[en] Boronic acids are important for effective separation of biological active cis-diols. For the purpose of constructing a new type of saccharide-sensitive material which can not only provide convenient separation but also improve the access of boronic acid to guest molecules, the fluorogenic boronic acid terminated, thermo-sensitive polymers (BA-polyNIPAm) were grafted to an alkyne modified silica gel through the exploitation of click chemistry. The BA-polyNIPAm grafted silica gel (BA-polyNIPAm-SG) was characterized by FT-IR, fluorescence spectra, fluorescence microscopy, elemental analysis (EA), thermal gravimetric analysis (TGA), scanning electron microscope (SEM) and so on. BA-polyNIPAm-SG displayed affinity binding ability for saccharides under physiological pH value and allowed saccharides to be conveniently separated from solution. The maximum binding capacities for fructose and glucose are 83.2 μmol/g and 70.4 μmol/g polymer, respectively. The intensity of fluorescence emission of BA-polyNIPAm-SG increased with the increasing of fructose concentration. The present study provides a new kind of composite material which contains moveable and flexible grippers for recognizing and binding guest molecules. - Highlights: • Fluorogenic boronic acid terminated polymers were conjugated to silica particle. • The prepared material can conveniently separate saccharides from solution. • The prepared material displays increased fluorescence emission upon binding fructose

[en] Highlights: • Molecularly imprinted material (MIM) for 2,4-D was prepared via Click reaction. • Alkyne-β-CD and propargyl amine were used as the combinatorial functional monomers. • The imprinting sites of MIM were fabricated in the nano-pores of SBA-15. • The imprinting approach can improve site accessibility for the template effectively. -- Abstract: In order to improve the diffusion kinetics of molecularly imprinted materials (MIMs), applying imprinting technology to mesoporous materials is a promising strategy. In the present study, an imprinting approach based on the combination of mesoporous silica materials and molecular imprinting technology is reported. Molecularly imprinted material (MIM) for 2,4-dichlorophenoxyacetic acid (2,4-D) was prepared by using 2,4-D as the template molecule, alkyne-modified β-cyclodextrin and propargyl amine as the combinatorial functional monomers and SBA-15 as the supporter. The functional monomers were anchored to the azide-modified SBA-15 by azide–alkyne Click reaction. The synthesized MIM was characterized by transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), elemental analysis (EA), thermal gravimetric analysis (TGA), low-angle X-ray diffraction (XRD) and N₂ adsorption–desorption analysis. The interactions between template and functional monomers were studied by proton NMR analysis and UV–vis experiments. The results of the equilibrium binding experiments and selective tests showed that the prepared MIM has binding affinity and specificity for a group of analytes which have similar size and shape to those of template. Binding kinetic experiments demonstrated that the present imprinting approach can effectively enhance the mass transfer rate. The solid phase extraction of 2,4-D using MIM as the adsorbent was investigated. The extraction conditions for the processes of loading, washing and eluting were optimized. The recoveries of the molecularly imprinted solid phase extraction (MISPE) column for 2,4-D were 76.3–88.9% with relative standard deviations (RSD) of 3.48–7.64%.

[en] Highlights: • FRET-based molecularly imprinted probe for detection of doxorubicin was prepared. • The detection limit of the probe was 13.8 nM for doxorubicin. • The FRET-based probe had a higher selectivity for the template than ordinary MIMs. - Abstract: In this work, a new type of fluorescent probe for detection of doxorubicin has been constructed by the combined use of fluorescence resonance energy transfer (FRET) technology and molecular imprinting technique (MIT). Using doxorubicin as the template, the molecularly imprinted polymer thin layer was fabricated on the surfaces of carbon dot (CD) modified silica by sol-gel polymerization. The excitation energy of the fluorescent donor (CDs) could be transferred to the fluorescent acceptor (doxorubicin). The FRET based fluorescent probe demonstrated high sensitivity and selectivity for doxorubicin. The detection limit was 13.8 nM. The fluorescent probe was successfully applied for detecting doxorubicin in doxorubicin-spiked plasmas with a recovery of 96.8–103.8%, a relative standard deviation (RSD) of 1.3–2.8%. The strategy for construction of FRET-based molecularly imprinted materials developed in this work is very promising for analytical applications.

[en] Highlights: • The Pd−[email protected]₂O/N-RGO hybrid was synthesized via a facile wet chemical route. • An enhanced electrocatalytic property of the hybrid has been demonstrated. • The constructed sensor displays super performances for the tryptophan detection. • Advantages include excellent practicability with remarkable reliability. - Abstract: In this work, the N doping together with Pd−[email protected]₂O hybridization for graphene oxide was achieved by a combined process of hydrothermal treatment and chemical reduction, based on which a novel Pd−[email protected]₂O cubes decorated N-doped reduced graphene oxide (Pd−[email protected]₂O/N-RGO) hybrid was obtained. The synthesized Pd−[email protected]₂O/N-RGO was detailedly characterized by various technologies. The results show that the low Pd loading [email protected]₂O cubes with the sizes of 300–500 nm are well dispersed on N-RGO sheets, thereby avoiding the serious aggregation and maintaining a large electroactive surface area of the attained hybrid. Benefiting from the synergistic effect of the properties of Pd−[email protected]₂O particles and N-RGO sheets, the Pd−[email protected]₂O/N-RGO modified electrode exhibits remarkable electrocatalytic performance on the oxidation of tryptophan with the enhanced oxidation response and the lowered oxidation overpotential. Under the optimal conditions for the electrochemical detection of tryptophan, the constructed sensor displays a wide linear range (0.01–40.0 μM) and a low detection limit (1.9 nM), outperforming most of the reported hybrid-based sensors. The proposed sensor also features good selectivity, stability and reproducibility, which has been successfully applied for the detection of tryptophan in the urine and milk samples with satisfactory recoveries. All these results suggest that the Pd−[email protected]₂O/N-RGO hybrid could be a promising and convenient material for the fabrication of high-performance electrochemical sensors.