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American Chemical Society primary journals, production, 131 Apple Macintosh advantages, 22 short learning curve, 22 software, 23 switcher utility, 23-24 Application interface definition, 132 example, 132,133f Attachment point, description, 71 Automated patent system, software development, I4l... [Pg.155]

Figure 15.10 Primary (a) and secondary (b) separation of unleaded gasoline, where (a) shows the IRD chromatogram, and (b) shows the MSD total ion chromatogram of heart cut c. Adapted from Analytical Chemistry, 65, N. Ragunathan et al., Multidimensional gas chromatography with parallel cryogenic tr aps , pp. 1012-1016, copyright 1993, with permission from the American Chemical Society. Figure 15.10 Primary (a) and secondary (b) separation of unleaded gasoline, where (a) shows the IRD chromatogram, and (b) shows the MSD total ion chromatogram of heart cut c. Adapted from Analytical Chemistry, 65, N. Ragunathan et al., Multidimensional gas chromatography with parallel cryogenic tr aps , pp. 1012-1016, copyright 1993, with permission from the American Chemical Society.
The primary literature has grown so much in recent years that attempts have been made to reduce the volume. One such attempt is the Journal of Chemical Research, begun in 1977. The main section of this journal, called the Synopses , publishes synopses, which are essentially long abstracts, with references. The full texts of most of the papers are published only in microfiche and miniprint versions. For some years, the American Chemical Society journals, including J. Am. Chem. Soc. and J. Org. Chem., have provided supplementary material for some of their papers. This material is available from the Microforms and Back Issues Office at the ACS Washington office, either on microfiche or as a photocopy. These practices have not yet succeeded in substantially reducing the total volume of the world s primary chemical literature. [Pg.1607]

Fry SC, Miller JG. Toward a working model of the growing plant cell wall. Phenolic cross-linking reactions in the primary cell walls of dicotyledons. American Chemical Society, Washington, DC, 1989. [Pg.31]

FIGURE 5.26. Antigen-antibody construction of a monolayer glucose oxidase electrode with an attached ferrocenium cosuhstrate and cyclic voltammetric response in a phosphate buffer (pH 8) at 25°C and a scan rate of 0.04 V/s. a Attached ferrocene alone, h Addition of the substrate, c Primary plots, d Secondary plot. The numbers on the curves in parts h and c are the values of the substrate concentration in mM. Adapted from Figure 2 in reference 24, with permission from the American Chemical Society. [Pg.337]

Fig. 2.1.3. Selected ion chromatograms for C14-C17-SAS homologues in (a) primary effluent and (b) secondary effluent collected from a sewage treatment plant. Reproduced with permission from Ref. [35]. 1994 by American Chemical Society. Fig. 2.1.3. Selected ion chromatograms for C14-C17-SAS homologues in (a) primary effluent and (b) secondary effluent collected from a sewage treatment plant. Reproduced with permission from Ref. [35]. 1994 by American Chemical Society.
FIGURE 4. (Top) plot of log k for the reactions of primary and secondary amine nucleophiles with picryl chloride against their pK3 values in aqueous solution at 25 °C. (Bottom) plot of log k for the reactions of a series of substituted quinuclidine ions with picryl chloride against the pA a values of the nucleophiles. In aqueous solution at 25 °C77. Reprinted with permission from Reference 77. Copyright (1992) American Chemical Society... [Pg.1234]

In Writing on Your Own task2B, you generated a list of three to five keywords related to your paper topic. Use these keywords to search for peer-reviewed journal articles about your topic. The goal is to find at least four articles relevant to your research area. Search scientific databases such as American Chemical Society Publications or ScienceDirect be cautious with general Internet search engines, such as Google, because they do not limit searches to the primary literature. [Pg.44]

Figure 14.8 (Left) Primary sequence of peptide MAXI with /8-hairpin promoted intramolecular folding, leading to the reversible formation of self-assembled /8-sheets. (Right) Cryo-TEM image of self-assembled peptide scaffolds. Scale bar = 200 nm. Reprinted from Schneider et al. (2002). Copyright 2002 American Chemical Society. Figure 14.8 (Left) Primary sequence of peptide MAXI with /8-hairpin promoted intramolecular folding, leading to the reversible formation of self-assembled /8-sheets. (Right) Cryo-TEM image of self-assembled peptide scaffolds. Scale bar = 200 nm. Reprinted from Schneider et al. (2002). Copyright 2002 American Chemical Society.
Fig. 24 a Primary adsorption of small proteins and b Secondary adsorption of large proteins. Reproduced with permission from [200] (Copyright 1999 American Chemical Society)... [Pg.39]

Fig. 8 Diagram depicting three-dimensional tunneling model. Dj is the total ET distance along the primary double strand. Dj is the distance of migration on the neighboring double strand Dj=Di-Dds where D s is the center-to-center interduplex distance [7b]. Reprinted with permission from the J. Phys. Chem. Copyright (2000) American Chemical Society... Fig. 8 Diagram depicting three-dimensional tunneling model. Dj is the total ET distance along the primary double strand. Dj is the distance of migration on the neighboring double strand Dj=Di-Dds where D s is the center-to-center interduplex distance [7b]. Reprinted with permission from the J. Phys. Chem. Copyright (2000) American Chemical Society...
Many resources were used to compile the information in this book. The hazardous chemicals listed here are taken from Sittig, 4th Edition. For a few chemicals in Sittig, their makers are not listed, perhaps because they are made in such limited quantities that they are sold through specialty middlemen and catalog houses. The primary resources for preparing the list of manufacturers in this book were (1) the Web sites of the companies, (2) membership in special sections of United States chemical societies, the European Chemical Industry Council (CEFIC) and societies in India, Japan, Asia, Italy and elsewhere, and (3) sites in which companies register themselves as producers of particular products, such as the Thomas Directories in the U.S. and Europe, the American Chemical Society ChemCyclopedia, and the British Chemical Industries Association Chemextra. Direct access to these sites are quickly available to any Internet user. They are listed in Section VII - Hotlines, Databases and Useful Web Sites. [Pg.355]

Stanley E. Manahan is a professor of chemistry at the University of Missouri-Columbia, where he has been on the faculty since 1965, and is president of ChemChar Research, Inc., a firm developing nonincinerative thermochemical waste treatment processes. He received his A.B. in chemistry from Emporia State University in 1960 and his Ph.D. in analytical chemistry from the University of Kansas in 1965. Since 1968, his primary research and professional activities have been in environmental chemistry, toxicological chemistry, and waste treatment. He teaches courses on environmental chemistry, hazardous wastes, toxicological chemistry, and analytical chemistry. He has lectured on these topics throughout the United States as an American Chemical Society local section tour speaker, in Puerto Rico, at Hokkaido University in Japan, at the National Autonomous University in Mexico City, and at the University of the Andes in Merida, Venezuela. He was the recipient of the Year 2000 Award of the environmental chemistry division of the Italian Chemical Society. [Pg.6]

Figure 13. Schematic representations of the geometries of host-guest complexes, (a) Two possible geometries of the host-guest complex between calix[6]arene hexaester (29) and a protonated primary amine guest, (b) Plausible geometry of the host-guest complex between dibenzo-18-crown-6 (32) and a protonated primary amine guest (reprinted with permission from Anal. Chem. 1993, 65, 1077. Copyright 1993 American Chemical Society). Figure 13. Schematic representations of the geometries of host-guest complexes, (a) Two possible geometries of the host-guest complex between calix[6]arene hexaester (29) and a protonated primary amine guest, (b) Plausible geometry of the host-guest complex between dibenzo-18-crown-6 (32) and a protonated primary amine guest (reprinted with permission from Anal. Chem. 1993, 65, 1077. Copyright 1993 American Chemical Society).
Fig. 14.5 Proposed mechanism for primary and secondary spillover hydrogen binding with carbon nanotube. Reproduced with permission from [10], copyright 2006 American Chemical Society... Fig. 14.5 Proposed mechanism for primary and secondary spillover hydrogen binding with carbon nanotube. Reproduced with permission from [10], copyright 2006 American Chemical Society...
Fig. 8. (a) Primary structure of the cyclic endothelin antagonist BE18257B and (b) a family of 36 NMR structures which demonstrates the well-defined nature of the cyclic peptide backbone. (Reprinted with permission from Coles et a/.148 Copyright (1993) American Chemical Society.)... [Pg.128]

The use of proper chemical nomenclature is essential for effective scientific communication. More than one million new substances are reported each year, each of which must be identified clearly, unambiguously, and completely in the primary literature. Chemical compounds are named according to the rules established by the International Union of Pure and Applied Chemistry (IUPAC), the International Union of Biochemistry and Molecular Biology (IUBMB) [formerly the International Union of Biochemistry (IUB)], the Chemical Abstracts Service (CAS), the Committee on Nomenclature, Terminology, and Symbols of the American Chemical Society, and other authorities as appropriate. For more information on naming chemical compounds, refer to the bibliography in Chapter 18. This chapter gives the editorial conventions and style points for chemical compound names. [Pg.233]

The following chapters in this book represent, in the main, the proceedings of a 1973 American Chemical Society symposium which focused on the fundamental protein chemistry and enzymology of many enzymes used in food processing. In addition to the primary literature, there are a large number of good books and review articles available, since the broad subject of food-related enzymes has been of both academic and commercial interest for many years. [Pg.27]

Figure 1.4 Life cycle flow chart for solvent usage. Primary life cycle stages are represented by rectangles. [Reprinted with permission from Org. Proc. Dev., 2007, 11, 149-155. Copyright 2007 American Chemical Society.]... Figure 1.4 Life cycle flow chart for solvent usage. Primary life cycle stages are represented by rectangles. [Reprinted with permission from Org. Proc. Dev., 2007, 11, 149-155. Copyright 2007 American Chemical Society.]...
The materials, safety information, and procedures contained in this book are believed to be reliable. This information and these procedures should serve only as a starting point for laboratory practices, and they do not purport to specify minimal legal standards or to represent the policy of the American Chemical Society. No warranty, guarantee, or representation is made by the American Chemical Society as to the accuracy or specificity of the information contained herein, and the American Chemical Society assumes no responsibility in connection therewith. The added safety information is intended to provide basic guidelines for safe practices. Therefore, it cannot be assumed that all necessary warnings and precautionary measures are contained in this document and that other or additional information and measures may not be required. Users of this book and the procedures contained herein should consult the primary literature and other sources of safe laboratory practices for more exhaustive information. [Pg.446]

Figure 5. Cross-sectional view of fully differentiated wood fibers. (A) SE M of a Douglas-fir. Note the thick secondary walls (S) and the fiher lumen (L). (Reproduced from Ref 39. Copyright 1982, American Chemical Society.) (B) TEM of two adjacent fibers in white spruce. Key P, primary wau, S, secondary wall L, lumen and ML, middle lamella. (Reproduced with permission from Ref. 38. Copyright 1974, Forest Products... Figure 5. Cross-sectional view of fully differentiated wood fibers. (A) SE M of a Douglas-fir. Note the thick secondary walls (S) and the fiher lumen (L). (Reproduced from Ref 39. Copyright 1982, American Chemical Society.) (B) TEM of two adjacent fibers in white spruce. Key P, primary wau, S, secondary wall L, lumen and ML, middle lamella. (Reproduced with permission from Ref. 38. Copyright 1974, Forest Products...

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