The title compounds, di-μ-chlorido-bis-({2-[(η-2,3)-(prop-2-en-1-yl)sulfan-yl]pyridine-κ}copper(I)), [CuCl(CHNS)], and di-μ-bromido-bis-({2-[(η-2,3)-(prop-2-en-1-yl)sulfan-yl]pyridine-κ}copper(I)), [CuBr(CHNS)], were obtained by alternating-current electrochemical synthesis starting from an ethano-lic solution of 2-[(prop-2-en-1-yl)sulfan-yl]pyridine () and the copper(II) halide. The isostructural crystals are built up from centrosymmetric [Cu ()] dimers, which are formed due to the π,σ-chelating behavior of the organic ligand. In the crystals, the dimers are linked by C-H⋯ hydrogen bonds as well as by aromatic π-π stacking inter-actions into a three-dimensional network.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8587979PMC
http://dx.doi.org/10.1107/S2056989021011002DOI Listing

Publication Analysis

Top Keywords

syntheses crystal
4
crystal structures
4
structures copperi-halide
4
copperi-halide πσ-coordination
4
πσ-coordination compounds
4
compounds based
4
based 2-[prop-2-en-1-ylsulfan-yl]pyridine
4
2-[prop-2-en-1-ylsulfan-yl]pyridine title
4
title compounds
4
compounds di-μ-chlorido-bis-{2-[η-23-prop-2-en-1-ylsulfan-yl]pyridine-κ}copperi
4

Similar Publications

Magnetic nanoparticles of Nd2Fe14B prepared by ethanol-assisted wet ball milling technique.

Sci Rep

January 2025

Environmental and Occupational Hazards Control Research Center, Research Institute for Health Sciences and Environment, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

The magnetic material Nd2Fe14B is one of the strongest magnetic materials found in nature. The demand for the production of these nanoparticles is significantly high due to their exceptional properties. The aim of the present study is to synthesize magnetic nanoparticles of Nd2Fe14B using ethanol in the wet ball milling technique (WBMT).

View Article and Find Full Text PDF

Hydroxyapatite (HA) is an important constituent of natural bone. The properties of HA can be enhanced with the help of various ionic substitutions in the crystal lattice of HA. Iron (Fe) is a vital element present in bones and teeth.

View Article and Find Full Text PDF

High-temperature structural disorders stabilize hydrous aluminosilicates in the mantle transition zone.

Nat Commun

January 2025

Center for High Pressure Science, State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao, 066004, China.

Hydrous aluminosilicates are important deep water-carriers in sediments subducting into the deep mantle. To date, it remains enigmatic how hydrous aluminosilicates withstand extremely high temperatures in the mantle transition zone. Here we systematically investigate the crystal structures and chemical compositions of typical hydrous aluminosilicates using single-crystal X-ray diffraction, electron probe microanalyzer, and nanoscale secondary ion mass spectrometry.

View Article and Find Full Text PDF

The mechanical properties of metal-organic frameworks (MOFs) are of high fundamental and practical relevance. A particularly intriguing technique for determining anisotropic elastic tensors is Brillouin scattering, which so far has rarely been used for highly complex materials like MOFs. In the present contribution, we apply this technique to study a newly synthesized MOF-type material, referred to as GUT2.

View Article and Find Full Text PDF

A new Donor-Acceptor type pyrazinacene derivative (1) featuring strong ICT was synthesized by linking electron-donating triphenylamine (TPA) and electron-accepting CN groups via a pyrazinacene core. The compound exhibits a dramatic color change from greenish blue to red-violet upon selective recognition of naphthalene (3) to form a 1:1 co-crystal (1•3). This color change is induced by intermolecular CT between pyrazinacene and naphthalene's aromatic moieties, driven by π-hole···π interactions.

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!