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28 C Masters, Homogeneous Transition-Metal Catalysis: a Gentle Art, Chapman & Hall, London, 1981, p 40 29 R S Dickson, Homogeneous Catalysis with Compounds of Rhodium and Iridium, Reidel, Dordrecht, 1985, 3, p 40 30 P A Chaloner, Handbook of Coordination Catalysis in Organic Chemistry, Butterworths, London, 1986, 2, p 9 31 A Spencer, in Comprehensive Coordination Chemistry, Vol 6: Applications, G Wilkinson, R G Gillard, and J A McCleverty, eds, Pergamon Press, Oxford, 1987, 612, p 229 32 H Takaya and R Noyori, in Comprehensive Organic Synthesis, B M Trost and 1 Fleming, eds, Vol 8: Reduction, 1 Fleming, ed, Pergamon Press, Oxford, 1991, 32, p 443 33 G W Parshall and S D Ittel, Homogeneous Catalysis, Wiley-Interscience, New York, 1992, 3, p 25 34 D J Pasto, in Comprehensive Organic Synthesis, B M Trost and 1 Fleming, eds, Vol 8: Reduction, 1.

The list in the Pattern Brush Options dialog box allows you to choose from four existing patterns instead of the selected artwork: None, Original, Polka Dot Pattern, and Waves Pattern. Any pattern in your document is listed here.

Fleming, ed, Pergamon Press, 1991, 33, p 471 35 P W Rabideau, Tetrahedron 45, 1579 (1989) 36 P W Rabideau and Z Marcinow, Org React (NY) 42, 1 (1992) 37 L N Mander, in Comprehensive Organic Synthesis, B M Trost and 1 Fleming, eds, Vol 8: Reduction, 1 Fleming, ed, Pergamon Press, 1991, 34, p 489 38 D N Kursanov and Z N Parnes, Russ Chem Rev (Engl transl) 38, 812 (1969) 39 D N Kursanov and Z N Parnes, N M Loim, Synthesis 633 (1974) 40 D N Kursanov, Z N Parnes, M 1 Kalinkin, and N M Loim, Ionic Hydrogenation and Related Reactions, Harwood, Chur, 1985 41 W A Lazier and H R Arnold, Org Synth, Coli Vol 2, 142 (1943) 42 J Oudar, Catal Rev-Sci Eng 22, 171 (1980) 43 C H Bartholomew, P K Agrawal, and J R.

Katzer, Adv Catal 31, 135 (1982) 44 J Barbier, E Lamy-Pitara, P Marecot, J P Boitiaux, J Cosyns, and F Vema, Adv Catal 37,279 (1990) 45 W J Kirkpatrick, Adv Catal 3, 329 (1951) 46 P C H Mitchell, in Catalysis, A Specialist Periodical Report, Vol 1, C Kemball, senior reporter, The Chemical Society, Burlington House, London, 1977, 6, p 204; Vol 4, C Kemball and D A Dowden, senior reporters, The Royal Society of Chemistry, Burlington House, London, 1981, 7, p 175 47 R Adams, V Voorhees, and R L Shriner, Org Synth, Coli Vol 1,463 (1941) 48 H R Billica and H Adkins, Org Synth, Coli Vol 3, 176 (1955) 49 S V Lebedev, G G Kobliansky, and A O Yakubchik, J Chem Soc 417 (1925) 50 J Horiuti, G Ogden, and M Polanyi, Trans Faraday Soc 30, 663 (1934) 51 J Horiuti and M.

Quite often in tables, a column or row functions as the heading for that section of the table, labeling all the information in that particular section. Dreamweaver has an option for designating these cells: the Header option. Table header cells are usually rendered in boldface and centered in each cell. Figure 13-16 shows an example of a table in which both the first row and first column are marked as table header cells.

Polanyi, Trans Faraday Soc 30, 1164 (1934) 52 M Bartok and A Molnar, in Stereochemistry of Heterogeneous Metal Catalysis, Wiley, Chichester, 1985, 3, p 53 53 S Nishimura, H Sakamoto, and T Ozawa, Chem Lett 855 (1973) 54 J J Rooney and G Webb, J Catal 3, 488 (1964) 55 P B Wells and G R Wilson, Disc Faraday Soc 41, 237 (1966)..

An additional routing circuit is needed if the amount of shifting is not fixed. The design of a barrel shifter is discussed in Section 3.7.3.

Figure 15-5 Sampling errors introduced by an end-sampling thief differ from those introduced by a side-sampling thief, but persist nonetheless. In this type of thief, a window is opened at the bottom of the sampling tube, and particles are forced into a cavity by further insertion of the thief. This eliminates the bias toward particles that passively ll a cavity more easily than others, but on the other hand, (a) these thieves entrain more particles during insertion, and (b) their performance again suffers from substantial systematic error.