Search results for "Phosphazene"
showing 10 items of 15 documents
A PH-functionalized polyphosphazene: a macromolecule with a highly flexible backbone.
2006
Solution processable high band gap hosts based on carbazole functionalized cyclic phosphazene cores for application in organic light‐emitting diodes
2011
A new class of solution processable dendrimers based on cyclic phosphazene (CP) cores have been prepared and used as host materials for blue and green organic light emitting diodes (OLEDs). The dendrimers are prepared in high yield from minimal step reactions, are soluble in common solvents for solution processing, are amorphous, and have excellent thermal properties necessary for application in OLEDs. OLED efficiencies of 10.3 cd/A (4.2 Im/W) and 35.3 cd/A (33.5 Im/W) were achieved using commercially available Flrpic and Ir(mppy) 3 as blue and green phosphorescent emitters, respectively. These efficiencies were 2x higher than control devices prepared using poly(N-vinylcarbazole), the most …
On the Preparation and Characterization of Polyethylene/Polyamide Blends by Melt Processing in the Presence of an Ethylene/Acrylic Acid Copolymer and…
2006
Samples of HDPE and PA6 have been melt-processed in the presence of two new phosphazene compounds, CP-2EPOX and CP-20XA together with an ethylene/acrylic acid copolymer. The blends have been prepared in an industrial twin-screw extruder by using PA6 and PE in weight ratios of 25/75 and 75/25. When used, 5 phr of EAA and 0.2 phr of CP have been added. The materials have been completely characterized from a rheological, morphological, and mechanical point of view. The results indicate that the additives used caused an increase in the rupture tensile properties, of the impact strength and viscosity especially in the PE-rich blend in the presence of CP-2EPOX. This result can be attributed both …
Solution processable phosphorescent dendrimers based on cyclic phosphazenes for use in organic light emitting diodes (OLEDs)
2008
A novel solution processable phosphorescent dendrimer based on cyclic phosphazene (CP) cores has been prepared and used as emissive layers in simple OLED architectures, providing efficiencies of 24.0 cd A^-1 and 16.7 lm W^-1. Bolink, Henk, Henk.Bolink@uv.es ; Garcia Santamaria, Sonsoles Amor, Sonsoles.Garcia@uv.es
Efficient blue emitting organic light emitting diodes based on fluorescent solution processable cyclic phosphazenes
2008
Solution processable blue fluorescent dendrimers based on cyclic phosphazene (CP) cores incorporating amino-pyrene moieties have been prepared and used as emissive layers in organic light emitting diodes (OLEDs). These dendrimers have high glass transition temperatures, are monodisperse, have high purity via common chromatographic techniques, and form defect-free amorphous films via spin/dip coating. The solution processable blue light emitting OLEDs reach current efficiencies of 3.9 cd/A at brightness levels near 1000 cd/m2. Depending on the molecular bridge used to attach the fluorescent dendron to the inorganic core, the emission wavelength changes from 470 to 545 nm, corresponding to bl…
Phosphorylated micro- vs. nano-cellulose: a comparative study on their surface functionalisation, growth of titanium-oxo-phosphate clusters and remov…
2019
Controlled cellulose disassembly affords many variants including amorphous micro-sized cellulose crystals (MCC) and cellulose nano-sized crystals (CNC), which have emerged recently as green and sustainable nanomaterials. Unfortunately, their lower reactivity and thermal and chemical instability constitute an impediment for multifaceted nanoscience and nanotechnology usage. Herein, MCC and CNC are functionalised using two phosphorus derivatives (phosphoryl chloride and hexachlorocyclotriphosphazene), under acid-free, urea-free and corrosive-free, gentle experimental conditions. Notably, CNC can accommodate more phosphorus species compared to MCC, with the bulky phosphazene precursor being le…
Effect of adding new phosphazene compounds to poly(butylene terephthalate)/polyamide blends. I: Preliminary study in a batch mixer
2005
Abstract Poly(butylene terephthalate) (PBT) and a sample of polyamide have been melt processed in the presence of two new phosphazene compounds, namely 2,2-dichloro-4,4,6,6-bis[spiro(2′,2″dioxy-1′,1″biphenyl)]cyclotriphosphazene (2Cl-CP) and 2,2-bis-(2-methoxy-4-methyleneoxy-phenoxy)-4,4,6,6,-bis[spiro(2′,2″dioxy-1′,1″biphenyl)]cyclophosphazene (CP-2EPOX). The blends were prepared by using polyamide 6 (PA6) at 25/75 w/w and 75/25 w/w composition. In order to perform a preliminary analysis on the behaviour of the blends, the materials were prepared in a batch mixer. The materials have been completely characterized from a rheological, morphological, mechanical point of view. The results indic…
New phosphazene-based chain extenders containing allyl and epoxide groups
2003
In this paper we present the synthesis and the characterization of cyclophosphazenes substituted with allyl groups, their transformation in epoxide-containing cyclophosphazenes and the final utilization of these compounds as chain extenders in combination with polyamides. The reaction at high temperature of Nylon-6 with epoxy-functionalized cyclophosphazenes leads to the opening of the epoxy units by the action of both amino (--NH2) and carboxylic (--COOH) end-groups of the polymer to enhance the final molecular weight of this material. The consequences of this fact on the thermal, mechanical and visco-elastic properties of treated Nylon-6 have been also evaluated and compared to those of t…
Chemical Reactions occurring in the molten state between Ny6 and Oxazoline groups linked to a Cyclophosphazene moiety
2009
Spin Trapping of Carbon-Centered Ferrocenyl Radicals with Nitrosobenzene
2015
In contrast to metal centered 17 valence electron radicals, such as [Mn(CO)5]•, ferrocenium ions [Fe(C5H5)2]+ (1+), [Fe(C5Me5)2]+ (2+), [Fe(C5H5)(C5H4Et)]+ (3+), [Fe(C5H5)(C5H4NHC(O)Me)]+ (4+), and [Fe(C5H5)(C5H4NHC(S)Me)]+ (5+) do not add to nitrosobenzene PhNO to give metal-coordinated stable nitroxyl radicals. In the presence of the strong and oxidatively stable phosphazene base tert-butylimino-tris(dimethylamino)phosphorane, the quite acidic ferrocenium ions 1+–5+ are deprotonated to give a pool of transient and persistent radicals with different deprotonation sites [1–Hx]•–[5–Hx]•. One rather persistent iron-centered radical [4–HN]•, deprotonated at the nitrogen atom, has been detected…