Search results for "Ionic"

1979

The kinetics of the anionic polymerization of styrene were investigated under pressure (1≤p/bar < 1800) with Na+ as counter ion in tetrahydropyran (THP) as solvent and with Cs+ as counter ion in 1,2-dimethoxyethane (DME) as solvent. The results yielded the activation volume of the contact ion pair ΔV and the sum (ΔV + ΔVcs) of the activation volume of the solvent separated ion pair ΔV and the volume change upon formation of solvent separated ion pairs from contact ion pairs ΔVcs. The numerical values are negative. The activation volume of the solvent separated ion pairs could be estimated.

Novel one-pot synthesis of quaternary ammonium halides: new route to ionic liquids

2004

Treatment of an amide with an alkyl or substituted alkyl halide in the presence of a weak base in a one-pot reaction leads to crystalline quaternary ammonium halides with reasonable chemical yields; some of the compounds show low melting points and a liquid range of over 50–100 °C before decomposition.

Understanding the impact of poly(allylamine) plasma grafting on the filtration performances of a commercial polymeric membrane

2019

Abstract Commercial membranes often exhibit difficulties in rejecting specific ionic species, and especially multivalent cations, due to their usual negative charge. To face this drawback, it is proposed here to functionalize the membrane surface by allylamine plasma polymerization. The impact of this modification on both permeation flux and ion rejection is investigated for single salt solutions and ion mixtures. It is shown that the membrane behaves like a positive membrane from the point of view of cation rejection but the negative charge (and the corresponding electrical field) inside pores leads to high rejection of divalent anions like a negative membrane. This allows a high selectivi…

Progress in Understanding of the Interactions between Functionalized Polyolefins and Organo-Layered Double Hydroxides

2013

The dispersion of organo-layered double hydroxides (O-LDH) in functionalized polyolefins (POs) is investigated. Two different polyethylene matrices (maleic anhydride (MAH) and diethyl maleate functionalized) are tested and a hydrogenated fatty acid modified LDH is used. The attention is focused on evidencing the interaction between the functional groups of the polymer and the O-LDH through FT-IR. Moreover, a combination of solvent fractionation, morphological, and rheological characterizations enables to gain a deeper insight into the structure of these composites. In particular, the formation of bridging bonds between the particles and MAH functionalized macromolecules is assumed, possibly…

The ionic liquid effect on the Boulton-Katritzky reaction: a comparison between substrates of different structure

2015

The mononuclear rearrangement of heterocycles, also called Boulton–Katritzky reaction, was studied in ionic liquid solution using N-(5-phenyl-1,2,4-oxadiazol-3-yl)-N′-(4-nitrophenyl)-formamidine as substrate. The investigation was carried out using piperidine as basic catalyst and several ionic liquids differing in both cation and anion structure. Kinetic data collected were compared with the ones previously reported using (Z)-phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole to have information about the effect due to the different structure of the alkyl chain borne on the substrate. Furthermore, data were analysed on the grounds of polarity, Kamlet–Taft solvent parameters, but taking…

Structure and reactivity of a mononuclear gold(II) complex.

2017

Mononuclear gold(II) complexes are very rare labile species. Transient gold(II) species have been suggested in homogeneous catalysis and in medical applications, but their geometric and electronic structures have remained essentially unexplored: even fundamental data, such as the ionic radius of gold(II), are unknown. Now, an unprecedentedly stable neutral gold(II) complex of a porphyrin derivative has been isolated, and its structural and spectroscopic features determined. The gold atom adopts a 2+2 coordination mode in between those of gold(III) (four-coordinate square planar) and gold(I) (two-coordinate linear), owing to a second-order Jahn–Teller distortion enabled by the relativistical…

Competing salt effects on phase behavior of protein solutions: tailoring of protein interaction by the binding of multivalent ions and charge screeni…

2014

The phase behavior of protein solutions is affected by additives such as crowder molecules or salts. In particular, upon addition of multivalent counterions, a reentrant condensation can occur; i.e., protein solutions are stable for low and high multivalent ion concentrations but aggregating at intermediate salt concentrations. The addition of monovalent ions shifts the phase boundaries to higher multivalent ion concentrations. This effect is found to be reflected in the protein interactions, as accessed via small-angle X-ray scattering. Two simulation schemes (a Monte Carlo sampling of the counterion binding configurations using the detailed protein structure and an analytical coarse-grain…

Mechanism of anionic polymerization of methyl methacrylate in the presence of aluminium alkyls

1995

Methyl methacrylate was polymerized with tert-butyl lithium in the presence of triethylaluminium or triisobutylaluminium at 78°C in toluene. As indicated by GPC and MALDI-TOF mass spectrometry, the polymerization is accompanied by side reactions. The lower oligomers were fractionated by distillation and characterised by NMR, FT-IR, UV and electron impact (EI) mass spectrometry. All these data show that part of the polymer chains are carrying exactly one tert-butyl isoprenyl ketone unit. In order to avoid the formation of tert-butyl isoprenyl ketone a molar ratio of Al/Li>2 is necessary.

Properties of Hydrophobic Polymer Melts Tethered to the Water Surface As Determined with in Situ X-ray Reflectivity

1997

Insoluble monolayers of hydrophobic polymers with low glass transition temperature (perfluoropolyethers, polyisoprenes) and a single ionic head group (carboxylic acid, sulfonate) have been characterized at the air/water interface via X-ray reflectivity measurements. The films are considerably thicker (30−420 A) than conventional Langmuir monolayers of low molecular weight substances or polymers with surface active repeat units. The thickness is inversely proportional to the area per head group and is in accordance with a model assuming a solvent-free hydrophobic layer of the same density as the bulk material.

The first structurally characterized cationic lanthanide–alkyl complexesElectronic supplementary information (ESI) available: experimental and spectr…

2002

Reaction of rare earth metal–alkyl complexes [Ln(CH2SiMe3)3(THF)2] (Ln = Y, Lu) with B(C6X5)3 (X = H, F) in the presence of crown ethers gives crystallographically characterized ion pairs [Ln(CH2SiMe3)2(CE)(THF)n]+[B(CH2SiMe3)(C6X5)3]– (CE = [12]-crown-4, n = 1; CE = [15]-crown-5 and [18]-crown-6, n = 0).