The rod-shaped Au25 nanocluster possesses a low photoluminescence quantum yield (QY=0.1%) and hence is not of practical use in bioimaging and related applications. Herein, we show that substituting silver atoms for gold in the 25-atom matrix can drastically enhance the photoluminescence. The obtained Ag(x)Au(25-x) (x=1-13) nanoclusters exhibit high quantum yield (QY=40.1%), which is in striking contrast with the normally weakly luminescent Ag(x)Au(25-x) species (x=1-12, QY=0.21%). X-ray crystallography further determines the substitution sites of Ag atoms in the Ag(x)Au(25-x) cluster through partial occupancy analysis, which provides further insight into the mechanism of photoluminescence enhancement.
A metal exchange method based upon atomically precise gold nanoclusters (NCs) as templates is devised to obtain alloy NCs including CuxAu25-x(SR)18, AgxAu25-x(SR)18, Cd1Au24(SR)18, and Hg1Au24(SR)18 via reaction of the template with metal thiolate complexes of Cu(II), Ag(I), Cd(II), and Hg(II) (as opposed to common salt precursors such as CuCl2, AgNO3, etc.). Experimental results imply that the exchange between gold atoms in NCs and those of the second metal in the thiolated complex does not necessarily follow the order of metal activity (i.e., galvanic sequence). In addition, the crystal structure of the exchange product (Cd1Au24(SR)18) is successfully determined, indicating that the Cd is in the center of the 13-atom icosahedral core. This metal exchange method is expected to become a versatile new approach for synthesizing alloy NCs that contain both high- and low-activity metal atoms.
Fluorescent probes, as noninvasive tools for visualizing the metabolism of biomolecules, hold great potential to explore their physiological and pathological processes. For cysteine (Cys), however, none of the reported fluorescent probes could image the metabolic processes in living cells. To achieve this goal, we developed a coumarin derivative based on rational design of the dual recognition sites for Cys and its metabolite, SO. The probe displayed distinct two channels with turn-on fluorescent emission toward Cys and SO, which were successfully applied for imaging both A549 cells and zebrafish. Further, with reversible fluorescent responses toward Cys, the probe could image the enzymatic conversion of Cys to SO in living A549 cells in a ratiometric manner. The present work reports the first probe to image the endogenous generated SO without incubation of the SO donors.
Chirality in nanoparticles is an intriguing phenomenon. Herein, we have devised a well-defined gold nanoparticle system for investigating the origin of chirality in nanoparticles. We have designed chiral thiols (R- and S-isomers) and synthesized chiral gold nanoparticles composed of 25 gold atoms and 18 ligands, referred to as Au(25)(pet)(18), where pet represents chirally modified phenylethylthiolate -SCH(2)CH(CH(3))Ph at the 2-position. These optically active nanoparticles are close analogues of the optically nonactive phenylethylthioalte-capped Au(25)(pet)(18) nanoparticles, and the latter's crystal structure is known. On the basis of the atomic and electronic structures of these well-defined Au(25) nanoparticles, we have explicitly revealed that the ligands and surface gold atoms of Au(25)(pet)(18) play a critical role in effecting the circular dichroism responses from the nanoparticles. Similar effects are also observed in chiral Au(25) rods. The mixing of electronic states of ligands with those of surface gold atoms constitutes the fundamental origin of chirality in such nanoparticles.
We report the synthesis and characterization of selenophenolate-capped 25-gold-atom nanoclusters via a ligand-exchange approach. In this method, phenylethanethiolate (PhCH(2)CH(2)S) capped Au(25) nanoclusters are utilized as the starting material, which is subject to ligand-exchange with selenophenol (PhSeH). The as-obtained cluster product is confirmed to be selenophenolate-protected Au(25) nanoclusters through characterization by electrospray ionization (ESI) and matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS), thermogravimetric analysis (TGA), elemental analysis (EA), UV-Vis and (1)H/(13)C NMR spectroscopies. The ligand-exchange synthesis of [Au(25)(SePh)(18)](-)[(C(8)H(17))(4)N](+) nanoclusters demonstrates that the core size of gold nanoclusters is retained in the thiolate-to-selenolate exchange process and that the 18 surface thiolate ligands can be completely exchanged by selenophenolate, rather than giving rise to a mixed ligand shell on the cluster. The two types of Au(25)L(18) (L = thiolate or selenolate) nanoclusters also show some differences in stability and optical properties.
This work reports the first synthesis of selenophenolate-protected Au(18)(SePh)(14) nanoclusters. This cluster exhibits distinct differences from its thiolate analogue in terms of optical absorption properties. The Au(18)(SePh)(14) nanoclusters were obtained via a controlled reaction of Au(25)(SCH(2)CH(2)Ph)(18) with selenophenol. Electrospray ionization time-of-flight mass spectrometry (ESI-TOF-MS) revealed the crude product to contain predominantly Au(18)(SePh)(14) nanoclusters, and side products include Au(15)(SePh)(13), Au(19)(SePh)(15) and Au(20)(SePh)(16). High-performance liquid chromatography (HPLC) was employed to isolate Au(18)(SePh)(14) nanoclusters. The results of thermogravimetric analysis (TGA), elemental analysis (EA), and (1)H/(13)C NMR spectroscopy confirmed the cluster composition. To the best of our knowledge, this is the first report of selenolate-protected Au(18) nanoclusters. Future theoretical and X-ray crystallographic work will reveal the geometric structure and the nature of selenolate-gold bonding in the nanocluster.
We reported the first lysosome targeted two-photon fluorescent probe (Lyso-NP) as a viscosity probe for monitoring autophagy. The fluorescence lifetime of Lyso-NP exhibited an excellent linear relationship with viscosity value ( R = 0.99, x = 0.39). Lyso-NP also showed the specific capability for imaging lysosomal viscosity under two-photon excitation at 860 nm along with good biocompatibility. More importantly, Lyso-NP could be used to monitor the autophagy process in living cells by quantitatively detecting lysosomal viscosity changes during the membrane fusion process via two-photon fluorescence lifetime imaging.
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