Despite being weak attractive forces, closed-shell metallophilic interactions play important roles in the Group 11 metal complexes on their diverse structural and physical features. A plethora of experimental and computational studies has thus been dedicated to such weak attractive d -d interactions, particularly aurophilic and argentophilic interactions. Although d -d Cu -Cu forces had been recognized for four decades, cuprophilic interactions are less explored and they are best evidenced by single-crystal X-ray crystallographic analysis on Cu complexes and aggregates thereof, by which precise information about the Cu⋅⋅⋅Cu contacts, shorter than the sum of two van der Waals radii (3.92 Å) between the copper centers concerned can be obtained. Based on recently compelling experimental and spectroscopic evidence for intra- and intermolecular cuprophilic interactions in copper chemistry, the present Minireview summarizes recent progress in the past three decades in the synthesis and structures of multinuclear homometallic copper complexes, whereby supported and unsupported d -d Cu -Cu interactions are at work.
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http://dx.doi.org/10.1002/chem.201900332 | DOI Listing |
Inorg Chem
January 2025
Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, 3012 Bern, Switzerland.
Binuclear silver(I) and copper(I) complexes, and , with bridging diphenylphosphine ligands were prepared. In , the silver(I) center is located inside a trigonal plane composed of three phosphorus donors from three separate and bridging dppm ligands. The fourth coordination site is filled with neighboring silver(I) ions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
State Key Laboratory of Superhard Materials, College of Physics, Jilin University, Changchun, 130012, China.
Developing ionic copper-iodine clusters with multiple emitting is crucial for enriching lighting and display materials with various colors. However, the luminescent properties of traditional ionic copper-iodine clusters are often closely associated with low-energy cluster-centered triplet emission, which will redshift further as the Cu⋅⋅⋅Cu bond length decreases. This article utilizes a pressure-treated strategy to achieve an anomalous pressure-induced blue-shifted luminescence phenomenon in ionic CuI(4-dimethylamino-1-ethylpyridinium) crystals for the first time, which is based on dominant through-space charge-transfer (TSCT).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
University of Rennes, INSA Rennes, CNRS, ISCR (Institut des Sciences Chimiques de Rennes), UMR 6226, F-35000, Rennes, France.
A new luminescent Cu(I) tetrametallic metallacycle B is reported that features very rare semi-bridging aqua ligands. When heated markedly above room temperature, this compound undergoes a post-synthetic transformation in the solid-state, affording the new luminescent metallacycle C. Thermogravimetric analysis, IR spectroscopy and single-crystal X-ray diffraction reveal that this alteration preserves the gross tetrametallic macrocycle structure, but is caused by the release of the coordinated water molecules with the concomitant formation of cuprophilic interactions.
View Article and Find Full Text PDFInorg Chem
September 2024
Univ Rennes, CNRS, ISCR-UMR 6226, 35000 Rennes, France.
The properties of cuprophilic compounds and the underlying fundamental principles responsible for the Cu(I)···Cu(I) interactions have been the subject of intense research as their diverse structural and physical attributes are being explored. In this light, we performed a new study of the compound [CuO(Mes)] reported by Haakansson et al. using state of the art experimental and theoretical analysis techniques.
View Article and Find Full Text PDFSci Bull (Beijing)
September 2024
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China; Science & Technology Innovation Laboratory for Optoelectronic Information of China, Fuzhou 350108, China; University of Chinese Academy of Sciences, Beijing 100049, China. Electronic address:
One-dimensional (1D) semiconductor nanostructures exhibit exceptional performance in mitigating short-channel effects and ensuring low power consumption. However, the scarcity of high-mobility p-type 1D materials impedes further advancement. Molecular-based materials offer high designability in structure and properties, making them a promising candidate for 1D p-type semiconductor materials.
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