Publications by authors named "Yanglin Shen"

The advantages of two-stage warnings have been validated. This study investigated how drivers' expectations of automated driving system capabilities and cognitive load affect their attention allocation and takeover performance when using a two-stage warning system in a Level 3 automated driving system. Thirty-two drivers participated in a driving simulation study.

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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.

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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.

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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.

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Surface cracks could improve the optical and photoelectronic properties of crystalline materials as they increase specific surface area, but the controlled self-assembly of fullerene (C ) molecules into micro-/nanostructures with surface cracks is still challenging. Herein, we report the morphology engineering of novel C microstructures bearing surface cracks for the first time, selecting phenetole and propan-1-ol (NPA) as good and poor solvents, respectively. Our systematic investigations reveal that phenetole molecules initially participate in the formation of the ends of the C microstructures, and then NPA molecules are involved in the gradual growth of the sidewalls of the microstructures.

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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.

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Article Synopsis
  • The study focuses on how adding a sulfido template to a specific silver cluster enhances its light-emitting properties.
  • This modification resulted in a new silver cluster with a longer wavelength emission (716 nm) compared to the original cluster (660 nm).
  • The changes in emission are attributed to alterations in the cluster's structural and electronic properties, especially the interactions between the sulfido template and the silver metal core.
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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.

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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.

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Article Synopsis
  • Four silver thiolate clusters were isolated, each featuring unique configurations based on different templating anions: BF4, CF3COO, MoO4, and CrO4.
  • These clusters share a similar nestlike structure built around a silver-sulfide [AgS] core, highlighting the importance of the anion in their formation.
  • The luminescent properties of clusters 2-4 can be adjusted from green to orange to red by altering the templating anion, indicating a relationship between the anion's charge transfer and the clusters' emission colors.
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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.

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