Anthracene labeled poly(pyridine methacrylamide) as a polymer-based chemosensor for detection of pyrophosphate (PO) in semi-aqueous media.

To develop fluorophore-labelled pyridinium-based macromolecular architectures for fluorometric and colorimetric detection of anions, two polymers P1 and P2 are synthesized. Linear polymer P1 and cross-linked polymer P2, prepared from N-methacryloyl-3-aminopyridine monomers via free radical polymerization followed by quaternization of the pyridine ring nitrogen with anthracene as a fluorescent marker, have been successfully employed in anion sensing. P1 exhibits excellent sensing of HPPi in aqueous DMSO.

Uptake and Release of Species from Carbohydrate Containing Organogels and Hydrogels.

Hydrogels are used for a variety of technical and medical applications capitalizing on their three-dimensional (3D) cross-linked polymeric structures and ability to act as a reservoir for encapsulated species (potentially encapsulating or releasing them in response to environmental stimuli). In this study, carbohydrate-based organogels were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization of a -D-glucose pentaacetate containing methacrylate monomer (Ac-glu-HEMA) in the presence of a di-vinyl cross-linker; these organogels could be converted to hydrogels by treatment with sodium methoxide (NaOMe). These materials were studied using solid state C cross-polarization/magic-angle spinning (CP/MAS) NMR, Fourier transform infrared (FTIR) spectroscopy, and field emission scanning electron microscopy (FE-SEM).

Synthesis of a polymer bearing several coumarin dyes along the side chain and study of its fluorescence in pure and binary solvent mixtures as well as aqueous surfactant solutions.

A copolymer bearing several pendent dyes (coumarin derivatives) along the side chain has been synthesized, and its fluorescence parameters have been monitored in pure solvents and also as a function of composition of binary solvent mixtures. Fluorescence parameters (the maximum energy of fluorescence, quantum yield, and rate constant for the decay of the excited state) of the free fluorophore show significant dependence on the nature of the immediate environment around it. The value of a parameter measured in neat solvent for the fluorophore covalently bound to the polymer is different from that of the free fluorophore, indicating that the polymer chain influences the spectroscopic properties of the dye.

Remarkable swelling capability of amino acid based cross-linked polymer networks in organic and aqueous medium.

This work reports design and synthesis of side chain amino acid based cross-linked polymeric gels, able to switch over from organogel to hydrogel by a simple deprotection reaction and showing superabsorbancy in water. Amino acid based methacrylate monomers, tert-butoxycarbonyl (Boc)-l/d-alanine methacryloyloxyethyl ester (Boc-l/d-Ala-HEMA), have been polymerized in the presence of a cross-linker via conventional free radical polymerization (FRP) and the reversible addition-fragmentation chain transfer (RAFT) technique for the synthesis of cross-linked polymer gels. The swelling behaviors of these organogels are investigated in organic solvents, and they behave as superabsorbent materials for organic solvents such as dichloromethane, acetone, tetrahydrofuran, etc.

CdS quantum dots doped tuning of deswelling kinetics of thermoresponsive hydrogels based on poly(2-(2-methoxyethoxy)ethyl methacrylate).

Thermoresponsive poly(2-(2-methoxyethoxy)ethyl methacrylate) (PMEO2MA) based hybrid nanocomposite hydrogels (NCH) were synthesized by dispersing preformed cadmium sulfide (CdS) quantum dots (QDs) in the reaction mixture followed by polymerization via reversible addition-fragmentation chain transfer (RAFT) technique. High doping capacity and negligible QDs leakage were observed for hydrophilic QDs doped hydrogels (hpl-NCH) due to H-bonding interactions between QDs and pendant groups of hydrogel network. The hpl-NCH networks showed improved structural/orientational order and swelling ratios with increasing doping concentration compared to the organic hydrogel (OH).

Controlled synthesis of amino acid-based pH-responsive chiral polymers and self-assembly of their block copolymers.

Leucine/isoleucine side chain polymers are of interest due to their hydrophobicity and reported role in the formation of α-helical structures. The synthesis and reversible addition-fragmentation chain transfer (RAFT) polymerization of amino acid-based chiral monomers, namely Boc-L-leucine methacryloyloxyethyl ester (Boc-L-Leu-HEMA, 1a), Boc-L-leucine acryloyloxyethyl ester (Boc-L-Leu-HEA, 1b), Boc-L-isoleucine methacryloyloxyethyl ester (Boc-L-Ile-HEMA, 1c), and Boc-L-isoleucine acryloyloxyethyl ester (Boc-L-Ile-HEA, 1d), are reported. The controlled nature of the polymerization of the said chiral monomers in N, N-dimethylformamide (DMF) at 70 °C is evident from the formation of narrow polydisperse polymers, the molecular weight controlled by the monomer/chain transfer agent (CTA) molar ratio and the linear relationship between molecular weight and monomer conversion.