The identification of insect specific iAANAT inhibitors.

An important aspect of food security is the development of innovative insecticides, particularly ones that specifically target insect pests and exhibit minimal toxicity to mammals. The insect arylalkylamine N-acyltransferases (iAANATs) could serve as targets for novel insecticides that satisfy these criteria. There exists a wealth of structural and biochemical information for the iAANATs and iAANAT knockdown experiments show that these enzymes are critical to insect health.

Role of H in Solvent Extraction of Am(III) and Eu(III) Using a Polydentate Bipyridine N-,O-Donor Ligand: Chemical Equilibrium States and Kinetic Aspects.

In this work, the influence of protonation on the kinetics and thermodynamics of extraction of the Am/Eu pair using N-heterocyclic dicarboxylic acid diamide ,'-diethyl-,'-bis(4-ethylphenyl)-[2,2'-bipyridine]-6,6'-dicarboxamide () was investigated. The extraction efficiency of the ligand did not decrease, even at a nitric acid concentration 4 times higher than that of the ligand in the organic phase. X-ray diffraction analysis established that protonation leads to the preorganization of the ligand due to the reversal of bipyridyl rings into the binding conformation when both nitrogen atoms are turned to one side.

Coordination of Fluorine-Substituted 1,10-Phenanthroline Diphosphonates with Americium(III) and Lanthanides(III): Solvent Extraction, Complexation, XRD, and Theoretical Study.

Hybrid N,O-donor ligands based on 1,10-phenanthroline are a promising class of compounds for processing high-level waste. Here, we synthesized novel phenanthroline-based diphosphonates containing electron-withdrawing fluorine atoms in alkyl substituents. We studied their extraction properties for Am(III) and, for the first time, for the entire series of lanthanides(III).

Bipyridyldicarboxamides and f-metals: the influence of electron effects on the structure, stability, separation, and photophysical properties of their complexes.

In this work, three isomeric fluorinated bipyridyldicarboxamides were studied to evaluate the impact of the fluorine atom position on the structure, stability, Am(III)/Ln(III) separation, and photophysical properties of their complexes. The complexes of the fluorinated amides have a metal-to-ligand composition of 1 : 1, which is independent of the fluorine atom position or lanthanide metal. The bipyridyl fragments in the fluorinated complexes are flattened compared with those in unsubstituted ones.

Pyridine Diphosphonate Ligand for Stabilization of Tetravalent Uranium and Neptunium in Aqueous Medium under Aerobic Conditions.

Though uranium is usually present in its +6 oxidation state (as uranyl ion) in aqueous solutions, its conversion to oxidation states such as +4 or +5 is a challenging task. Electrochemical reduction and axial oxo activation are the preferred methods to get stable unusual oxidation states of uranium in an aqueous medium. In previous studies, dicarboxylic acid has been used to stabilize UO in aqueous alkaline solutions.