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Detection of methoxylated anions of fullerenes by electrospray ionization mass spectrometry

Journal Article · · Journal of the American Chemical Society; (United States)
DOI:https://doi.org/10.1021/ja00075a057· OSTI ID:5116219
;  [1]
  1. New York Univ., NY (United States)

Electrospray ionization mass spectrometry (ESI-MS) has been applied to the study of the reactions of fullerenes in solution. The C[sub 60][sup [minus]] and other anionic species are readily examined directly in 1:1 toluene/methanol by negative ion ESI-MS. Addition of a NaOMe/MeOH solution to C[sub 60] in toluene leads to formation of C[sub 60][sup [minus]] and C[sub 60](OMe)[sub n][sup [minus]] (n = 1, 3, 5, 7) as major anions as well as a product derived from coupling and oxidation with toluene, C[sub 60]O[sub 2](CH[sub 2]C[sub 6]H[sub 5])[sup [minus]]. The expected isotopic shifts of the peaks in deuteriomethanol or deuteriotoluene confirmed the proposed formulas. Similar experiments on C[sub 70] gave the same types of anions. A crown ether tagged fulleroid was also used for the same reaction, but the ESI-MS study could be done in both positive and negative ion modes. Our results showed that fulleroids do have chemical properties similar to those of fullerenes themselves. 21 refs., 4 figs.

OSTI ID:
5116219
Journal Information:
Journal of the American Chemical Society; (United States), Journal Name: Journal of the American Chemical Society; (United States) Vol. 115:22; ISSN JACSAT; ISSN 0002-7863
Country of Publication:
United States
Language:
English