Impact Factor 3.782 | CiteScore 3.51
More on impact ›

Original Research ARTICLE

Front. Chem., 22 May 2019 |

Stereoselective Ring-Opening (Co)polymerization of β-Butyrolactone and ε-Decalactone Using an Yttrium Bis(phenolate) Catalytic System

  • 1Department of Chemistry, Faculty of Science, Mahidol University, Bangkok, Thailand
  • 2Department of Materials Science and Engineering, School of Molecular Science and Engineering, Vidyasirimedhi Institute of Science and Technology, Rayong, Thailand
  • 3Chimie ParisTech, PSL University, CNRS, Institut de Recherche de Chimie Paris, Paris, France
  • 4CNRS UPR2301, Institut de Chimie des Substances Naturelles, Université Paris-Sud, Université Paris-Saclay, Gif-sur-Yvette Cedex, France
  • 5INSTM Research Unit, Department of Chemistry and Biology A. Zambelli, University of Salerno, Fisciano, Italy

An effective route for ring-opening copolymerization of β-butyrolactone (BBL) with ε-decalactone (ε-DL) is reported. Microstructures of the block copolymers characterized by 13C NMR spectroscopy revealed syndiotactic-enriched poly(3-hydroxybutyrate) (PHB) blocks. Several di- and triblock copolymers (PDL-b-PHB and PDL-b-PHB-b-PDL, respectively) were successfully synthesized by sequential addition of the monomers using (salan)Y(III) complexes as catalysts. The results from MALDI-ToF mass spectrometry confirmed the presence of the copolymers. Moreover, thermal properties of the block copolymers were also investigated and showed that the microphase separation of PDL-b-PHB copolymers into PHB- and PDL-rich domains has an impact on the glass transition temperatures of both blocks.


Polyhydroxyalkanoates (PHAs) comprise a group of naturally occurring aliphatic polyesters produced by bacteria and other living organisms (Reddy et al., 2003; Tan et al., 2017). These biodegradable and hydrophobic materials combine the film-barrier properties of polyesters with the mechanical performances of petroleum-based polyethylene and polypropylene. Thanks to their interesting properties, these polymers are already used in packaging, automotive, hygienic, agricultural, and biomedical applications (Costa et al., 2013; Khosravi-Darani, 2015; Luef et al., 2015; Ali and Jamil, 2016; Yeo et al., 2018). The most common PHA is poly(3-hydroxybutyrate) (PHB), which is a linear, isotactic, high-molecular-weight polymer. However, this polymer has poor mechanical properties due to its brittleness and a susceptibility to thermal degradation slightly above its melting temperature. Therefore, development of a synthesis method producing PHBs with controlled molecular weight, lower melting temperature, and lower brittleness would be a solution for industrial manufacturing and practical use of ideal bio-based polymers (Li et al., 2016). One of the most effective approaches for the controlled synthesis of PHB is ring-opening polymerization (ROP) of β-butyrolactone (BBL) (Kricheldorf and Eggerstedt, 1997; Hori and Hagiwara, 1999; Rieth et al., 2002; Ajellal et al., 2010; Brulé et al., 2011, 2013; Li et al., 2016). ROP of β-butyrolactone mediated by metal systems has attracted much attention in recent years and had considerable achievements (Kricheldorf and Eggerstedt, 1997; Hori and Hagiwara, 1999; Rieth et al., 2002; Ajellal et al., 2010; Brulé et al., 2011). A major point of interest for some of these catalysts is the high degree of (stereo)control they exhibit under suitable conditions.

Various modification methods have been reported to improve the performance of PHB (Thomas, 2010; Aluthge et al., 2013; Lin et al., 2013; Olsén et al., 2013; Barouti and Guillaume, 2016). In particular, the formation of PHB-based copolymers might be a promising strategy but still remains a considerable synthetic challenge (Aluthge et al., 2013; Barouti and Guillaume, 2016). In this regard, poly(ε-decalactone) (PDL), a bio-based polymer synthesized by ROP of ε-decalactone (ε-DL), might be a good candidate to copolymerize with PHB in order to improve its mechanical properties (Lin et al., 2013; Olsén et al., 2013). Indeed, this polymer has been shown to be amorphous, with a low Tg value (i.e., −53°C) (Olsén et al., 2013). Although some initiators (co)polymerize ε-decalactone with good control, (Chuang et al., 2013; Lin et al., 2013; Olsén et al., 2013; Jasinska-Walc et al., 2014, 2015; Martello et al., 2014; Schneiderman et al., 2014, 2015; Lee et al., 2015; Zhu et al., 2015, 2018; Mannion et al., 2016; Tang et al., 2017) copolymerization of ε-DL with rac-BBL is still unknown. In this paper, we present the first example of an effective block copolymerization of BBL and DL initiated by a group 3 metal system to produce high-molecular-weight polymers with narrow molecular weight distributions.

Results and Discussion

In our search for new copolymerization catalysts, we focused our efforts on investigating the catalytic activity of (salan)Y(III) complexes known to be active for PHB formation (Fang et al., 2013). Therefore, we decided to study the potential of such a catalytic system in a copolymerization procedure, aiming to produce PDL-PHB block copolymers with a one-pot sequential methodology. In accordance with previous observations, the reaction of commercially available Y(OiPr)3 with the salan ligand L produces a mixture of bimetallic complexes [(L)Y(μ-OiPr)]2 (1) and (L)2Y2(μ-OiPr)(μ-OH) (2) (Scheme 1). Only volatile by-products are then removed between the yttrium alkoxide formation step and the polymerization step so that the resulting complexes are ready for polymerization without purification.


Scheme 1. Synthesis of complexes 1 and 2.

Firstly, we investigated the homopolymerization of ε-decalactone using complexes 1 and 2. The results are summarized in Table 1. These complexes are active initiators for the controlled ROP of ε-DL under mild conditions. The corresponding polymers formed had narrow polydispersities (PDI = Mw/Mn), and GPC chromatograms of the isolated polymers are monomodal, suggesting that only one species in solution is active for the ROP of DL (Figure S1). As was already demonstrated for rac-BBL (Fang et al., 2013), we hypothesize that excess monomer cleaves the dimeric structure of both yttrium alkoxide complexes. When these species are exposed to excess DL, the monomer is coordinated and allows the formation of a mononuclear (salan)Y(OiPr)(DL) complex and a (salan)Y(OH)(DL) species, presumably inactive for polymerization.


Table 1. Polymerization of ε-decalactone using (salan)Y(III) complexesa.

The resulting catalytic system proved to be active at 50°C in either C6D6 or toluene solutions. For [DL]/[Y] = 62.5, polymerization in C6D6 reached 92% conversion in 10 h (Table 1, Entry 2), while polymerization in toluene achieved 80% conversion within 14 h (Table 1, Entry 3). Reducing or increasing the monomer concentration resulted in no significant change of the polymerization control (Table 1, Entries 3 and 4). Although our yttrium-based system was also active at 50°C in neat DL, low catalytic activities were observed, probably due to viscosity issues (Table 1, Entry 5) (Moritz, 1989). All other polymerization reactions were therefore preferably conducted in C6D6 at [ε-DL] = 2.5 M. Interestingly, this system proved to be active in the presence of 125–625 equiv. of lactone (Table 1, Entries 6–8), resulting in a TOF of 6 h−1.

For [DL]/[Y] < 100, the polymers produced have narrow molecular weight distributions and experimental number-average molecular masses (Mn) close to the theoretical ones. However, for higher ratios, experimental Mn values do not correspond well with calculated Mn values. This mismatch possibly arises from suppression of hydrodynamic volume of PDL chains in THF or poor correlation between the polystyrene calibration of the GPC and the actual molecular weights of the PDL chains, as already reported by Olsén et al. (2013).

To confirm the mechanism, PDL was characterized by NMR spectroscopy. The results showed the polymer chain having isopropoxide and hydroxyl as end groups (Figure 1 and Figure S2), suggesting that the polymerization occurs through a coordination–insertion mechanism. The mechanism is similar to the mechanism reported in ROP of lactones or lactide catalyzed by metal alkoxide complexes (Thomas, 2010; Chuang et al., 2013; Fang et al., 2013). Matrix Assisted Laser Desorption Ionisation - Time of Flight (MALDI-ToF) mass spectrometry analysis was also performed in order to determine structure of the resulting polymer. The sample from Table 1, Entry 1, was chosen to be characterized by MALDI-ToF-MS. The spectrum reveals a repeating mass series of linear PDL having isopropoxide as an end group (OiPr[ε-DL]nH + Cs+) (Figure S3). The result is consistent with the end-group analysis by 1H NMR spectroscopy. All of the PDL samples are transparent viscous liquids under ambient temperature, indicating the amorphous nature of PDL (Lin et al., 2013; Olsén et al., 2013). Having an amorphous nature, it could be a great choice to copolymerize PDL with brittle polymers to improve the performance of the resulting copolymer. Then, we investigated the catalytic activity of our yttrium system toward diblock copolymerization of ε-DL and rac-BBL. The copolymerization was first attempted through addition of monomer mixture to a C6D6 solution of the precursor at 60°C. However, this method failed to give block copolymers, as GPC analysis showed multimodal distributions. The copolymerization was therefore carried out by one-pot sequential copolymerization of first ε-DL and then rac-BBL at room temperature. The results are summarized in Table 2. For [monomers]/[Y] < 100, the copolymerization nearly reached completion for both monomers in < 5 h in C6D6 (Table 2, Entries 1 and 2). By doubling the monomer-to-metal ratio, the resultant polymer revealed a double experimental Mn value, indicating a controlled polymerization reaction (Table 2, Entries 1 and 2). The copolymerization was then conducted in toluene with high amounts of rac-BBL (Table 2, Entries 3–7). The resulting copolymers having 5–59 mol% of ε-DL were synthesized with TOF up to 44 h−1. Interestingly, the catalytic system also proved to be active for synthesizing PDL-b-PHB-b-PDL triblock copolymers by one-pot sequential copolymerization. The copolymerization achieved ~60% conversion of ε-DL and 99% conversion of rac-BBL (Table 2, Entries 8 and 9). GPC analysis of all the copolymers showed a monomodal peak with narrow molecular weight distributions Mw/Mn (Figure S1). As observed for the homopolymerization of ε-DL, lower experimental Mn values were obtained, probably due to poor correlation between the polystyrene calibration of the GPC and the actual molecular weights. In order to determine the diffusion coefficients of two copolymers of different sizes (Table 2, Entries 1 and 7), DOSY NMR experiments were performed. For the low-molecular-weight copolymer sample (Table 2, Entry 1), we measured a diffusion coefficient of 2.32 × 10−10 m2.s−1, while the higher-molecular-weight copolymer corresponded to a diffusion coefficient of 1.88 × 10−10 m2.s−1 (Table 2, Entry 7). As the rate of diffusion is inversely related to the molecular weight/size, these results are consistent with GPC analyses (Figures S12, S13).


Figure 1. 1H NMR (500 MHz, CDCl3) of PDL prepared by ROP of ε-DL with (salan)Y(III) complexes.


Table 2. Copolymerization of ε-DL and BBL using (salan)Y(III) complexesa.

In order to determine topology and end groups of the block copolymers, a diblock copolymer (PDL-b-PHB) (Table 2, Entry 1) and a triblock copolymer (PDL-b-PHB-b-PDL) (Table 2, Entry 8) were characterized by MALDI-ToF-MS (Figure 2 and Figure S4). The highest-intensity isotope distribution corresponds to linear PDL with an isopropoxide end group. Also, analysis of the minor isotope distributions confirmed the presence of the block copolymers. For instance, in Figure 2, the peak at m/z 1,980.31 corresponds to (OiPr[ε-DL]10[BBL]1H + Cs+). Similar MALDI-ToF-MS spectra showing minor series of isotope distribution of block copolymers were previously reported for poly(ε-decalactone)-b-poly(ω-pentadecalactone) copolymers (Jasinska-Walc et al., 2015). For PDL-b-PHB-b-PDL, similar isotope patterns are observed with mass higher than PDL-b-PHB (Figure S4).


Figure 2. MALDI-ToF-MS spectrum of PDL-b-PHB copolymer synthesized by ring-opening copolymerization of ε-DL and BBL with cesium trifluoroacetate as a cationizing agent.

Microstructural and Statistical Analysis of the Copolymers

Microstructural analysis of PDL-b-PHB was studied by 13C NMR spectroscopy. The resonances were assigned at the diad and triad levels. Ring-opening copolymerization of ε-DL and rac-BBL promoted by the yttrium complexes allowed the formation of syndiotactic PHB in PDL-b-PHB copolymers. By comparing 13C NMR of the block copolymers with a prior 13C NMR assignment for syndiotactic PHBs (Ajellal et al., 2009a; Fang et al., 2013), expansion of both carbonyl and methylene regions of PHB in PDL-b-PHB copolymer showed resonances that corresponded to triad sensitivities. The most intense resonances of the carbonyl and methylene regions at δ 169.32 and δ 40.79 ppm, respectively, were correlated to rr-centered triads. The lower-intensity resonances at δ 169.22 (carbonyl region) and δ 40.93 ppm (methylene region) were assigned to rm triads, and the others at δ 40.88 and δ 40.73 (methylene region) were mm and mr triads, respectively (Figure 3).


Figure 3. 13C NMR spectrum (125 MHz, CDCl3) of (A) carbonyl region and (B) methylene region, (C) methyl region of PHB in PDL-b-PHB copolymers (Table 2, entry 6).

Notably, the resonance attributed to mm triad is almost negligible, as expected for syndiotactic-enriched polymers (Amgoune et al., 2006; Ajellal et al., 2009a,b). The methyl region shows two resonances at the diad level. The resonance at δ 19.89 ppm was correlated to r diad, and the one at δ 19.84 ppm was assigned to m diad. Therefore, probability of racemic linkages between monomer units (Pr) can be calculated (Amgoune et al., 2006; Ajellal et al., 2009a,b). As expected for syndiotactic PHBs, Pr values of PHB in PDL-b-PHB are high (up to 0.90 syndiotacticity), for all diblock copolymers with 5–25 mol% ε-DL (Table 3, Entries 2–5), although we observed slight differences in the PHB microstructures depending on the reaction conditions (e.g., the concentration of monomer) (Amgoune et al., 2006; Ajellal et al., 2009b; Kramer et al., 2009). Finally, the microstructure of PDL blocks was not determined, due to insufficient resolution of ε-DL resonances at 125.0 MHz (Figure S5).


Table 3. Thermal data of selected syndiotactic-enriched PDL-b-PHB copolymers obtained by using (salan)Y(III) complexes. Data of a PHB homopolymer are also reported for comparison.

Thermal and X-Ray Analyses

Differential scanning calorimetry (DSC) and wide-angle x-ray diffraction (WAXD) analyses were performed to evaluate the influence of ε-DL content on the thermal and structural properties of the copolymers. The main thermal properties [i.e., glass transition temperatures (Tg), melting temperatures (Tm), and melting enthalpies (ΔHm)] of the selected PDL-b-PHB copolymers (corresponding to polymers of Table 2, Entries 3–6) are reported in Table 3. Thermal data of a PHB sample are also shown in Table 3 for comparison. All analyzed samples crystallize from melt during the DSC cooling run, and only small differences are observed for both Tm and ΔHm between first and second DSC heating runs. Second DSC heating thermograms of Entries 1–5 in Table 3 are reported in Figures S6S11.

The detected high values of Tm (ranging from 144 to 156°C) and ΔHm (ranging from 42 to 59 J/g) of copolymers are in good agreement with those observed for other syndiotactic-enriched PHB homopolymers (0.8 < Pr < 0.9) (Ajellal et al., 2009a; Ebrahimi et al., 2016). This hypothesis was confirmed by the WAXD patterns of all copolymers (Figure 4). Positions and intensity ratios of Bragg reflections detected in the spectra correspond to those observed for the syndiotactic PHB crystalline form (Kemnitzer et al., 1993, 1995). Moreover, WAXD spectra confirm that PDL blocks are amorphous, since no other Bragg reflection, except those of the syndiotactic PHB crystal form, was detected. Both thermal (Table 3) and structural (Figure 4) data suggest that ε-DL content ranging from 5 to 25 mol% has less effect on crystallinity of PHB blocks of PDL-b-PHB copolymers. It is worth noting that even by increasing ε-DL content to 59 mol% (Table 2, Entry 7), the Tm of the PHB block remains high (i.e., 143°C). Based on these data, it appears that the PDL block, probably due to its high flexibility, has no influence on the ability of the PHB block to crystallize.


Figure 4. WAXD patterns of PHB homopolymer and PDL-b-PHB samples (entries 1–5 in Table 3) produced via ROP of rac-BBL and copolymerization of rac-BBL and DL with (salan)Y(III) complexes.

The observed small differences in Tm of copolymers reported in Table 3 are possibly due to small differences in stereoregularity of the BBL unit sequences rather than to the PDL block lengths (Figure S14). These differences could explain why, in the second DSC heating run, the copolymer with 25 mol% of DL units (Table 3, Entry 5) has a Tm higher than the one of the PHB homopolymer having similar Mn (Table 3, Entry 1). In addition, PDL-b-PHB copolymers exhibited two Tg values (Tg values were evaluated by second DSC heating runs and reported in Table 3), one in the range −5, +4°C, similar to the Tg of a PHB homopolymer (Ajellal et al., 2009a), and the second in the range −52, −48°C, comparable to the Tg of a PDL homopolymer (Olsén et al., 2013). This probably results in the immiscibility of PHB and PDL blocks (Olsén et al., 2013). In Figure 5, Tg of both PDL and PHB blocks of the polymers reported in Table 3 was plotted as a function of ε-DL mol% content. A roughly linear behavior for both glass transition temperatures is observed. Therefore, increasing the length of the PDL blocks increases the glass transition temperatures of the PHB blocks while slightly decreasing the ones of the PDL blocks.


Figure 5. Plot of Tg(second run) vs. ε-DL mol% content of polymers from Table 3 (entries 1–5).

The behavior of both glass transition temperatures does not match the typical Flory–Fox (Fox and Flory, 1950) behavior, which, for low Mn values,1 predicts the Tg increase with increasing Mn. For the PDL block, the Tg decreases from −48 to −52°C when Mn, calc increases from 1.6 to 12.5 kDa. For the PHB block, copolymers (Table 3, Entries 2–5) have Tg ranging from 4 to −5°C, while the homopolymer (Table 3, Entry 1) has both the lowest Tg (−8°C) and the highest Mn,calc (25.5 kDa). This behavior can be explained assuming that PDL-b-PHB copolymers are constituted by immiscible blocks arranged in separated microphases. Based on this assumption, the reduction of the volume fraction2 of the PHB phase (f PHB), which decreases from 0.9 to 0.55 with increasing ε-DL content from 5 to 25 mol%, corresponds to a size decrease of PHB-rich domains. Moreover, we can also assume that the PHB blocks have a decreasing mobility, as they are segregated in gradually decreasing space and surrounded by an immiscible phase. As it is generally accepted that Tg is inversely related to polymer flexibility and mobility, the observed increase of Tg of PHB can therefore be explained by the reduction of the PHB block mobility due to the microphase separation of PDL-b-PHB copolymers into PDL and PHB domains.

For the PDL block, with increasing volume fraction of the PDL phase (f PDL), which increases from 0.1 to 0.45 with increasing ε-DL content from 5 to 25 mol%, the size of PDL-rich domains, increases and the mobility of PDL blocks, segregated into increasing space, is assumed to increase. Consequently, with increasing f PDL, the PDL block mobility increases approaching the mobility of PDL homopolymer, and as a result, Tg of the PDL block approaches that of the homopolymer (i.e., −53°C) (Olsén et al., 2013).


We have reported for the first time the ring-opening copolymerization of ε-DL with rac-BBL catalyzed by an yttrium-based catalytic system. Di- and triblock copolymers, PDL-b-PHB and PDL-b-PHB-b-PDL, were synthesized by means of one-pot sequential polymerization of ε-DL and rac-BBL. In agreement with NMR observations, thermal and structural analyses of PDL-b-PHB copolymers suggested that the observed crystallinity is due to the syndiotactic PHB block. Our results demonstrated that the PHB block crystallizes even in the presence of long, amorphous, and highly flexible PDL blocks. Moreover, it has been also observed that the microphase separation of PDL-b-PHB copolymers into PHB- and PDL-rich domains has an impact on the glass transition temperature of both blocks, which is not in agreement with the Flory–Fox relationship. As observed for a thermoplastic elastomer, the physical behavior of these copolymers (i.e., stiffness/flexibility) can be tuned by changing the ε-DL/BBL ratio, thanks to the simultaneous presence of a highly flexible phase (PDL block) associated with a rigid crystalline phase (PHB block). Such tunable physical behavior makes these copolymers industrially relevant.

Author Contributions

JK, VG, and CR performed the experiments. CT, JK, and VV wrote the manuscript with support from the co-authors. All authors analyzed the data, discussed the results, and commented on the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


CNRS, ENSCP, and the French Ministry of Research and Higher Education are thanked for financial support of this work. We gratefully acknowledge financial support from Mahidol University, the Royal Golden Jubilee Ph.D. Program (PHD/0106/2556), the Thailand Research Fund, and the French government's contribution to the RGJ-Ph.D. program. CT is grateful to the Institut Universitaire de France.

Supplementary Material

The Supplementary Material for this article can be found online at:


1. ^More correctly, for Tg values lower than Tg of polymer with infinite molecular mass. Tg of a shortly branched polymer with Mn > 20–30 kDa is commonly considered to be independent of Mn.

2. ^The volume fraction (f), at different ε-DL mol%, was calculated by using Mn.calc of both polymer blocks and density values of 0.97 and 1.22 g/cm3 for PDL and PHB blocks, respectively.


Ajellal, N., Bouyahyi, M., Amgoune, A., Thomas, C. M., Bondon, A., Pillin, I., et al. (2009a). Syndiotactic-enriched poly(3-hydroxybutyrate)s via stereoselective ring-opening polymerization of racemic β-butyrolactone with discrete yttrium catalysts. Macromolecules 42, 987–993. doi: 10.1021/ma8022734

CrossRef Full Text | Google Scholar

Ajellal, N., Durieux, G., Delevoye, L., Tricot, G., Dujardin, C., Thomas, C. M., et al. (2010). Polymerization of racemic β-butyrolactone using supported catalysts: a simple access to isotactic polymers. Chem. Commun. 46, 1032–1034. doi: 10.1039/b923546a

PubMed Abstract | CrossRef Full Text | Google Scholar

Ajellal, N., Thomas, C. M., and Carpentier, J.-F. (2009b). Functional syndiotactic poly(β-hydroxyalkanoate)s via stereoselective ring-opening copolymerization of rac-β-butyrolactone and rac-allyl-β-butyrolactone. J. Polym. Sci. A Polym. Chem. 47, 3177–3189. doi: 10.1002/pola.23418

CrossRef Full Text | Google Scholar

Ali, I., and Jamil, N. (2016). Polyhydroxyalkanoates: current applications in the medical field. Front. Biol. 11, 19–27. doi: 10.1007/s11515-016-1389-z

CrossRef Full Text | Google Scholar

Aluthge, D. C., Xu, C., Othman, N., Noroozi, N., Hatzikiriakos, S. G., and Mehrkhodavandi, P. (2013). PLA–PHB–PLA triblock copolymers: synthesis by sequential addition and investigation of mechanical and rheological properties. Macromolecules 46, 3965–3974. doi: 10.1021/ma400522n

CrossRef Full Text | Google Scholar

Amgoune, A., Thomas, C. M., Ilinca, S., Roisnel, T., and Carpentier, J. F. (2006). Highly active, productive, and syndiospecific yttrium initiators for the polymerization of racemic β-butyrolactone. Angew. Chem. Int. Ed. 45, 2782–2784. doi: 10.1002/anie.200600058

PubMed Abstract | CrossRef Full Text | Google Scholar

Barouti, G., and Guillaume, S. M. (2016). Polyhydroxybutyrate (PHB)-based triblock copolymers: synthesis of hydrophobic PHB/poly(benzyl β-malolactonate) and amphiphilic PHB/poly(malic acid) analogues by ring-opening polymerization. Polym. Chem. 7, 4603–4608. doi: 10.1039/C6PY00910G

CrossRef Full Text | Google Scholar

Brulé, E., Gaillard, S., Rager, M.-N., Roisnel, T., Guérineau, V., Nolan, S. P., et al. (2011). Polymerization of racemic β-butyrolactone using gold catalysts: a simple access to biodegradable polymers. Organometallics 30, 2650–2653. doi: 10.1021/om200271q

CrossRef Full Text | Google Scholar

Brulé, E., Guérineau, V., Vermaut, P., Prima, F., Balogh, J., Maron, L., et al. (2013). Polymerization of cyclic esters using N-heterocyclic carbene carboxylate catalysts. Polym. Chem. 4, 2414–2423. doi: 10.1039/c3py00108c

CrossRef Full Text | Google Scholar

Chuang, H.-J., Chen, H.-L., Huang, B.-H., Tsai, T.-E., Huang, P.-L., Liao, T.-T., et al. (2013). Efficient zinc initiators supported by NNO-tridentate ketiminate ligands for cyclic esters polymerization. J. Polym. Sci. A Polym. Chem. 51, 1185–1196. doi: 10.1002/pola.26486

CrossRef Full Text | Google Scholar

Costa, M. M., Cabral-Albuquerque, E. C., Alves, T. L., Pinto, J. C., and Fialho, R. L. (2013). Use of polyhydroxybutyrate and ethyl cellulose for coating of urea granules. J. Agric. Food Chem. 61, 9984–9991. doi: 10.1021/jf401185y

PubMed Abstract | CrossRef Full Text | Google Scholar

Ebrahimi, T., Aluthge, D. C., Hatzikiriakos, S. G., and Mehrkhodavandi, P. (2016). Highly active chiral zinc catalysts for immortal polymerization of β-butyrolactone form melt processable syndio-rich poly(hydroxybutyrate). Macromolecules 49, 8812–8824. doi: 10.1021/acs.macromol.6b01908

CrossRef Full Text | Google Scholar

Fang, J., Tschan, M. J.-L., Roisnel, T., Trivelli, X., Gauvin, R. M., Thomas, C. M., et al. (2013). Yttrium catalysts for syndioselective β-butyrolactone polymerization: on the origin of ligand-induced stereoselectivity. Polym. Chem. 4, 360–367. doi: 10.1039/C2PY20590D

CrossRef Full Text | Google Scholar

Fox, T. G., and Flory, P. J. (1950). Second-order transition temperatures and related properties of polystyrene. I. Influence of molecular weight. J. Appl. Phys. 21, 581–591. doi: 10.1063/1.1699711

CrossRef Full Text | Google Scholar

Hori, Y., and Hagiwara, T. (1999). Ring-opening polymerisation of β-butyrolactone catalysed by distannoxane complexes: study of the mechanism. Int. J. Biol. Macromol. 25, 237–245. doi: 10.1016/S0141-8130(99)00038-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Jasinska-Walc, L., Bouyahyi, M., Rozanski, A., Graf, R., Hansen, M. R., and Duchateau, R. (2015). Synthetic principles determining local organization of copolyesters prepared from lactones and macrolactones. Macromolecules 48, 502–510. doi: 10.1021/ma502262e

CrossRef Full Text | Google Scholar

Jasinska-Walc, L., Hansen, M. R., Dudenko, D., Rozanski, A., Bouyahyi, M., Wagner, M., et al. (2014). Topological behavior mimicking ethylene–hexene copolymers using branched lactones and macrolactones. Polym. Chem. 5, 3306–3310. doi: 10.1039/C3PY01754K

CrossRef Full Text | Google Scholar

Kemnitzer, J. E., Gross, R. A., McCarthy, S. P., Liggat, J., Blundell, D. J., and Cox, M. (1995). Crystallization behavior of predominantly syndiotactic poly(β-hydroxybutyrate). J. Environ. Polym. Degrad. 3, 37–47. doi: 10.1007/BF02067792

CrossRef Full Text | Google Scholar

Kemnitzer, J. E., McCarthy, S. P., and Gross, R. A. (1993). Preparation of predominantly syndiotactic poly β-hydroxybutyrate) by the tributyltin methoxide catalyzed ring-opening polymerization of racemic β-butyrolactone. Macromolecules 26, 1221–1229. doi: 10.1021/ma00058a004

CrossRef Full Text | Google Scholar

Khosravi-Darani, K. (2015). Application of poly(hydroxyalkanoate) in food packaging: improvements by nanotechnology. Chem. Biochem. Eng. Q. 29, 275–285. doi: 10.15255/CABEQ.2014.2260

CrossRef Full Text | Google Scholar

Kramer, J. W., Treitler, D. S., Dunn, E. W., Castro, P. M., Roisnel, T., Thomas, C. M., et al. (2009). Polymerization of enantiopure monomers using syndiospecific catalysts: a new approach to sequence control in polymer synthesis. J. Am. Chem. Soc. 131, 16042–16044. doi: 10.1021/ja9075327

PubMed Abstract | CrossRef Full Text | Google Scholar

Kricheldorf, H. R., and Eggerstedt, S. (1997). Polylactones. 41. polymerizations of β-d,l-butyrolactone with dialkyltinoxides as initiators. Macromolecules 30, 5693–5697. doi: 10.1021/ma970244c

CrossRef Full Text | Google Scholar

Lee, S., Lee, K., Kim, Y. W., and Shin, J. (2015). Preparation and characterization of a renewable pressure-sensitive adhesive system derived from ε-decalactone, l-lactide, epoxidized soybean oil, and rosin ester. ACS Sustain. Chem. Eng. 3, 2309–2320. doi: 10.1021/acssuschemeng.5b00580

CrossRef Full Text | Google Scholar

Li, Z., Yang, J., and Loh, X. J. (2016). Polyhydroxyalkanoates: opening doors for a sustainable future. NPG Asia Mater. 8, e265–e265. doi: 10.1038/am.2016.48

CrossRef Full Text | Google Scholar

Lin, J. O., Chen, W., Shen, Z., and Ling, J. (2013). Homo- and block copolymerizations of ε-decalactone with L-lactide catalyzed by lanthanum compounds. Macromolecules 46, 7769–7776. doi: 10.1021/ma401218p

CrossRef Full Text | Google Scholar

Luef, K. P., Stelzer, F., and Wiesbrock, F. (2015). Poly(hydroxy alkanoate)s in medical applications. Chem. Biochem. Eng. Q. 29, 287–297. doi: 10.15255/CABEQ.2014.2261

PubMed Abstract | CrossRef Full Text | Google Scholar

Mannion, A. M., Bates, F. S., and MacOsko, C. W. (2016). Synthesis and rheology of branched multiblock polymers based on polylactide. Macromolecules 49, 4587–4598. doi: 10.1021/acs.macromol.6b00792

CrossRef Full Text | Google Scholar

Martello, M. T., Schneiderman, D. K., and Hillmyer, M. A. (2014). Synthesis and melt processing of sustainable poly(ε-decalactone)-block-poly(lactide) multiblock thermoplastic elastomers. ACS Sustain. Chem. Eng. 2, 2519–2526. doi: 10.1021/sc500412a

CrossRef Full Text | Google Scholar

Moritz, H. U. (1989). Increase in viscosity and its influence on polymerization processes. Chem. Eng. Technol. 12, 71–87. doi: 10.1002/ceat.270120112

CrossRef Full Text | Google Scholar

Olsén, P., Borke, T., Odelius, K., and Albertsson, A. C. (2013). ε-Decalactone: a thermoresilient and toughening comonomer to poly(L-lactide). Biomacromolecules 14, 2883–2890. doi: 10.1021/bm400733e

PubMed Abstract | CrossRef Full Text | Google Scholar

Reddy, C. S. K., Rashmi, R. G., and Kalia, V. C. (2003). Polyhydroxyalkanoates: an overview. Bioresour. Technol. 87, 137–146. doi: 10.1016/S0960-8524(02)00212-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Rieth, L. R., Moore, D. R., Lobkovsky, E. B., and Coates, G. W. (2002). Single-site β-diiminate zinc catalysts for the ring-opening polymerization of β-butyrolactone and β-valerolactone to poly(3-hydroxyalkanoates). J. Am. Chem. Soc. 124, 15239–15248. doi: 10.1021/ja020978r

PubMed Abstract | CrossRef Full Text | Google Scholar

Schneiderman, D. K., Gilmer, C., Wentzel, M. T., Martello, M. T., Kubo, T., and Wissinger, J. E. (2014). Sustainable polymers in the organic chemistry laboratory: synthesis and characterization of a renewable polymer from δ-decalactone and L-lactide. J. Chem. Edu. 91, 131–135. doi: 10.1021/ed400185u

CrossRef Full Text | Google Scholar

Schneiderman, D. K., Hill, E. M., Martello, M. T., and Hillmyer, M. A. (2015). Poly(lactide)-block-poly(ε-caprolactone-co-ε-decalactone)-block-poly(lactide) copolymer elastomers. Polym. Chem. 6, 3641–3651. doi: 10.1039/C5PY00202H

CrossRef Full Text | Google Scholar

Tan, D., Yin, J., and Chen, G. Q. (2017). “Production of polyhydroxyalkanoates,” in Current developments in biotechnology and bioengineering: production, isolation and purification of industrial products, eds A. Pandey, S. Negi, and C. R. Soccol (Cambridge, MA: Elsevier), 655–692. doi: 10.1016/B978-0-444-63662-1.00029-4

CrossRef Full Text | Google Scholar

Tang, B., Schneiderman, D. K., Zare Bidoky, F., Frisbie, C. D., and Lodge, T. P. (2017). Printable, degradable, and biocompatible ion gels from a renewable aba triblock polyester and a low toxicity ionic liquid. ACS Macro Lett. 6, 1083–1088. doi: 10.1021/acsmacrolett.7b00582

CrossRef Full Text | Google Scholar

Thomas, C. M. (2010). Stereocontrolled ring-opening polymerization of cyclic esters: synthesis of new polyester microstructures. Chem. Soc. Rev. 39, 165–173. doi: 10.1039/B810065A

PubMed Abstract | CrossRef Full Text | Google Scholar

Yeo, J. C. C., Muiruri, J. K., Thitsartarn, W., Li, Z., and He, C. (2018). Recent advances in the development of biodegradable PHB-based toughening materials: approaches, advantages and applications. Mater. Sci. Eng. C Mater. Biol. Appl. 92, 1092–1116. doi: 10.1016/j.msec.2017.11.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, Y., Radlauer, M. R., Schneiderman, D. K., Shaffer, M. S. P., Hillmyer, M. A., and Williams, C. K. (2018). Multiblock polyesters demonstrating high elasticity and shape memory effects. Macromolecules 51, 2466–2475. doi: 10.1021/acs.macromol.7b02690

CrossRef Full Text | Google Scholar

Zhu, Y., Romain, C., and Williams, C. K. (2015). Selective polymerization catalysis: controlling the metal chain end group to prepare block copolyesters. J. Am. Chem. Soc. 137, 12179–12182. doi: 10.1021/jacs.5b04541

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: yttrium complex, ring-opening copolymerization, ε-decalactone, β-butyrolactone, tacticity

Citation: Kiriratnikom J, Robert C, Guérineau V, Venditto V and Thomas CM (2019) Stereoselective Ring-Opening (Co)polymerization of β-Butyrolactone and ε-Decalactone Using an Yttrium Bis(phenolate) Catalytic System. Front. Chem. 7:301. doi: 10.3389/fchem.2019.00301

Received: 22 November 2018; Accepted: 15 April 2019;
Published: 22 May 2019.

Edited by:

Pimpa Hormnirun, Kasetsart University, Thailand

Reviewed by:

Tanin Nanok, Kasetsart University, Thailand
Mina Mazzeo, University of Salerno, Italy

Copyright © 2019 Kiriratnikom, Robert, Guérineau, Venditto and Thomas. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Vincenzo Venditto,
Christophe M. Thomas,