Surface Modification of Ultra-high Molecular Weight Polyethylene Membranes Using Underwater Plasma Polymerization

Ultra-high molecular weight polyethylene membranes were modified and subsequently polymer coated using the underwater plasma produced by glow discharge electrolysis. This plasma pretreatment generated various O-functional groups among them OH groups have dominated. This modified inner (pore) surface of membranes showed complete wetting and strong adhesion to a hydrogel copolymerized by glow discharge electrolysis also. The deposited hydrogel consists of plasma polymerized acrylic acid crosslinked by copolymerization with the bifunctional N,N′-methylenebis(acrylamide). Tuning the hydrogel hydrophilicity and bio-compatibility poly(ethylene glycol) was chemically inserted into the copolymer. Such saturated polymer could only be inserted on a non-classic way by (partial) fragmentation and recombination thus demonstrating the exotic properties of the underwater plasma. The modification of membrane was achieved by squeezing the reactive plasma solution into the pores by plasma-induced shock waves and supported by intense stirring. The deposited copolymer hydrogel has filled all pores also in the inner of membrane as shown by scanning electron microscopy of cross-sections. The copolymer shows the characteristic units of acrylic acid and ethylene glycol as demonstrated by infrared spectroscopy. A minimum loss in carboxylic groups of acrylic acid during the plasma polymerization process was confirmed by X-ray photoelectron spectroscopy. Additional cell adhesion tests on copolymer coated polyethylene using IEC-6 cells demonstrated the bio-compatibility of the plasma-deposited hydrogel.     

SUBSTITUENT EFFECTS ON CONFORMATIONAL EQUILIBRIA IN THIANE-1-N-ARYL-SULFIMIDES

Abstract

Compounds of the general type shown have been synthesized and their conformational equilibria 13 have been established by low temperature ¹³C nmr spectroscopy.     

Phosphate-Phosphonate Rearrangement of Aliphatic Phosphates

Abstract

Phosphorylation of various aliphatic alcohols gives phosphates 1 which are deprotonated by sBuLi/TMEDA in diethyl ether, THF or hexane at ?78 °C. The organo-lithiurns 2 and 4 formed isornerize to α-hydroxy- phosphonates 3 and 5 (phosphate-phosphonate rearrangement^[1.2]     

Core–shell nanogels by RAFT crosslinking polymerization: Synthesis and characterization

A synthetic methodology is described for the preparation of core–shell nanogels by reversible addition‐fragmentation chain transfer. Well‐defined macro chain transfer agents (macro‐CTA's) were prepared in a first step using monomers that yield sensitive polymers. In the second step, a crosslinker alone or with the addition of a functionalized comonomer were used to form a crosslinked core. The ratio of crosslinker to macro‐CTA is crucial to yield nanogels. Furthermore, the polymerization time has an impact in the architecture of the nanomaterial obtained: it evolves from a core‐crosslinked star to a core–shell nanogel. Controlling the molecular weight of the macro‐CTA and the type of comonomer in the core forming step, core–shell nanogels with hydrodynamic diameters from 22 to 168 nm and a core that represents from 35 to 77% of the size, were prepared containing functional groups in the core which could be used as catalytic scaffolds. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012.     

Biologically Active 1-Aminodeoxy and 1-O-Alkyl Derivatives of The Powerful D-Glucosidase Inhibitor 2,5-Dideoxy-2,5-Imino-D-Mannitol

ABSTRACT

By an Amadori rearrangement of easily available 5-azido-5-deoxy-D-glucofuranose with dibenzylamine and subsequent catalytic hydrogenation of the resulting 5-azido-1-(N,N-dibenzyl)amino-1,5-dideoxy-D-fructopyranose, 1-amino-1,2,5-trideoxy-2,5-imino-D-mannitol was obtained in only two steps and in excellent overall yield. Likewise, other amines were employed to introduce extended side chains ultimately suitable for attachment of the inhibitor to solid supports. The reported rearrangement reaction is a high yielding, convenient and apparently general entry to 1-aminodeoxyketopyranoses modified at C-5, facilitated by the ring enlargement of the aldofuranose to the ketopyranose as an additional driving force. A range of selected chain extended analogues was prepared by acylation of N-1. Inhibitors obtained exhibit K _i-values with D-glucosidases in the micromolar range. Interestingly, 1-N-acylation resulted in superior inhibitory activities, as did the addition of a hexyl chain.