Peculiar holes on checkerboard facets of a trigonal prismatic AuAg(SPhCl)(PPh) cluster caused by steric hindrance and magic electron count.

Dalton Trans

Collaborative Innovation Center of Chemistry for Energy Materials, State Key Laboratory for Physical Chemistry of Solid Surfaces, and Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.

Published: February 2017

We report herein the synthesis and structure of a 45-atom trigonal-prismatic Au-Ag bimetallic nanocluster, formulated as AuAg(SPhCl)(PPh), based on single-crystal X-ray crystallographic determination. The structure can be described as a core-shell structure with a tricapped trigonal prismatic (ttp1) Au core encaged in a larger (frequency-two) tricapped trigonal prismatic (ttp2) Ag shell. The cluster is terminated by six Ag(PPh) moieties which, along with ttp2 and 27 thiolates, constitute the outer trigonal-prismatic (TP) shell. Each of the three nearly coplanar yet severely distorted "square" faces of TP contains 13 Ag atoms which are arranged in a way reminiscent of the (100) face of a face-centered cubic (fcc) structure. Of the 30 edges formed by these quasi-(100) faces of the TP, only 27 are bridged by the thiolate ligands; three are vacant, one on each "square" face. It is believed that these peculiar vacant ligand sites are caused by steric hindrance of the thiolate ligands in combination with the superatomic electronic shell closing of 1S1P1D rendering 9(ttp1) + 30(ttp2) + 6(TP) - 27(SR) = 18 jellium electrons.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c6dt04419kDOI Listing

Publication Analysis

Top Keywords

trigonal prismatic
12
caused steric
8
steric hindrance
8
tricapped trigonal
8
thiolate ligands
8
peculiar holes
4
holes checkerboard
4
checkerboard facets
4
facets trigonal
4
prismatic auagsphclpph
4

Similar Publications

Self-assembly of 1T/1H superlattices in transition metal dichalcogenides.

Nat Commun

December 2024

International Center for Quantum Design of Functional Materials (ICQD), Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui, 23026, China.

Heterostructures and superlattices composed of layered transition metal dichalcogenides (TMDs), celebrated for their superior emergent properties over individual components, offer significant promise for the development of multifunctional electronic devices. However, conventional fabrication techniques for these structures depend on layer-by-layer artificial construction and are hindered by their complexity and inefficiency. Herein, we introduce a universal strategy for the automated synthesis of TMD superlattice single crystals through self-assembly, exemplified by the NbSeTe 1T/1H superlattice.

View Article and Find Full Text PDF

We report a detailed structural study of a series of five new quaternary Eu(II)-containing mixed chalcogenide phases, EuSiSeS, EuSiSeS, EuSiSeS, EuSiSeS, and EuSiSe, synthesized using the flux-assisted boron chalcogen mixture (BCM) method. High-quality crystals were grown, and their crystal structures were determined by single-crystal X-ray diffraction. All members of the EuSiSeS series crystallize in the monoclinic crystal system with space group 2/, except EuSiSe, which crystallizes in the 2 space group.

View Article and Find Full Text PDF

Unveiling Trigonal Anti-Prismatic Structure and Stacking Sequences in InTe.

Small

December 2024

Department of Materials Science & Engineering and Research Institute of Advanced Materials, Seoul National University, Seoul, 08826, Republic of Korea.

Polymorphic phases of 2D van der Waals layered materials attract significant research interest due to their diverse properties. There is a growing need to synthesize novel polymorphs and explore their atomic-level structures. In this study, molecular beam epitaxy (MBE) is used to grow indium telluride, a III-VI metal chalcogenide with promising applications, on graphene substrates.

View Article and Find Full Text PDF

Multifunctional chiral metal hydrogen-bonded organic frameworks constructed from lanthanide ions with a trigonal prismatic coordination environment.

Dalton Trans

December 2024

State Key Laboratory of Materials-Oriented Chemical Engineering, School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 211816, P. R. China.

Two pairs of chiral enantiomers D/L-Dy(PMP)·2HO (D-1/L-1) and D/L-Yb(PMP)·2HO (D-2/L-2) were synthesized by the introduction of enantiomerically pure D/L-PMP (PMP = (phosphonomethyl)proline) ligands into lanthanide coordination chemistry. The chiral characteristics of these products were confirmed by single crystal X-ray diffraction, second harmonic generation (SHG) measurements and circular dichroism (CD) spectroscopy. These complexes are composed of 1D chains constructed from lanthanide ions with a trigonal prismatic coordination geometry and PMP ligands.

View Article and Find Full Text PDF

Sulfur dioxide (SO) is an important industrial feedstock that can be directly utilized or catalytically transformed to value-added chemicals such as sulfuric acid. The development of regenerable porous sorbents for the highly efficient storage and energy-minimal release of toxic SO operating under ambient conditions has attracted growing interest. Herein, we report the topology-guided construction of highly porous -type metal-organic frameworks (MOFs) through a counterintuitive modulator-directed catenation control approach.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!