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Volumn 15, Issue 36, 2009, Pages 8955-8960

Rational monomer design towards 2D polymers: Synthesis of a macrocycle with three 1,8-anthn lene units

Author keywords

Anthracenes; Cross coupling; Macrocycles; Photodiraerization; Topochemical polymerization

Indexed keywords

BUILDING BLOCKES; CONNECTION SITES; CROSS-COUPLING; ETHYNYL; MACROCYCLES; OH GROUP; PALLADIUM-CATALYZED CROSS-COUPLINGS; PHOTODIRAERIZATION; SONOGASHIRA CROSS-COUPLING; TARGET COMPOUND; TOPOCHEMICAL POLYMERIZATION; TRIMETHYLSILYL;

EID: 70349093168     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200900781     Document Type: Article
Times cited : (31)

References (65)
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    • 3h conformation is also possible. The solution conformation of 1 is under investigation. This includes complexation studies with guest molecules such as carborane or fullerenes. Such host-guest complexes may also be of direct interest as monomers for 2D polymer synthesis
    • 3h conformation is also possible. The solution conformation of 1 is under investigation. This includes complexation studies with guest molecules such as carborane or fullerenes. Such host-guest complexes may also be of direct interest as monomers for 2D polymer synthesis.
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    • note
    • For the Sonogashira reaction without cuprous iodide two different names are being used in the literature, namely the "copper-free Sonogashira reaction" and the "Heck alkynylation." For a comment on this matter, see: T. Ljungdahl, K. Pettersson, B. Albinsson, J. Martensson, J. Org. Chem. 2006, 71, 1677-1687. We tend to agree with this comment, however, and as the former name is used much more often in the literature we will use it here as well.
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    • Ljungdahl, T.1    Pettersson, K.2    Albinsson, B.3    Martensson, J.4
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    • 1H NMR spectroscopy as a side reaction upon the UV irradiation
    • 1H NMR spectroscopy as a side reaction upon the UV irradiation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.