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Gold complexes, in carbonylation, 391 Green chemistry, 807 Grignard reagent carbomagnesation with, 331 metallation with, 250, 598 Gross formylation, 416 Group IA cations, as promoters in methane coupling, 110 Group IIA oxides, in methane coupling, 110 Group III halides, as additives in hydrosilylation, 326 Groups I-IV organometallics and hydrides, as cocatalysts in metathesis, 699 Group IV halides, as additives in hydrosilylation, 326 Group IVB halides, as additives in carboxylation, 382 in hydroformylation, 372 Group VIA oxides on alumina, in butylenes-isobutylene isomerization, 176 Group VIII metals activity of, in hydrogenolysis, 656, 657 in carboxylation of alkenes, 381 in catalytic hydrosilylation, 323 in CO reduction, 102 in dissociative adsorption of CO, 116 in hydroformylation, 371 in hydrogenation of dienes, 627 in isomerization of n-butenes, 187 methanation activity of, 108 Grubbs catalyst, 712, 714 Halcon-Arco process, for manufacture of propylene oxide, 508 Halcon process for manufacture of maleic anhydride, 515 for manufacture of propionic acid, 385 Half-hydrogenated intermediate, in CO hydrogenation, 105 Half-hydrogenated state, 185,621 N-Halo amides, halogenation with, 580 Haloboranes, addition of, to alkynes, 327 Haloboration, 327 Halogenation of alkanes, 577, 585, 592 of alkenes, 304, 337 addition complexes in, 337, 338 free-radical, 307 of alkynes, 310 allylic, 590, 594 of aromatics, 580, 584, 585, 589, 594 of dienes, 308 Halometallation, 327, 345

Description ID value unique to this document Space-separated list of classes useful for selecting this element for style and other purposes Local style information Advisory title, typically rendered by a graphical browser when the pointer is over the element

To access a glyph set, simply click the desired glyph set from the Show pop-up menu in the Glyph panel. Make sure the Type tool is active and that the text cursor (text-insertion point) is active in a text frame or path. Double-click the desired glyph in the Glyphs panel; InDesign will insert it at the text cursor location.

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Click the New button to define a new custom function or select an existing custom function from the displayed list and then click the Edit button to modify that function. If you wish to create a slightly modified version of an existing function, you can make a copy of an existing custom function by selecting that function and then clicking the Duplicate button. The Edit Custom Function dialog is shown in Figure 26-4, as it would appear if you were creating a new function. If you re editing an existing function, the Function Name text box, the Function Parameters list, and the New Function text box display the function s current name, parameter list, and definition (as it does in the top part of Figure 26-2). Proceed as follows to define your new function.

than are known by other methods to be present in any particular sample. The observation of membrane proteins by standard 2D gels is hindered by solubility. First, these proteins are not solubilised in the buffer (for the rst dimension). Second, solubilised membrane proteins will all too easily precipitate again at their isoelectric point pI. One approach to solving the initial problem is solubilising membrane proteins in either organic solvents or non-ionic/zwitterionic detergents. The pI problem may be avoided by just using 1D gels. However, even if membrane proteins are clearly resolved within a gel, further problems are encountered during the digestion steps because oligo-/polypeptides in digests tend to be particularly hydrophobic (Figure 9.23). An alternative to using gels is shotgun proteomics (i.e., in situ digestion of complex mixtures of proteins followed by 2D liquid chromatography mass spectrometry (2D LC-MS) to identify proteins in particular samples (Figure 9.24). Again, initial solubilisation is an

As you can see, there are a few twists to this notion of making HTML both human- and machine-readable, but it s still a workable proposition. Now, you can find the conclusion of this module in Listing 18-13.

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The structure of the parse tree is important for the Code Generator to be able to generate the bytecodes in the correct order for execution When the Code Generator has nished examining the parse tree, the result is a complete VDBE program that can be passed to the Virtual Machine for execution An important function of the Code Generator is that it tries to optimize the program that it produces by using its knowledge of the target databases to ensure that the code makes the most ef cient use of the database schemas and indices This key part of the Code Generator is referred to as the Query Optimizer.

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The following three scripts, taken from Adobe s InDesign script examples, do the same thing in JavaScript, AppleScript, and VBA they rotate an EPS graphic and its frame.

2. Open the Bevels.ai file. 3. Create the path you want to be your bevel in the Bevels.ai document. 4. Turn that path into a symbol. Do this by choosing Window Symbols. Either drag the path to the Symbols panel or select the path and then click the New Symbol button in the Symbols panel. Or with the path selected, choose New Symbol from the Symbols panel s pop-up menu.

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