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Volumn 11, Issue 13, 2005, Pages 3968-3978

Maleimido-terminated self-assembled monolayers

Author keywords

Conjugate addition; Maleimide; Monolayers; Self assembly; Silanes

Indexed keywords

ATOMIC FORCE MICROSCOPY; CONTACT ANGLE; DNA; INFRARED SPECTROSCOPY; OLIGOMERS; SILANES; SILICON; SURFACE STRUCTURE; X RAY PHOTOELECTRON SPECTROSCOPY;

EID: 21244486260     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200400896     Document Type: Article
Times cited : (34)

References (42)
  • 5
    • 84956068026 scopus 로고
    • b) M. Grunze, Phys. Scr. 1993, T49B, 711-717;
    • (1993) Phys. Scr. , vol.T49B , pp. 711-717
    • Grunze, M.1
  • 7
    • 0345979435 scopus 로고    scopus 로고
    • A. Ulman, Chem. Rev. 1996, 96, 1533-1554.
    • (1996) Chem. Rev. , vol.96 , pp. 1533-1554
    • Ulman, A.1
  • 27
    • 0012241210 scopus 로고
    • The reverse Diels-Alder reaction is thought to be a very useful method for the preparation of N-substituted maleimides that can not be obtained by direct dehydration of maleimic acids owing to the formation of the corresponding isomaleimides. See, M. Narita, T. Teramoto, M. Okawara, Bulleid Meml. Lect. Bulletin Chem. Soc. Japan 1971, 44, 1084-1089.
    • (1971) Bulleid Meml. Lect. Bulletin Chem. Soc. Japan , vol.44 , pp. 1084-1089
    • Narita, M.1    Teramoto, T.2    Okawara, M.3
  • 34
    • 21244459753 scopus 로고    scopus 로고
    • note
    • Numbers in parenthesis are the relative areas obtained by fitting the peak with Gauss-Lorentz peaks, as indicated in Figure 6a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.