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By P.G. Kistemaker and N.M.M. Nibbering (Eds.)

ISBN-10: 0444888713

ISBN-13: 9780444888716

Those complaints, containing the texts of the invited lectures, conceal all facets of mass spectrometry together with conception, basic stories, purposes and instrumentation. Emphasis is put on contemporary advancements. an entire directory of the posters is incorporated

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Biol. , 57 (1986) 295. (b) I. -Y. G. Cooks, W. -G. -J. Chang, Biomed. Environ. , 14 (1987) 17. -G. M. G. -J. Chang, Biol. , 20 (1991) 503. M. H. G. -G. -J. Chang, Int. J. Mass Spectrom. Ion Processes, in press. , A m s t e r d a m 118/119 (1992) 37-70 37 Fourier transform ion cyclotron resonance mass spectrometry: technique developments* Alan G. Marshall*'b and Lutz Schweikhard3'' 3 Department of Chemistry, The Ohio State University, 120 West 18th Avenue, Columbus OH 43210 (USA) h Department of Biochemistry, The Ohio State University, 120 West 18th Avenue, Columbus OH 43210 (USA) (Received 26 August 1991) ABSTRACT In the three years since the 11th International Mass Spectrometry Conference, Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometry has advanced both theoretically and experimentally with respect to ion formation and transfer to the ion trap, ion trap design and operation, ion excitation and detection, data reduction, and in chemical and analytical applications.

Soc. , 2 (1991) 487. N. V. E. , Rapid Commun. , 5 (1991) 260. 7 O. Grizzi, M. Shi, H. W. Rabalais, Phys. Rev. B, 40 (1989) 10129. D. W. G. A. Walton, Mass Spectrom. , 7 (1988) 465. 9 T. A. G. Cooks, Int. J. Mass Spectrom. Ion Processes, 82 (1988) 131. E. D. Thesis, Purdue University, 1990. E. J. R. K. A. E. Riederer, Jr. G. Cooks, submitted for publication. 11 K. Quian, A. L. G. H. Futrell, J. Phys. , 93 (1989) 3889. K. G. L. H. Futrell, Int. J. Mass Spectrom. Ion Processes, 86 (1988) 61. 13 C D .

28. Toluene derivatives of C60 generated in the presence of FeCl3 and observed by electron attachment [61]. G. Cooks et ail Int. J. Mass Spectrom. o I ■ ■ ■ ■ ■ , 0 20 40 60 —-r^, 80 , , ■ , 1 100 120 140 160 180 200 Lab Collision Energy (eV) Fig. 29. Dissociation efficiency curve (Ar target) of the toluene adduct showing that toluene binds strongly to C60. Carbon-carbon bond formation is of particular interest and the formation of derivatives of buckminsterfullerene with simple aromatic compounds in the presence of FeCl3 (Fig.

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Advances in Mass Spectrometry by P.G. Kistemaker and N.M.M. Nibbering (Eds.)


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