Acid-Basic and Complexing Properties of Compounds with a C(X)NHP(Y) Fragments

Abstract

N-(thio)carbonyl(thio)amidophosphates, their open-chain and crown-containing analogues with a C (X) NHP (Y) fragments are NH acids with pKa 8–11 and the effective complexing agents for “soft” ion metals.     

The Analyticity Breakdown for Frenkel-Kontorova Models in Quasi-periodic Media: Numerical Explorations

We study numerically the “analyticity breakdown” transition in 1-dimensional quasi-periodic media. This transition corresponds physically to the transition between pinned down and sliding ground states. Mathematically, it corresponds to the solutions of a functional equation losing their analyticity properties. We implemented some recent numerical algorithms that are efficient and backed up by rigorous results so that we can compute with confidence even close to the breakdown. We have uncovered several phenomena that we believe deserve a theoretical explanation: (A) The transition happens in a smooth surface. (B) There are scaling relations near breakdown. (C) The scaling near breakdown is very anisotropic. Derivatives in different directions blow up at different rates. Similar phenomena seem to happen in other KAM problems.     

Experimental NMR and MS study of benzoylguanidines. Investigation of E/Z isomerism

Molecules containing the guanidinic nuclei possess several pharmacological applications, and knowing the preferred isomers of a potential drug is important to understand the way it operates pharmacologically. Benzoylguanidines were synthesized in satisfactory to good yields and characterized by NMR, Electrospray Ionization Mass Spectrometry (ESI‐MS) and Fourrier Transform InfraRed Spectroscopy techniques (FTIR). E/Z isomerism of the guanidines was studied and confirmed by NMR analysis in solution (¹H‐¹³C Heteronuclear Single Quantum Coherence (HSQC) and Heteronuclear Multiple‐Bond Correlation (HMBC), ¹H‐¹⁵N HMBC, ¹H‐¹H Correlation Spectroscopy (COSY) and Nuclear Overhauser Effect Spectroscopy (NOESY) experiments) at low temperatures. Compounds with p‐Cl and p‐Br aniline moiety exist mainly as Z isomer with a small proportion of E isomer, whereas compounds with p‐NO2 moiety showed a decrease in proportion of isomer Z. The results are important for the application of these molecules as enzymatic inhibitors. Copyright © 2013 John Wiley & Sons, Ltd.     

Synthesis and characterization of cellulose acetate from cellophane industry residues. Application as acetaminophen controlled-release membranes

Journal of Thermal Analysis and Calorimetry - Cellophane film production generates cellulosic residues from scraps, edges, and low-quality films. In this work, cellophane was used as a raw material...     

Double Orthogonal Click Reactions for the Development of Antimicrobial Peptide Nanotubes

A new class of amphipathic cyclic peptides, which assemble in bacteria membranes to form polymeric supramolecular nanotubes giving them antimicrobial properties, is described. The method is based on the use of two orthogonal clickable transformations to incorporate different hydrophobic or hydrophilic moieties in a simple, regioselective, and divergent manner. The resulting cationic amphipathic cyclic peptides described in this article exhibit strong antimicrobial properties with a broad therapeutic window. Our studies suggest that the active form is the nanotube resulted from the parallel stacking of the cyclic peptide precursors. Several techniques, CD, FTIR, fluorescence, and STEM, among others, confirm the nanotube formation.     

Basicity and Reactivity of Alpha-Aminophosphonates: Theoretical Investigation

Abstract

Previously [1] we have found the possibility of the mechanism alteration for addition of substituted aminophosphonates (RO)₂P(O)CHR¹NHR² to PhNCO (where R = alkyles). which depends on the substituents at phosphorus and carbon atoms. We have performed theoretical investigation of basicity and reactivity of alpha- arninophosphonates by PM3 method using HyperChem molecular modeling package, We found that the calculated basicity parameters are in good correlation with our previous experimental data. From the results of the calculations, the whole series can be divided into three subsets: S1 with R¹=H and R²=n-Bu; S2 with RI=Ar with electronodonating substituent, R²=cycloHex. S3 with R¹=Ar with acceptor substituents, R²=cycloHex. The molecules, which belong to different series, differ in MO distribution on the reaction center NH. The aminophosphinates. containing electrono- withdrawing substituents at both centers (nitrogen and alpha-carbon) are deactivated completely.     

Intramolecular [2+2] Photocycloaddition of 3‐ and 4‐(But‐3‐enyl)oxyquinolones: Influence of the Alkene Substitution Pattern,Photophysical Studies,and Enantioselective Catalysis by a Chiral Sensitizer

The intramolecular [2+2] photocycloaddition of four 4‐(but‐3‐enyl)oxyquinolones (substitution pattern at the terminal alkene carbon atom: CH₂, Z‐CHEt, E‐CHEt, CMe₂) and two 3‐(but‐3‐enyl)oxyquinolones (substitution pattern: CH₂, CMe₂) was studied. Upon direct irradiation at λ=300 nm, the respective cyclobutane products were formed in high yields (83–95 %) and for symmetrically substituted substrates with complete diastereoselectivity. Substrates with a Z‐ or E‐substituted terminal double bond showed a stereoconvergent reaction course leading to mixtures of regio‐ and diastereomers with almost identical composition. The mechanistic course of the photocycloaddition was elucidated by transient absorption spectroscopy. A triplet intermediate was detected for the title compounds, which–in contrast to simple alkoxyquinolones such as 3‐butyloxyquinolone and 4‐methoxyquinolone–decayed rapidly (τ≈1 ns) through cyclization to a triplet 1,4‐diradical. The diradical can evolve through two reaction channels, one leading to the photoproduct and the other leading back to the starting material. When the photocycloaddition was performed in the presence of a chiral sensitizer (10 mol %) upon irradiation at λ=366 nm in trifluorotoluene as the solvent, moderate to high enantioselectivities were achieved. The two 3‐(but‐3‐enyl)oxyquinolones gave enantiomeric excesses (ees) of 60 and 64 % at ?25 °C, presumably because a significant racemic background reaction occurred. The 4‐substituted quinolones showed higher enantioselectivities (92–96 % ee at ?25 °C) and, for the terminally Z‐ and E‐substituted substrates, an improved regio‐ and diastereoselectivity.