Layered synthetic multilayers

Layer-by-layer Ru3 cluster-based multilayers were fabricated onto preorganized self-assembled monolayer gold electrode surfaces by Abe et al. [15], in which [Ru3(q3-0)( i-0Ac)6(4,4/-bpy)2(C0)] was utilized as the synthetic precursor. The stepwise connection of oxo-centered triruthenium cluster units onto the gold electrode surface is a feasible approach for construction of Ru3 cluster-based oligomers on a solid surface, in which the bridging ligand 4,4 -bipyridine appears to mediate weak cluster-cluster electronic interaction between the Ru3 cluster centers. 

A somewhat curious effect arises when additional water is dosed on top of this synthetic inner layer, in that the work function is observed to exhibit substantial further decreases. This implies that the water molecules in the multilayers above the inner layer assume some measure of preferential orientation, induced by the presence of the adsorbed bromide in the first layer. This result is probably connected to structure making and structure breaking, or hydrophobic and hydrophilic, properties of soild surfaces, but will not be discussed in detail here. 

In addition, the separator must have a low electrical resistance, good thermal and chemical stability and must be light in order to retain the high energy density characteristics of the cell. Practical separators have a composite multilayer configuration. A silver-stopping layer of cellophane or non-woven synthetic polyamide is located next to the positive electrode which reduces soluble silver species back to the metal. A potassium titanate paper layer may be placed next to the zinc electrode, and a number of cellophane layers which swell in aqueous KOH make up the middle section. In most cells the separators are fabricated as envelopes or sacks which completely enclose the zinc electrodes. 

Modified processing techniques have been useful for thermoplastic starch polymers. Recent work [45, 46] has examined the use of coextruded sheet processing to produce polyester / thermoplastic wheat starch / polyester multilayer films. They found that adhesion strength between the layers and stability of the interface were crucial properties in controlling the final performance properties of the films. Work by Sousa [47] has examined use of the novel shear controlled orientation injection molding (SCORIM) process to control morpholoiges and provide tensile property increases of thermoplastic starch/synthetic blends. 

In the following sections, we give an overview of the various attempts to fabricate crosslinked layers for use in multilayer OLEDs categorized by the reactive group used in the precursor materials. We start with the [2+2] cycloaddition of cinna-mates and the radical polymerization of acrylates and styrene derivatives. The emphasis of the chapter is on our own work, which is focused on the cationic ringopening polymerization (CROP) of oxetane-functionalized materials. Finally, we summarize the less-frequently employed synthetic routes. 

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