Towards sixfold functionalization of buckminsterfullerene (C60) at fully addressable octahedral sites

被引:0
|
作者
Qian, WY [1 ]
Rubin, Y [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
关键词
cycloadditions; Diels-Alder reactions; diimines; fullerenes; semiempirical calculations;
D O I
10.1002/(SICI)1521-3773(19990816)38:16<2356::AID-ANIE2356>3.0.CO;2-Y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Selective C60-functionalizations that provide access to unusual multifunctional molecules are of interest in the construction of highly organized three-dimensional assemblies. The temporary 'masking' of three of the most reactive sites on C60 by a bisdiene tether has allowed the facile and high-yielding formation of the fully differentiated trisadduct I and the interesting hexaadduct 2.
引用
收藏
页码:2356 / 2360
页数:5
相关论文
共 50 条
  • [1] Toward sixfold functionalization of fullerene C60 with fully addressable octahedral locations.
    Qian, WY
    Rubin, Y
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1999, 218 : U154 - U155
  • [2] C60 - BUCKMINSTERFULLERENE
    KROTO, HW
    ALLAF, AW
    BALM, SP
    CHEMICAL REVIEWS, 1991, 91 (06) : 1213 - 1235
  • [3] A MULTIPLY-SUBSTITUTED BUCKMINSTERFULLERENE (C60) WITH AN OCTAHEDRAL ARRAY OF PLATINUM ATOMS
    FAGAN, PJ
    CALABRESE, JC
    MALONE, B
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (24) : 9408 - 9409
  • [4] Stability of buckminsterfullerene, C60
    Tomita, S
    Andersen, JU
    Hansen, K
    Hvelplund, P
    CHEMICAL PHYSICS LETTERS, 2003, 382 (1-2) : 120 - 125
  • [5] Is C60 buckminsterfullerene aromatic?
    Chen, Zhongfang
    Wu, Judy I.
    Corminboeuf, Clemence
    Bohmann, Jonathan
    Lu, Xin
    Hirsch, Andreas
    Schleyer, Paul von Rague
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2012, 14 (43) : 14886 - 14891
  • [6] THE FRONTIER ORBITALS OF BUCKMINSTERFULLERENE C60
    Ji Min YAN
    Xue Qi YI Institute of Chemistry. Academia Sinica
    ChineseChemicalLetters, 1992, (06) : 445 - 448
  • [7] Local σ-π mixing in C60 buckminsterfullerene
    Azami, S. M.
    Pooladi, R.
    Sheikhi, M. H.
    JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, 2009, 901 (1-3): : 153 - 156
  • [8] Vapor pressure of C60 buckminsterfullerene
    Piacente, V., 1600, ACS, Washington, DC, United States (99):
  • [9] THE HEAT OF FORMATION OF BUCKMINSTERFULLERENE, C60
    SCHULMAN, JM
    DISCH, RL
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1991, (06) : 411 - 412
  • [10] A CRYSTALLOGRAPHIC ANALYSIS OF C60 (BUCKMINSTERFULLERENE)
    HAWKINS, JM
    LEWIS, TA
    LOREN, SD
    MEYER, A
    HEATH, JR
    SAYKALLY, RJ
    HOLLANDER, FJ
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1991, (11) : 775 - 776