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Volumn 15, Issue 23, 1999, Pages 8288-8291

Improved method for the preparation of organic monolayers of 1-alkenes on hydrogen-terminated silicon surfaces

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; CHEMICAL MODIFICATION; FILM PREPARATION; MIXTURES; ORGANIC SOLVENTS; SILICON; SURFACE TREATMENT;

EID: 0033323843     PISSN: 07437463     EISSN: None     Source Type: Journal    
DOI: 10.1021/la9904962     Document Type: Article
Times cited : (200)

References (31)
  • 13
    • 0032542694 scopus 로고    scopus 로고
    • The presence of negligible but apparently detectable amounts of Mg has been reported in ref 2a. Larger amounts of Li and Mg have been shown to be present in the case of the reaction of porous silicon with Grignard reagents. See: (a) Song, J. H.; Sailor, M. J. J. Am. Chem. Soc. 1998, 120, 2376-2381.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 2376-2381
    • Song, J.H.1    Sailor, M.J.2
  • 15
    • 0000818886 scopus 로고    scopus 로고
    • See, for example, the effect of trace amounts of several of the transition metals on the minority-carrier recombination velocity: Itsumi, M.; Sato, Y.; Imai, K.; Yabumoto, N. J. Appl. Phys. 1997, 82, 3250-3255.
    • (1997) J. Appl. Phys. , vol.82 , pp. 3250-3255
    • Itsumi, M.1    Sato, Y.2    Imai, K.3    Yabumoto, N.4
  • 16
    • 0000807285 scopus 로고    scopus 로고
    • For some recent examples of the reaction of organic compounds with nanocrystalline silicon, resulting in the formation of covalent Si-C bonds, see: (a) Buriak, J. M.; Allen, M. J. J. Am. Chem. Soc. 1998, 120, 1339-1340.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 1339-1340
    • Buriak, J.M.1    Allen, M.J.2
  • 19
    • 0033076248 scopus 로고    scopus 로고
    • (d) Buriak, J. M. Adv. Mater. 1999, 11 (3), 265-267.
    • (1999) Adv. Mater. , vol.11 , Issue.3 , pp. 265-267
    • Buriak, J.M.1
  • 28
    • 0342602865 scopus 로고    scopus 로고
    • note
    • One of the reviewers suggested that the odd behavior of anisole-the only oxygenated solvent in the series investigated-could also be the result of a higher residual water content. As traces of residual water are indeed an important factor in the modification of hydrogen-terminated silicon surfaces this explanation can currently not be excluded, although distilled anisole was dried over NaOH prior to use.
  • 29
    • 0343908664 scopus 로고    scopus 로고
    • note
    • 3.
  • 30
    • 0343908665 scopus 로고    scopus 로고
    • note
    • Although the free volume of tert-butylbenzene is larger than that of mesitylene, the diameter of the molecule with respect to that of the phenyl ring is only slightly increased by the tert-butyl group. This group has a diameter of approximately 4.4 Å, which is similar to the diameter of approximately 4.3 Å of a phenyl ring. As mesitylene has a diameter of 5.4 Å, this difference in the width of the two molecules, combined with the presence of a relatively large alkyl group in tert-butylbenzene, may explain the observed differences between the two solvents at lower 1-hexadecene concentrations.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.