A simple and efficient approach to endow the controllable multi-stimuli-responsive property for the supramolecular polymer was successfully developed by rationally introducing iodine into a novel naphthalimide-functionalized pillar[5]­arene-based supramolecular polymer (PNA⊃GBP). Interestingly, by introducing iodine into the supramolecular polymer PNA⊃GBP, the iodine could not only control the optical properties and self-assembly states of PNA⊃GBP via electronic donor–acceptor effect but also control the molecular recognition properties by competitive redox reaction. Benefiting from these excellent iodine controlled multiresponse properties, the PNA⊃GBP showed selective fluorescent response for cyanide, cysteine, and mercury in supramolecular polymer gels, water solutions, and living cells with high sensitivities. The supramolecular polymer PNA⊃GBP could act as a novel smart material for selective detection CN–, Hg2+, and l-Cys.

A novel approach to achieve ultrasensitive response was successfully developed by rationally introducing the competition between cation-π and exo-wall π-π interactions into a pillar[5]arene-based supramolecular organogel (P5N-OG). Interestingly, the P5N-OG could be used for ion detection and separation, fluorescent display materials as well as ultrasensitive logic gates.

Light-harvesting is a key step in photosynthesis, but it is still a challenge to create an efficient artificial light harvesting system in the broader solar spectrum to mimic natural processes....

A novel approach for the design of multi-stimuli-responsive supramolecular functional materials was successfully developed by introducing the competition of π–π stacking and cation–π interactions into a pillar[5]arene-based supramolecular π-gel (MP5-G).

An efficient perovskite-quantum-dot light-harvesting system with NIR emission was fabricated based on passivation CH3NH3PbBr3 QDs in the supramolecular self-assembly of Zn(II) carboxyl functionalized-pillar[5]arene coordination polymer and two different fluorescence dyes,...

Ultrasensitive response properties are an intriguing concern for stimuli-responsive materials. Herein, we report a novel method to achieve an ultrasensitive response by introducing the competition of cationπ and ππ interactions into a pillar[5]arene-based supramolecular organic framework (SOF-AMP). SOF-AMP was constructed with a novel bis-naphthalimide functionalized pillar[5]arene, which was able to form a stable supramolecular gel (SOF-AMP-G) in cyclohexanol. Interestingly, SOF-AMP-G shows an ultrasensitive response to Fe3+ through the competition of cationπ and ππ interactions. Meanwhile, the Fe3+ coordinated SOF (MSOF-Fe) shows an ultrasensitive response to H2PO4-. SOF-AMP-G displayed yellow fluorescence whereas, after the addition of 0.5 equiv. of Fe3+ to SOF-AMP-G, the yellow fluorescence was quenched. The detection limit of SOF-AMP-G for Fe3+ is 7.54 × 10-9 M. More interestingly, the Fe3+ coordinated SOF gel (MSOF-Fe-G) could sense H2PO4- with a fluorescence "turn-on". The detection limit of MSOF-Fe-G for H2PO4- is 4.21 × 10-9 M. Simultaneously, the Fe3+ and H2PO4- responsive thin films based on these SOF gels were prepared. Moreover, these SOF gels could be used as ultrasensitive ion sensors, fluorescent display materials and sensitive logic gates.

A bifunctional supramolecular pseudorotaxane chemosensor (G-WAP) based on pillar[5]arene and phenazine imidazole was constructed, which could detect Hg2+ and Ag+ in water.

A novel water soluble fluorescent sensor was synthesized by employing the carboxyl and imidazolyl moiety as the hydrophilic group site and Hg2+ binding site, whereas a naphthalimide moiety was used as the signal group.