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Volumn 2, Issue 9, 2011, Pages 1677-1681

Powering reductive charge shift reactions - Linking fullerenes of different electron acceptor strength to secure an energy gradient

Author keywords

[No Author keywords available]

Indexed keywords

CHARGE RECOMBINATIONS; CHARGE SEPARATIONS; CHARGE SHIFT; ELECTRON ACCEPTOR; ELECTRON DONORS; ENERGY GRADIENTS; PICOSECONDS; PRIMARY ELECTRONS; SECONDARY ELECTRONS;

EID: 81355138445     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c1sc00331c     Document Type: Article
Times cited : (27)

References (55)
  • 14
    • 60949108369 scopus 로고    scopus 로고
    • Compound 1 is formed in moderate yield (40%). Since typical click-chemistry reactions take place with high yields, this result could be accounted for by the competition between the cycloaddition reaction of the azide derivative on the terminal alkyne group and on the fullerene units. Nevertheless, in order to minimize this competitive process, the reaction is carried out at room temperature. See supporting information
    • M. A. Fazio O. P. Lee D. I. Schuster Org. Lett. 2008 10 4979
    • (2008) Org. Lett. , vol.10 , pp. 4979
    • Fazio, M.A.1    Lee, O.P.2    Schuster, D.I.3
  • 40
    • 0002325264 scopus 로고    scopus 로고
    • K. M. Kadish, R. S. Ruoff, ed.; John Wiley and Sons: New York
    • D. M. Guldi, P. V. Kamat, In Chemistry, Physics and Technology;, K. M. Kadish, R. S. Ruoff, ed.; John Wiley and Sons: New York, 2000, p 225-282
    • (2000) Chemistry, Physics and Technology , pp. 225-282
    • Guldi, D.M.1    Kamat, P.V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.