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Volumn 15, Issue 3, 1996, Pages 1067-1070

Synthesis and electronic properties of 9,10-disilylanthracenes

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EID: 4243108515     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om950776m     Document Type: Article
Times cited : (116)

References (31)
  • 1
    • 85025776609 scopus 로고
    • For reviews, see: (a) Sakurai, H. J. Organomet. Chem. 1980, 200, 261. (b) Bock, H. Angew. Chem., Int. Ed. Engl. 1989, 28, 1627. (c) Bock, H.; Solouki, B. Chem. Rev. 1995, 95, 1161.
    • (1980) J. Organomet. Chem. , vol.200 , pp. 261
    • Sakurai, H.1
  • 2
    • 0024802840 scopus 로고
    • For reviews, see: (a) Sakurai, H. J. Organomet. Chem. 1980, 200, 261. (b) Bock, H. Angew. Chem., Int. Ed. Engl. 1989, 28, 1627. (c) Bock, H.; Solouki, B. Chem. Rev. 1995, 95, 1161.
    • (1989) Angew. Chem., Int. Ed. Engl. , vol.28 , pp. 1627
    • Bock, H.1
  • 3
    • 0000369605 scopus 로고
    • For reviews, see: (a) Sakurai, H. J. Organomet. Chem. 1980, 200, 261. (b) Bock, H. Angew. Chem., Int. Ed. Engl. 1989, 28, 1627. (c) Bock, H.; Solouki, B. Chem. Rev. 1995, 95, 1161.
    • (1995) Chem. Rev. , vol.95 , pp. 1161
    • Bock, H.1    Solouki, B.2
  • 13
    • 0011755790 scopus 로고
    • Although Suzuki and co-workers have quite recently reported that the copolymers of 9,10-bis(chloromethylpropylsilyl)anthracene and dichloromethylphenylsilane have strong emission properties, the structure and the emission properties of the monomer 9,10-bis-(chloromethylpropylsilyl)anthracene itself have not been described. See: Suzuki, H.; Satoh, S.; Kimata, Y.; Kuriyama, A. Chem. Lett. 1995, 451.
    • (1995) Chem. Lett. , pp. 451
    • Suzuki, H.1    Satoh, S.2    Kimata, Y.3    Kuriyama, A.4
  • 16
    • 85033844041 scopus 로고    scopus 로고
    • note
    • 20 However, we could obtain 1-4 with butyllithium in diethyl ether or tertbutyllithium in THF without using TMEDA.
  • 19
    • 0001580762 scopus 로고
    • Photoelectron Spectra of Silicon Compounds
    • Patai, S., Rappoport, Z., Eds.; Wiley: Chichester, U.K., Chapter 9
    • The ionization potentials of 1,4-bis(trimethylsilyl)benzene (8.7 eV) and 1,4-bis(trimethylsilyl)naphthalene (7.85 eV) have been reported to be smaller than those of benzene (9.25 eV) and naphthalene (8.15 eV). See: Bock, H.; Solouki, B. Photoelectron Spectra of Silicon Compounds. In The Chemistry of Organic Silicon Compounds; Patai, S., Rappoport, Z., Eds.; Wiley: Chichester, U.K., 1989; Chapter 9.
    • (1989) The Chemistry of Organic Silicon Compounds
    • Bock, H.1    Solouki, B.2
  • 21
    • 85033857683 scopus 로고    scopus 로고
    • note
    • 22


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.