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After you set polar tracking settings, discussed earlier in this chapter in the Polar tracking section, you can snap to increments along the polar angles you have set. When PolarSnap is on, the polar tooltip only shows distances in increments of the snap setting. When you see the distance you want, just click. PolarSnap makes it easy to draw accurately without having to type coordinates. To use PolarSnap, follow these steps: 1. Right-click the SNAP button on the status bar and click Settings to open the Drafting Settings dialog box with the Snap and Grid tab displayed, as just explained. 2. Check PolarSnap in the Snap type & style section of the dialog box (refer to Figure 4-18). 3. Type a number in the Polar Distance text box. 4. Click OK to close the dialog box. 5. Click SNAP on the status bar. Note that PolarSnap and Grid snap are mutually exclusive. If PolarSnap is on, the cursor will not snap to the grid. Used with polar tracking, PolarSnap is a powerful tool. Remember that you can polar track along orthogonal as well as other angles.
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he promise of a brand is the idea that it can be trusted and will make your life better. Everyone from banks to your sneaker to your morning orange juice maker want to develop a long-term relationship with you. Brands promise you value. They work to develop an impression that will lodge so powerfully in your mind that you unconsciously turn to them, engage in their story, and adopt the set of values upon which pivots their relationship with you. Building a long-term relationship is the goal of all brands. Put simply, a brand is an organization s story. It promises value to you for the purpose of building a relationship. Because people can interact with your organization online, nonprofits have tremendous potential to create relationships that will sustain your work. The key to building this relationship is an emotional engagement with your audience. In order to mobilize the audience into becoming involved as either a donor, a volunteer or member, a nonprofit must first understand that the audience they are trying to reach and engage receives many hundred messages a day asking them in one way or another to buy into a relationship. This is because building relationships that deliver value is the very lifeblood that pumps through the heart of the branding exercise. Virtually all keepers of brands have recognized the power that the Internet holds in building relationships with their different audiences. It is a noisy landscape to be sure, but nonprofit organizations have a story to tell that sets them apart from consumer-product driven brands. (i.e. Ivory Snow, Levis, and Ford). Consumer-driven brands must create a story that has some value to you for the sole purpose of building a relationship that is predicated on you purchasing their product. Nonprofits, by contrast, have embedded in their very culture, articulated with their mission statements, and delivered through their programs, brands that are saturated with values that can serve to build relationships that are instead based on you as a member of
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MECHANICAL MOLECULAR MODELS AND QUANTUM ASPECTS OF CHEMISTRY
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65. P. G. Ryan, A. D. Connell, and B. D. Gardner, Marine Pollution Bull. 19, 174 176 (1988). 66. K. W. Kenyon and E. Kridler, Auk 86, 339 343 (1969). 67. R. H. Day, D. H. S. Wehle, and F. C. Coleman, in R. S. Shomura and H. O. Yoshida, eds., Proceedings of the Workshop on the Fate and Impact of Marine Debris, Honolulu, Hawaii, 1984. U.S. Department of Commerce. NOAA-TMNMFS-SWSFC-54, 1985, pp. 344 386. 68. D. G. Ainley, L. B. Spear, and C. A. Ribic, in R. S. Shomura and M. L. Godfrey, eds., Proceedings of the Second International Conference on Marine Debris, Honolulu, Hawaii, 1989, U.S. Department of Commerce. NOAA-TM-NMFS-SWSFC154, 1990, pp. 653 664. 69. S. Reed, Notornis 28, 239 240 (1981). 70. D. G. Ainley, W. R. Fraser, and L. B. Spear, in R. S. Shomura and M. L. Godfrey, eds., Proceedings of the Second International Conference on Marine Debris. Honolulu, Hawaii, 1989, U.S. Department of Commerce, NOAA-TM-NMFS-SWSFC154, 1990, pp. 682 691. 71. P. A. Prince, Ibis, 122, 476 488 (1980). 72. C. J. R. Robertson and B. D. Bell, in J. P. Croxall, P. G. H. Evans, and R. W. Schreiber, eds., Status and Conservation of the World s Seabirds, International Council for Bird Protection, Technical Publication, No. 2, Cambridge, England, 1984, pp. 573 586. 73. M. P. Morin, Elepaio, 47, 107 108 (1987). 74. Z. Lucas, Marine Pollution Bull. 24, 192 199 (1992). 75. J. E. Winston, M. R. Gregory, and L. M. Stevens, in J. M. Coe and D. B. Rogers, eds., Marine Debris: Sources, Impacts and Solutions, Springer, New York, 1997, pp. 81 97. 76. M. R. Gregory, Marine Environ. Res. 10, 399 414 (1983). 77. J. E. Winston, Marine Pollution Bull. 13, 348 351 (1982). 78. D. K. A. Barnes and W. G. Sanderson, Proceedings of the 11h International Bryozoology Association Conference, Panama City, Panama, 2000, pp. 154 160. 79. A. Ing lfsson, Marine Biol. 122, 13 21 (1995). o 80. P. Uneputty and S. M. Evans, Marine Environ. Res. 44, 233 242 (1997). 81. E. J. Carpenter and K. L. Smith, Science 175, 1240 1241 (1972). 82. E. J. Carpenter, S. J. Anderson, G. R. Harvey, H. P. Miklas, and B. B. Peck, Science 178, 749 750 (1972). 83. Y. Mato, T. Isobe, H. Takada, H. Kanehiro, C. Ohtake, and T. Kaminuma, Environ. Sci. Tech. 35, 318 324 (2001). 84. P. G. Ryan, Marine Environ. Res. 25, 249 273 (1988). 85. J. P. Ludwig, C. L. Summer, H. J. Auman, V. Gauger, D. Bromley, J. P. Giesy, R. Rolland, and T. Colborn, in G. Robertson and R. Gales, eds., Albatross Biology and Conservation, Surrey Beatty, Norton, Australia, 1998, pp. 225 238. 86. J. T. Hardy, Prog. Oceanogra. 11, 307 328 (1982). 87. J. T. Hardy, Marine Environ. Res. 23, 223 225 (1987). 88. J. N. Cross, J. T. Hardy, J. E. Hose, G. P. Hershelman, L. D. Antrim, R. W. Gossett, and E. A. Crecelius, Marine Environ. Res. 23, 307 323 (1987).
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In the last couple of decades a lot of attention has focused on the research of molecules as a potential future component in electronic devices; this research is motivated, as covered earlier, by the possible economical and physical limits of the minimization of the current solid-state electronic devices, including, among a host of other issues, the increasingly complex and expensive lithography processes, the doping uctuations, and the short inversion-channel e ect [237]. Molecular electronics is a potentially interesting alternative to traditional silicon-based semiconductors because the proposed molecular electronic structures occupy an area less than thousand times of the area currently used in solid-state semiconductor integrated circuits [237]. Key structures of interest include: (i) molecules as wires/switches and (ii) recti ers, diodes, rectifying diodes, and resonant tunneling diodes. Molecular nanoelectronics was proposed by Aviram and Ratner in 1974 as a way to produce a recti er from organic molecules. The rst example of a single molecular electronic device appeared in 1990. Several approaches have been studied in the past few years. The major challenge relates to the di culty of making individual electrical contacts to molecules, these being only be a few nanometers in size. The development of the scanning tunneling microscope (STM) enabled the rst advancements in this eld and has remained one of the major tools for characterizing single molecules. Some of the rst demonstrations of electronic properties of single molecules by Purdue University included Coulomb blockade and Coulomb staircase. A second set of experiments at IBM have demonstarted a STM tip deforming a C60 buckyball; the resulting mechanical deformation modi es the resonance tunneling bands of the molecule and produces electromechanical ampli cation. While these devices demonstrate functionality that may be used in circuits, the scaling to the level of present CMOS circuits appears to be out-of-reach at this time. Another approach to molecular electronics is the use of organic molecules. Yale and South Carolina Universities have reported the conduction through a benzene molecule attached to two gold electrodes using thiol groups to bind the molecule to the gold. Benzene rings have delocalized electrons out of the plane of the molecule through which electrons can be transported when an appropriate bias is applied across the molecule. Carbon carbon double and triple bonds provide similar orbitals out of the plane and, therefore, combinations of these polyphenylene molecules create conducting wires now known as Tour wires (named after James Tour). Molecules
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23 Creating 3D Surfaces
(5.23)
Figure 8-12: The Viewports dialog box makes it easy to choose a configuration. The Viewport dialog box is usually the best place to start creating viewports. However, if the standard configurations do not meet your needs, you can use one of them as a starting point and then use the other options. Notice the Apply To drop-down list at the bottom-left corner of the Viewports dialog box in Figure 8-12. By default, the tiled viewport configurations apply to the entire display, meaning that they replace your current configuration. You can also choose to apply the configuration to the current viewport. The active viewport has a bold border and crosshairs. To make a viewport active, click anywhere inside that viewport. Then choose View Viewports New Viewports, choose Current Viewport from the Apply To drop-down list, and choose the configuration that you want for that viewport. Let s say that you have four equal viewports, and the top-left viewport is active. If you choose the Four: Equal configuration from the Viewports dialog box while the top-left viewport is active and apply it to the current viewport, the top-left viewport is divided into four viewports. Now you have seven viewports in the drawing.
our attention to a rst-order ODE IVP here, and so it is actually enough to assume that R. Finally, observe that AB and AM methods can be combined to yield predictor correctors. An mth-order AB method can act as a predictor for an mth-order AM method that is the corrector. A Runge Kutta method can initialize the procedure.
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