AI Article Synopsis

  • The study involves the synthesis of metal complexes (Palladium, Platinum, Ruthenium, and Iridium) using a specific macrocyclic ligand derived from 2,6-diaminopyridine and 3-ethyl 2,4-pentanedione.
  • Characterization of the ligand and complexes was performed using a variety of techniques, including elemental analysis and various spectral methods, revealing that most complexes are diamagnetic except for the Ruthenium(III) complex, which has one unpaired electron.
  • The synthesized compounds were also tested for their effectiveness against plant pathogenic fungi and bacteria, demonstrating potential biocidal properties.

Article Abstract

Palladium(II), platinum(II), ruthenium(III) and iridium(III) complexes of general stoichiometry [PdL]Cl(2), [PtL]Cl(2), [Ru(L)Cl(2)]Cl and [Ir(L)Cl(2)]Cl are synthesized with a tetradentate macrocyclic ligand, derived from 2,6-diaminopyridine with 3-ethyl 2,4-pentanedione. Ligand was characterized on the basis of elemental analyses, IR, mass, and (1)H NMR and (13)C NMR spectral studies. All the complexes were characterized by elemental analyses, molar conductance measurements, magnetic susceptibility measurements, IR, mass, electronic spectral techniques and thermal studies. The value of magnetic moments indicates that all the complexes are diamagnetic except Ru(III) complex which shows magnetic moments corresponding its one unpaired electron. The macrocyclic ligand and all its metal complexes were also evaluated in vitro against some plant pathogenic fungi and bacteria to assess their biocidal properties.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.saa.2011.01.041DOI Listing

Publication Analysis

Top Keywords

macrocyclic ligand
12
palladiumii platinumii
8
platinumii rutheniumiii
8
rutheniumiii iridiumiii
8
iridiumiii complexes
8
elemental analyses
8
magnetic moments
8
complexes
5
synthesis structural
4
structural spectral
4

Similar Publications

2-Cyanopyrimidine-Containing Molecules for N-Terminal Selective Cyclization of Phage-Displayed Peptides.

ACS Chem Biol

January 2025

Texas A&M Drug Discovery Center, Department of Chemistry, Texas A&M University, College Station, Texas 77843, United States.

Current methods for the macrocyclization of phage-displayed peptides often rely on small molecule linkers that nonspecifically react with targeted amino acid residues. To expand tool kits for more regioselective macrocyclization of phage-displayed peptides, this study explores the unique condensation reaction between an N-terminal cysteine and nitrile along with the reactivity of an internal cysteine. Five 2-cyanopyrimidine derivatives were synthesized for this purpose and evaluated for their selective macrocyclization of a protein-fused model peptide.

View Article and Find Full Text PDF

Conformational Plasticity and Binding Affinity Enhancement Controlled by Linker Derivatization in Macrocycles.

Angew Chem Int Ed Engl

January 2025

Darmstadt University of Technology: Technische Universitat Darmstadt, Clemens-Schöpf-Institute of Organic Chemistry and Biochemistry, Alarich-Weiss-Strasse 4, 64287, Darmstadt, GERMANY.

Article Synopsis
  • Macrocycles are natural and synthetic compounds that can enhance the ability of bioactive molecules to penetrate cells, with emerging guidelines for their design.
  • Even medium-sized macrocycles exhibit significant flexibility in shape, even while attached to target proteins, which allows for diverse conformations.
  • Minor linker modifications in these macrocycles can lead to new ligand formations with improved binding properties for important therapeutic targets, highlighting the unique benefits of macrocyclic structures in drug development.
View Article and Find Full Text PDF

Gadopiclenol: A q = 2 Gadolinium-Based MRI Contrast Agent Combining High Stability and Efficacy.

Invest Radiol

October 2024

From the Research and Innovation Department, Guerbet, Roissy, France (I.M., M.-C.D.G., J.-F.M., A.D., Y.B., N.D., I.S., G.B., C.M., C.F., O.R., S.C.); General, Organic, and Biomedical Chemistry Unit, NMR and Molecular Imaging Laboratory, University of Mons, Mons, Belgium (C.H., S.L.); and Institute of Inorganic and Analytical Chemistry, University of Münster, Münster, Germany (C.K., T.J.M., U.K.).

Objectives: Gadopiclenol is a q = 2 pyclen gadolinium-based contrast agent (GBCA) recently approved by the Food and Drug Administration, European Medicines Agency, and other European countries. The aim of this report is to demonstrate its stability in multiple stressed in vitro conditions and in vivo, in rat kidney, while maintaining its higher relaxivity compared with conventional GBCAs on the market.

Materials And Methods: Both gadopiclenol and its chemical precursor Pi828-Gd were characterized and compared with q = 1 gadolinium (Gd) complexes.

View Article and Find Full Text PDF

Tunability in Heterobimetallic Complexes Featuring an Acyclic "Tiara" Polyether Motif.

Inorg Chem

December 2024

Department of Chemistry, University of Kansas, 1567 Irving Hill Road, Lawrence, Kansas 66045, United States.

Both cyclic "crown" and acyclic "tiara" polyethers have been recognized as useful for the binding of metal cations and enabling the assembly of multimetallic complexes. However, the properties of heterobimetallic complexes built upon acyclic polyethers have received less attention than they deserve. Here, the synthesis and characterization of a family of eight redox-active heterobimetallic complexes that pair a nickel center with secondary redox-inactive cations (K, Na, Li, Sr, Ca, Zn, La, and Lu) bound in acyclic polyether "tiara" moieties are reported.

View Article and Find Full Text PDF

Arraying and Guest Inclusion of Soluble Metal-Organic Nanotubes Composed of Macrocyclic Paddle-Wheel Metal Complexes.

Angew Chem Int Ed Engl

December 2024

Nagoya University: Nagoya Daigaku, Department of Chemistry, Graduate School of Science, Furo-cho, Chikusa-ku, 464-8602, Nagoya, JAPAN.

A new series of metal-organic nanotubes was constructed through one-dimensional assembly using molecular triangles or molecular squares composed of paddlewheel dirhodium complexes and bidentate axial ligands. The metal-organic nanotubes were significantly different from conventional solid metal-organic framework (MOF) motifs. They exhibit good solubility owing to the branched side chains at their periphery and demonstrate high orientation capabilities in thin films owing to their anisotropic structure.

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!