Poly , solution deposition

In this chapter, we will discuss the formation of various mesoscale crystalline morphologies and molecular orientation of HT-PATs, specifically HT-PHTs in solution-deposited films. Also, we will introduce poly(3,3 "-dialkylquaterthiophene)... 

In a more recent approach, polyelectrolyte multilayers of poly(butanyl viologen) dibromide (PBV) and poly(styrene sulfonate) sodium salt (PSS) have been prepared (52) using an alternating polyion solution deposition technique. In this technique, the ITO substrate is alternatively exposed to positive and negative polyelectrolytes, with spontaneous polymer deposition via coulombic interactions between surface and polyion of opposite charge. In this layer-by-layer deposition technique, all redox material is electrochemically addressable, with good electrochromic performance characteristics. 

The beater additive process starts with a very dilute aqueous slurry of fibrous nitrocellulose, kraft process woodpulp, and a stabilizer such as diphenylamine in a felting tank. A solution of resin such as poly(vinyl acetate) is added to the slurry of these components. The next step, felting, involves use of a fine metal screen in the shape of the inner dimensions of the final molded part. The screen is lowered into the slurry. A vacuum is appHed which causes the fibrous materials to be deposited on the form. The form is pulled out after a required thickness of felt is deposited, and the wet, low density felt removed from the form. The felt is then molded in a matched metal mold by the appHcation of heat and pressure which serves to remove moisture, set the resin, and press the fibers into near final shape (180—182). 

Since multiple electrical and optical functionality must be combined in the fabrication of an OLED, many workers have turned to the techniques of molecular self-assembly in order to optimize the microstructure of the materials used. In turn, such approaches necessitate the incorporation of additional chemical functionality into the molecules. For example, the successive dipping of a substrate into solutions of polyanion and polycation leads to the deposition of poly-ionic bilayers [59, 60]. Since the precursor form of PPV is cationic, this is a very appealing way to tailor its properties. Anionic polymers that have been studied include sulfonatcd polystyrene [59] and sulfonatcd polyanilinc 159, 60]. Thermal conversion of the precursor PPV then results in an electroluminescent blended polymer film. 

The substituted five-ring OPVs have been processed into poly crystal line thin films by vacuum deposition onto a substrate from the vapor phase. Optical absorption and photolumincscence of the films are significantly different from dilute solution spectra, which indicates that intermolecular interactions play an important role in the solid-state spectra. The molecular orientation and crystal domain size can be increased by thermal annealing of the films. This control of the microstruc-ture is essential for the use of such films in photonic devices. 

Polylactides, 18 Poly lactones, 18, 43 Poly(L-lactic acid) (PLLA), 22, 41, 42 preparation of, 99-100 Polymer age, 1 Polymer architecture, 6-9 Polymer chains, nonmesogenic units in, 52 Polymer Chemistry (Stevens), 5 Polymeric chiral catalysts, 473-474 Polymeric materials, history of, 1-2 Polymeric MDI (PMDI), 201, 210, 238 Polymerizations. See also Copolymerization Depolymerization Polyesterification Polymers Prepolymerization Repolymerization Ring-opening polymerization Solid-state polymerization Solution polymerization Solvent-free polymerization Step-grown polymerization processes Vapor-phase deposition polymerization acid chloride, 155-157 ADMET, 4, 10, 431-461 anionic, 149, 174, 177-178 batch, 167 bulk, 166, 331 chain-growth, 4 continuous, 167, 548 coupling, 467 Friedel-Crafts, 332-334 Hoechst, 548 hydrolytic, 150-153 influence of water content on, 151-152, 154... 

Zinc sulfide, with its wide band gap of 3.66 eV, has been considered as an excellent electroluminescent (EL) material. The electroluminescence of ZnS has been used as a probe for unraveling the energetics at the ZnS/electrolyte interface and for possible application to display devices. Fan and Bard [127] examined the effect of temperature on EL of Al-doped self-activated ZnS single crystals in a persulfate-butyronitrile solution, as well as the time-resolved photoluminescence (PL) of the compound. Further [128], they investigated the PL and EL from single-crystal Mn-doped ZnS (ZnS Mn) centered at 580 nm. The PL was quenched by surface modification with U-treated poly(vinylferrocene). The effect of pH and temperature on the EL of ZnS Mn in aqueous and butyronitrile solutions upon reduction of per-oxydisulfate ion was also studied. EL of polycrystalline chemical vapor deposited (CVD) ZnS doped with Al, Cu-Al, and Mn was also observed with peaks at 430, 475, and 565 nm, respectively. High EL efficiency, comparable to that of singlecrystal ZnS, was found for the doped CVD polycrystalline ZnS. In all cases, the EL efficiency was about 0.2-0.3%. 

In a typical reaction 100 - 200 mg of metal [Cr or Ni] was evaporated from a preformed alumina crucible over a period of 60 - 90 min and deposited into a mixture of 2 in poly(dimethylsiloxane) [Petrarch Systems 0.1 P.] within a rotary solution metal vapor reactor operating at 10 4 torr. The reaction flask was cooled to approximately 270 K by an iced-water bath. For a description of the apparatus see Chapter 3 of reference 4. The product in each case was a dark orange viscous liquid and was characterized as obtained from the reaction vessel. 

Nanocapsules of biodegradable polymers, such as PLA and PLA copolymers or poly (e-caprolactone), have been prepared by an interfacial polymer deposition mechanism [163-166], An additional component, a water-immiscible oil, is added to the drug-polymer-solvent mixture. A solution of the polymer, the drug, and a water-immiscible oil in a water-miscible solvent such as acetone is added to an external... 

Thin polymer films have been prepared by surface catalysis in ultrahigh vacuum and electrochemical deposition from solution. These two routes of synthesis result in poly(thiophene), poly(aniline) and poly(3,5-lutidine) films that have similar infrared spectra. These polymer films are highly orientationally ordered the rings are perpendicular to the surface in poly(thiophene) and poly(3,5-lutidine) films, and the phenyl rings are parallel to the surface in poly(aniline). 

Poly(thiophene) films have also been formed on a Pt foil potentiostatically from 1 M thiophene in 1M LiC104/CH3CN at 1.74 V vs. Ag/AgCl(lM). The films were then removed from the thiophene solution and placed in 1M LiC104/CH3CN and cycled between 0 V to 2.0 V vs. Ag/AgCl to test for the presence of polymer films. At deposition potentials below 1.74 V no film deposition was detected, at higher... 

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