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Intermediate connectivity

Fe2L2) and longer chain the monomeric (FeL) form. When the intermediate connecting chain is -(CH2)6- (39), a crossover point between Fe2L2 and FeL is reached where both are present (52). [Pg.207]

Figure 16-31 (A) Structure of molybdopterin cytosine dinucleotide complexed with an atom of molybdenum. (B) Stereoscopic ribbon drawing of the structure of one subunit of the xanthine oxidase-related aldehyde oxidoreductase from Desulfo-vibrio gigas. Each 907-residue subunit of the homodimeric protein contains two Fe2S2 clusters visible at the top and the molybdenum-molybdopterin coenzyme buried in the center. (C) Alpha-carbon plot of portions of the protein surrounding the molybdenum-molybdopterin cytosine dinucleotide and (at the top) the two plant-ferredoxin-like Fe2S2 clusters. Each of these is held by a separate structural domain of the protein. Two additional domains bind the molybdopterin coenzyme and there is also an intermediate connecting domain. In xanthine oxidase the latter presumably has the FAD binding site which is lacking in the D. gigas enzyme. From Romao et al.633 Courtesy of R. Huber. Figure 16-31 (A) Structure of molybdopterin cytosine dinucleotide complexed with an atom of molybdenum. (B) Stereoscopic ribbon drawing of the structure of one subunit of the xanthine oxidase-related aldehyde oxidoreductase from Desulfo-vibrio gigas. Each 907-residue subunit of the homodimeric protein contains two Fe2S2 clusters visible at the top and the molybdenum-molybdopterin coenzyme buried in the center. (C) Alpha-carbon plot of portions of the protein surrounding the molybdenum-molybdopterin cytosine dinucleotide and (at the top) the two plant-ferredoxin-like Fe2S2 clusters. Each of these is held by a separate structural domain of the protein. Two additional domains bind the molybdopterin coenzyme and there is also an intermediate connecting domain. In xanthine oxidase the latter presumably has the FAD binding site which is lacking in the D. gigas enzyme. From Romao et al.633 Courtesy of R. Huber.
To install streams for feeds, product, and intermediate connections, click the arrow to the right of the Material Streams box on the bottom left of the window and select Material. Moving the cursor to the flowsheet produces a number of arrows on the inlets and outlets of the various blocks. A feedstream is installed by first clicking the flowsheet and then clicking the arrow pointing to a feed valve. Figure 2.32 shows stream 1 connected to valve VI. Figure 2.33 shows the final flowsheet with all lines installed and some streams renamed for clarity. Save the file in an appropriate directory. [Pg.74]

The (conjugated-diene)zirconocene and -hafnocene systems reviewed above are unique in that three isomeric organometallic species can be distinguished by physical and/or chemical means. Two of these, 3 and 5, represent stable isolable molecules, while the third, (T) -diene)MCp2 (4), functions as a chemically detectable intermediate connecting the (rf-diene)metallocene isomers (see Scheme 1). [Pg.33]

Intermediate connective tissues, muscle, blood, cartilage, cholesterol stones, uric acid stones. [Pg.486]

Entry 6 reminds us that the furanose and pyranose forms of carbohydrates are specialized examples of hemiacetals and capable of interconversion. Entries 7 and 8 connect enolization of the open-chain form to interconversion of C-2 epimers. Entry 9 illustrates another reaction involving the enol of the open-chain form. Here, the enediol intermediate connects aldose and ketose isomers. In entry 10, an enzyme-catalyzed reverse aldol reaction cleaves a 6-carbon chain to two 3-carbon fragments. [Pg.976]

Figure 146 is a diagram of the equipment showing intermediate connections between the various parts and the path of the carrier gas. The oven contains the preliminary partition column, a ten-way valve, and two adsorption columns. Nickel catalyst remains ouside, as its working temperature is different from that within the oven. [Pg.387]

Figure 7. The relative contribution of isolated W to the interfacial area depends strongly on W connectivity. Under intermediate connectivity, significant quantities of W become isolated as pendular rings only small W saturation. Figure 7. The relative contribution of isolated W to the interfacial area depends strongly on W connectivity. Under intermediate connectivity, significant quantities of W become isolated as pendular rings only small W saturation.

See other pages where Intermediate connectivity is mentioned: [Pg.2]    [Pg.569]    [Pg.332]    [Pg.208]    [Pg.12]    [Pg.103]    [Pg.159]    [Pg.3]    [Pg.356]    [Pg.3872]    [Pg.84]    [Pg.501]    [Pg.723]    [Pg.525]    [Pg.3871]    [Pg.116]    [Pg.119]    [Pg.413]    [Pg.83]    [Pg.34]    [Pg.35]    [Pg.36]   
See also in sourсe #XX -- [ Pg.32 ]




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