Chemical generation of the dianion of C-60 followed by the reaction of monoiodo- or alpha,omega-diiodo-alkanes leads to the high-yield and regioselective formation of 1,2- and 1,4- dialkyl C-60 or 1,2-fused ring C-60 adducts. C-13 NMR studies including proton-carbon correlations were used to ascertain the geometry of the products while the new closed adducts were also characterized by MS, W-vis and voltammetric measurements. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.
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Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, JapanOsaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan
Fukuzumi, S
Suenobu, T
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机构:Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan
Suenobu, T
Hirasaka, T
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机构:Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan
Hirasaka, T
Arakawa, R
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机构:Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan
Arakawa, R
Kadish, KM
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机构:Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan
机构:
Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, JapanOsaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan
Fukuzumi, S
Suenobu, T
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机构:Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan
Suenobu, T
Hirasaka, T
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机构:Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan
Hirasaka, T
Arakawa, R
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机构:Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan
Arakawa, R
Kadish, KM
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机构:Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, Suita, Osaka 5650871, Japan