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Volumn 136, Issue 14, 2012, Pages

Using heavy atom rare gas matrix to control the reactivity of 4-methoxybenzaldehyde: A comparison with benzaldehyde

Author keywords

[No Author keywords available]

Indexed keywords

AR-MATRIX; ARGON MATRICES; AROMATIC ALDEHYDE; DECARBONYLATE; DECARBONYLATIONS; HEAVY ATOM EFFECTS; HEAVY ATOMS; INTERSYSTEM CROSSING; METHANONE; METHOXY; METHOXYBENZENE; P-ANISALDEHYDE; PARENT COMPOUNDS; PHOTOCHEMICAL BEHAVIORS; PHOTOCHEMICAL TRANSFORMATIONS; PHOTOPRODUCTS; RARE GAS MATRIX; REACTION CHANNELS; ULTRAVIOLET IRRADIATIONS; XENON MATRICES;

EID: 84859939811     PISSN: 00219606     EISSN: None     Source Type: Journal    
DOI: 10.1063/1.3701734     Document Type: Article
Times cited : (10)

References (79)
  • 29
    • 77952721686 scopus 로고    scopus 로고
    • Light induced reactions in cryogenic matrices
    • (Ed. Angelo Albini), Royal Society of Chemistry, Chap. 3
    • See also R. Fausto and A. Gómez-Zavaglia, "Light induced reactions in cryogenic matrices," in "Specialistic Reports in Photochemistry" (Ed. Angelo Albini), Royal Society of Chemistry, Vol. 37 (2009), Chap. 3, pp.72-99;
    • (2009) Specialistic Reports in Photochemistry , vol.37 , pp. 72-99
    • Fausto, R.1    Gómez-Zavaglia, A.2
  • 53
    • 84859947129 scopus 로고    scopus 로고
    • See supplementary material at for this article: Figure S1, with fragments of difference spectra comparing the photoproducts generated upon irradiation of benzaldehyde isolated in xenon and argon matrices; Figures S2 and S3, with the B3LYP/6-311++G(d,p) calculated optimized structures, relative energies, and μC = C wavenumber (for central ethylenic bond) of the conformers of E and Z open-ring ketene isomeric of p-anisaldehyde; Tables S1 and S3 with vibrational data for p-methoxybenzoyl and benzoyl radicals; Table S2 with observed bands of benzene valence isomers and benzoyl radical in the spectra of photolysed benzaldehyde matrices; Table S4, with B3LYP/6-311++G(d,p) calculated wavenumbers and IR intensities for the different calculated forms of the open-ring ketene isomeric of p-anisaldehyde
    • See supplementary material at http://dx.doi.org/10.1063/1.3701734 for this article: Figure S1, with fragments of difference spectra comparing the photoproducts generated upon irradiation of benzaldehyde isolated in xenon and argon matrices; Figures S2 and S3, with the B3LYP/6-311++G(d,p) calculated optimized structures, relative energies, and μC = C wavenumber (for central ethylenic bond) of the conformers of E and Z open-ring ketene isomeric of p-anisaldehyde; Tables S1 and S3 with vibrational data for p-methoxybenzoyl and benzoyl radicals; Table S2 with observed bands of benzene valence isomers and benzoyl radical in the spectra of photolysed benzaldehyde matrices; Table S4, with B3LYP/6-311++G(d,p) calculated wavenumbers and IR intensities for the different calculated forms of the open-ring ketene isomeric of p-anisaldehyde.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.