Two complexes of divalent samarium have been synthesized by electrochemical reduction in methanol-tetrahydrofuran solutions: [Sm(18-crown-6)(ClO4)2] and [Sm(15-crown-5)2](ClO4)2. In [Sm(18-crown-6)(ClO4)2] the metal cation is ten-coordinate and its coordination sphere comprises six oxygen atoms of the crown ligand and four oxygen atoms from two perchlorate anions. [Sm(15-crown-5)2](ClO4)2 shows a sandwich structure with decacoordinate samarium located between two 15-crown-5 molecules. At 77 K both compounds show f-f luminescence originating from the 5D0 level, and also the 15-crown-5 complex shows a weak luminescence in the range 20000-25000 cm(-1), which has been tentatively interpreted as originating from 3P0 and 5H3 levels. At room temperature the emission of [Sm(15-crown-5)2](ClO4)2 is dominated by broad f-d bands. In the excitation spectra some Fano resonances have been observed. The 18-crown-6 compound is unstable, but the 15-crown-5 compound is fairly stable in air.

Download full-text PDF

Source
http://dx.doi.org/10.1039/b316253bDOI Listing

Publication Analysis

Top Keywords

oxygen atoms
8
complexes smii
4
smii crown
4
crown ethers-electrochemical
4
ethers-electrochemical synthesis
4
synthesis structure
4
structure spectroscopy
4
spectroscopy complexes
4
complexes divalent
4
divalent samarium
4

Similar Publications

Radially Distributed Electron Transfer on Single-Crystalline Surface of Gold Microplates.

ACS Nano

January 2025

State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Chemistry and Chemical Engineering, Donghua University, Shanghai 201620, China.

Electron transfer is ubiquitous in many chemical reactions and biological phenomena; however, the spatial heterogeneities of electron transfer kinetics in electrocatalysis are so far insufficiently resolved. Measuring and understanding the localized electron transfer are crucial to deciphering the intrinsic activity of electrocatalysts and to achieving further improvements in performance. By using scanning electrochemical probe microscopy to spatially resolve redox electrochemistry across the single-crystalline surface of gold microplates, we discover an intriguing radially distributed electron transfer pattern, where the kinetics around the periphery region are significantly higher than those at the central region, regardless of the redox reaction types.

View Article and Find Full Text PDF

Modulating the structure of Cu in CuX/CNTs hollow tetrakaidecahedron to enhance high-efficiency HO production.

J Colloid Interface Sci

January 2025

School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China. Electronic address:

Regulation of active sites of electrocatalysts is critical in adjusting electronic structure and catalytic selectivity towards oxygen reduction reaction (ORR) to hydrogen peroxide (HO). Herein, the CuX/CNTs (X = Se, SSe, S) hollow tetrakaidecahedron catalysts were synthesized to facilitate the electrocatalytic reduction of O to HO. The introduction of S resulted in a shift from four-electron pathway on CuSe/CNTs to two-electron process on CuS/CNTs, ultimately leading to an enhancement in HO productivity.

View Article and Find Full Text PDF

High-energy metal deposition significantly impacts the performance and reliability of two-dimensional (2D) semiconductors and nanodevices. This study investigates the localized annealing effect in atomically thin InO induced during high-energy metal deposition. The localized heating effect alters the electronic performance of InO devices, especially in shorter channel devices, where heat dissipation is further constrained.

View Article and Find Full Text PDF

The studies on ionic liquids (ILs) and their interaction with different solvents have always been an interesting topic for experimental and computational chemists. Recently, however, deep insights on the molecular structures of the IL-water binary mixtures have been mainly performed through classical simulations. Here, a comprehensive quantum mechanical study is presented on seven 1-butyl-3-methylimidazolium-based ILs in the absence and presence of water.

View Article and Find Full Text PDF

Converting Fe-N-C single-atom catalyst to a new FeNxSey cluster catalyst for proton-exchange membrane fuel cells.

Angew Chem Int Ed Engl

January 2025

Tianjin University, School of Materials science and engineering, School of Materials Science and Engineering, Tianjin University, 300072, Tianjin, CHINA.

Fe-N-C catalyst is the most promising alternative to platinum catalyst for proton-exchange membrane fuel cells (PEMFCs), however its high performance cannot be maintained for a long enough time in device. The construction of a new Fe coordination environment that is different from the square-planar Fe-N 4 configuration in Fe-N-C catalyst is expected to break current stability limits, which however remains unexplored. Here, we report the conversion of Fe-N-C to a new FeNxSey catalyst, where the Fe sites are three-dimensionally (3D) co-coordinated by N and Se atoms.

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!