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/ic100254tDOI Listing

Publication Analysis

Top Keywords

decanuclear copper
8
tripodal adenine
8
adenine ligand
8
copper framework
4
framework supported
4
supported tripodal
4
ligand communication
4
communication describes
4
describes synthesis
4
synthesis crystal
4

Similar Publications

Article Synopsis
  • Defined arrays of transition metal ions with tailored ligands enhance the design of their physical properties, particularly for Group 11 metals like copper, which are efficient photoluminescence (PL) emitters due to unique interactions.
  • A study reveals a tetracuprous array that forms a helical Cu complex and can rearrange to create a nanosized Cu cluster, demonstrating various luminescent behaviors with varying quantum yields.
  • The research combines synthesis, crystallography, and computational methods to link molecular structure with photoluminescence properties, highlighting the potential of these materials in OLED applications.
View Article and Find Full Text PDF

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 PDF

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 PDF

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 PDF

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 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!