Synthesis of a short-chain fullerene dimer

Tetrahedron Letters

Volumn 47, Issue 42, 2006, Pages 7413-7415

  Hingston, Timothy J ^a   Sambrook, Mark R ^a   Porfyrakis, Kyriakos ^a   Briggs, G Andrew D ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

Cycloadditions; Dimers; Fullerenes

Indexed keywords

DIMER; FULLERENE DERIVATIVE;

ABSORPTION SPECTROSCOPY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLOADDITION; ISOLATION PROCEDURE; MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; ULTRAVIOLET SPECTROSCOPY;

EID: 33748427181     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.08.061     Document Type: Article

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19. - Calculated mass 399.7319.
20. 2O (125 ml). The toluene layer was collected, and dried over magnesium sulfate. After filtration and solvent exchange for fresh toluene, the products were separated using HPLC, giving monomer 1 in 75% yield (443 mg) and dimer 2 produced in 12% yield (112 mg).
21. -.
22. -.
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