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Volumn , Issue 24, 2002, Pages 3062-3063

Nucleophilic substitution of alkylchlorodihydro[60]fullerenes: Thermodynamic stabilities of alkylated C60 cation intermediates

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; CARBON 60; CATION; FULLERENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0036923190     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b210126b     Document Type: Article
Times cited : (9)

References (24)
  • 6
    • 0012252077 scopus 로고    scopus 로고
    • note
    • The synthesis and characterization of 2b and 2d have been described in ref. 1. Compounds 2a, 2c and 3a were synthesized in similar manners.
  • 7
    • 0012253132 scopus 로고    scopus 로고
    • note
    • 0 are the rate constants of solvolysis of tert-butyl chloride at 25°C in a given solvent and in 80 vol% aqueous ethanol, respectively;
  • 9
    • 0012331021 scopus 로고    scopus 로고
    • note
    • 60 in 11 and 30%, respectively;
  • 13
    • 0012348983 scopus 로고    scopus 로고
    • note
    • 70 was added before sample injection.
  • 14
    • 0012252294 scopus 로고    scopus 로고
    • note
    • The two isomers were not monitored separately because of their nearly identical HPLC retention times.
  • 17
    • 0012286074 scopus 로고    scopus 로고
    • note
    • 60 core with a staggered conformation in which the chlorine atom has a gauche orientation. Details of the theoretical results will be reported separately.
  • 22
  • 24
    • 0012253733 scopus 로고    scopus 로고
    • note
    • R+ values of 1a-d also indicated the similarity in stability between these cations and the tert-butyl cation. The result will be reported in due course.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.