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Volumn 113, Issue 42, 2009, Pages 11153-11160

Reactivity of C2H5+ with benzene: Formation of ethylbenzenium ions and implications for Titan's ionospheric chemistryt

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE CROSS SECTIONS; ALKYL CATIONS; ALTERNATIVE ROUTES; CENTER OF MASS; CHEMICAL PROCESS; COVALENTLY BOUND; CROSS SECTION; ETHYL CATIONS; HYDROCARBON MOLECULES; HYPERTHERMAL ENERGIES; LOW ENERGIES; PROTONATED; REACTION CHANNELS; SIDE REACTIONS; SINGLE-COLLISION; THEORETICAL APPROACH;

EID: 70350140203     PISSN: 10895639     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp905052h     Document Type: Article
Times cited : (15)

References (62)
  • 18
    • 33748300820 scopus 로고    scopus 로고
    • Protonated aromatics and arenium ions
    • Nibbering, N. M. M., Ed.; Elsevier: Amsterdam, Topic B16
    • (d) Kuck, D. Protonated Aromatics and Arenium Ions. In Encyclopedia of Mass Spectrometry; Nibbering, N. M. M., Ed.; Elsevier: Amsterdam, 2005; Vol.4, Topic B16, p 229.
    • (2005) Encyclopedia of Mass Spectrometry , vol.4 , pp. 229
    • Kuck, D.1
  • 19
    • 33748300820 scopus 로고    scopus 로고
    • H/D exchange in hydrocarbon ions
    • Nibbering, N. M. M., Ed.; Elsevier: Amsterdam, Topic B20
    • (e) Kuck, D. H/D Exchange in Hydrocarbon Ions. In Encyclopedia of Mass Spectrometry; Nibbering, N. M. M., Ed.; Elsevier: Amsterdam, 2005; Vol.4, Topic B20, p 270.
    • (2005) Encyclopedia of Mass Spectrometry , vol.4 , pp. 270
    • Kuck, D.1
  • 27
    • 63849138358 scopus 로고    scopus 로고
    • Addition/correction.
    • Addition/correction. J. Phys. Chem. A 2009, 113, 1869.
    • (2009) J. Phys. Chem. A , vol.113 , pp. 1869
  • 46
    • 70350139945 scopus 로고    scopus 로고
    • Protonated xylenes are predicted to be even more stable isomers, see ref 13d
    • Protonated xylenes are predicted to be even more stable isomers, see ref 13d.
  • 47
    • 33344458869 scopus 로고    scopus 로고
    • For combined spectroscopic/theoretical studies of the closely related case of protonated toluene, see
    • For combined spectroscopic/theoretical studies of the closely related case of protonated toluene, see: (a) Dopfer, O.; Lemaire, J.; Maitre, P.; Chiavarino, B.; Crestoni, M. E.; Fornarini, S. Int, J. Mass Spectrom. 2006, 249, 149.
    • (2006) Int, J. Mass Spectrom. , vol.249 , pp. 149
    • Dopfer, O.1    Lemaire, J.2    Maitre, P.3    Chiavarino, B.4    Crestoni, M.E.5    Fornarini, S.6
  • 51
    • 0001534054 scopus 로고    scopus 로고
    • Angew. Chem. 2000, 112, 129.
    • (2000) Angew. Chem. , vol.112 , pp. 129
  • 53
    • 33644852606 scopus 로고    scopus 로고
    • Proton affinity evaluation
    • -1 is taken, for the proton affinity of ethylbenzene. NIST Standard Reference Database Number 69; Linstrom, P. J., Mallard, W. G., Eds.; National Institute of Standards and Technology: Gaithersburg, MD 20899, retrieved June 30
    • -1 is taken, for the proton affinity of ethylbenzene. Hunter, E. P. Lias, S. G. Proton Affinity Evaluation. In NIST Chemistry Webbook; NIST Standard Reference Database Number 69; Linstrom, P. J., Mallard, W. G., Eds.; National Institute of Standards and Technology: Gaithersburg, MD, 20899, http://webbook.nist.gov (retrieved June 30, 2009).
    • (2009) NIST Chemistry Webbook
    • Hunter, E.P.1    Lias, S.G.2
  • 58
    • 70350161868 scopus 로고    scopus 로고
    • + as suggested in ref 35. NIST Standard Reference Database Number 69, Gaithersburg
    • + as suggested in ref 35. NIST Standard Reference Database Number 69, Gaithersburg, 2008, see: http://webbook. nist.gov/chemistry/.
    • (2008)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.