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materials was obtained by using azobenzene derivatives with different types of the electron-withdrawing groups in the para-position of the azobenzene units It has been shown that the SRG formation is more effective in materials having strong electron-donating substituents in azobenzene moiety Two published works reviewed in the following text demonstrated additional possibilities given by supramolecular approach, and with these works the review of reported results on the surface relief structures in supramolecular azobenzenecontaining materials is completed The supramolecular approach based on the ionic interactions (Kulikovska et al, 2007; Stumpe et al, 2006a) was additionally extended to polyelectrolytes formed in situ by sol gel reaction of alkoxysilanes (Kulikovska et al, 2008a; Stumpe et al, 2006a) The complex is shown in Fig 217 Similarly, different commercially available ionic azobenzene derivatives were used as active components (Stumpe et al, 2006a).

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The aminosubstituted alkoxysilane (3-aminopropyl)triethoxysilane (APTES) was used as an example of a passive component The materials were produced by mixing of alcoholic solutions of the azobenzene derivatives and APTES followed by sol gel reaction catalyzed by HCl No glass transition has been observed for the investigated materials (Kulikovska et al, 2008a) In addition to the ionic azobenzene polyelectrolyte complexes here, the charged chromophores form the ionic complexes with amino groups of polymer chains But at the same time the polysiloxane network is formed by polycondensation This additional irreversible cross-linking of polymer backbones differ the materials from all other supramolecular materials used for SRG formation The degree of condensation and the degree of cross-linking could be tuned by the choice and amount of catalyst, by the choice of the solvent, and by the thermal treatment or aging of lms Up to 12-mm deep SRGs were inscribed into these materials.

(5.2.43)

Rackable is focused on large-scale customers who are very technically sophisticated and know exactly what they want in a blade system: what processors, what speed I/O, how much memory, and so on. This allows Rackable to build a customized solution to fit their customers specific application and infrastructure requirements.

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a,l c,2 (5.2.44)

Figure 218 presents an example of 2-D relief structure induced by successive recording of linear gratings The reported polarization dependence of.

This condition expresses the fact that reaction (5.2.39) determines the rate of the overall process. On neglecting kal in the denominator of Eq. (5.2.43), substitution of

Rackable s high-density, side-to-side, and back-to-back design efficiently uses all possible space within a rack to provide more processing power in a smaller footprint. For customers who want many of the benefits of blades with the standardization of rack servers, Rackable s Scale Out Series provides an extremely customizable hybrid solution.

Figure 2.17. Schematic presentation of supramolecular Methyl Red sol gel material. Source: Kulikovska, 2008a. Reprinted with permission from American Chemical Society.

(5.2.45)

500 0

Verari Systems is making its mark in the blade market using commercial offthe-shelf (COTS) components, putting their value-add into the chassis, power, and cooling design. Verari has been around since 1996 and shipped their first blade product, the BladeRack, in 2002. With only 250 employees, they have worked hard to be ranked sixth in the market by IDC and Gartner (2005). Their high-end blade solution can accommodate up to 176 processors with more than 1.4 Teraflops (Tflops) of computing power in a standard seven-foot (48U) cabinet, making them the first to offer this level of power in a standard rack configuration (see Figure 16.6). The bulk of their sales have been to three customers who have deployed more than 10,000 Verari blades.

(5.2.47)

Figure 2.18. Relief structure recorded in lm of the Methyl Red sol gel material (Fig. 2.17). Topology of the grating is presented on the left, cutting of the grating in 3-D view in the middle, and photograph of diffraction by the grating on the right. Source: Kulikovska et al., 2008b. Reprinted with permission from 2008 SPIE. See color insert.

converts Eq. (5.2.46) to Eq. (5.2.24) for n = 2. A similar result would be obtained if the rate of the overall reaction were controlled by the reaction (5.2.40). Thus, assuming the validity of Eqs. (5.2.42) and (5.2.44), the stepwise transfer of electrons can formally yield the same dependence of the current on the potential as for direct transfer of several electrons in one step. This is a very common case in irreversible, multielectron electrode reactions. The rate-controlling process is often the first step in which, for example, a single electron is accepted, while the other reactions connected with the acceptance of further electrons are very fast and the rate of the reverse (here oxidation) reaction is negligible. Equation (5.2.46) gives

Verari offers everything on a blade, from workstations (thin clients or client blades), to servers, to storage. All BladeRack solutions are built with COTS components, eliminating the cost associated with building and servicing proprietary hardware. They currently have a patent pending on their design that allows the use of standard motherboards, positioned vertically in the chassis and using standard interface cards, NICs, HBAs, and HCAs, with all cables built into the rack. The motivation for building the BladeRack architecture around COTS components was to impose no limitations on the configurations, or as Verari describes it, blades without boundaries. To sustain the power requirements of the BladeRack, Verari uses high-voltage DC power to the blade to mitigate power loss. The BladeRack supports up to 25kVA, 208V three-phase power with automatic balancing.

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