Synthesis of a series of oligo(ethylene glycol)-terminated alkanethiol amides designed to address structure and stability of biosensing interfaces.

A strategy for the synthesis of a series of closely related oligo(ethylene glycol)-terminated alkanethiol amides (principally HS(CH(2))(m)CONH(CH(2)CH(2)O)(n)H; m = 2, 5, 11, 15, n = 1, 2, 4, 6, 8, 10, 12) and analogous esters has been developed. These compounds were made to study the structure and stability of self-assembled monolayers (SAMs) on gold in the prospect of designing new biosensing interfaces. For this purpose, monodisperse heterofunctional oligo(ethylene glycols) with up to 12 units were prepared. Selective monoacylation of the symmetrical tetra- and hexa(ethylene glycol) diols as their mesylates with the use of silver(I) oxide was performed. The synthetic approach was based on carbodiimide couplings of various oligo(ethylene glycol) derivatives to omega-(acetylthio) carboxylic acids via a terminal amino or hydroxyl function. SAM structures on gold were studied with respect to thickness, wettability (water contact angles approximately 30 degrees ), and conformation. A good fit was obtained for the relation between monolayer thickness (d) and the number of units in the oligo(ethylene glycol) chain (n): d = 2.8n + 21.8 (A). Interestingly, the corresponding infrared spectroscopy analysis showed a dramatic change in conformation of the oligomeric chains from all-trans (n = 4) to helical (n > or = 6) conformation. A crystalline helical structure was observed in the SAMs for n > 6.     

Synthesis of a polymerizable metal-ion-chelating lipid for fluid bilayers.

Hydrated lipid structures, such as liposomes, that display tethered metal-ion-chelating groups have proven useful in peptide and protein binding, as well as 2D protein crystallization through molecular recognition of accessible histidine sites in proteins and peptides. Polymerizable metal-ion-chelating lipids bearing a reactive diacetylene group have been described. These interesting compounds can be polymerized in the solid-analogous phase. Here we describe the design of the first polymerizable metal-ion-chelating lipid that can be used in the fluid, i.e., liquid analogous, phase of lipid bilayers. The synthesis of 1-palmitoyl-2-[8-[(E,E)-2',4'-hexadienoyloxy]octanoyl]-sn-glycero-3-N-[11-[N',N'-bis[carboxymethyl]imino]-3,6,9-trioxaundecanoyl] phosphatidylethanolamine (1) is described. The chelator moiety, iminodiacetate (IDA), was linked to the polymerizable phosphatidylethanolamine (PE) with a terminal 2,4-hexadienoyl (sorbyl) group through an oligo(ethylene glycol)-based spacer. Lipid 1-Cu complex is designed to be combined with the corresponding polymerizable matrix lipids (bis-SorbPC) to form functionalized liposomes that can be stabilized by various polymerization methods.     

Control of protein structure and function through surface recognition by tailored nanoparticle scaffolds

Thioalkyl and thioalkylated oligo(ethylene glycol) (OEG) ligands with chain-end functionality were used to fabricate water-soluble CdSe nanoparticle scaffolds. Surface recognition of chymotrypsin (ChT) was achieved using these functionalized nanoparticle scaffolds, with three levels of interaction demonstrated: no interaction (OEG terminated with hydroxyl group), inhibition with denaturation (carboxylate-terminated thioalkyl ligands), and inhibition with retention of structure (carboxylate-terminated OEG). The latter process was reversible upon an increase in ionic strength, with essentially complete restoration of enzymatic activity.     

Highly water-soluble neutral BODIPY dyes with controllable fluorescence quantum yields

A series of novel highly water-soluble neutral BODIPY dyes have been obtained by functionalization of BODIPY dyes with branched oligo(ethylene glycol)methyl ether groups at positions 8, 2 and 6 or 4 and 4'. Use of an ortho-substituent group of branched oligo(ethylene glycol)methyl ether on the meso-phenyl ring of BODIPY dyes and replacement of the fluorine atoms of BODIPY dyes at positions 4 and 4' with methyloxy or ethynyl subunits significantly enhance fluorescence quantum yields of BODIPY dyes.     

Synthesis and optical and electrochemical properties of polycyclic aromatic compounds based on bis(benzothiophene)-fused fluorene

Novel polycyclic aromatic compounds (FBTPhO3 and FBTPhO4), which are based on bis(benzothiophene)-fused fluorene functionalized with oligo(ethylene glycol)-substituted phenyl, were synthesized through an intramolecular electrophilic cyclizing reaction. Thermal measurements revealed their excellent thermal stability and amorphous state. Photoluminescence spectra suggested that they both show deep blue light emission. Cyclic voltammetry tests exhibited that the ionization potentials of FBTPhO3 and FBTPhO4 are 5.67 and 5.68 eV, respectively, implying their good inoxidizability. These compounds may be promising building blocks for high-performance optoelectronic functional materials.     

Hydrophilic polymethacrylates containing cholic acid‐ethylene glycol derivatives as pendant groups

In an effort to improve the hydrophilicity of bile acid containing polymers, we have synthesized new methacrylate monomers by incorporating ethylene glycol and oligo(ethylene glycol) spacers of different lengths between cholic acid and methacrylate residues. The monomers were subsequently polymerized by free radical reaction in solution. The methyl ester protecting groups on the cholic acid residue were selectively hydrolyzed to restore the carboxylic acid group of cholic acid. Water absorption tests showed that the hydrophilicity of the polymers was improved with increasing length of oligo(ethylene glycol) spacers and upon restoration of the carboxylic acid group of the cholic acid residue.     

meso-C6F5 substituted BODIPYs with distinctive spectroscopic properties and their application for bioimaging in living cells

A series of meso-C₆F₅ BODIYs have been successfully synthesized and characterized. Some of them displayed excellent spectroscopic properties, such as relatively large Stokes shift, high fluorescence quantum yield, far-red or near infrared region (NIR) emission, and good photostability. In particular, the dye functionalized with oligo(ethylene glycol) ether-phenyl groups at the 3,5-position of BODIPY core became water-soluble and its emission located in the NIR region with large Stokes shift. Time-dependent density functional theory calculations were conducted to understand the structure–optical properties relationship. Furthermore, cell staining tests demonstrated that the meso-C₆F₅ BODPY derivative with oligo(ethylene glycol) ether-phenyl group was membrane permeable and selectively stained cytosol in living cells.     

Determination of glycols by HPLC with refractive index detection

A simple and fast HPLC method for the determination of glycols is described. It is characterized by a reversed-phase separation using water as eluent and a refractive index detection. The method was applied to investigate the biodegradation of glycols in a laboratory activated sludge plant and to determine the content of glycols or alcohols in detergents. The detection limit is 4 mg/l ethylene glycol or propylene glycol in an aqueous sample.     

Differentiation of O-H and C-H bond scission mechanisms of ethylene glycol on Pt and Ni/Pt using theory and isotopic labeling experiments

Understanding and controlling bond-breaking sequences of oxygenates on transition metal catalysts can greatly impact the utilization of biomass feedstocks for fuels and chemicals. The decomposition of ethylene glycol, as the simplest representative of biomass-derived polyols, was studied via density functional theory (DFT) calculations to identify the differences in reaction pathways between Pt and the more active Ni/Pt bimetallic catalyst. Comparison of the computed transition states indicated three potentially feasible paths from ethylene glycol to C1 oxygenated adsorbates on Pt. While not important on Pt, the pathway to 1,2-dioxyethylene (OCH(2)CH(2)O) is favored energetically on the Ni/Pt catalyst. Temperature-programmed desorption (TPD) experiments were conducted with deuterated ethylene glycols for comparison with DFT results. These experiments confirmed that decomposition of ethylene glycol on Pt proceeds via initial O-H bond cleavage, followed by C-H and the second O-H bond cleavages, whereas on the Ni/Pt surface, both O-H bonds are cleaved initially. The results are consistent with vibrational spectra and indicate that tuning of the catalyst surface can selectively control bond breaking. Finally, the significant mechanistic differences in decomposition of polyols compared to that of monoalcohols and hydrocarbons serve to identify general trends in bond scission sequences.     

Novel antifouling oligo(ethylene glycol) methacrylate particles via surfactant-free emulsion polymerization

The use of particle formulations with antifouling surface properties attracts increasing interest in several biotechnological applications. Majority of these studies utilize a poly(ethylene glycol) coating to render the corresponding surface nonrecognizable to biological macromolecules. Herein, we report a simple way to prepare novel antifouling colloids composed of oligo(ethylene glycol) backbones via surfactant-free emulsion polymerization. Monodisperse cross-linked poly(ethylene glycol) ethyl ether methacrylate particles were characterized by dynamic light scattering and transmission electron microscopy. The effects of monomer, cross-linker and initiator on particle characteristics were investigated. More importantly, a prominent blockage of bovine serum albumin adsorption was obtained for the poly(ethylene glycol)-based sub-micron (~200 nm) particles when compared with similar-sized poly(methyl methacrylate) counterparts.     

Proton-ionizable acyclic dibenzopolyethers and their polymers for use in selective lead(II) separation

Abstract

2,2′-[1,2-Ethanediylbis(oxy)]bisbenzoic acid (1), 2,2′-[oxybis(1,2-ethanediyloxy)]bisbenzoic acid (2), 1,2-[2′-(acetoxy)phenoxy] ethane (3), and 1,5-[2′-(acetoxy)phenoxy]-3-oxopentane (4) have been prepared for use in selective Pb(II) separation. The extraction of Pb(II) and Cu(II) from buffered aqueous solutions of varying pH into chloroform by 1–4 is examined in relation to their molecular structure. Compound 1 with an ethylene glycol spacer unit exhibits excellent extraction selectivity for Pb(II) over Cu(II). Lengthening the spacer group to a diethylene glycol unit diminishes the extraction efficiency and selectivity. For 3 and 4, extraction was inefficient due to low lipophilicity and solubility of the ligands in chloroform. Condensation polymerization of compounds 3 and 4 with formaldehyde in formic acid provides stable chelating resins 5 and 6 which contain both ion-exchange and polyether binding sites for metal complexation. Resin 5 with an ethylene glycol spacer group is found to be an effective chelating resin for Pb(II) separation. The sorption mechanism and selectivity are studied and compared with the commercially available iminodiacetic acid resin CR-10.     

Tethered bilayer lipid membranes based on monolayers of thiolipids mixed with a complementary dilution molecule. 1. Incorporation of channel peptides

Tethered bilayer lipid membranes (tBLMs) are described based on the self-assembly of a monolayer on template stripped gold of an archea analogue thiolipid, 2,3-di-o-phytanyl-sn-glycerol-1-tetraethylene glycol-d,l-alpha-lipoic acid ester lipid (DPTL), and a newly designed dilution molecule, tetraethylene glycol-d,l-alpha-lipoic acid ester (TEGL). The tBLM is completed by fusion of liposomes made from a mixture of diphytanoylphosphatidyl choline (DPhyPC), cholesterol, and 1,2-diphytanoyl-sn-glycero-3-phosphate (DPhyPG) in a molar ratio of 6:3:1. Melittin and gramicidin are incorporated into these tBLMs as shown by surface plasmon resonance (SPR) and electrochemical impedance spectroscopy (EIS) studies. Ionic conductivity at 0 V vs Ag|AgCl, 3 M KCl, measured by EIS measurements are comparable to the results obtained by other research groups. Admittance plots as a function of potential are discussed on a qualitative basis in terms of the kinetics of ion transport through the channels.     

Synthesis of oligo(ethylene glycol) toward 44-mer

A synthetic method for oligo(ethylene glycol) toward 44-mer (FW = 1956.35) is described. Reiteration of Williamson's ether synthesis and hydrogenation to remove protecting benzyl group affords desired oligo(ethylene glycol) toward 44-mer in moderate yields. The advantages in this method are use of commercially easily available materials as starting materials and procedures avoiding difficulty in purification of the products as much as possible.     

Synthesis,self-assembly,and photomechanical actuator performance of a sequence-defined polyviologen crosslinker

ABSTRACT

Although it is well known that viologen radical cations can self-assemble into stacks or complexes on account of radical-radical pairing interactions, it has only recently been demonstrated that reduction of main-chain polyviologens integrated into hydrogel networks can trigger actuation. In these earlier examples, hydrogels comprising oligoethylene glycol-based polyviologens and poly(ethylene glycol) were functionalized with terminal azide groups to prepare ‘click’-based gels. Here, we report a new structural design for the functional polyviologen that consists of main-chain viologen subunits separated by hexamethylene groups instead of glycols and is capped at each end with styrene groups. Activation of this viologen-based macrocrosslinker was achieved using chemical- and photoreduction methods and its ability to undergo intramolecular chain-folding was monitored by absorption spectroscopy. Acrylate-based organogels and hydrogels were also prepared and a comparison was carried out to assess the actuator performance in each gel in terms of the rate of contraction and changes in stiffness.     

Highly Efficient Synthesis of Monodisperse Poly(ethylene glycols) and Derivatives through Macrocyclization of Oligo(ethylene glycols)

A macrocyclic sulfate (MCS)‐based approach to monodisperse poly(ethylene glycols) (M‐PEGs) and their monofunctionalized derivatives has been developed. Macrocyclization of oligo(ethylene glycols) (OEGs) provides MCS (up to a 62‐membered macrocycle) as versatile precursors for a range of monofunctionalized M‐PEGs. Through iterative nucleophilic ring‐opening reactions of MCS without performing group protection and activation, a series of M‐PEGs, including the unprecedented 64‐mer (2850 Da), can be readily prepared. Synthetic simplicity coupled with versatility of this new strategy may pave the way for broader applications of M‐PEGs.     

NMR spectroscopy and free volume analysis of the effects of copolymer composition on the swelling kinetics and chain dynamics of highly crosslinked copolymers of acrylic acid with PEG‐containing multiacrylates

Novel ionizable polymer networks were prepared from oligo(ethylene glycol) (OEG) multiacrylates and acrylic acid (AA), employing bulk radical photopolymerization techniques. The properties of these materials exhibited a complex dependence on the network structure and composition. Penetrant sorption experiments demonstrated that the crosslinked structure of the copolymers depended very strongly on the AA content as well as the number of ethylene glycol groups. The impact of varying the AA content and the oligo(ethylene glycol) chain length on the polymer chain dynamics was examined using diffusion and ¹³C NMR relaxation studies. The penetrant uptake studies indicated a coupling of Fickian and relaxation‐driven contributions to the swelling behavior. The effect of increasing the AA content on the characteristic chain relaxation time was reversed as the oligo(ethylene glycol) chain length was varied, indicating that chain relaxation is controlled by structural considerations, for shorter oligo(ethylene glycol) chains, and by compositional considerations, for longer oligo(ethylene glycol) chains. Measured compositional effects on solid state ¹³C NMR relaxation times supported these conclusions. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 1953–1968, 1999     

Excess molar enthalpies of binary mixtures containing ethylene glycols or poly(ethylene glycols) + ethyl alcohol at 308.15 K and atmospheric pressure

Excess molar enthalpies, , of binary mixtures containing ethylene glycols and poly(glycols) + ethyl alcohol were measured by a flow microcalorimeter at 308.15 K and at atmospheric pressure over the whole composition range. Binary mixtures contain ethyl alcohol + ethylene glycol, + di(ethylene glycol), + tri(ethylene glycol), + tetra(ethylene glycol), + poly(ethylene glycol)-200, + poly(ethylene glycol)-300, + poly(ethylene glycol)-400, + poly(ethylene glycol)-600. Effects of the molecular weight distribution (MWD), of the polymer were investigated too, by preparing three additional samples of poly(ethylene glycol) with the same number average molecular weight (M_n ≈ 300), but different MWD. For all mixtures, results were fitted to the Redlich–Kister polynomial. curves are asymmetrical, showing positive values which vary from 280 J mol⁻¹ (diethylene glycol + ethyl alcohol) to 1034 J mol⁻¹ (mixture containing PEGs (200 + 400) + ethyl alcohol). Effects of changes in the glycols chain length and in MWD on the molecular interactions among the mixture components are discussed.     

Soluble-polymer-supported synthesis of beta-lactams on a modified poly(ethylene glycol)

A modified poly(ethylene glycol) (PEG) has been developed for the soluble-polymer-supported synthesis of beta-lactams. The monomethylether of PEG (MeOPEG) with an average M(W) of 5000 was used as the support, a 4-(3-propyl)phenyl residue as the spacer, and a 4-oxyphenylamino group as the moiety with the reactive functionality. From this modified PEG representative aromatic, heteroaromatic, unsaturated, and aliphatic imines were obtained in high yields by different procedures. The polymer-supported imines were then employed to prepare several beta-lactams by enolate/imine condensation and ketene/imine cycloaddition. Examples of the control of the absolute stereochemistry during the azetidinone ring formation are also reported. The reactions carried out on the polymer-bound imines showed a remarkable similarity to those performed on nonimmobilized imines, both in terms of yields and stereoselectivities. Removal of the beta-lactams from the polymer has also been accomplished to directly deliver the N-unsubstituted azetidinones.     

含四硫富瓦烯大环化合物的合成与研究进展

简要介绍了含有四硫富瓦烯(TTF)单元的大环化合物的分类, 概括了各类含四硫富瓦烯大环化合物的合成方法, 主要包括含有1,3-二硫杂环戊烯-2-硫酮单元的大环化合物在亚磷酸三烷基酯参与下的偶合反应, 以及带有氰乙基硫等取代基的预先合成的官能化TTF与二卤代低聚醚的反应. 综述了含四硫富瓦烯大环化合物的电化学性能及其在分子识别方面应用研究的最新进展, 提出了含四硫富瓦烯大环化合物的发展趋势.     

Reversible protection of oligomeric ethylene glycols by bis (2,4-dinitrophenylation) and basic ethanolysis

Bis-(2,4-dinitrophenyl)glycols are stable in the presence of triethylamine but undergo ethanolysis in the presence of hydroxide ions. The quantitative removal of the DNP blocking group allows an integrated scheme to pure glycols from commercially available polyethylene glycol mixtures

1 Mixtures of ethylene glycol oligomers are obtained by anionic polymerization of ethylene oxide. See, for example, G. O. Curme and F. Johnston, Glycols, Reinhold, New York, 1953. They are commercially available (as PEG-200, PEG-400, etc., to indicate the average molecular weight of the major components).

by bis-dinitrophenylation, chromatographic separation, and end-group removal, using high performance liquid chromatography (HPLC) of the bis-(2,4-dinitrophenyl)glycols for purity monitoring. A facile synthetic method for the production of penta-to dodecaglycols in a mixed, aqueous, dioxane solvent system, with fair yields, is also described. The bis-(2,4-dintrophenyl) protection of glycols is a reversible reaction that can be used as (1) a preparative method for pure glycols from readily available commercial polyethylene glycol mixtures; (2) a highly sensitive and accurate analytical method

2 A. Warshawsky, A. Tishbee, and N. Shoef, J. Liq. Chromatogr., submitted for publication.

coupled with HPLC.