Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Aromatic amine-containing polymer

Aromatic-Amine-Containing Polymers for Organic Electroluminescent Devices... [Pg.381]

In this paper, some of the aromatic amine-containing polymers synthesized in our group are introduced and the devices using these polymers are summarized. Examples of the devices using these polymers as a hole transport layer as well as an emitter layer are discussed. [Pg.382]

KIDO ETAL. Aromatic-Amine-Containing Polymers... [Pg.385]

Accordion polymers—Continued orientational and chemical stability, 139 synthesis by Knoevenagel condensation polymerization, 135-136 waveguide construction, 139-140 Aluminum metal electrode, deposition on polymer in LED, 411,412/ Aromatic amine-containing polymers dye-dispersed poly(N-vinylcarbazole), 387, 390-393... [Pg.548]

Organic electroluminescent device with aromatic amine-containing polymer as a hole transport layer (II) Poly(arylene ether sulfone)-containing tetraphenylbenzidine.. Polym. Adv. Technol., 7, 31. [Pg.220]

The design of single-component polymer transport materials continues to interest researchers in this field. The use of such materials will completely eliminate solvent extraction, diffusional instability, and crystallization of the small molecules. One obvious route that has not been successful to date is the design of yet another aromatic-amine-containing carbon-backbone polymer. An alternative may be to explore the large class of glassy silicon-backbone polymers, such as polysilylenes (14) and polyphosphazenes (iS). [Pg.472]

Stolka, M., Pai, D.M., Refner, D.S., and Yanus, J.C. (1983) Photoconductivity and hole transport in polymers of aromatic amine-containing methacrylates. [Pg.220]

They show good to excellent resistance to highly aromatic solvents, polar solvents, water and salt solutions, aqueous acids, dilute alkaline solutions, oxidative environments, amines, and methyl alcohol. Care must be taken in choice of proper gum and compound. Hexafluoropropylene-containing polymers are not recommended for use in contact with ammonia, strong caustic (50% sodium hydroxide above 70°C), and certain polar solvents such as methyl ethyl ketone and low molecular weight esters. However, perfluoroelastomers can withstand these fluids. Propylene-containing fluorocarbon polymers can tolerate strong caustic. [Pg.509]

The susceptibility of cyclodisilazanes to nucleophilic attack by aromatic amines has also been used to prepare silazane containing polymers. Polysilazane cyclo-linear chains with aromatic spacing groups, synthesized by polycondensations of difunctional cyclodisilazanes with bis-phenols and N.N -diorganosilane diamines, have been reported (13). [Pg.175]

Cyclic chain termination by antioxidants. Oxidation of some substances, such as alcohols or aliphatic amines, gives rise to peroxyl radicals of multiple (oxidative and reductive) activity (see Chapters 7 and 9). In the systems containing such substances, antioxidants are regenerated in the reactions of chain termination. In other words, chain termination occurs as a catalytic cyclic process. The number of chain termination events depends on the proportion between the rates of inhibitor consumption and regeneration reactions. Multiple chain termination may take place, for instance, in polymers. Inhibitors of multiple chain termination are aromatic amines, nitroxyl radicals, and variable-valence metal compounds. [Pg.490]

Aromatic compounds, 13 108-109 13 680. See also Aromatics acylation of, 12 173-181 amination of, 12 184 arylation of, 12 170-171 Cycloalkylation of, 12 169 in diesel fuel, 12 425 formylation of, 12 178 Friedel-Crafts acylation of, 12 174 Friedel-Crafts alkylation of, 12 164 nitration of, 12 182-183 oxidative coupling of, 19 654 sulfonation of, 12 181 sulfonation reagents for, 23 521-524 Aromatic-containing polymers, sulfonation of, 23 535-536... [Pg.70]

In order to demonstrate the use of laser flash photolysis in elucidation of the MDI based polyurethane photolysis mechanism, three polyurethanes, two aryl biscarbamate models, an aryl monocarbamate model, and an aromatic amine were selected. Two of the polyurethanes are based on MDI while the third is based on TDI (mixture of 2,4 and 2,6 isomers in 80/20 ratio). The MDI based polyurethanes all have the same basic carbamate repeat unit. The MDI elastomer (MDI-PUE) is soluble in tetrahydrofuran (THF). The simple polyurethane (MDI-PU) based on MDI and 1,4-butanediol is used in the tert-butoxy abstraction reactions since it does not contain a polyether backbone. (See page 47 for structures of polymers and models.)... [Pg.46]

A recent development31 is the preparation of metal polymer complexes directly on the electrode via the electrochemically induced polymerization of the metal complex. Ruthenium(II) and osmium(II) complexes with ligands containing aromatic amines, e.g. 3- or 4-aminopyridine or 5-amino-1,10-phenanthroline, are electrochemically polymerized to yield a film of the metal polymer on the electrode surface. The polymerization involves free radicals, which are formed via the initial oxidation of the metal complex to a radical cation and subsequent reaction of the radical cation with a base to yield the free radical. [Pg.488]

The following photoconductive polymers can also be clarified as polymers of aromatic amines poly(N-vinylphenothiazine) and poly(N-vinylphenoxazine ° and poly(N-acrylodibenzazepine) ° Poly(N-vinylcarbazole) is basically a modified vinyldiphenylamine polymer . It has yet to be detemined if the transport characteristics of PVK with the diphenyl amino group forced into planarity are different from those of poly(N-vinyldiphenylamine) which would possess a greater freedom of rotation. The properties of PVK have been discussed in many articles and reviews [for example see Ref. ]. Several articles and patents have been published recently which deal with carbazole containing polymers other than PVK, and copolymers of N-vinylcarbazole with some other monomers. [Pg.28]


See other pages where Aromatic amine-containing polymer is mentioned: [Pg.381]    [Pg.393]    [Pg.309]    [Pg.381]    [Pg.393]    [Pg.309]    [Pg.145]    [Pg.71]    [Pg.170]    [Pg.379]    [Pg.488]    [Pg.370]    [Pg.489]    [Pg.322]    [Pg.490]    [Pg.213]    [Pg.249]    [Pg.84]    [Pg.379]    [Pg.862]    [Pg.784]    [Pg.170]    [Pg.311]    [Pg.16]    [Pg.28]    [Pg.31]    [Pg.266]    [Pg.112]    [Pg.266]    [Pg.335]    [Pg.122]    [Pg.135]    [Pg.153]    [Pg.16]    [Pg.31]   


SEARCH



Aromatic amination

Aromatic amine-containing polymer structures

Aromatic amines

Aromatics amination

© 2024 chempedia.info