Benzoic acid (4-(2-propoxy)-3-vinylphenyl) ester (1), the divinyl compounds terephthalic acid bis(4-(2-propoxy)-3-vinylphenyl) ester (2) and bis(4-(2-propoxy)-3-vinylphenoxy)diphenylsilane (3), and the trivinyl compound benzene-1,3,5-tricarboxylic acid tris(4-(2-propoxy)-3-vinylphenyl) ester (4) were used for the synthesis of a series of ruthenium-based mono-, bi-, and trinuclear metathesis catalysts, i.e., RuX and 1,3,5, where the corresponding trifluoroacetatederived systems were prepared from the parent dichloro-substituted initiators via reaction with CF 3 COOAg. Initiators I1a-I4a and I1b-I4b were used for the cyclopolymerization of a series of 1,6-heptadiynes, i.e., dimethyl dipropargylmalonate (M1), diethyl dipropargylmalonate (M2), di-tert-butyl dipropargylmalonate (M3), 4-(ethoxycarbonyl)-1,6-heptadiyne (M4), 4,4-(bishydroxymethyl)-1,6-heptadiyne (M5), and 4-(hydroxymethyl)-1,6-heptadiyne (M6), to yield the corresponding A n -X-A n type block and (A n ) 3 X type tristar copolymers. Cleavage of the A n -X-A n type block copolymerwith tetrabutylammonium fluoride resulted in the formation of the low-PDI telechelic homopolymer M2 25 -CH-[2-(2-PrO)-1,5-C 6 H 3 ]-OH with half the molecular weight of the parent block copolymer, indicative for an equal activity of both initiator sites in I3b. An interesting finding was the fact that monomers with reduced steric demands in the 4-position (M1, M4, M5, and M6) could even be polymerized with chlorine-based initiators; however, values for M n were in general lower than the calculated ones. In contrast to Mo-based initiators, no influence of monomer size on the structure of the final polymer in terms of the ratio of 1,2-(cyclopent-1-ene)vinylene and 1,3-(cyclohex-1-ene)methylidene units, respectively, was observed.