Continuing research on the preparation and structural determination of monolayer-protected silver clusters has been performed. The compounds include mixed-valence Ag
0/1+
clusters and single-valence ...Ag
1+
clusters, which contain a few to tens or hundreds of Ag atoms that are protected by organic ligands. Sometimes, counter ions and extraneous species appear in their crystalline state. These non-metal parts define the shell layers of silver clusters. Strong coordination bonds and weak supramolecular interactions have been employed not only to modify the shell configurations and components of discrete silver clusters but also to hierarchically assemble silver clusters, producing novel cluster-based functional materials with unexpected physical and chemical properties. Atomically-precise structures help to map out definite electronic structures and structure-property correlations, enabling precise control of shell layers to achieve desired stability and specific functionalities. In this Tutorial Review, based on classic silver cluster paradigms, we first summarize the strategies and recent advances in precise modification and hierarchical assembly of well-defined silver clusters through shell engineering. Second, the correlations of structure-property and structure-functionality are summarized. Of these, the most important is structure-luminescence relationship, which is discussed in detail. In this topic, the uniqueness and prospect of silver clusters as potential lighting materials are scrutinized. Finally, the existing challenges and perspectives of functional silver clusters are presented. The general strategic design presented in this Review will motivate researchers to exploit the development of functionality-oriented materials based on nanosized building blocks in the enrichment of nanotechnology and material science.
This tutorial review focuses on the modification and assembly of atomically-precise silver clusters by changing shell layers for more stability and functionalities, especially for brighter luminescence.
A polar homochiral 3D MOF {Co2(L)(bpe)(H2O)}·5H2O n constructed with cobalt(II) and a new ligand N-(1,3-dicarboxy-5-benzyl)-carboxymethylglycine (H4L) accommodates ordered helical water streams in ...its helical grooves. It provides the first example of switchable ferroelectric and optical behavior through two-step reversible single-crystal to single-crystal transformation (SCSC) upon desorption/adsorption of water spirals and coordinated water molecules, respectively.
Silver chalcogenolate cluster assembled materials (SCAMs) are a category of promising light‐emitting materials the luminescence of which can be modulated by variation of their building blocks ...(cluster nodes and organic linkers). The transformation of a singly emissive Ag12(SBut)8(CF3COO)4(bpy)4n (Ag12bpy, bpy=4,4′‐bipyridine) into a dual‐emissive (Ag12(SBut)6(CF3COO)6(bpy)3)n (Ag12bpy‐2) via cluster‐node isomerization, the critical importance of which was highlighted in dictating the photoluminescence properties of SCAMs. Moreover, the newly obtained Ag12bpy‐2 served to construct visual thermochromic Ag12bpy‐2/NH2 by a mixed‐linker synthesis, together with dichromatic core–shell Ag12bpy‐2@Ag12bpy‐NH2‐2 via solvent‐assisted linker exchange. This work provides insight into the significance of metal arrangement on physical properties of nanoclusters.
Tandem varying of Ag cluster structure and tuning mixed linkers in a stepwise fashion are used to achieve dual‐emitting homogeneous and core–shell silver chalcogenolate cluster assembled materials. The arrangements of silver in the cluster are demonstrated to play a fundamentally important role in luminescence.
The dispersive sweep of fast radio bursts (FRBs) has been used to probe the ionized baryon content of the intergalactic medium
, which is assumed to dominate the total extragalactic dispersion. ...Although the host-galaxy contributions to the dispersion measure appear to be small for most FRBs
, in at least one case there is evidence for an extreme magneto-ionic local environment
and a compact persistent radio source
. Here we report the detection and localization of the repeating FRB 20190520B, which is co-located with a compact, persistent radio source and associated with a dwarf host galaxy of high specific-star-formation rate at a redshift of 0.241 ± 0.001. The estimated host-galaxy dispersion measure of approximately Formula: see text parsecs per cubic centimetre, which is nearly an order of magnitude higher than the average of FRB host galaxies
, far exceeds the dispersion-measure contribution of the intergalactic medium. Caution is thus warranted in inferring redshifts for FRBs without accurate host-galaxy identifications.
Recently, research on metal–organic frameworks (MOFs) serving as a new type of proton conductive material has resulted in many exciting achievements. However, direct observation of a well-established ...proton-transfer mechanism still remains challenging in MOFs and other crystalline compounds, let alone other conductive materials. Herein we report the solvothermal synthesis of a new proton-conducting MOF, (Me2NH2)Eu(L) (H4L = 5-(phosphonomethyl)isophthalic acid). The compound consists of a layered anionic framework Eu(L)− and interlayer-embedded counter cations (Me2NH2)+, which interact with adjacent uncoordinated O atoms of phosphonate groups to form strongly (N–H···O) hydrogen-bonded chains aligned parallel to the c-axis. Facile proton transfer along these chains endows the compound with single-crystal anhydrous conductivity of 1.25 × 10–3 S·cm–1 at 150 °C, and water-assisted proton conductivity for a compacted pellet of microcrystalline crystals attains 3.76 × 10–3 S·cm–1 at 100 °C and 98% relative humidity (RH). Proton dynamics (vibrating and transfer) within N–H···O chains of the compound are directly observed using a combination of anisotropic conductivity measurements and control experiments using large single-crystals and pelletized samples, in situ variable-temperature characterization techniques including powder X-ray diffraction (PXRD), single-crystal X-ray diffraction (SCXRD), diffuse reflectance infrared Fourier transform spectrum (DRIFTS), and variable-temperature photoluminescence. In particular, a scarce single-crystal to single-crystal (SCSC) transformation accompanied by proton transfer between an anionic structure (Me2NH 2)Eu(L) and an identical neutral framework Eu(HL) has been identified.
Abstract
Ratiometric luminescent oxygen sensing based on dual fluorescence and phosphorescence emission in a single matrix is highly desirable, yet the designed synthesis remains challenging. ...Silver-chalcogenolate-cluster-based metal-organic frameworks that combine the advantages of silver clusters and metal-organic frameworks have displayed unique luminescent properties. Herein, we rationally introduce −NH
2
groups on the linkers of a silver-chalcogenolate-cluster-based metal-organic framework (Ag
12
bpy-NH
2
) to tune the intersystem crossing, achieving a dual fluorescence-phosphorescence emission from the same linker chromophore. The blue fluorescence component has a 100-nm gap in wavelength and 8,500,000-fold difference in lifetime relative to a yellow phosphorescence component. Ag
12
bpy-NH
2
quantifies oxygen during hypoxia with the limit of detection of as low as 0.1 ppm and 0.3 s response time, which is visualized by the naked eye. Our work shows that metal cluster-based MOFs have great potential in luminescent sensing, and the longer-lived charge-separated states could find more photofunctional applications in solar energy transformation and photocatalysis.
Convenient generation of stable superatomic silver clusters and their systematic site-specific tailoring and directional assembly present an enduring and significant challenge. In this work, we ...prepared a face-centered cubic (fcc) array of Ag14 superatoms protected by face-capping 1,2-dithiolate-o-carborane (C2B10H10S2) ligands, each produced from 1-thiol-o-carborane in crystallization with simultaneous reduction of Ag+ to Ag0. We find that the corner N-donor ligands contribute predominately to the stability and luminescence of the Ag14 superatom. As the first-formed nanocluster Ag14(C2B10H10S2)6(CH3CN)8·4CH3CN (NC-1) with labile vertex-coordinated CH3CN ligands is highly unstable, monodendate pyridine ligands were used to replace these CH3CN species site-specifically, giving Ag14(C2B10H10S2)6(pyridine/p-methylpyridine)8 (NCs-2,3) in gram scale with its core structure intact, which features ultrastability up to 150 °C in air. Moreover, using bidentate N-containing ligands to bridge the superatomic Ag14 building blocks, we constructed an unprecedented hierarchical series of 1D-to-3D superatomic silver cluster-assembled materials (SCAM-1,2,3,4), and SCAM-4 is air-stable up to 220 °C. Furthermore, this series of stable solid-state superatomic-nanocluster materials exhibit tunable dual emission with wide-range thermochromism. The present study constitutes a major step toward the development of ligand-modulation of the structure, stability, assembly, and functionality of superatomic silver nanoclusters.
Silver cluster-assembled materials (SCAMs), by virtue of their tunable structure, accessible surface area and excellent stability, hold great promise as highly efficient catalysts. Herein, we report ...a new SCAM Ag12(S t Bu)6(CF3COO)3(TPyP) n (denoted as Ag12TPyP) composed of a Ag12 chalcogenolate cluster core stabilized by porphyrinic ligands. Ag12TPyP showed superior sulfur mustard simulant (2-chloroethyl ethyl sulfide, CEES) degradation efficiency and achieved a half lifetime (t 1/2) of 1.5 min with 100% selectivity. The experimental results demonstrated that synergistic effects between the silver cluster and photosensitizer ligand promote the efficiency of the generation of singlet oxygen (1O2), which accelerates the decontamination rate. Additionally, benefiting from strong affinity between the silver cluster and CEES, Ag12TPyP exhibits a CEES uptake of 74.2 mg g–1. This work demonstrates that SCAMs offer a new route to the rational design of novel materials for the detoxification of mustard gas.
Active participation in intellectual leisure activities such as calligraphy helps prevent cognitive decline and dementia, but the underlying mechanisms are not fully understood. With disrupted ...functional connectivity (FC) of default mode network (DMN) associated with cognitive decline, we speculate that intellectual activities might optimize cognitive function through modulating FC of DMN. This two-arm single-blind randomized controlled trial aims to identify the effects of increasing practice of calligraphy on cognitive function and FC of DMN in people with subjective cognitive decline (SCD).
One hundred twelve community-living Chinese aged 55 to 75 years old with SCD but without mild cognitive impairment or dementia and with prior practice of calligraphy as defined by 1 h of calligraphy per week will be recruited through elderly social centres in Hong Kong and randomized into either control or intervention group. The control group will continue with their usual practice of calligraphy, whereas the intervention group will double their practice of calligraphy. Measurement of cognitive outcomes and neuroimaging on resting-state FC will be performed at baseline and in 6 months. Repeated measures analysis of variance will be used to assess cognitive and FC changes, with time being the within-group factor, control/intervention as the between-group measure, and important covariates (age, sex, educational and occupational attainment, health, and other lifestyle factors) controlled for.
This study will shed light on the underlying neurocognitive mechanisms of how intellectual activities promotes cognitive maintenance. Our anticipated findings will provide evidence that reversing or slowing FC disruption by actively participating in intellectual activities is still possible for the at-risk individuals.
Chinese Clinical Trial Registry ChiCTR1900024433 . Registered on 11 July 2019.
We report a new enantiomeric pair of superatomic silver clusters, R/S-Ag 17 , prepared from chiral alkynyl ligands. R-Ag 17 and S-Ag 17 possess C 3 symmetry and emit near-infrared (NIR) light with a ...quantum yield (QY) of 8.0% under ambient condition as well as NIR circularly polarized luminescence (CPL) as a result of the chirality of the excited states. Both experiments and theoretical calculations indicate for the first time that the CPL originates from transitions between superatomic 1P z (along the C 3 axis) and 1S orbitals. This work opens a new avenue for CPL-active metal nanoclusters by utilizing chiral alkynyl ligands and enlightens the chirality transfer from chiral protecting ligands to superatomic states in metal clusters.
PDF
