Search results for "Ionic polymerization"

Wide-Bite-Angle Diphosphine Ligands in Thermally Activated Delayed Fluorescent Copper(I) Complexes: Impact on the Performance of Electroluminescence …

2021

We report a series of seven cationic heteroleptic copper(I) complexes of the form [Cu(P^P)(dmphen)]BF4, where dmphen is 2,9-dimethyl-1,10-phenanthroline and P^P is a diphosphine chelate, in which the effect of the bite angle of the diphosphine ligand on the photophysical properties of the complexes was studied. Several of the complexes exhibit moderately high photoluminescence quantum yields in the solid state, with ΦPL of up to 35%, and in solution, with ΦPL of up to 98%. We were able to correlate the powder photoluminescence quantum yields with the % Vbur of the P^P ligand. The most emissive complexes were used to fabricate both organic light-emitting diodes and light-emitting electrochem…

Enhancing the photoluminescence quantum yields of blue-emitting cationic iridium(iii) complexes bearing bisphosphine ligands

2016

EZ-C acknowledges the University of St Andrews for financial support. We thank Johnson Matthey and Umicore AG for the gift of materials and Cihang Yu for the preparation of isopropxantphos. We thank Dr. Nail Shaveleev for the synthesis of NMS25. IDWS and AKB acknowledge support from EPSRC (EP/J01771X). This work has been supported by the Spanish Ministry of Economy and Competitiveness (MINECO) MAT2014-55200. Herein we present a structure-property relationship study of thirteen cationic iridium (III) complexes of the form of [Ir(C^N)2(P^P)]PF6 in both solution and the solid state through systematic evaluation of six bisphosphine (P^P) ligands (xantphos, dpephos, dppe, Dppe, nixantphos and is…

Green phosphorescence and electroluminescence of sulfur pentafluoride-functionalized cationic iridium(III) complexes

2015

EZ-C acknowledges the University of St Andrews for financial support. We report four cationic iridium(III) complexes [Ir(C^N)2(dtBubpy)](PF6) that have sulfurpentafluoride-modified 1-phenylpyrazole and 2-phenylpyridine cyclometalating (C^N) ligands (dtBubpy = 4,4'-di-tert-butyl-2,2'-bipyridyl). Three of the complexes were characterized by single-crystal X-ray structure analysis. In cyclic voltammetry, the complexes undergo reversible oxidation of iridium(III) and irreversible reduction of the SF5 group. They emit bright green phosphorescence in acetonitrile solution and in thin films at room temperature, with emission maxima between 482–519 nm and photoluminescence quantum yields of up to 7…

Micelles of polyisobutylene-block-poly(methacrylic acid) diblock copolymers and their water-soluble interpolyelectrolyte complexes formed with quater…

2004

The micellization of ionic amphiphilic diblock copolymers, polyisobutylene-block-poly(methacrylic acid) (PIB-b-PMAA), with a constant degree of polymerization of the non-ionic block ðDPn ¼ 20Þ and various degrees of polymerization of the polyelectrolyte block ðDPn ¼ 100 – 425Þ was examined in aqueous media by means of fluorescence spectroscopy using pyrene as a polarity probe. The molar values of the critical micellization concentration (cmc) were found to be around 2 £ 10 26 mol/l, being nearly independent of the length of the polyelectrolyte block as well as pH (in the range 6 – 9) and ionic strength (# 0.5 M NaCl) while the specific cmc values varied from 20 to 100 mg/l. Small-angle neut…

1990

It is shown that the block-like structure of the polyampholyte poly(methacrylic acid)-block-poly(1-methyl-4-vinylpyridinium chloride) considerably influences its conformational behaviour. This specific behaviour is explained by the formation of intra-macromolecular polyelectrolyte complexes stabilized by cooperative ionic contacts between acidic and basic units near the isoelectric point (i. e. p.). The structure of the block-polyampholyte at the i. e. p. is suggested to be close to the structure of non-stoichiometric polyelectrolyte complexes. The complex formation ability of the block-polyampholyte with respect to anionic, cationic, and nonionic polymers is also studied. By means of poten…

Gold nanostars coated with neutral and charged polyethylene glycols: A comparative study of in-vitro biocompatibility and of their interaction with S…

2015

Gold nanostars (GNS) have been coated with four different polyethylene glycols (PEGs) equipped with a -SH function for grafting on the gold surface. These PEGs have different chain lengths with average MW = 2000, 3000, 5000 and average number of -O-CH2-CH2 - units 44, 66, and 111, respectively. Two are neutral and two are terminated with -COOH and -NH2 functions, thus bearing negative and positive charges at physiological pH, thanks to the formation of carboxylate and ammonium groups. The negative charge of the GNS coated with PEG carboxylate has also been exploited to further coat the GNS with the PAH (polyallylamine hydrochloride) cationic polymer. Vitality tests have been carried out on …

Hyperbranched polyethylenimines as versatile precursors for the preparation of different type of unimolecular micelles

2007

Abstract Hyperbranched polyethylenimine (HPEI) was successfully employed as precursor for the preparation of unimolecular inverted and aqueous micelles. The unimolecular inverted micelles (UIMs) obtained by the amidation of HPEI with 1,1′-carbonyldiimidazole (CDI) activated palmitic acid exhibited high encapsulation efficiency for hydrophilic anionic dyes and the efficiency could be enhanced significantly by decreasing the degree of amidation or quaternizing the residual amines. The weight ratio of loaded guests to the amidated HPEIs was not dependent on the molecular weight of HPEI core when the degree of amidation was kept constant. Decreasing the length of the aliphatic chain from 16 to …

Polymerisation und Kettenverknüpfung von Alkenyl-1,2,3-thiadiazolen

1986

4- und 5-Vinyl-1,2,3-thiadiazole 1, 2 lassen sich in radikalischen oder kationischen Kettenreaktionen polymerisieren. Die dabei vollstandig intakt bleibenden Thiadiazolringe konnen photochemisch abgebaut werden, wobei es zur Kettenvernetzung uber substanzeigene S-Brucken kommt. Das 5-Vinylsystem 2 kann mit 4,4′-(1,6-Hexandiyl)bis(4H-1,2,4-triazol-3,5-dion) unter Denitrogenierung copolymerisiert werden. Polymerization and Cross-Linking of Alkenyl-1,2,3-thiadiazoles 4- and 5-Vinyl-1,2,3-thiadiazoles 1, 2 can be polymerized in radical or cationic chain processes. The completely intact remaining thiadiazole ring systems can be photochemically cleaved yielding a cross-linking of the polymer chai…

Rotationsdispersion bei monomeren und polymeren L-bornylestern

1962

L-Bornylacrylat und -methacrylat wurden unter verschiedenen Bedingungen radikalisch und ionisch polymerisiert. Die Wellenlangenabhangigkeit der Drehwerte last sich durch eine eintermige DRUDE-Gleichung beschreiben. Die DRUDE-Konstanten fur Poly-L-bornylacrylat hangen nur wenig vom Losungsmittel ab. Sie werden aber, ebenso wie die Lage der COTTON-Effekte, vom Polymerisationsmechanismus beeinflust. The radical and ionic polymerization of L-bornylacrylate and -methacrylate was studied under varying conditions. The optical rotatory dispersion is represented by a simple one-term DRUDE equation. The solvents have little effect on the DRUDE constants for poly-L-bornylacrylate. However, these const…

The apparently anomalous effects of surfactants on interfacial tension in the IBA/water system near its upper critical solution temperature

2016

We studied the effect of anionic, cationic, and nonionic surfactants on the interfacial tension between the two phases of the isobutyric acid/water system using spinning drop tensiometry. It has been found that interfacial tension decreases with increasing concentration of the surfactant in the case of sodium dodecyl sulfate (SDS) and of dodecyltrimethylammonium chloride (DTAC). However, in the case of Triton X-100 an increase of surfactant concentration leads to an increase of the interfacial tension. Such results are consistent with the upper critical solution temperature (UCST) in the presence of these surfactants: the UCST decreases with increasing SDS and DTAC concentrations while it i…