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M. L. Gross and R. Caprioli, ISBN (set) 0-08-043850-4); for a fascinating account of the history of mass spectrometry see:
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The Encyclopedia of Mass Spectrometry, Ed.
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B. Asamoto, VCH, New York, NY
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FT-ICR/MS: Analytical Applications of Fourier Transform Ion Cyclotron Resonance Mass Spectrometry, ed., B. Asamoto,, VCH, New York, NY, 1991
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FT-ICR/MS: Analytical Applications of Fourier Transform Ion Cyclotron Resonance Mass Spectrometry, Ed.
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J. M. Farrar and W. H. Saunders, Wiley, New York
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P. Kebarle, in Techniques for the study of ion-molecule reactions, ed., J. M. Farrar, and, W. H. Saunders,, Wiley, New York, 1988, ch. 5
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S. A. McLuckey, G. J. Van Berkel, G. L. Glish and J. C. Schwartz, in Practical Aspects of Ion Trap Mass Spectrometry, ed., R. E. March, and, J. F. J. Todd,, CRC, Boca Raton, FL, 1995, vol. 2, p. 89
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McLuckey, S.A.1
Van Berkel, G.J.2
Glish, G.L.3
Schwartz In, J.C.4
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Electrospray Ionization Mass Spectrometry: Fundamentals, Instrumentation, and Applications, ed., R. B. Cole,, Wiley, New York, 1997
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McIndoe, J.S.2
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For a detailed series of reviews on quadrupole ion trap mass spectrometry, see the books, Practical Aspects of Ion Trap Mass Spectrometry:
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http://nobelprize.org/physics/laureates/1989/paul-lecture.html
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R. E. March and J. F. J. Todd, CRC, Boca Raton, FL
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Beynon coined the phrase "the modern mass spectrometer - a complete chemical laboratory" to highlight the ability of mass spectrometers to provide fundamental information of gas-phase chemical reactions:
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and the quadrupole ion trap does suffer some disadvantages, chief of which is the difficulty of trapping low mass fragment ions under CID conditions. This can lead to inaccurate branching ratios for fragment products
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C. Brunnee Int. J. Mass Spectrom. Ion Processes 1987 76 121
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A. de Meijere and F. Diederich, Wiley-VCH, Weinheim, 2nd edn, Interestingly, the reverse situation holds for the condensed phase, where there are fewer examples of C-C bond activation (see:
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Metal-Catalyzed Cross-Coupling Reactions, ed., A. de Meijere, and, F. Diederich,, Wiley-VCH, Weinheim, 2nd edn, 2004
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This difference can be explained by the fact that it is easier to form bare or poorly ligated metal ions in the gas phase, which are highly reactive and often undergo either C-H or C-C bond activation
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10.1016/j.ijms.2005.08.015 (invited contribution to Professor Bohme Honor Issue), in press
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A. Jacob P. F. James R. A. J. O'Hair Do Alkali and Alkaline Earth Acetates Form Organometallates via Decarboxylation? A Survey Using Electrospray Ionization Tandem Mass Spectrometry And DFT Calculations Int. J. Mass Spectrom. 10.1016/j.ijms.2005.08.015
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Academic Press, London, pp. 98-107 Gregor has previously noted the challenges with mass spectrometry nomenclature of inorganic systems. In mass spectrometry, M is used to designate the molecule, while in inorganic chemistry, M is used to designate a metal. Here we use the nomenclature suggested by Gregor to define metal complexes in the gas phase:
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R. C. Mehrotra and R. Bohra, Metal Carboxylates, Academic Press, London, 1983, pp. 98-107
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(1983)
Metal Carboxylates
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Mehrotra, R.C.1
Bohra, R.2
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Decarboxylation of simple inorganic carboxylates can also occur in solution. For reviews, see:
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235U for atomic bomb manufacture. See: pp. 13-18 of
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235U for atomic bomb manufacture. See: pp. 13-18 of
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L. Benz X. Tong P. Kemper Y. Lilach A. Kolmakov H. Metiu M. T. Bowers S. K. Buratto J. Chem. Phys. 2005 122 081102
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Bowers, M.T.7
Buratto, S.K.8
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