A flexible polycyclic chemosensor for simultaneous discernment of Ni2+ and Cd2+ depending on distinct coordination
Ziyu Chen1, Qianxin Long1, Wen Li1
1Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, East China University of Science & Technology, 130 Meilong Road, Shanghai 200237 China.
Abstract:
Herein, we present a paradigm of a flexible molecular system for simultaneous discernment of Ni2+ and Cd2+, depending on distinct chemical coordination manners. By incorporating two functional pyridine groups at different positions on the flexible DPAC framework (9,14-diphenyl-9,14-Dihydrodibenzo [a,c]phenazine), two derivatives are prepared as 27Py-DPAC and 36Py-DPAC. The results show that 27Py-DPAC can chemically coordinate with Ni2+ (intermolecular coordination) and Cd2+ (intramolecular coordination), generating fluorescence turn-off and -on behaviors, respectively. The key factors leading to the different coordination ways are the ionic radius and the substituted positions of pyridine groups. Demonstrably, 36Py-DPAC can respond to Ni2+ abiding by the principle of the 27Py-DPAC sensor, but it cannot sense Cd2+ because of the difficulty in forming an effective intramolecular coordination resulted from the large distance between two nitrogen atoms on pyridine and the central heterocyclic ring. Based on the ionic response properties of the two compounds, logic circuits were developed to simulate logical operations and facilitate ion detection. This research expands the applicability of flexible polycyclic conjugated molecules in chemical sensing and underscores the influence of different modification sites of functional groups on ion binding mechanisms.
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