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Referred to in the Text

Table 2 contains an alphabetical listing of carbides referred to in the text. [Pg.438]

The chemistry of vomicine is dealt with in a series of papers by Wieland and collaborators published in LiMg s Annalen. These parts are referred to in the text of the article where necessary. Part I (with Oertei.), 1929, 469, 198 VI, VII, VIII (with CA1.TET and Moyer), 1981, 491, 107, 117, 129 EX, X (with HfimcBEB and... [Pg.595]

Figure 9-96. Vapor-liquid equilibrium showing X and application cases referred to in the text. Used by permission, Koshy, T. D., and Rukovena, F. Jr., Hydrocarbon Processing V. 85, No. 5 (1986) p. 64 all rights reserved. Figure 9-96. Vapor-liquid equilibrium showing X and application cases referred to in the text. Used by permission, Koshy, T. D., and Rukovena, F. Jr., Hydrocarbon Processing V. 85, No. 5 (1986) p. 64 all rights reserved.
This rule can then Ik alternatively referred to in the text as R90. [Pg.44]

Figure 8.20 (Solid + liquid) phase equilibria for [.viQHf, +. yl.4-C6H4(CH,)2 - The circles are the experimental results the solid lines are the fit of the experimental results to equation (8.31) the dashed lines are the ideal solution predictions using equation (8.30) the solid horizontal line is at the eutectic temperature and the diamonds are (.v, T) points referred to in the text. Figure 8.20 (Solid + liquid) phase equilibria for [.viQHf, +. yl.4-C6H4(CH,)2 - The circles are the experimental results the solid lines are the fit of the experimental results to equation (8.31) the dashed lines are the ideal solution predictions using equation (8.30) the solid horizontal line is at the eutectic temperature and the diamonds are (.v, T) points referred to in the text.
Figure 3. Comparison of the amino acid sequence of RHG of A. aculeatus with polygalacturonases PGI, PGII and PGC of A. niger. The most homologous region of the proteins is shown. Numbering is from the first amino acid of the signal peptide. Identical amino acids similar amino acids. The amino acid residues in bold type are referred to in the text. Figure 3. Comparison of the amino acid sequence of RHG of A. aculeatus with polygalacturonases PGI, PGII and PGC of A. niger. The most homologous region of the proteins is shown. Numbering is from the first amino acid of the signal peptide. Identical amino acids similar amino acids. The amino acid residues in bold type are referred to in the text.
Designations used by companies to distinguish their products are often claimed as trademarks. All brand names and product names used in this book are trade names, service marks, trademarks or registered trademarks of their respective owners. The Publisher is not associated with any product or vendor mentioned in this book. All trademarks referred to in the text of this publication are the property of their respective owners. [Pg.7]

Figure 5.11 Individual transferrin receptor domains. Ribbon diagrams for domain I, the protease-like domain (a) domain II, the apical domain (b) and domain III, the helical domain (c). Secondary structure elements are labelled and are referred to in the text first with respect to the domain number, then with respect to the linear order of the elements within the domain. For example aI-3 refers to the third helix in the first domain. In (a), the two grey spheres indicate the positions that would be occupied by Zn2+ in an authentic protease. Reprinted with permission from Lawrence et ah, 1999. Copyright (1999) American Association for the Advancement of Science. Figure 5.11 Individual transferrin receptor domains. Ribbon diagrams for domain I, the protease-like domain (a) domain II, the apical domain (b) and domain III, the helical domain (c). Secondary structure elements are labelled and are referred to in the text first with respect to the domain number, then with respect to the linear order of the elements within the domain. For example aI-3 refers to the third helix in the first domain. In (a), the two grey spheres indicate the positions that would be occupied by Zn2+ in an authentic protease. Reprinted with permission from Lawrence et ah, 1999. Copyright (1999) American Association for the Advancement of Science.
Adapted from Farhataziz et al. (1966). Note that these are observed yields from which the primary yields are calculated and referred to in the text. [Pg.154]

FIGURE 1.1 Structures of organic compounds referred to in the text (a) sucrose (also known as saccharose), (b) dimethyl sulfoxide (DMSO), (c) dimethylformamide (DMF), (d) sorbitol, (e) mannitol, (f) nitrilotriacetic acid (NTA), (g) citric acid, (h) N,N,N, N -fran,s-1,2-diaminocyclohexane-tetraacetic acid (CyTA), (i) saccharic acid, (j) glutamic acid. [Pg.5]

Figure I. Unear absorption spectra for polydiacetylene solutions. The three solutions are referred to in the text as blue, red, and yellow (from left to right in the figure). (Reproduced with permission from Ref. 24. Copyright 1979, American Institute of... Figure I. Unear absorption spectra for polydiacetylene solutions. The three solutions are referred to in the text as blue, red, and yellow (from left to right in the figure). (Reproduced with permission from Ref. 24. Copyright 1979, American Institute of...
Figure 16 Schematic layout of microchip designs for (a) PCRD1 and (b) PCRD2 dimensions in mm. Letters are referred to in the text and identify the solution introduction reservoirs and points where potentials were applied. Indicated channels dimensions are for 10-pm-deep devices, and are not repeated in (b) except where differing from those in (a). (From Ref. 107, with permission.)... Figure 16 Schematic layout of microchip designs for (a) PCRD1 and (b) PCRD2 dimensions in mm. Letters are referred to in the text and identify the solution introduction reservoirs and points where potentials were applied. Indicated channels dimensions are for 10-pm-deep devices, and are not repeated in (b) except where differing from those in (a). (From Ref. 107, with permission.)...
For convenience, the structures discussed in the following sections are listed in Table 3. In many cases, the compounds do not have common or trivial names and are referred to in the text by number. [Pg.188]

Reviews and texts relevant to the early transition elements which have not been referred to in the text include ... [Pg.177]

Label only those compounds (and other structures) in a scheme that are referred to in the text. Do not label all compounds. Use bolded numbers and/or letters (e.g., 2, 3a). Center the labels just below the compounds. [Pg.540]

Citation An authoritative source referred to in the text to indicate work that has influenced the current work or that provides essential background information. [Pg.543]

Hales method was to heat a wide variety of materials and to measure the volume of air given off. His quantitative approach was itself inspired by the example of Isaac Newton, whose Queries in the Opticks he frequently referred to in the text. But his ultimate justification went slightly beyond Newtons authority, to that of God. [Pg.118]

This table includes only those systems for which the kinetics of hydrogen activation have been established a number of other systems are referred to in the text. [Pg.307]

The tie lines between the atomic and molecular orbitals in Figure 5.10 (and all other MO diagrams i i this text) do not take the mixing of MOs into account. The MO diagrams in this book are simplified as far as possible and. wherever there is orbital mixing, the contributions from the vanous atomic orbitals are not always fully indicated by the tie lines. Whenever orbital mixing is important, it is referred to in the text. [Pg.96]

The oxides and oxyacids of boron as well as a variety of hydrated and anhydrous metal borates are discussed herein. An alphabetical list of compounds referred to in the text is given in Table 1. [Pg.188]

Figure 9.1 Spectrum recorded during the decomposition of a solution of propionyl benzoyl peroxide and iodine in o-dichlorobenzene at 100°C. The numbers in parentheses below the formulas indicate the relative spectrum amplitudes for the underlined protons. Spectrum groups referred to in the text are indicated at the top of the figure. Reprinted with permission from H. R. Ward, Accts. Chem. Res., 5, 18 (1972). Copyright by the American Chemical Society. Figure 9.1 Spectrum recorded during the decomposition of a solution of propionyl benzoyl peroxide and iodine in o-dichlorobenzene at 100°C. The numbers in parentheses below the formulas indicate the relative spectrum amplitudes for the underlined protons. Spectrum groups referred to in the text are indicated at the top of the figure. Reprinted with permission from H. R. Ward, Accts. Chem. Res., 5, 18 (1972). Copyright by the American Chemical Society.
Figure 1. The Cs geometry of the pentamethylbenzenium cation with carbons labeled as referred to in the text. Selected bond lengths in A are also shown. (Reproduced from reference 13. Copyright 1995 American Chemical Society.)... Figure 1. The Cs geometry of the pentamethylbenzenium cation with carbons labeled as referred to in the text. Selected bond lengths in A are also shown. (Reproduced from reference 13. Copyright 1995 American Chemical Society.)...
Figure 2. Mutations of PMCA2. Mutations are named as referred to in the text and shown on the structural schematic from Figure 1. Approximate locations of mutations are indicated by circles for point (missense) mutations or triangles for frameshift (truncation) mutations... Figure 2. Mutations of PMCA2. Mutations are named as referred to in the text and shown on the structural schematic from Figure 1. Approximate locations of mutations are indicated by circles for point (missense) mutations or triangles for frameshift (truncation) mutations...
Scheme 8 Proposed dioxygen evolution mechanism for Mnm complexes of LI 1C and formal analogy to Kok states. The (CH2) group is the variable backbone link referred to in the text. (From Ref. 163b.)... Scheme 8 Proposed dioxygen evolution mechanism for Mnm complexes of LI 1C and formal analogy to Kok states. The (CH2) group is the variable backbone link referred to in the text. (From Ref. 163b.)...
Unpublished work referred to in the text has been supported by grants from the United States Public Health Service, the Playtex Park Foundation, and the National Science Foundation. [Pg.135]

Tables II to X give the melting points and, where applicable, the optical rotations of the inositols, inososes, inosamines, and quercitols, and of all of their known O-substituted derivatives. Anhydroinositols, although not substitution products in the strict sense, are included, as are the carbonyl-functional derivatives of the inososes. Halogen- and nitro-substituted cyclitols, and the C-methyl-inositols and their derivatives, are not included most of these compounds are referred to in the text. The derivatives are arranged in the following order salts (inosamines) or functional derivatives (inososes), carboxylic esters, borates, nitrates, sulfonic esters, phosphates, glycosides, acetals (and Schiff bases), ethers (and IV-alkyl derivatives), and anhydrides. Tables II to X give the melting points and, where applicable, the optical rotations of the inositols, inososes, inosamines, and quercitols, and of all of their known O-substituted derivatives. Anhydroinositols, although not substitution products in the strict sense, are included, as are the carbonyl-functional derivatives of the inososes. Halogen- and nitro-substituted cyclitols, and the C-methyl-inositols and their derivatives, are not included most of these compounds are referred to in the text. The derivatives are arranged in the following order salts (inosamines) or functional derivatives (inososes), carboxylic esters, borates, nitrates, sulfonic esters, phosphates, glycosides, acetals (and Schiff bases), ethers (and IV-alkyl derivatives), and anhydrides.
Figure 14.3 A neighbor-joining tree of most OBPs listed in Table 14.2 bootstrap support is based on 1000 replicates and only branches with >50% support are shown. A single tree is shown, broken into thirds to fit the page. Insert A is a key to the taxa. Insert B is the uncollapsed tree (taxa not shown) to illustrate full branch lengths (percent sequence differences). A size bar indicating 10% sequence difference is shown. Named clusters (e.g. ABPX) are referred to in the text. Figure 14.3 A neighbor-joining tree of most OBPs listed in Table 14.2 bootstrap support is based on 1000 replicates and only branches with >50% support are shown. A single tree is shown, broken into thirds to fit the page. Insert A is a key to the taxa. Insert B is the uncollapsed tree (taxa not shown) to illustrate full branch lengths (percent sequence differences). A size bar indicating 10% sequence difference is shown. Named clusters (e.g. ABPX) are referred to in the text.
Figure 1. Sketch of a general electrochemical cell, as referred to in the text, with the mixed conductor MX as the central phase. The currentcollecting metal is denoted by m .3 Reprinted from J. Maier, Z. Phys. Chem. NF (1984) 191-215. Copyright 1984 with permission from Oldenbourg Verlagsgruppe. Figure 1. Sketch of a general electrochemical cell, as referred to in the text, with the mixed conductor MX as the central phase. The currentcollecting metal is denoted by m .3 Reprinted from J. Maier, Z. Phys. Chem. NF (1984) 191-215. Copyright 1984 with permission from Oldenbourg Verlagsgruppe.
Certain experimental difficulties (e. g., high temperatures, low reaction rates) have prevented the production of homogeneous compounds37,46,62. These problems still remain, but new insight has been gained via the simple experimental techniques referred to in the text. [Pg.148]

The sequences have been derived from references referred to in the text. Two examples of enzymes from the amylase family are shown for comparison. Over 40 enzymes ranging from amylases, glucosidases, various a-1,6-debranching enzymes, and 4 examples of branching enzymes have been compared by Svensson.286 The invariant amino acid residues believed to be involved in catalysis are in bold letters)... [Pg.135]

Figure 8. Planar structure of dieldrin and partial structures of some dieldrin analogs (each containing six chlorine atoms) referred to in the text. Table below gives toxicities for dechlorinated derivatives of dieldrin (see key in figure) to adult female blowflies, Calliphora erythrocephala. Similar superscripts indicate significant difference at 95%... Figure 8. Planar structure of dieldrin and partial structures of some dieldrin analogs (each containing six chlorine atoms) referred to in the text. Table below gives toxicities for dechlorinated derivatives of dieldrin (see key in figure) to adult female blowflies, Calliphora erythrocephala. Similar superscripts indicate significant difference at 95%...
Figure 4.2 An example from the G-BASE project of a gridded image for arsenic in stream sediments (top) and stream waters (bottom) from eastern England. Note The maps show how stream water and stream sediment maps can be used in combination to explain the distribution and behaviour of elements in the surface environment. The Mesozoic sedimentary ironstone referred to in the text is shown by the white outline. Figure 4.2 An example from the G-BASE project of a gridded image for arsenic in stream sediments (top) and stream waters (bottom) from eastern England. Note The maps show how stream water and stream sediment maps can be used in combination to explain the distribution and behaviour of elements in the surface environment. The Mesozoic sedimentary ironstone referred to in the text is shown by the white outline.

See other pages where Referred to in the Text is mentioned: [Pg.291]    [Pg.6]    [Pg.169]    [Pg.229]    [Pg.82]    [Pg.16]    [Pg.620]    [Pg.958]    [Pg.61]    [Pg.135]    [Pg.181]    [Pg.1016]    [Pg.407]    [Pg.30]   


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