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One-step synthesis of fullerene hydride C60H2 via hydrolysis of acylated fullerenes

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Tzirakis, Manolis D., Alberti, Mariza N., Nye, Leanne C., Drewello, Thomas and Orfanopoulos, Michael. (2009) One-step synthesis of fullerene hydride C60H2 via hydrolysis of acylated fullerenes. Journal of Organic Chemistry, Vol.74 (No.15). pp. 5746-5749. ISSN 0022-3263

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Official URL: http://dx.doi.org/10.1021/jo900934j

Abstract

The hitherto unexplored class of acylated fullerene compounds has been shown to be excellent C60H2 precursors. Upon a simple treatment with basic Al2O3, they are hydrolyzed quantitatively into C60H2, This key feature led to the development of a new, straightforward protocol for the selective synthesis of the simplest [60] fullerene hydride, C60H2. This protocol may offer an advantageous alternative to previously known methods for the synthesis of C60H2 allowing for a rapid access to C60H2 in good yield and high purity without tedious separating processes.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Divisions: Faculty of Science > Chemistry
Journal or Publication Title: Journal of Organic Chemistry
Publisher: American Chemical Society
ISSN: 0022-3263
Date: 7 August 2009
Volume: Vol.74
Number: No.15
Number of Pages: 4
Page Range: pp. 5746-5749
Identification Number: 10.1021/jo900934j
Status: Peer Reviewed
Publication Status: Published
Access rights to Published version: Restricted or Subscription Access
Funder: The Greek National Scholarships Foundation (IKY)
URI: http://wrap.warwick.ac.uk/id/eprint/17514

Data sourced from Thomson Reuters' Web of Knowledge

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