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Volumn 12, Issue , 2008, Pages 390-413

Oligo-and poly(2,5-thienylene-ethynylene)s

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Indexed keywords


EID: 84888857416     PISSN: 17249449     EISSN: None     Source Type: Book Series    
DOI: None     Document Type: Article
Times cited : (1)

References (101)
  • 2
  • 15
  • 24
    • 31144477360 scopus 로고    scopus 로고
    • Meier, H. Angew. Chem. 2005, 117, 2536-2561.
    • (2005) Angew. Chem. , vol.117 , pp. 2536-2561
    • Meier, H.1
  • 25
    • 18044382149 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 2482-2506.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 2482-2506
  • 27
    • 24944516927 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 5592-5629.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 5592-5629
  • 29
    • 85043573957 scopus 로고    scopus 로고
    • Wiley-VCH: Weinheim, Germany
    • Haley, M. M.; Tykwinski, R. R., Eds.; Wiley-VCH: Weinheim, Germany, 2006; pp. 476-528.
    • (2006) , pp. 476-528
    • Haley, M.M.1    Tykwinski, R.R.2
  • 38
    • 85043604895 scopus 로고    scopus 로고
    • Società Chimica Italiana: Rome
    • Attanasi, O. A.; Spinelli, D., Eds.; Società Chimica Italiana: Rome, 1997; Vol. 1, pp. 277-302.
    • (1997) , vol.1 , pp. 277-302
    • Attanasi, O.A.1    Spinelli, D.2
  • 78
    • 85043581082 scopus 로고    scopus 로고
    • Chem. Abstr. 2001, 135, 61784.
    • (2001) Chem. Abstr. , vol.135 , pp. 61784
  • 82
    • 85043573494 scopus 로고    scopus 로고
    • One or two coupled catalytic circles were suggested.50-52 Depending on electron-poor or electron-rich alkynes, a change of mechanisms seems to be reasonable.52 A major problem consists in the deprotonation of terminal alkynes by tert. amines as weak bases. In order to overcome this difficulty, the primary formation of Pd or Cu π-complexes was postulated. However, neither their intermediate formation nor their deprotonation by tert. amines was really proved
    • One or two coupled catalytic circles were suggested.50-52 Depending on electron-poor or electron-rich alkynes, a change of mechanisms seems to be reasonable.52 A major problem consists in the deprotonation of terminal alkynes by tert. amines as weak bases. In order to overcome this difficulty, the primary formation of Pd or Cu π-complexes was postulated. However, neither their intermediate formation nor their deprotonation by tert. amines was really proved.
  • 85
  • 87
    • 85043601778 scopus 로고    scopus 로고
    • Therefore dialkynes as oxidation products are often minor by-products
    • Therefore dialkynes as oxidation products are often minor by-products.
  • 88
    • 85043582125 scopus 로고    scopus 로고
    • 1-I
    • 1-I.
  • 89
    • 85043597989 scopus 로고    scopus 로고
    • Highly polar triple bonds can add primary or secondary amines under these conditions. In such cases, only tertiary amines can be used
    • 38
  • 90
    • 85043592733 scopus 로고    scopus 로고
    • 2,3 Nowadays this group is seldom used.30,31
    • 2,3 Nowadays this group is seldom used.30,31
  • 91
    • 85043597059 scopus 로고    scopus 로고
    • 3 is possible. Fluoride as base cleaves both silyl groups
    • 3 is possible. Fluoride as base cleaves both silyl groups.
  • 97
    • 85043606748 scopus 로고    scopus 로고
    • max values. See for example Ref.14
    • max values. See for example Ref.14
  • 98
    • 85043586385 scopus 로고    scopus 로고
    • F ≤0.1%.
    • F ≤0.1%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.