水中卤化物、拟卤化物和一系列含氧阴离子的发光化学传感器进行了研究。基于在亚微摩尔浓度范围内的完全猝灭(λ = 434 nm),该聚合物能够定量检测CN离子,并且对诸如乙酸根、溴离子和碘离子等常见阴离子具有明显的选择性。在pH = 7.0的缓冲水中,在存在典型干扰阴离子的情况下,添加CN时也观察到猝灭响应(K = 9.7(±0. _ 2) × 10 M),检测限低至0.9 μmol L。基于晶体结构、固态CPMAS C - NMR相关性以及H NMR、IR - ATR、MS - ESI(+)和SEM - EDS实验,光学变化归因于其相应的二叔丁基 - 联吡啶的有效释放,同时形成了氰化锌配合物。配位聚合物的CPMAS C - NMR光谱与晶体结构的对称性一致。迄今为止,尚未探索使用柔性配位聚合物作为荧光传感器在纯水溶液中快速、选择性地检测氰离子。