Linear aliphatic oligoesters derived from ε-caprolactone (CL) were synthesized by ring-opening polymerization (ROP) using terpene alcohols that have antibacterial activity as initiators (nerol, geraniol, β-citronellol and farnesol). Ammonium decamolybdate (NH4)8[Mo10O34] was used as a catalyst. From previous oligoesters, monodisperse species of monomers, dimers, and trimers were isolated by flash column chromatography (FCC). Poly(ε-caprolactone) (PCL) oligoesters [oligo(CLs)] and monodisperse oligomeric species were characterized by different analytical techniques, such as nuclear magnetic resonance (NMR) spectroscopy, electrospray ionization quadrupole time-of-flight mass spectrometry (ESI/MS-QTOF), and Fourier-transform infrared (FTIR) spectroscopy to determine the chemical nature of the samples. The thermal properties were analyzed by differential scanning calorimetry (DSC), which showed significant differences between the olefin and alkyl terminal groups. The end-groups affected crystalline domains according to the crystallization temperatures (T c), melting temperatures (T m), and glass transition temperature (T g) of the oligo(CLs) and monodisperse oligomeric species. In addition, the results of thermogravimetric analysis (TGA) suggest that the thermal degradation in the case of the monomer and dimer species with olefin terminal groups is similar compared to that with the alkyl terminal group. Due to the antimicrobial properties of olefinic initiators, microbiological tests were carried out on the monodisperse oligomeric species through studies of the minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and antibiograms. This is the first time in the literature that monodisperse oligomers derived from PCL functionalized with terpenes and alkyl end-groups were tested in terms of their antibacterial properties. The results indicated that these monodisperse species could lead to new antibiotic compounds with potential applications.
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