A family of lanthanide mixed-valent vanadium(III/IV) oxosilicates Ln4V(5-x)Zn(x)Si4O22 (Ln = La, Ce, Pr, and Nd) was synthesized as high-quality single crystals via a high-temperature molten salt method. An in situ reduction of V(V) to V(III/IV) as well as of Ce(IV) to Ce(III) was achieved utilizing Zn metal as the reducing agent, some of which is incorporated into the crystal structure. Ce4V(4.77)Zn(0.23)Si4O22, to the best of our knowledge, is the first example of a cerium-containing mixed-valent vanadium silicate. The crystal structures were determined by single-crystal X-ray diffraction, and the four isostructural oxosilicates were determined to crystallize in the chevkinite-structure type in the monoclinic space group I2/a. The unit cells of the Ln4V(5-x)Zn(x)Si4O22 (Ln = La, Ce, Pr, and Nd) series are related to the reported C2/m phases Ln4V5Si4O22 (Ln = La, Pr, and Nd) by a doubling of the c-axis and a loss of a mirror plane. The three-dimensional crystal structure consist of two-dimensional rutile-based vanadium oxide and lanthanide oxide layers linked via Si2O7 groups. The temperature dependence of the magnetic susceptibility of these compounds was measured, and only the Nd analogue exhibited a magnetic transition at 5 K; all samples displayed a discontinuity or deviation from linearity at ca. 130-150 K.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.inorgchem.5b02735 | DOI Listing |
Dalton Trans
October 2024
Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee - 247667, India.
High- ferro-/ferrimagnetic quadruple perovskites constitute an important class of oxides that has garnered a lot of research attention in recent times, but their synthesis is commonly achieved under high-pressure conditions. Thus, the development of high- quadruple perovskites that can be synthesized under ambient pressure can be a key to the above problem. Herein, we report ambient pressure synthesis of a series of new A-site ordered quadruple perovskites, LnCuMnTiO (Ln = La, Nd; = 0, 0.
View Article and Find Full Text PDFLuminescence
June 2024
School of Physics and Chemistry, Hunan First Normal University, Changsha, People's Republic of China.
Utilizing the structure characteristic of KCaY (PO) crystal, the site distribution of Eu in KCaY (PO):Eu phosphor coactivated with Eu and Eu ions is tuned. Upon 393-nm excitation, the as-prepared phosphor exhibits a broadband emission of Eu peaked at ~ 475 nm and a typical red emission of Eu with a strong D-F emission at ~ 591 nm. The luminescence color of the phosphor can be adjusted from blue to green, white, yellow, and red.
View Article and Find Full Text PDFChem Commun (Camb)
July 2024
P. Roy and Diana T. Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104, USA.
Complex (CpCe)(TCNQ)(CeCp) (1) was prepared by reducing neutral TCNQ (tetracyanoquinodimethane) with CpCe(THF). Two types of cerium centres with a dianionic TCNQ moiety are present in 1, wherein each of the four cyano-groups are bound by a cation. Formation of this trapped-valent organocerium compound 1 is facilitated by metal-ligand redox cooperativity.
View Article and Find Full Text PDFJ Am Chem Soc
March 2024
Laboratory of Nuclear Energy Chemistry, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China.
Dilanthanide complexes with one-electron delocalization are important targets for understanding the specific 4f/5d-bonding feature in lanthanide chemistry. Here, we report an isolable azide-bridged dicerium complex [{(Trapen)Ce}(μ-N)] [Trapen = tris (2-aminobenzyl)amine; TMS = SiMe], which is synthesized by the reaction of tripodal ligand-supported (Trapen)CeCl complex with NaN. The structure and bonding nature of are fully characterized by X-ray crystal diffraction analysis, electron paramagnetic resonance (EPR), magnetic measurement, cyclic voltammetry, X-ray absorption spectroscopy, and quantum-theoretical studies.
View Article and Find Full Text PDFJ Chem Crystallogr
June 2022
Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, MI, 48202, USA.
The title metallacrown (MC) complexes Ln[15-MC-5](OAc)CI(CHN) (), where OAc is acetate, shi is salicylhydroximate, and Ln = Gd and Dy, were synthesized via a self-assembly reaction in methanol and pyridine. Single crystals were grown using slow evaporation and characterized using X-ray diffraction. Seven-coordinate capped octahedron geometries were observed for the lanthanide ion in both complexes, which is uncommon for trivalent lanthanide species.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!