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In the last section you looked at ways of presenting your XML files to human consumers. Often the clients for your XML documents are other machines. You've seen that if you know the DTD for a given XML file then you can easily write an application that extracts the information you need. If you are processing hundreds of resumes each day, you may want to pre screen the submissions to make certain that they meet some minimal qualification before you hand process them. Consider the difficulties that will arise when you interact with another organization that is processing r sum s that have been validated against a different DTD, one that the organization has developed in house. In this section, you are concerned with transforming XML documents so that they can be read and understood. This time, however, you aren't concerned with how they look but in how the data is structured. Although this type of transformation is usually applied to data centric XML documents, you can continue with the Richard III example by converting a document that conforms to the existing play.dtd to a document that conforms to a new DTD that you'll define.

Transition metal coordination compounds of metals with two or more oxidation states have proven particularly versatile in photopolymerizations of unsaturated organic compounds (38) and should be useful for polymerizing vinyl derivatives of both nonmetal and metal inorganic species. To illustrate, a photoactivated platinum-catalyzed hydrosilylation polymerization of vinyldimethylsilane (Fig. 2.24) has been shown to remain catalytically active for an extended time period. The vinyl and hydride end-groups continue to link for several months, with the weight-average molecular mass (M W increasing from 5500 to 12,300 during that time (39). A ring-opening carbosilane photopolymerization will be discussed below (Section 2.3). Mesogenic metal Schiff-base derivatives with monoacrylate end groups (Fig. 2.24) can be polymerized photochemically in a melt blend with 3% of a uorinated diaryltitanocene photoinitiator that generates radicals for the polymerization (40). The insoluble nature of the products means that the polymerization results were based on optical properties and the evolution of heat

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26 Mittal, K L Silanes and Other Coupling Agents; Mittal, K L, Ed, VSP: Utrecht, 1992 27 Plueddemann, E P Silane Coupling Agents; 2nd ed, Plenum Press: New York, 1991 28 Arkles, B CHEMTECH 1977, 7, 766 29 McCarthy, T J, Chimia 1990, 44, 316 and references cited therein 30 Wang, B, Archer, R D Polym Mater Sci Engr 1988, 59, 120; 1988, 60, 710 31 Archer, R D, Wang, B Polym Mater Sci Engr 1989, 61, 101 32 Archer, R D, Wang, B Chem Mater 1993, 5, 317 33 Archer, R D, Tong, W, Tan, U-K Poly Mater Sci Engr 1996, 75, 383 34 Byrd, H, Hollowary, C E, Pogue, J Polym Prepr 1999, 40(1), 167 35 Katz, H E, Schilling, M L, Chidsey, C E D, Putvinski, T M, Hutton, R S.

= {W (t) : t 0} {BH (t) : t 0} M 0 M 0 MT Mu,1 (X, S), Mu,2 (X, S), Hn (x), Hn (x), GOE, In , d {e1 , . . . , en } u (Z, B)

Chem Mater 1991, 3, 699 36 Tesk, J A, Antonucci, J M, Eichmiller, F C, Kelly, J R, Rupp, N W, Waterstrat, R W, Fraker, A C, Chow, L C, George, L A, Stansbury, J W, Parry, E E in Kirk-Othmer Encyclopedia of Chemical Technology; Kroschwitz, J I and Howe-Grant, M, Ed, John Wiley & Sons: NY, 1993; Vol 7, pp 996 1022 37 Teraoka, F, Takahashi, J Dent Mater 2000, 16, 145 and references cited therein 38 Haug, S P, Andres, C J, Moore, B K J Prosthetic Dentistry 1999, 81, 431 39 Matsumura, H in Polymer Materials Encyclopedia; Salamone, J C, Ed, CRC Press: Boca Raton, 1996, pp 1834, 1836 lists 16 silanes and 1 siloxane oligomer used as dental adhesives 40 Zhang, C, Laine, R M Polym Prepr.

The usual argument to compute det(C s,t ) as the square of the volume in of the set of linear combinations of the form i=n i us,t with 0 i 1 i=3 i (i = 3, . . . , n) shows that E det(C s,t ) 1 + M = (n 2)!