A Bis-Chelating / Ligand for the Synthesis of Heterobimetallic Platinum(II)/Rhenium(I) Complexes: Tools for the Optimization of a New Class of Platinum(II) Anticancer Agents

The two independent and coordination sites of a newly synthesized bis[2-(hydroxyphenyl)-1,2,4-triazole] platform have been exploited to prepare four monometallic neutral ()Pt^II complexes carrying DMSO, pyridine, triphenylphosphine, or N-heterocyclic carbene as the fourth ligand. Then, the second coordination site was used to introduce an IR-active rhenium tricarbonyl entity, affording the four corresponding heterobimetallic neutral Pt^II/Re^I complexes, as well as a cationic Pt^II/Re^I derivative. X-ray crystallographic studies showed that distortion of the organic platform occurred to accommodate the coordination geometry of both metal centers. No ligand exchange or transchelation occurred upon incubation of the Pt^II complexes in aqueous environment or in the presence of Fe^III, respectively. The antiproliferative activity of the ligand and complexes was first screened on the triple-negative breast cancer cell line MDA-MB-231. Then, the IC₅₀ values of the most active candidates were determined on a wider panel of human cancer cells (MDA-MB-231, MCF-7, and A2780), as well as on a nontumorigenic cell line (MCF-10A). Low micromolar activities were reached for the complexes carrying a DMSO ligand, making them the first examples of highly active, but hydrolytically stable, Pt^II complexes. Finally, the characteristic mid-IR signature of the {Re(CO)₃} fragment in the Pt/Re heterobimetallic complexes was used to quantify their uptake in breast cancer cells.     

Photolysis of Phosphoniums and Phosphoranes Azides

Abstract

First evidence for a Curtius type rearrangement involving a pentacoordinated atom and charged species are described     

Efficient Synthesis of 3‐Pyrrolylquinolines via an 1,3‐Dipolar Cycloaddition/Oxidation Sequence

The synthesis of some new functionalized quinolyl derivatives relies on the 1,3‐dipolar cycloaddition of an azomethine ylide, generated from sarcosine and paraformaldehyde, to quinolyl α,β‐unsaturated esters, followed by oxidation of the pyrrolidinyl moiety to pyrrole with activated MnO₂.     

Synthesis,Photophysics and Nonlinear Optical Properties of Stilbenoid Pyrimidine‐Based Dyes Bearing Methylenepyran Donor Groups

The nonlinear properties and the photophysical behavior of two π‐conjugated chromophores that incorporate an electron‐deficient pyrimidine core (A) and γ‐methylenepyrans as terminal donor (D) groups have been thoroughly investigated. Both dipolar and quadrupolar branching strategies are explored and rationalized on the basis of the Frenkel exciton model. Even though a cooperative effect is clearly observed if the dimensionality is increased, the nonlinear optical (NLO) response of this series is moderate if one considers the nature of the D/A couple and the size of the chromophores (as measured by the number of π electrons). This effect was attributed to a disruption in the electronic conjugation within the dyes’ scaffold for which the geometry deviates from planarity owing to a noticeable twisting of the pyranylidene end‐groups. This latter structural parameter also has a strong influence on the excited‐state dynamics, which leads to a very efficient fluorescence quenching.     

N-Glycosidase treatment with 18O labeling and de novo sequencing argues for flagellin FliC glycopolymorphism in Pseudomonas aeruginosa

In prokaryote organisms, N-glycosylation of proteins is often correlated to cell–cell recognition and extracellular events. Those glycoproteins are potential targets for infection control. To date, many surface-glycosylated proteins from bacterial pathogens have been described. However, N-linked Pseudomonas surface-associated glycoproteins remain underexplored. We report a combined enrichment and labeling strategy to identify major glycoproteins on the outside of microorganisms. More precisely, bacteria were exposed to a mix of biotinylated lectins able to bind with glycoproteins. The latter were then recovered by avidin beads, digested with trypsin, and submitted to mass spectrometry. The targeted mixture of glycoproteins was additionally deglycosylated in the presence of H₂ ¹⁸O to incorporate ¹⁸O during PNGase F treatment and were also analyzed using mass spectrometry. This approach allowed us to identify a few tens of potential N-glycoproteins, among which flagellin FliC was the most abundant. To detect the possible sites of FliC modifications, a de novo sequencing step was also performed to discriminate between spontaneous deamidation and N-glycan loss. This approach led to the proposal of three potential N-glycosylated sites on the primary sequence of FliC: N26, N69, and N439, with two of these three asparagines belonging to an N-X-(S/T) consensus sequence. These observations suggest that flagellin FliC is a heterogeneous protein mixture containing both O- and N-glycoforms.

Oligo (p -phenylene)s substituted with long alkoxy chains I. Thermotropic liquid crystalline properties and UV absorption/emission characteristics

A series of linear oligo (p-phenylene)s containing three, five and seven phenylene groups, modified with short lateral and long terminal alkoxy chains, were synthesized via Palladium complex-catalysed cross-coupling reactions. The thermotropic liquid crystalline and UV absorption/emission properties of these compounds were studied. It was observed that tri (p -phenylene)s develop a rich mesomorphism including tilted smectic type mesophases (SmC and SmF/SmI) and the nematic phase, whereas penta- and hepta-(p-phenylene)s substituted with short lateral chains develop only the nematic phase. From these observations it is clear that the short lateral chains hinder the layered molecular packing typical of smectic phases and promote the formation of the less ordered liquid-like nematic phase. Mesophases appeared at lower temperatures when longer end chains were used. The optical properties studied by UV-Vis and emission spectroscopy indicate that these systems are promising candidates for blue-emitting layers in electroluminescent devices.     

Mild addition of carbon nucleophiles to pyridine and quinoline N-oxides under different activation conditions

In the course of our syntheses of functionalised pyridine and quinoline derivatives, we examined the reactivities of pyridine and quinoline N-oxides towards the nucleophilic addition of acidic carbon derivatives. Different activating reagents were used, such as PyBroP, triflic anhydride and a combination of pyrrolidine phosphoramide and triflic anhydride.     

Particle-hole symmetry and the Pfaffian state

We show that the particle-hole conjugate of the Pfaffian state-or "anti-Pfaffian" state-is in a different universality class from the Pfaffian state, with different topological order. The two states can be distinguished easily by their edge physics: their edges differ in both their thermal Hall conductance and their tunneling exponents. At the same time, the two states are exactly degenerate in energy for a nu=5/2 quantum Hall system in the idealized limit of zero Landau level mixing. Thus, both are good candidates for the observed sigma_{xy}=5/2(e;{2}/h) quantum Hall plateau.