This Communication describes the synthesis, crystal structure, and magnetic properties of a unique decanuclear copper complex of a tripodal adenine ligand built around a phenyl ring core. This complex comprises two mu(4)-oxo tetranuclear copper(II) units of the type Cu(4)OCl(6)L(4), bridged together by two pentacoordinated copper centers. Variable-temperature magnetic susceptibility data reveal the possibility of interaction between copper sites.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/ic100254t | DOI Listing |
Inorg Chem
July 2024
Department of Chemistry and Biochemistry, Kennesaw State University, 370 Paulding Avenue NW, MD # 1203, Kennesaw, Georgia 30144, United States.
Chem Asian J
July 2024
Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka, 560-0043, Japan.
Here, we report the reactivity of copper(I) clusters toward sulfide ions; these sulfide copper(I) clusters have attracted much attention due to their relevance to biologically active centers and their fascinating structural and photophysical properties. Treatment of the Cu Rh pentanuclear complex, [Cu{Rh(aet)}] (aet=2-aminoethanethiolate), in which a {Cu } cluster moiety is bound by two fac-[Rh(aet)] metalloligands, with NaSH in water produced the Cu Rh decanuclear complex, [CuS{Rh(aet)}], accompanied by the dimerization of [Cu{Rh(aet)}] and the incorporation of a sulfide ion at the center. While similar treatment using the analogous Cu Ir complex with fac-[Ir(aet)] metalloligands, [Cu{Ir(aet)}], produced the isostructural Cu Ir decanuclear complex, [CuS{Ir(aet)}], the use of the Cu Rh complex with fac-[Rh(apt)] metalloligands, [Cu{Rh(apt)}] (apt=3-aminopropanethiolate), resulted in the removal of one of the three Cu atoms from {Cu } to afford the Cu Rh tetranuclear complex, [Cu{Rh(apt)}].
View Article and Find Full Text PDFMolecules
September 2021
Department of Chemistry, National Dong Hwa University, Hualien 974301, Taiwan.
A decanuclear silver chalcogenide cluster, [Ag(Se){SeP(OPr)}] () was isolated from a hydride-encapsulated silver diisopropyl diselenophosphates, [Ag(H){SeP(OPr)}], under thermal condition. The time-dependent NMR spectroscopy showed that was generated at the first three hours and the hydrido silver cluster was completely consumed after thirty-six hours. This method illustrated as cluster-to-cluster transformations can be applied to prepare selenide-centered decanuclear bimetallic clusters, [CuAg(Se){SeP(OPr)}] (x = 0-7, ), via heating [CuAg(H){SeP(OPr)}] (x = 1-6) at 60 °C.
View Article and Find Full Text PDFDalton Trans
September 2021
Functional Inorganic Materials Lab (FIML), Department of Chemistry, Aligarh Muslim University, Aligarh 202002, India.
Two new copper clusters, {Cu} and {CuCd}, with polydentate aminoalcohol ligands, diethanol propanolamine (HL) and bis-tris{2-[bis(2-hydroxyethyl)amino]-2-(hydroxymethyl)propane-1,3-diol} (HL), have been synthesized under mild conditions and characterized thoroughly by single-crystal X-ray diffraction (XRD), infrared spectroscopy, elemental analysis, powder XRD, magnetic and DFT studies, and absorption and fluorescence spectroscopy. The cluster {Cu} exhibits a rare tetranuclear copper cubane core whereas {CuCd} forms an unusual heterometallic cage owing to the introduction of the second metal Cd into the ligand. A hexapodal ligand (HL) with N and O donor atoms was chosen deliberately for the construction of a high-nuclearity cluster, i.
View Article and Find Full Text PDFMolecules
November 2020
Department of Chemistry, Memorial University, St. John's Newfoundland, NL A1B 3X7, Canada.
The self-assembly of 2,6-diformyl-4-methylphenol () and 1-amino-2-propanol ()/2-amino-1,3-propanediol () in the presence of copper(II) ions results in the formation of six new supramolecular architectures containing two versatile double Schiff base ligands (HL and HL1) with one-, two-, or three-dimensional structures involving diverse nuclearities: tetranuclear [Cu(HL)(N)]·4CHOH·56HO () and [Cu(L)(OH)(HO)] (), dinuclear [Cu(HL1)(N)(HO)(NO)] (), polynuclear {[Cu(HL1)(HO)(BF)(N)]·HO} (), heptanuclear [Cu(HL1)(O)(CHCO)]·6CHOH·44HO (), and decanuclear [Cu(HL1)(O)(OH)(CHCO)] (CHCO)·20HO (). X-ray studies have revealed that the basic building block in , , and is comprised of two copper centers bridged through one μ-phenolate oxygen atom from HL or HL1, and one μ-1,1-azido (N) ion and in , , and by μ-phenoxide oxygen of L or HL1 and μ-O or μ-O ions. H-bonding involving coordinated/uncoordinated hydroxy groups of the ligands generates fascinating supramolecular architectures with 1D-single chains ( and ), 2D-sheets (), and 3D-structures ().
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!