Arylacylhydrazones of 2,3-dihydroxybenzaldehyde are appropriate ligands for the preparation of heterodinuclear triple-stranded helicates involving high coordinated lanthanide(III) ions. In the present study, three different kinds of substituents are introduced at the ligands in order to modify the organic periphery of the coordination compounds: (1) alkoxy groups are attached to the terminal phenyl groups, (2) NH protons of the hydrazones are substituted by phenyl moieties and (3) amino acid bearing units are attached to the terminus of the ligand. The new ligands nicely form the desired triple-stranded gallium(III)-lanthanum(III) complexes [(5a-c,7,12,15)(3)GaLa] of which the highly phenylated derivative was crystallized and studied by X-ray diffraction.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c1dt10775eDOI Listing

Publication Analysis

Top Keywords

decorating lanthanide
4
lanthanide terminus
4
terminus self-assembled
4
self-assembled heterodinuclear
4
heterodinuclear lanthanumiii/galliumiii
4
lanthanumiii/galliumiii helicates
4
helicates arylacylhydrazones
4
arylacylhydrazones 23-dihydroxybenzaldehyde
4
23-dihydroxybenzaldehyde appropriate
4
appropriate ligands
4

Similar Publications

Rare earth elements (REEs) are essential for many clean energy technologies. Yet, they are a limited resource currently obtained through carbon-intensive mining. Here, bio-scaffolded proteins serve as simple, effective materials for the recovery of REEs.

View Article and Find Full Text PDF

This work presents the synthesis and characterization of three isomorphous lanthanide-based metal-organic frameworks (Ln-MOFs) (Ln=Eu (1), Tb (2), and Sm (3)) supported by a pyridine-2,6-dicarboxamide-based linker offering appended arylcarboxylate groups. Single crystal X-ray diffraction studies highlight that these Ln-MOFs present three-dimensional porous architectures offering large cavities decorated with hydrogen bonding (H-bonding) groups. These Ln-MOFs display noteworthy luminescent characteristics.

View Article and Find Full Text PDF

A new type of lanthanide-sodium metalloring organic framework featuring high proton conduction in a wide temperature range and detection of Fe ions.

Dalton Trans

December 2024

Key Laboratory of Polymer Materials and Products of Universities in Fujian, Department of Materials Science and Engineering, Fujian University of Technology, Fuzhou 350118, P. R. China.

We present the design and synthesis of two novel isostructural metalloring organic frameworks (MROFs) {[(MeNH)(HO)NaX(μ-OH)(HO)(SIP)]·sol} (FUT-2-X, X = Eu and Sm), which are composed of the sulfonate-carboxylate ligand 5-sulfoisophthalic acid monosodium salt (NaHSIP) and an unprecedented lanthanide-sodium metalloring [XNa(HO)(SIP), X = Eu and Sm]. The two MROFs possess channel walls decorated with uncoordinated sulfonic acid groups and filled with abundant guest molecules residing within the framework, which support the proton conductivity of the materials by expanding the intermolecular hydrogen bonding network. FUT-2-Eu exhibits exceptional proton conductivity over a wide temperature range, achieving conductivity from 1.

View Article and Find Full Text PDF

A Hollowed-Out Heterometallic Cluster for Catalytic Knoevenagel Condensation.

Angew Chem Int Ed Engl

November 2024

Department of Chemistry and Key University Laboratory of Rare Earth Chemistry of Guangdong, Southern University of Science and Technology, Shenzhen, 518055, China.

Lanthanide-containing clusters are synthetically challenging and with significant chemical and materials applications. Herein, two isostructural heterometallic clusters of the formula (NO)@[LnNi(OH)(IDA)(CHCOO)(NO)(HO)]Cl⋅xHO⋅yCHOH (IDA=iminodiacetate; Ln=Gd 1, x=110, y=0; Ln=Eu 2, x=95, y=40) were obtained via co-hydrolysis of Ln (Gd or Eu) and Ni in the presence of iminodiacetate (IDA). Crystallographic studies show that each features a truncated tetrahedral core of LnNi within which a void of 1.

View Article and Find Full Text PDF

Target-Engineered Liposomes Decorated with Nanozymes Alleviate Liver Fibrosis by Remodeling the Liver Microenvironment.

ACS Appl Mater Interfaces

November 2024

School of Pharmacy, Chengdu University of Traditional Chinese Medicine, State Key Laboratory of Southwestern Chinese Medicine Resources, Chengdu 611137, China.

Liver fibrosis is a pathological repair response that occurs after sustained liver damage, and prompt intervention is necessary to prevent liver fibrosis from developing into a potentially life-threatening condition. In long-term liver injury, damaged hepatocytes produce excessive amounts of reactive oxygen species (ROS), which activate hepatic stellate cells (HSCs). This activation leads to excessive accumulation of extracellular matrix proteins in liver tissue.

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!