Shi Dongjian, Ni Ming, Luo Jing, Akashi Mitsuru, Liu Xiaoya, Chen Mingqing
The Key Laboratory of Food Colloids and Biotechnology Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, P. R. China.
Analyst. 2015 Feb 21;140(4):1306-13. doi: 10.1039/c4an01991a.
Although many rhodamine based fluorescence sensors were reported to detect metal ions with high sensitivity and selectivity, there are very few reports available to study the mechanisms of detection and the interaction between probe and metal ions. This paper aims to detect ferric ions by novel fluorescence chemosensors and study the mechanisms in detail. A novel probe AD-MAH-RhB was designed and synthesized from rhodamine B (RhB), adamantyl (AD), ethylene diamine and maleic anhydride (MAH). AD-MAH-RhB could detect Fe(3+) in aqueous solutions. The mechanism was explored by the HSAB principle, FTIR and mass spectra. The results suggested that Fe(3+) bound with amine and oxygen atoms in AD-MAH-RhB to form a complex composed of a 2 : 1 stoichiometry of Fe(3+) and the probe. Moreover, computational simulations were employed to further investigate the detection mechanism. The calculated results showed that Fe(3+) could conjugate with AD-MAH-RhB probe to form a stable complex, which was induced by synergetic effects of the suitable space and distance of van der Waals forces. However, Hg(2+) was found to disturb this detection and form a complex with 1 : 2 stoichiometry of Hg(2+) and AD-MAH-RhB. Then, another probe, β-cyclodextrin modified polymaleic anhydride (PMAH-CD) including AD-MAH-RhB (PMAH-CD/AD-MAH-RhB) was fabricated by inclusion interaction between CD and AD. PMAH-CD@AD-MAH-RhB showed high selectivity and sensitivity to Fe(3+) in the aqueous solution by eliminating the interruption of Hg(2+) possibly due to the high hydrogen interaction among the probes to inhibit the stable form complex with Hg(2+).
尽管有许多基于罗丹明的荧光传感器被报道能够高灵敏度和高选择性地检测金属离子,但关于检测机制以及探针与金属离子之间相互作用的研究报道却非常少。本文旨在通过新型荧光化学传感器检测铁离子并详细研究其机制。由罗丹明B(RhB)、金刚烷基(AD)、乙二胺和顺丁烯二酸酐(MAH)设计合成了一种新型探针AD-MAH-RhB。AD-MAH-RhB能够在水溶液中检测Fe(3+)。通过软硬酸碱(HSAB)原理、傅里叶变换红外光谱(FTIR)和质谱对其机制进行了探究。结果表明,Fe(3+)与AD-MAH-RhB中的胺基和氧原子结合,形成了一种由Fe(3+)与探针以2∶1化学计量比组成的配合物。此外,还采用了计算模拟进一步研究检测机制。计算结果表明,Fe(3+)能够与AD-MAH-RhB探针共轭形成稳定的配合物,这是由范德华力合适的空间和距离的协同效应诱导产生的。然而,发现Hg(2+)会干扰这种检测,并与Hg(2+)和AD-MAH-RhB以1∶2化学计量比形成配合物。然后,通过环糊精(CD)与AD之间的包合作用制备了另一种探针,即包含AD-MAH-RhB的β-环糊精修饰的聚马来酸酐(PMAH-CD)(PMAH-CD/AD-MAH-RhB)。PMAH-CD@AD-MAH-RhB通过消除Hg(2+)的干扰,在水溶液中对Fe(3+)表现出高选择性和高灵敏度,这可能是由于探针之间的高氢键相互作用抑制了与Hg(2+)形成稳定的配合物。