N, B-doped carbon dots as a sensitive fluorescence probe for Hg(2+) ions and 2,4,6-trinitrophenol detection for bioimaging.

Nitrogen and boron co-doped carbon dots (BCNDs1-3) were prepared from three kinds of borate via a facile hydrothermal method. The as-prepared BCNDs did not shift with the change of excitation wavelength and possess good water dispersibility, strong fluorescence emission with high fluorescent quantum yield of 29.01%, 51.42%, 68.28%, respectively. Subsequently, these BCNDs were exploited as excellent Hg(2+) ion and 2,4,6-trinitrophenol (TNP) probe. The efficient selective detection of Hg(2+) can be attributed to non-radiative electron/hole recombination annihilation through an effective electron transfer process and the detection of TNP can be attributed to the fluorescence resonance energy transfer process (FRET). The results show that the BCNDs2 is the most sensitive fluorescence probe for Hg(2+) ions and TNP detection as low as Hg(2+) 7.3nM and TNP 0.35µM compared with BCNDs1 and BCNDs3. The as-prepared BCNDs possess the advantages of good selectivity, fast response and a broad linear detection. They were applied to sensing and imaging of human umbilical vein endothelial cells, showing low cytotoxicity and good biocompatibility.

New fluorescence probe for Fe³âº with bis-rhodamine and its application as a molecular logic gate.

A bis-rhodamine based fluorescent probe R1 for naked-eye detection of Fe(3+) with enhanced sensitivity compared to a mono-rhodamine derivative that shows selectivity for Hg(2+), has been synthesized. The 1:1 stoichiometric structure of R1 and Fe(3+) is confirmed using a Job's plot estimation and density functional theory calculations. The reversibility of R1 is verified through its spectral response toward Fe(3+) and S(2-) titration experiments. Using Fe(3+) and S(2-) as chemical inputs and the fluorescence intensity signal as outputs, R1 can be utilized as an INHIBIT logic gate at molecular level. Fluorescent imaging for Fe(3+) in living HL-7702 cells have also been successfully performed.

Highly luminescent organosilane-functionalized carbon dots as a nanosensor for sensitive and selective detection of quercetin in aqueous solution.

The organosilane-functionalized carbon dots (SiCDs) were synthesized using citric acid with N-(b-aminoethyl)-g-aminopropyl methyldimethoxy silane (AEAPMS). The as-synthesized SiCDs were characterized by IR, TEM, XPS, NMR and fluorescence. The SiCDs showed a strong emission at 455 nm with excitation at 365 nm. The SiCDs exhibited analytical potential as sensing probes for quercetin (QCT) determination. pH effect, temperature effect, interferences, and analytical performance of the method were investigated. It suggested that SiCDs exhibited high sensitivity and selectivity toward QCT: the linear ranges of SiCDs were estimated to be 0-40 µM while the limit of detection (LOD) was calculated to be 79 nM.