Assembly of silver(I)-copper(I) bimetallic thiolate complexes assisted by phenylacetylene stabilizers.

Ag/Cu bimetallic clusters have been widely reported, but synthesis of such clusters simple self-assembly of heterometallic ions in air remains challenging due to the susceptibility of Cu ions to oxidation. In this study, protected by the phenylacetylene auxiliary ligand, we utilized [Cu(CHCN)]PF in conjunction with the (PrSAg) polymer to form Ag(I)-Cu(I) oligomer precursors, serving as the starting point for constructing a new [AgCu(PrS)(DPPM)](PF) cluster (DPPM = bis(diphenylphosphino)methane, Ag11-xCux, = 5-9). When the (PrSAg) precursor was replaced by (BuSAg), another cluster [AgCuS(BuS)(CHCN)](CHOH)(HO)(PF) (Ag21Cu4) was obtained.

Template-assisted synthesis of isomeric copper(i) clusters with tunable structures showing photophysical and electrochemical properties.

A comparative study of structure-property relationships in isomeric and isostructural atomically precise clusters is an ideal approach to unravel their fundamental properties. Herein, seven high-nuclearity copper(i) alkynyl clusters utilizing template-assisted strategies were synthesized. Spherical Cu and Cu clusters are formed with a [M@(V/PO)] (M: Cu, Na, K) skeleton motif, while peanut-shaped Cu clusters feature four separate PO templates.

Ag Cu (C=CAr) (DPPB) : A Rigid Ligand Co-Protected Bimetallic Silver(I)-Copper(I) Cluster with Room-Temperature Luminescence.

Metal clusters have become increasingly important in various applications, with ligands playing a crucial role in their construction. In this study, we synthesized a bimetallic cluster, Ag Cu (C=CAr) (DPPB) (Ag Cu ), using a rigid acetylene ligand, 3,5-bis(trifluoromethyl)phenylacetylide. Through single-crystal structure characterization, we discovered that the butterfly-shaped Ag Cu motifs were subject to distortion due to steric hindrance imposed by the rigid ligand.

Copper(I) Alkynyl Clusters with Crystallization-Induced Emission Enhancement.

Four copper(I) alkynyl complexes incorporating phosphate ligands, namely, [Cu(BuC≡C)(PhOPO)] (; PhOPO = phenyl phosphate), [Cu(BuC≡C)(1-NaphOPO)] (; 1-NaphOPO = 1-naphthyl phosphate), [VO@Cu(BuC≡C)(1-NaphOPO)](PF)(F) (), and [PO@Cu(BuC≡C)(1-NaphOPO)](PF)(F) (), were solvothermally synthesized and well-characterized by IR spectroscopy, powder X-ray diffraction, and single-crystal X-ray diffraction. Single-crystal X-ray analysis revealed that the Cu cluster-based coordination chain polymers and are formed by assembly during crystallization, while and contain high-nuclearity copper(I) composite clusters enclosing orthovanadate and phosphate template ions, respectively, that are supported by ROPO ligands. Complexes - exhibit crystallization-induced emission enhancement.

Construction of Silver Clusters Capped by Zwitterionic Ethynide Ligands.

A zwitterionic ligand 3-(triethylammonio)propyne (TAP) has been employed to construct nine silver ethynide compounds for the first time. Single-crystal X-ray analyses reveal that compounds and are silver ethynide assemblies based on the Ag subunits and clusters - are small discrete clusters of Ag, Ag, Ag, and Ag, respectively, ligated by the bulky TAP ligand with different auxiliary ligands. In addition, upon acquiring the tripod-like BuPO, a unprecedented 80 nuclei silver ethynide cluster was isolated and determined to be [(CFCO)@Ag(TAP)(BuPO)(CFCO)] by crystallography and thermogravimetric analysis.

Controllable synthesis of porous tubular carbon by a Ag-ligand-assisted Stöber-silica/carbon assembly process.

Herein, in this study, we utilized Ag+-ligand interactions for critically regulating the morphology of carbon by the Stöber-silica/carbon co-assembly method for the first time. Tetraethyl orthosilicate (TEOS) and resorcinol/formaldehyde (RF) assemble upon dictation by Ag+ and pyridyl-functionalized surfactants, producing porous carbon tubes (RF1) with a high surface area of 696 m2 g-1 and accessible mesopores ∼15 nm in size. Furthermore, when using tetrapropyl orthosilicate (TPOS) with a slower hydrolysis rate than that of TEOS, carbon tubes (RF2) with enhanced uniformity and a surface area as high as 2112 m2 g-1 are generated.

-Butyl thiol and pyridine ligand co-protected 50-nuclei clusters: the effect of pyridines on Ag-SR bonds.

Constructing silver(i)-thiolate clusters from simple building blocks usually involves elusive self-assembly processes and remains a long-standing challenge. In this work, we report 6 silver(i)-thiolate clusters protected by pyridines, namely, [Ag3(tBuS)2(Py)(NO3)]n (Py = pyridine) (1), [Ag10(tBuS)6(Py)6(CF3CO2)4]·3Py (2), [Ag12(iPrS)6(Py)8(NO3)6]·2H2O (3), Ag12(iPrS)6(Py)8(CF3CO2)6 (4), Ag12(iPrS)6(4-ap)6(NO3)6 (4-ap = 4-aminopyridine) (5), and [Ag50S13(tBuS)20(Py)12]·4BF4·4Py·4CH3OH·2H2O (6). Single-crystal X-ray crystallography analysis reveals that six clusters are constructed by four types of structural blocks, including the PyAg(tBuS)2 monomer, Py2Ag2(tBuS)2 dimer, Py3Ag3(tBuS)3 trimer and (4-ap)6Ag6(iPrS)6 hexamer.

Historical long-term exposure to pentachlorophenol causing risk of cancer--a community study.

Background: Pervious studies suggested occupational workers exposure to pentachlorophenol (PCP) might contribute to increased risk of cancer. However, few studies have focused on associations between PCP and cancer risk at the community level.

Objective: The present study was to explore the cancer risk for the community population living long-term in a PCP contaminated area.