Controlled Ring-Opening Polymerization of Methyl Glycolide with Bifunctional Organocatalyst.

A bifunctional thiourea-amine-based organocatalyst (Takemoto's catalyst), employing a metal-free approach, is presented for the regioselective ring-opening polymerization (ROP) of optically active (D and L) methyl glycolide (MG). In this study, a chiral version of Takemoto's catalyst efficiently promotes the ROP of MG at room temperature, yielding poly(lactic-co-glycolic acids) (PLGAs) with predicted molecular weights and narrow polydispersity indices (PDI≤1.2).

Enantioselective Separation of Amino Acids Using Chiral Polystyrene Microspheres Synthesized by a Post-Polymer Modification Approach.

The enantioselective separation of a racemic mixture of amino acids was achieved by chiral amino acid-modified polystyrene (PS) that was developed by a post-polymer modification approach. Styrene was polymerized using the reversible addition-fragmentation chain-transfer (RAFT) polymerization technique and further post-polymer modification was applied by Friedel-Crafts acylation reaction with chiral -phthaloyl-l-leucine acid chloride to obtain the protected PS-l-Leu. The chiral PS (protected PS-l-Leu) was assembled into microspheres using a surfactant and was used for carrying out the enantioselective separation of amino acid racemic mixtures by enantioselective adsorption followed by a simple filtration process.

Five concomitant polymorphs of a green fluorescent protein chromophore (GFPc) analogue: understanding variations in photoluminescence with π-stacking interactions.

The synthetically modified green fluorescent protein chromophore analogue 3,4,5-trimethoxybenzylidene imidazolinone (1) yielded five polymorphs (I, II, III, IV, V) concomitantly irrespective of the solvent used for crystallization. The pentamorphic modification of 1 is solely due to the interplay of iso-energetic weak intermolecular interactions in molecular associations as well as the conformational flexibility offered by a C-C single bond, which connects the electron-deficient moiety imidazolinone with the electron-rich trimethoxybenzylidene group. A common structural feature observed in all the polymorphs is the formation of a `zero-dimensional' centrosymmetric dimeric unit through a short and linear C-H.

Enantioselective Separation Using Chiral Amino Acid Functionalized Polyfluorene Coated on Mesoporous Anodic Aluminum Oxide Membranes.

Homochiral mesoporous anodic aluminum oxide membranes (AAO) were prepared by coating protected chiral D/L aspartic acid appended polyfluorene in the pores. These chiral AAO membranes successfully demonstrated enantioselective recognition and separation of a range of amino acids from their aqueous racemic mixture by simple filtration. Enantioselective separation was achieved by selective adsorption of one enantiomer from the aqueous racemic mixture into the chiral pores of the AAO membrane leaving the filtrate enriched with the other enantiomer.

Orientation effect induced selective chelation of Fe to a glutamic acid appended conjugated polymer for sensing and live cell imaging.

Intracellular detection and imaging of labile iron(ii) pools is very important in tracking physiological processes that demand new and rapid sensing probes. In this report, we present a water soluble polymer based probe for the fluorescence sensing and live cell imaging of labile Fe ions with high selectivity for the first time. The polymer probe was based on conjugated polyfluorene which was appended with amino acid (l-glutamic acid).