A convenient method for the preparation of fluoroalkyl-modified C60 using fluoroalkyl halides with Bu3SnH under radical conditions has been developed; 1-fluoroalkyl-2-hydro[60]fullerenes at 6,6-junction (C60(RF)H : RF = CF2CO2Et, n-C6F13, CF2Br, n-C12F25, and (CF2)6I) were synthesized effectively.
No takes yet. Share an insight, caveat, or question.
Yoshida et al. (1996) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: