This article reports for the first time about a novel category of mono-substituted acetylene monomers (1-4, M1-M4) (C≡CCH 2 NHCSNHR, R for M1 = CH 2 CH 3 ; M2 = (CH 2 ) 3 CH 3 ; M3 = (CH 2 ) 5 CH 3 ; M4 = C 6 H 5 ). The four monomers were identified by FT-IR, 1 H-NMR, 13 C-NMR spectroscopy and elementary analysis. In the presence of a rhodium catalyst ((nbd)Rh + B − (C 6 H 5 ) 4 (nbd = 2,5-norbornadiene)), M1-M4 underwent polymerization and provided the expected poly(N-propargylthiourea)s in a moderate to high yield (58-92%) and with a high cis content ( 91%) in the polymer backbones. The substituents had a big influence on the solubility of poly(N-propargylthioureas). Among the four polymers, polymer 4 (poly(4)) showed good solubility and relatively higher number-average molecular weight (up to 12 000). This polymer was further characterized by FT-IR and UV-Vis spectroscopy. TGA analysis demonstrated that the polymer remained stable up to 175 • C. Poly(4) exhibited considerable adsorption ability toward to Fe 3+ ions. The novel substituted polyacetylenes are also expected to exhibit some unique properties, such as inhibition of bacteria, chiral recognition, metal extraction and metal detection, derived from a combination of conjugated polymer backbones and highly functional thiourea groups in the side-chains.