Xiaolin Guan

Fluorophore-functionalized graphene oxide with application in cell imaging

In this work, we fabricated a novel triphenylamine-derivative (DNDT)-modified nanographene oxide by following a simple gram-scale method. The product showed interesting optical properties and good potential for use in bioimaging applications. This fluorescent carbon material could be readily internalized by HepG2 cells and was clearly visualized to accumulate mainly in the nucleus.

Intriguingly tuning the fluorescence of AIEgen using responsive polyelectrolyte microspheres

In this study, we present a practical approach to tune the fluorescence of AIEgen (the luminogens exhibiting AIE attributes) based on counterion-sensitive polyelectrolyte microspheres. The tunable fluorescence is induced by counterion-driven interactions in polyelectrolyte microspheres by a simple exchange of the counterions. The effects of different types of opposite counterions on the fluorescent properties of a new polyelectrolyte tetraphenylethene-graft-poly[2-(methacryloyloxy)-ethyltrimethylammonium chloride] (TPE–PMETAC), which was synthesized by Atom Transfer Radical Polymerization (ATRP) using a TPE derivative containing four arms as an initiator, were systematically investigated. For cationic microspheres with quaternary ammonium groups, the fluorescence intensity progressively increased according to the counterion series Cl− < ClO4− < PF6− < TFSI−, which is in accord with the ability of exchanged hydrophilic Cl− by hydrophobic anions in the order of ClO4− < PF6− < TFSI−. The mechanism of tuning fluorescence was determined by dynamic light scattering (DLS), zeta-potentials and scanning electron microscopy (SEM). We proved that the size of the microspheres and electrostatic repulsive forces between the microspheres were decreased by the addition of counterions due to the hydrophobic-induced collapse of the surfaces of the microspheres. As a result, the obvious increase in the fluorescence of AIEgen was obtained based on the aggregation of microspheres.

Efficient Detection of Trace Hg2+ in Water Based on the Fluorescence Quenching of Environment-friendly Thiol-functionalized Poly(vinyl alcohol) Capped CdS Quantum Dots Nanocomposite

Using environment-friendly materials for sensing toxic metal ions has drawn significant attention in recent research. Herein, we present an aqueous synthesis of stable CdS quantum dots (QDs) using thiol-functionalized poly(vinyl alcohol) (PVA) as the unique capping ligand for the detection of trace Hg(2+) in environmental water samples. The CdS QDs with an average size of 3.3 nm had good water-solubility and favorable fluorescence with a quantum yield of 32.8% and a longer luminescence lifetime of 31.9 ns. The fluorescence intensity of QDs aqueous solution in the 520 nm wavelength was quenched upon the addition of Hg(2+). Under the optimal conditions, the ratio of the blank fluorescence intensity to the quenched fluorescence intensity was linearly proportional to the Hg(2+) concentration from 2 to 4000 nM with a detection limit of 1 nM. Also, many co-existing metal ions were not interfered with the detection of Hg(2+). This nanomaterial was successfully applied to the measurement of Hg(2+) in water samples.

A direct crossed polymerization of triphenylamines and cyclohexanones via CC bond formation: the method and its bioimaging application

The effective polymerization process is very desirable in the field of macromolecule science. In this study, we present a facile synthetic method via aldol addition and condensation (AAC) that leads to the formation of fluorescent linear and branched polymers by cross coupling triphenylamines (TPA) and cyclohexanones (CYC) via CC bond formation. The methodology has the advantage of easy operations, mild reaction conditions, and high yield. Via the analysis of NMR, FT-IR, GPC, PL, UV, SEM, and theoretical calculation, the structure, physical properties, and optical behaviors of both polymers were well-characterized. The understanding of cell transplantation, migration, division, fusion, and lysis is a very challenging task. In this study, the linear polymer (LP) exhibits excellent biocompatibility and low cytotoxicity, which can be readily internalized by living cells in a noninvasive manner. The images of MPC5 cells indicate that LP can be a promising emissive fluorescence probe for bioimaging application.