Spiro fullerenes formed from homofullerenes and fullerenes fused to organic rings follow the normal procedures for naming organic spiro systems that contain at least one polycyclic ring system (ref. 11). Spiro fullerene parent hydrides will not necessarily have unprimed numbers as locants.
Examples:
2",7"-Dinitrospiro[cyclopropa[1,9](C60-Ih)[5,6]fullerene-3',9"-fluorene]
Dispiro[cyclopropane-1,3"-cyclobuta[1,9](C60-Ih)[5,6]fullerene-4",2'''-[1,3]dioxane]
Dispiro[cyclohexane-1,3"-dicyclopropa[1,9:52,60](C60-Ih)[5,6]fullerene-3''',1''' '-cyclohexane]
11. International Union of Pure and Applied Chemistry. Division of Organic Chemistry. Commission on Nomenclature of Organic Chemistry, "Extension and Revision of the Nomenclature for Spiro Compounds (IUPAC Recommendations 1999)". Pure Appl. Chem. 1999, 71, 531-558.