Quinolone and isoquinolone alkaloids: the structural-electronic effects and the antioxidant mechanisms

Structural Chemistry - Quinolone and isoquinolone alkaloids, which were found in the plant kingdom, are now potential antioxidants. In this case study, a quantum calculated procedure utilizing the...     

Metal-Templated,Tight Loop Conformation of a Cys-X-Cys Biomimetic Assembles a Dimanganese Complex

With the goal of generating anionic analogues to MN₂S₂ ⋅ Mn(CO)₃Br we introduced metallodithiolate ligands, MN₂S₂²⁻ prepared from the Cys-X-Cys biomimetic, ema⁴⁻ ligand (ema=N,N′-ethylenebis(mercaptoacetamide); M=Ni^II, [V^IV≡O]²⁺ and Fe^III) to Mn(CO)₅Br. An unexpected, remarkably stable dimanganese product, (H₂N₂(CH₂C=O(μ-S))₂)[Mn(CO)₃]₂ resulted from loss of M originally residing in the N₂S₂⁴⁻ pocket, replaced by protonation at the amido nitrogens, generating H₂ema²⁻. Accordingly, the ema ligand has switched its coordination mode from an N₂S₂⁴⁻ cavity holding a single metal, to a binucleating H₂ema²⁻ with bridging sulfurs and carboxamide oxygens within Mn-μ-S-CH₂-C-O, 5-membered rings. In situ metal-templating by zinc ions gives quantitative yields of the Mn₂ product. By computational studies we compared the conformations of “linear” ema⁴⁻ to ema⁴⁻ frozen in the “tight-loop” around single metals, and to the “looser” fold possible for H₂ema²⁻ that is the optimal arrangement for binucleation. XRD molecular structures show extensive H-bonding at the amido-nitrogen protons in the solid state.     

[2+2] Photodimerization of Stilbazoles Promoted by Oxalic Acid in Suspension

In this study, a very simple technique to perform efficiently photodimerization of some vinylpyridines is reported. By irradiating a stirred mixture of several stilbazoles with solid oxalic acid dihydrate dispersed in a nonpolar (i.e., cyclohexane) or moderately polar (benzene, dichloromethane, dioxane) solvent, the corresponding dimeric cyclobutane adducts were obtained in high yields and excellent regio- and stereoselectivities. The strategy could also be applied successfully to oily, waxy, or even insoluble stilbazoles. Moreover, the oxalic acid loading could be lowered to substoichiometric amounts. When further optimizations were needed, our strategy was found to be highly flexible to identify other oligocarboxylic acids as alternative additives to improve, or even overturn, the regioselectivity. Oxalic acid and other oligocarboxylic acids were found to be capable of orienting more than 50 stilbazoles toward photodimerization under these conditions.     

Efficient Synthesis of α‐Trifluoromethyl Carboxylic Acids and Esters through Fluorocarboxylation of gem‐Difluoroalkenes

A facile synthetic procedure for the preparation of α‐trifluoromethyl carboxylic acids and esters was achieved through multicomponent coupling reactions between gem‐difluoroalkenes, cesium fluoride, and carbon dioxide. The products were generated in moderate to excellent yields, and the synthetic utility of this method was demonstrated through the preparation of trifluoromethylated versions of popular nonsteroidal anti‐inflammatory drugs (NSAIDs).     

Interaction between excitons in 3D and 2D laser-excited semiconductors

Analytical expressions of the exciton-exciton interaction in 3D and 2D laser-excited semiconductors are approximately derived in rather easy-to-handle forms which enable us to study in detail their dependences on the exciton momenta, the momentum transferred between two excitons and the electron-hole mass ratio.We would like to thank Prof. Nguyen Van Hieu and Prof. Dao Vong Due for their support given to us in the research of highly excited media.     

Ferro- and antiferromagnetism in oxychalcogenides LnCrOX2 (Ln = La or Nd and X = S or Se)

The two isomorphous compounds LaCrOS₂ and LaCrOSe₂ are ferromagnetic (T_c = 35 and 51 K, respectively). This implies ferromagnetic super-superexchange interactions. NdCrOS₂ is antiferromagnetic (T_N = 72 K) and undergoes a spin-flop transition (H_c = 54 KOe at 20 K). The study of the thermal variation of Cr³⁺ and Nd³⁺ magnetic moments below T_N allows a rough estimate of the Cr---Nd and Cr---Cr exchange fields ratio (0.1).     

Can the pentazole anion (N5−) be isolated and/or trapped in metal complexes?

The 1,3-dipolar cycloreversion pathway of the pentazole anion (N₅^?) to the azide anion (N₃^?) plus dinitrogen (N₂) has been investigated using ab initio methods. At the MP4SDQ/6–31 + G* level of theory plus zero-point energy contributions, the pentazole anion is predicted to lie at 31 kcal mol^?1 above the N₃^? + N₂ system but the energy barrier for decomposition is 22 kcal mol^?1. This indicates that the pentazole anion could be isolated in an inert matrix at low temperature. Comparison between extended Hückel calculations on the (N₅)M(CO)₃ and (C₅H₅)M(CO)₃ complexes (with M = Fe²⁺, Mn⁺ and Cr) suggests that the N₅^? complexes would be formed if the fragments could be brought together. Predicted vibrational frequencies of the N₅^? anion are also reported.     

Two-phonon processes in Heisenberg ferromagnet

Using the method of double-time retarded Green function, an expression for the spin energy spectrum including the contributions of one-phonon and two-phonon processes has been derived. Calculations have been performed using the spin wave approximation. The broadening of the energy level is roughly estimated in a peculiar case.I would like to thank Dr. Dagmat Fraitová for her advice and help.