The [2 + 2 + 2] cycloaddition reactions of 1,6-diynes and alkynes with a functional group(s), such as epoxide, oxetane, ester, alcohol, phenol, amine, borate, styrene, and methacrylate, catalyzed by it dipimp/CoCl(2 center dot)6H(2)O/Zn reagent [dipimp: 2-(2,6-diisopropylphenyl)-iminomethyl-pyridine] yielded a variety of polymerizable molecules (monomers) having a 2,3-dillydi-o-1H-indene core Structure. Similarly, the [2 + 2 + 2] cycloaddition reactions of 1,6-diynes and nitriles with a functional group(s) catalyzed by a dppe/CoCl2 center dot 6H(2)O/Zn reagent [dppe: 1,2-bis(diphenylphosphino)ethane] gave a variety of polymerizable molecules (monomers) with a 6,7-dihydro-5H-cyclopenta[c]pyridine core Structure. Among the resulting monomers, 5-phenyl-1,3-dihydrospiro[indene-2,3'-oxetane] prepared from 3,3-di(prop-2-ynyl)oxetane and phenylacetylene was representatively polymerized ill the presence of BF3 catalyst. A cationic random copolymerization of one of 1,3-dihydrospiro[indene-2,3'-oxetane] derivatives with 3-ethyl-3-(phenoxymethyl)oxetane and radical random copolymerization of diethyl 5-(4-vinylphenyl)-1H-indene-2,2(3H)-dicarboxylate with styrene have also been demonstrated.