Reprints, filing

Both the literature and patents are continuously classified and filed by use of this classification system. A card file, a reprint file, and a patent file are maintained. The card file contains references to all or almost all of the existing material on each subject the reprint file contains the full text of a large number of the best articles on each subject ... 

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Bruno, Leonard C. Landmarks of science from the collections of the Library of Congress foreword by Daniel J. Boorstin. Washington (DC) Library of Congress, 1987 reprint, New York Facts on File, 1989. xi, 351 p. ISBN 0816021376... 

Ibid., p. 16. See also the entire university file reprinted in ibid., pp. 153-66. 

Fig. 4. Spectra acquired for a 0.55 pmol sample of the indoloquinoline alkaloid cryptolepine (1) dissolved in 25 pL J6-DMSO. (a) Proton-carbon (HMQC) direct correlation spectrum recorded in 12m (16 x 2048 point files, 16 transients/ increment) shown with no linear prediction, (b) Long-range 1H-13C HMBC spectrum of the same sample optimized for 8 Hz. The data were acquired as 64 x 4096 files with 16 transients accumulated/ increment. Data are again shown without any linear prediction. (Reprinted with permission from Ref. 11. Copyright 1998, John Wiley Sons, Ltd.)...

Figure 9 Plot of nk as a function of free energy for electron-transfer reactions of Ru-65-c)d 65 labeled with different ruthenium polypyridine complexes. The solid tine shows the theoretical dependence of equation (1) calculated with a reorganizational energy of 0.94 eV and a distance r of 13 A. The open boxes are for the reactions involving the excited state, = ki, and the filed boxes are for the thermal back reactions, ki-i = k2, all determined at 22 °C. (Reprinted with permission from Ref. 55. 1993 American Chemical Society)...

Figure 27 (a) Stress versus strain curves of different SWNTs ropes obtained in tensile-loading experiments carried out using AFM for eight ropes of SWNTs having diameter from 19 to 41 nm. (Reprinted with permission from M.-F. Yu, B.S. Files, S. Arepalli, and R.S. Ruoff, Phys. Rev. Lett., 2000, 84, 5552. 2000 by the American Physical Society.) (b) Stress versus strain curves for individual MWNTs. (Reprinted with permission from M.-F. Yu, O. Lourie, M.J. Dyer, K. Moloni, T.F. Kelly, and R.S. Ruoff, Science, 2000, 287, 637. 2000 AAAS)... 

Information on Rosengarten and Sons can be found in the Merck Archives, P W files and Williams Haynes, Chemical Pioneers The Founders of the American Chemical Industry (1931 reprinted, Freeport, NY Books for Libraries Press, 1970), pp. 26-41. 

Fig. 4.4 (a) Mean residence times of water molecules solvating the folded protein ubiquitin. Residue numbering follows the file PDB.1UBI. b PDB structure of ubiquitin highlighting the dehydrons (displayed in green). Reprinted with permission from American Institute of Physics [20]. Copyright 2007... 

Figure 28. Smgle-crysl l electron Tpifl two nance (ESR) speemi of TCNQ t/il7 complex, showing ihe orientation dcpeiukitte of die iriplei splitting (outer lines). The orientation of the crystal with respect to the direction of ihr applied magnetic filed is indicated on each spcctmm. The center line is assigned to the monoradicaL (Reprinted from Ref. -47 with permission of the American Chemical Society.)...

The "certified parties" entitled to obtain a deposit under the Budapest Treaty are determined by the laws and regulations of the country or countries in which a patent application is filed. See Rule II, Regulations Under the BudapestTreaty on the International Recognition of Microorganisms for the Purposes of Patent Procedure of April 28, 1977, reprinted in E. Hanellin (Ed.), Patents Throughout the World, App. C (2001). 

FIGURE 10. Alkanethiolate adlayer (large circles) on the Au(lll) surface (small circles). The diagonal slash in the large circles represents the azimuthal orientation of the plane defined by file all-trans hydrocarbon chain. Reprinted with permission from Reference 54. Copyright (1997) American Chemical Society... 

Figure 6.6-3 (Reprinted with permissinn from 0. A. Hougen, K. M. Watson, and R. A. Ragatz, Chemical Process Principles Charts, 2nd ed., John Wiley Sons, New York, I960. This figure appears as an Adobe PDF file on the CD-ROM accompanying this book, and may be enlarged and printed for easier reading and for use in solving problems.)...

Fig. 4.4. Aciylamide and CsCI quenching ecls on the ascorbate oxidase em ssion properties. Steady-state (open squares) and dynamic (Filed squares) quenching of ascoibale oxidase by aciylamide (A) and CsCI (B) upon excitation at 293 nm. Source Di Venerc, A, Mei, C.. Gibrdi, G.. Ros, N., Oe MatteE, F., McKs. R.. Cralton. E. and Finazzi Agro, A. I99S. Fur J. Bioclicm 257. 337-343. AudxHization of reprint accorded by Blackwell PuUisliing.

FIGURE 7.1 Menu pages in the Acrobat 8 Professional program, relating to document information and meta-data for (a) a typical journal reprint, with (b) the standard metadata schemas and (c) the advanced menu, where additional, more chemically relevant, metadata schemas can be added. The values, or more accurately, the absence of values for the various fields are typical for most Web-resident PDF files. 

Figure 31. A model system developed by Parkin and co-workers (a), Tris(2-mercapto-l-phenylimidazolyl)hydroborato lead complex, [Tm ]Pb [C104] (197), is strikingly similar in structure to the lead bound in the active site of the target protein ALAD (b), (only lead and coordinated cysteines are shown) (245). In both systems, lead is bound in a trigonal pyramidal geometry by three sulfurs. Metal-binding studies on the model system (198) and inhibition studies on the enzyme reveal that lead has a higher affinity for this type of site than the native zinc ion. [Part (a) reprinted with permission from B. M. Bridgewater and G. Parkin, J. Am. Chem. Soc., 122, 7140-7141 (2000). Copyright 1999 American Chemical Society. Coordinates for figure part b) were downloaded from the Protein Databank (pdb file id IQNV).]...

Figure 3.17 Proposed mechanism of the stabilization and induction of the i-motif structure by GQDs. Folded i-motif structure is generated from the PDB file (PDB id 1EL2). Reprinted with permission from ref. 167. Copyright 2012 American Chemical Society.

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