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Volumn 13, Issue 4, 2007, Pages 1129-1141

Amination of [60]fullerene by ammonia and by primary and secondary aliphatic amines - Preparation of amino[60]fullerene peroxides

Author keywords

Amines; Fullerenes; Peroxides; Radicals; Single electron transfer

Indexed keywords

AMINATION; AMINES; AMINO ACIDS; PEROXIDES; SINGLE CRYSTALS;

EID: 33846681357     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200600932     Document Type: Article
Times cited : (30)

References (50)
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    • c) For a recent review see: G. P. Miller, C. R. Chim. 2006, 9, 952.
    • (2006) C. R. Chim , vol.9 , pp. 952
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    • F. Wudl, A. Hirsch, K. C. Khemani, T. Suzuki, P.-M. Allemand, H. E. Koch, G. Srdanov, H. M. Webb, Fullerenes: Synthesis, Properties and Chemistry of Large Carbon Clusters (Eds. : G. S. Hammond, V. J. Kuck), ACS Symp. Ser. 1992, 48, Chapter 11, p. 161;
    • a) F. Wudl, A. Hirsch, K. C. Khemani, T. Suzuki, P.-M. Allemand, H. E. Koch, G. Srdanov, H. M. Webb, Fullerenes: Synthesis, Properties and Chemistry of Large Carbon Clusters (Eds. : G. S. Hammond, V. J. Kuck), ACS Symp. Ser. 1992, Vol. 48, Chapter 11, p. 161;
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    • Isomerically pure products were isolated, but it is not possible to assign their structures at present
    • Isomerically pure products were isolated, but it is not possible to assign their structures at present.
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    • 33846692000 scopus 로고    scopus 로고
    • Crystal data for 4a: C87H55NO12, M, 1306.32, triclinic, P1̄, a, 9.961(2, b, 13.569(3, c, 24.135(5) Å, α, 91.30(3, β= 91.51(3, γ, 109.84(3)°, V, 3065.8(11) A°3, T, 143(2) K, Z, 2, ρcalcd, 1.415 Mgm-3, graphite monochromatized MoKα radiation, λ, 0.71073 A°, crystal size 0.60×0.40×0.12 mm3. Data collected on a Rigaku RAXIS RAPID IP diffractometer, 10659 unique reflections (Rint, 0.04579, Refinement on F2, final residuals R1, 0.0693 for 4640 reflections with I>2σI, wR2, 0.1913 for all data. CCDC-284233 (4a, 284234 (6d, and -290716 (14a) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • 2, final residuals R1 = 0.0693 for 4640 reflections with I>2σI), wR2 = 0.1913 for all data. CCDC-284233 (4a), -284234 (6d), and -290716 (14a) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
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    • 2, final residuals R1 = 0.0558 for 3408 reflections with I>2σI), wR2 = 0.1103 for all data.
    • 2, final residuals R1 = 0.0558 for 3408 reflections with I>2σI), wR2 = 0.1103 for all data.
  • 32
    • 33846670565 scopus 로고    scopus 로고
    • Crystal data for 14a: C79H37C19N 2O7, M, 1445.16, triclinic, P1̄, a, 9.7211(19, b, 13.513(3, c, 23.003(5) Å, α, 88.89(3, β= 87.79(3, γ, 76.64(3)°, V, 2969.9(10) Å3, T, 143(2) K, Z, 2, ρcalcd, 1-616 Mg m-3, graphite monochromatized MoKα radiation, λ, 0.71073 Å, crystal size 0.40×0.20×0.12 mm3. Data collected on a Rigaku RAXIS RAPID IP diffractometer, 13297 unique reflections Rint, 0.0363, Refinement on F2, final residuals R1, 0.0553 for 7966 reflections with I > 2σI, wR2, 0.1620 for all data
    • 2, final residuals R1 = 0.0553 for 7966 reflections with I > 2σI), wR2 = 0.1620 for all data.
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    • Only the depicted enantiomer has been named for the racemates following IUPAC Recommendations 2002: W. H. Powell, F. Cozzi, G. P. Moss, C. Thilgen, R. J.-R. Hwu, A. Yerin, Pure Appl. Chem. 2002, 74, 629.
    • Only the depicted enantiomer has been named for the racemates following IUPAC Recommendations 2002: W. H. Powell, F. Cozzi, G. P. Moss, C. Thilgen, R. J.-R. Hwu, A. Yerin, Pure Appl. Chem. 2002, 74, 629.
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    • For the preparation of aziridine see
    • For the preparation of aziridine see: H. Y. Kim, A. Talukdar, M. Cushman, Org. Lett. 2006, 8, 1085.
    • (2006) Org. Lett , vol.8 , pp. 1085
    • Kim, H.Y.1    Talukdar, A.2    Cushman, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.