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The third important source for infonnation on modem Raman spectroscopy are the books cataloguing the proceedings of the International Conference on Raman Spectroscopy (ICORS) [37]. ICORS is held every two years at various international locations and feahires hundreds of contributions from leading research groups covering all areas of Raman spectroscopy. Although the published presentations are quite limited in lengdi, they each contain references to the more substantial works and collectively provide an excellent overview of current trends m Raman spectroscopy. A snapshot or brief sununary of the 1998 conference appears at the end of this chapter. [Pg.1196]

The excellent electrical insulation properties of polyethylene have led to extensive use in cable and other wire-covering applications. Spectacular early uses included undersea cables and airborne radar and the materials continue to be used in substantial quantities. One particular trend is the increasing use of cross-linked polyethylene for this area of use. Such materials have improved heat resistance and in addition have given generally better resistance to stress cracking. Cellular polyethylene is used as the insulator for television downlead aerials. [Pg.244]

Two new sections on the protection of phosphates and the alkyne-CH are included. All other sections of the book have been expanded, some more than others. The section on the protection of alcohols has increased substantially, reflecting the trend of the nineties to synthesize acetate- and propionate-derived natural products. An effort was made to include many more enzymatic methods of protection and deprotection. Most of these are associated with the protection of alcohols as esters and the protection of carboxylic acids. Here we have not attempted to be exhaustive, but hopefully, a sufficient number of cases are provided that illustrate the true power of this technology, so that the reader will examine some of the excellent monographs and review articles cited in the references. The Reactivity Charts in Chapter 10 are identical to those in the first edition. The chart number appears beside the name of each protective group when it is first introduced. No attempt was made to update these Charts, not only because of the sheer magnitude of the task, but because it is nearly impossible in... [Pg.785]

In the cyclization of the corresponding cis-epoxides, with the aim of obtaining the corresponding cis-2,3-disubstituted tetrahydropyrans, a similar trend was observed. For these systems, however, the 6-endo pathway was less favored, which was ascribed to difficulties in attaining a TS conformation that would allow for maximum stabilization of the developing p-orbital with the adjacent 7t-system. Alternatively, palladium-catalyzed cyclization of the tetrabutylammonium alkoxide derived from 33b results in the corresponding ris-2,3-disubstituted tetrahydro-pyran in excellent yield and selectivity (90%, dr >99 1), while the ris-epoxide gives stereoisomer 37b (86%, dr 98 2) [112]. [Pg.333]

The basic reason for this migration trend is that RO systems are now available from a host of OEM manufacturers in a wide variety of relatively low-cost, skid-mounted, modular forms, and are excellent at bulkwater TDS removal. [Pg.361]

This area of reactivity has been the subject of excellent reviews (J5). Silyl enol ethers are not sufficiently nucleophilic to react spontaneously with carbonyl compounds they do so under the influence of either Lewis acids or fluoride ion, as detailed above. Few clear trends have emerged from the somewhat limited number of definitive studies reported so far, with ambiguities in diastereoisomeric assignments occasionally complicating the issue even further. [Pg.68]

An important source of reference is another excellent review by Stern [844] this one is concerned with the high temperature properties of oxy-halides. The following general trends are found in salts containing an XO anion (X = Cl, Br and I) there are variations in stabilities in the sequences (i) (X =) Cl > Br > I for halogens in the same oxidation state, and (ii) XO4 > XOJ > XO2 > XCT for the different oxidation states of a particular halogen. [Pg.186]

The overall trend is explainable, at least qualitatively, with simple unimolecular decay theory. When a correction term is incorporated into the theoretical collision limit to account for the intrinsic surface site reactivity in the bulk, excellent agreement is obtained with the overall reactivity. In considering the overall trends, certain clusters, namely Cu+, Cuj, and Cu in particular, displayed somewhat anomalous reactivities which might be associated with structural and/or electronic effects. [Pg.230]


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