Linear amphiphilic diblock copolymers of lactide and 2-dimethylaminoethyl methacrylate using bifunctional-initiator and one-pot approaches

Linear amphiphilic diblock copolymers of polylactide (PLA) and poly(2-dimethylaminoethyl methacrylate) (PDMAEMA) were synthesized by atom transfer radical polymerization (ATRP) of DMAEMA followed by ring-opening polymerization (ROP) of LLA using the bifunctional initiator, 2′-hydroxyethyl 2-bromoisobutyrate. NMR showed that the resulting PLA block was racemic and a quaternization/precipitation technique showed that there were significant amounts of racemic PLA homopolymer. In addition, simultaneous ATRP of DMAEMA and ROP of l-lactide by tin octoate were conducted at varied temperatures, indicating 90 °C as a suitable compromise temperature; this one-pot process also led to racemization and P(L)LA homopolymer. The racemization was attributed to reversible deprotonation of LLA by the N(CH₃)₂ moiety of (P)DMAEMA and the PLA homopolymer impurity was related to in situ formation of lactoyl lactate (LA–LA) due to nucleophilic ring opening of lactide by the amino moieties of (P)DMAEMA. The methods presented can be useful for the preparation of PDMAEMA–b–PLA/PLA composites in a two-step process or in a single step, one-pot process.     

Rapid Synthesis and Antiproliferative Properties of Polyazamacrocycle-Based Bi- and Tetra-Gold(I) Phosphine Dithiocarbamate Complexes

A family of bi- and tetrametallic gold(I) phosphine dithiocarbamate complexes were synthesized, starting from cyclam and dimethylcyclam polyazamacrocycles, respectively, along with their monometallic gold(I) chloridophosphine precursors. Their antiproliferative properties were evaluated on two cancer cell lines (A549 and NSCLC-N6-L16). Most of the mono- and bimetallic complexes displayed strong activities and, in particular, one bimetallic derivative showed antiproliferative properties in the low micromolar range. Insights into the structure–activity relationships are given, along with determination of the thioredoxin reductase inhibition potential, two-photon imaging of the fluorescent derivatives, and evaluation of gold uptake.     

Metal‐Free Synthesis of Chlorinated β‐Amino Ketones via an Unexpected Reaction of Imines with Arylacetylenes in 1,1,1,3,3,3‐Hexafluoro‐2‐propanol

The metal‐free reaction of terminal arylacetylenes with α,α‐dichloroaldimines in 1,1,1,3,3,3‐hexafluoro‐2‐propanol as the sole solvent results in the rapid and selective formation of γ,γ‐dichloro‐β‐amino ketones. In this solvent the expected dichlorinated propargylamines and/or allylic amines are not formed. The dichloromethylene moiety of the aldimine acts as an activating group and is essential to accomplish this transformation. Electron‐rich acetylenes lead to the best results and work well with all imines (with or without α′‐H at the nitrogen substituent), while electron‐deficient acetylenes only reacted with N‐tert‐butylaldimines (no α′‐H). The mechanistic pathway showed 1,1,1,3,3,3‐hexafluoro‐2‐propanol to protonate the aldimine, which in the rate‐determining step will react with the arylacetylene to form a resonance‐stabilized allene cation, which is trapped by a HFIP molecule giving rise to an enol ether, which promptly hydrolyzes to furnish exclusively the β‐amino ketones. Using DFT techniques we found that the first C C bond forming step is the rate‐determining step and is associated with a barrier of about 21 kcal mol⁻¹.

     

Stereoselective Monoamine Oxidase‐Catalyzed Oxidative Aza‐Friedel–Crafts Reactions of meso‐Pyrrolidines in Aqueous Buffer

We disclose the highly diastereoselective combination of monoamine oxidase‐catalyzed oxidation of meso‐pyrrolidines and aza‐Friedel–Crafts reactions in aqueous buffer to give valuable enantioenriched 2‐substituted pyrrolidines in a formal double C H activation process. A range of secondary as well as tertiary amines were shown to be suitable substrates for the biocatalytic oxidation and subsequent addition of a variety of C‐nucleophiles.

     

Copper‐Catalyzed Asymmetric Conjugate Addition of Dimethylzinc to Acyl‐N‐methylimidazole Michael Acceptors: Scope,Limitations and Iterative Reactions

An efficient copper‐catalyzed enantioselective conjugate addition of dimethylzinc to unsaturated 2‐acyl‐N‐methylimidazoles has been achieved using a chiral bidentate hydroxyalkyl‐NHC ligand. The reactions proceed with excellent regioselectivity (1,4 vs. 1,6 and 1,8) in extended conjugated systems to afford the 1,4‐adducts in high enantioselectivities. This regioselectivity could be ascertained by DFT studies highlighting the crucial role of the imidazole ring. Thanks to the development of efficient protocols to regenerate the unsaturated 2‐acyl‐N‐methylimidazole moiety, an iterative process has been developed ultimately leading to 3,5,7 all‐syn or anti‐anti polydeoxypropionate stereodiads.

     

Surface enrichment of biomimetic apatites with biologically-active ions Mg2+ and Sr2+: A preamble to the activation of bone repair materials

The surface activation of calcium phosphate-based biomaterials for bone repair is an emerging route for improving bone regeneration processes. One way for such activation is through the exchange of surface calcium ions with biologically-active cations such as Mg²⁺ or Sr²⁺. In this work, the interactions of non-carbonated and carbonated nanocrystalline apatites with Mg²⁺ and Sr²⁺ were investigated by means of ion exchange experiments in solution. Langmuir-type isotherms were determined. For both Sr and Mg, a greater uptake was observed on the carbonated sample, and on both types of apatites the maximum strontium uptake was greater than that of magnesium. Inverse exchanges showed that the proportion of reversibly fixed ions after surface exchange was close to 85% for Mg and 75–80% for Sr. The results are related to the presence of a surface hydrated layer on the nanocrystals and possible exchange mechanisms are discussed. Our results favor the hypothesis of hetero-ionic surface exchanges (Mg²⁺↔Ca²⁺, Sr²⁺↔Ca²⁺) within the hydrated layer, and some analogy with octacalcium phosphate (OCP) is considered. This work should prove helpful for the control and understanding of the activation of synthetic apatite-based powders or scaffolds with bioactive elements, as well as for the global understanding of biomineralization processes.     

Finite element modelling of passive damping with resistively shunted piezocomposites

This work aims at modelling passive damping in structures made of composites with embedded resistively shunted piezoelectric ceramic fibres. To this end, a 3D material model is implemented in the finite element (FE) code ABAQUS. Academical test cases as well as a structural case study are presented.     

Design of dedicated seven-port star dividers for sectored circular antenna array feeding

In order to mitigate the multipath propagation problems for high rate wlans such as Hiperlan (5 GHz) [2], we study an approach based on electronic beam steering over 360° in azimuth with the help of circular arrays of monopoles [3]. Design simplicity and size constraints intended for potential low-cost applications on the terminals has led us to favor a beam switching topology, using a single feeding-port [4]. Two competing configurations of the microstrip feeding circuit are presented and their principle of operation is experimentally validated through passive circuit configurations. The power distribution is achieved in the first one with the help of a pseudo-divider based on a modified 7-branch star junction, whose specific advantage is its very small size. Unfortunately, this design does not preserve the circular permutation invariance of the radiation patterns. The second circuit bypasses this problem in achieving a power distribution through a virtual point junction, at the cost of an appreciable increase in the circuit size.