8-Quinolinolato gallium complexes: iso-selective initiators for rac-lactide polymerization.

The synthesis and characterization of a series of 8-quinolinolato gallium complexes is presented, and the complexes are analogous to a series of aluminum complexes previously reported. The complexes have been shown to be active initiators for the ring-opening polymerization of rac-lactide. High degrees of polymerization control are demonstrated, as exemplified by the linear evolution of molecular weight as the polymerization progresses, narrow polydispersity indices, and molecular weights corresponding to those predicted on the basis of initiator concentration. Some of the initiators show iso-selective polymerization of rac-lactide, with Pi = 0.70. The polymerization rates have been monitored, and the pseudo first-order rate constants are compared to those of analogous aluminum compounds. The 8-quinolinolato gallium initiators show rates approximately 3 times higher than those of the series of aluminum compounds, while maintaining equivalently high iso-selectivity (Pi = 0.70) and polymerization control.

Introduction

As the demand and usage of polymers increases, so do issues associated with the sustainability of their source materials, their end of life fates, and costs. Economic and environmental concerns have driven the quest to replace some petroleum-derived materials with alternative polymers sourced from renewable raw materials and with improved end of life options.[1] Polylactic acid (PLA) is one such material: it is efficiently prepared from starch and after use can be either composted or recycled. Although current production is around 100 000 t/a, growth in manufacture is predicted, and its properties make it suitable for applications spanning packaging, fibers, composites, and medical devices. PLA is manufactured by the ring-opening polymerization (ROP) of lactide (LA) (Figure 1), a process that is initiated by Lewis acidic metal alkoxide complexes.[1b,2] Quite a range of metals have precedent for initiating ROP, and for further details on the scope of this catalysis, the reader is referred to several comprehensive reviews.[1b,2,3] There has been a long-standing academic interest in aluminum-based initiators, due to the excellent control conferred by this metal and the potential for some Al complexes to enable stereocontrolled ROP of rac-lactide.[4] From the materials property perspective, the production of stereoblock or stereocomplex PLA, via the iso-selective ROP of rac-LA, remains a high priority target. Such polymers exhibit significantly improved thermal-mechanical properties as compared to isotactic PLA; for example, the Tm for isotactic PLA is 170 °C, whereas that for stereoblock/stereocomplex PLA has been reported from 170 to 230 °C.[5] Such improvements in thermal stability could enable higher-value applications for PLA.

Figure 1

The isoselective ring-opening polymerization of rac-LA producing stereoblock PLA.

Aluminum initiators have a strong track record in the production of stereoblock/complex PLA from rac-LA. So far, the most iso-selective catn class="Chemical">alysts reported have been aluminum salen complexes. These are important academic targets, but the very slow rate of polymerization and high catalyst loadings required are significant drawbacks to these systems. Recently, several groups have reported improved activity and good iso-selectivities using indium catalysts.[6] For example, Mehrkhodavandi and co-workers reported the dinuclear complex, A (Figure 2), which polymerized 200 equiv of rac-LA in 30 min (298 K, methylene chloride, ∼0.5 M in [LA], 90% conversion, Pi = 0.62).[6a] This is a marked increase in rate as compared to the Al salen systems, which typically take hours to achieve high conversions and require increased temperatures.[4a−4c,4e−4g] Recently, the same group has extended the study of dinuclear and mononuclear indium complexes, resulting in efficient catalysis with a moderate-good isotactic bias (Pi = 0.77) in the best cases.[6a−6c] During the past 6 years, various other researchers have also reported promising indium-based catalysts, showing good rates and control.[6e,7] One attractive system was reported by Tolman and Hillmyer, where InCl3, in the presence of an equivalent each of an alcohol and triethylamine, polymerized rac-LA quite rapidly and with high heteroselectivity (Ps = 0.97, 1:100 [I]:[LA], 5 h).[8] Another example of an interesting indium complex was a racemic homoleptic species, B (Figure 2), reported by Okuda and Arnold, which was found to induce a slight isotactic bias (Pi = 0.63).[6d]

Figure 2

Examples of the structures of some stereoselective In and Ga initiators for rac-LA ROP.

Given the significant potential for n class="Chemical">Al and In initiators, it was somewhat surprising to discover that Ga complexes have been far less investigated in the ROP of LA. The first report of a dialkyl gallium alkoxide complex, C (Figure 2), demonstrated the potential of this group 13 congener for fast, controlled polymerization catalysis.[9] A recent comparative study of aluminum and gallium complexes, with the structures represented by compound D (Figure 2), showed that the Ga catalysts were faster and equally well controlled as the Al counterparts (Ga >99% conversion, 100 equiv of LA, 353 K, toluene 1 h, versus Al 45% conversion under the same conditions).[10] Despite the difference in rate, the change in metal center did not affect the polymerization stereoselectivity, with moderate iso-selectivity being observed for both the Al and the Ga initiators (Pi = 0.70).

We have previously reported a series of bis(8-quinolinolato) n class="Chemical">aluminum ethyl complexes, which, in the presence of iso-propyl alcohol, were efficient, iso-selective initiators (Pi = 0.76), for the ROP of rac-LA.[11] In this Article, the preparation and application of a series of gallium complexes, with some of the same 8-quinolinato ligands, is presented.

Results and Discussion

Two 8-hydroxyquinoline lin class="Chemical">gands, 1 and 2, were selected for investigation as ancillary ligands for gallium polymerization initiators (Figure 3). The ligands were selected as both are commercially available compounds, an attractive feature if polymerization activity of the initiators can be increased. Furthermore, the aluminum complexes of 1 and 2 showed distinct differences in polymerization activity with the halide substituents of ligand 2 enhancing activity and iso-selectivity.

Figure 3

The structures of the pro-ligands, 1 and 2.

Ga Complex Synthesis

Pro-ligands 1 and 2 were reacted with n class="Chemical">gallium(III)chloride, in toluene at 298 K, to form bis(8-quinolinolato) gallium chloride compounds, 1a and 2a (Figure 4). The compounds were isolated as yellow crystalline solids, in moderate yields. The completion of the complexation reaction was confirmed by 1H NMR spectroscopy where the resonances assigned to the quinolinolato protons were at higher chemical shift as compared to the pro-ligands, due to the Lewis acidic Ga center deshielding the nuclei. For each complex, the stoichiometry was further confirmed by elemental analysis and mass spectrometry. For compound 2a, single crystals suitable for X-ray diffraction experiments were obtained from a saturated toluene solution.

Figure 4

The preparation of compounds 1a, 2a, and 2b. Reagents and conditions: (i) GaCl3, toluene, 298 K, 12 h, 1a (51%), 2a (53%); (ii) KOtBu, benzene-d6, 298 K, 24 h, product not isolated.

The preparation of compounds 1a, 2a, and 2b. Reagents and conditions: (i) GaCl3, n class="Chemical">toluene, 298 K, 12 h, 1a (51%), 2a (53%); (ii) KOtBu, benzene-d6, 298 K, 24 h, product not isolated.

Compounds 1a and 2a were tested as initiators for the ROP of rac-LA (1 M solution of LA in THF, 298 K, 20 h) but showed no activity. This is in line with the findings of other researchers that n class="Chemical">metal halide complexes are rarely effective initiators, presumably due to the high M–Cl bond strength (481 kJ mol–1 versus 285 kJ mol–1 for Ga–O).[12] To prepare active initiators, the gallium chloride complexes were reacted further to generate new alkoxide and amide complexes. Thus, various salt metathesis reactions, with the relevant potassium salts (Figure 4), were attempted. The reactions of either compound 1a or 2a with potassium tert-butoxide, potassium ethoxide, or potassium bis(trimethylsilyl)amide all resulted in a mixture of products. As an illustrative example, the reaction between 2a and potassium tert-butoxide yielded a yellow powder whose 1H NMR spectrum indicated the presence of the desired alkoxide complex 2b (vide infra) together with another complex, showing only resonances for the quinolinate ligands. This second product was isolated and characterized by X-ray crystallography. The product was determined to be the oxo-bridged dimeric complex [(L2Ga)2(μ-O)], which formed due to undesired oxidation of the target alkoxide complex (see the Supporting Information). The oxygen/moisture necessary for such a degradation reaction is presumed to have arisen from residual oxygen/water in the reaction/NMR solvents. It should be noted that the same solvents were applied successfully for the isolation of aluminum and gallium alkyl complexes, without any such degradation, illustrating the high sensitivity of the alkoxide derivatives. The pure alkoxide complex 2b was prepared by an NMR scale reaction, in a Young’s tap NMR tube with centrifugation to remove the KCl byproduct (Supporting Information Figure S1). The 1H NMR spectrum shows that all of the quinolinate resonances are shifted to lower field, and furthermore the singlet at 1.17 ppm, with a relative integral of 9, confirms the presence of the tert-butyl alkoxide. The low intensity signal at 1.05 ppm corresponds to residual tert-butyl alcohol. Crystals suitable for X-ray diffraction analyses (vide infra) were grown by addition of hexane to this solution.

As an alternative route to n class="Chemical">gallium alkoxide complexes, gallium alkyl complexes [L2GaR] (R = alkyl) were targeted as suitable precursors for further reaction, via protonolysis, with various alcohols. The reaction of 2 equiv. of the pro-ligands, 1 and 2, with trimethylgallium resulted only in the formation of the monoligated complexes 1c and 2c [LGaMe2] together with the residual pro-ligands. It is relevant that the reaction was conducted under the same conditions as had previously enabled the isolation of the bis-ligated aluminum ethyl complexes [L2AlEt].[11] Changing the conditions, for example, by using more polar solvents such as THF or pyridine, resulted solely in the formation of the same monoligated product. It was only possible to form some of the desired bis-ligated gallium complexes, by refluxing the solutions in toluene for 24 h. Even under such forcing conditions, complex 2c was only partly converted, in low yield (25%), to the desired bis-ligated product 2d.

Given the preferential formation of monolin class="Chemical">gated complexes, these species were themselves directly targeted. Complexes 1c and 2c were prepared in high yields (74% and 87%, respectively) by reaction between equimolar quantities of trimethylgallium and the appropriate pro-ligands (Figure 5). The complex formation was confirmed by 1H NMR spectroscopy, where characteristic shifts in the quinolinolate resonances were observed. A singlet peak was observed between 0 and 0.1 ppm, with a total relative integral of 6, due to the two gallium coordinated methyl groups.

Figure 5

Synthetic routes attempted for the preparation of bis(8-quinolinolato) gallium methyl compounds, and the synthesis of compounds 1c, 2c, and 2d. Reagents and conditions: (i) 0.5 equiv of GaMe3, toluene, 298 K; (ii) GaMe3, toluene, 298 K (1c 74%, 2c 87%); (iii) 0.5 equiv of GaMe3, toluene, 393 K (25%).

Synthetic routes attempted for the preparation of bis(8-quinolinolato) gallium methyl compounds, and the synthesis of compounds 1c, 2c, and 2d. Reagents and conditions: (i) 0.5 equiv of n class="Chemical">GaMe3, toluene, 298 K; (ii) GaMe3, toluene, 298 K (1c 74%, 2c 87%); (iii) 0.5 equiv of GaMe3, toluene, 393 K (25%).

X-ray Crystallography

Crystals suitable for X-ray crystn class="Chemical">allographic analysis were isolated for compounds 2a and 2b from toluene and benzene-d6/hexane solutions, respectively. Both compounds crystallized in centrosymmetric (i.e., racemic) space groups. The structure of 2a has C2 symmetry about an axis that passes through the gallium and chlorine atoms (Figure 6), while the structure of 2b contains two crystallographically independent complexes, 2b-A (shown in Figure 7) and 2b-B (shown in Supporting Information Figure S4). All three molecules have pentacoordinate gallium centers with similar distorted trigonal bipyramidal coordination geometries, the τ values being 0.69, 0.57, and 0.57 for 2a, 2b-A, and 2b-B, respectively. The greater deviation of 2b-A and 2b-B from the trigonal bipyramidal geometry is due to the steric bulk of the tert-butoxide coligand. As with the aluminum complexes, in every case the only geometric isomer observed has the nitrogen atoms of the ligand coordinated trans to one another in the axial positions. The O-donors, from the quinolinolate rings, are coordinated at equatorial sites, with the remaining site being occupied by a chloride or alkoxide coligand, for 2a and 2b, respectively. The Ga–O and Ga–N bond lengths to the quinolinolato ligand differ between 2a and 2b (A and B) significantly; in the case of 2a, all of the Ga–O and Ga–N bonds are shorter than those in 2b-A and 2b-B. Again, this can be attributed to the larger tert-butoxide group versus chloride (Figure 6 and Table 1). In both cases, the Ga–N and Ga–O bonds of the ligand are longer than the Al–N and Al–O bonds previously observed for the aluminum quinolinolate complexes.[11]

Figure 6

The molecular structure of the C2-symmetric complex 2a. Selected bond lengths (Å): Ga–Cl(1) 2.1915(6), Ga–N(1) 2.1073(10), Ga–O(12) 1.8680(10).

Figure 7

The structure of one (2b-A) of the two independent complexes present in the crystals of 2b.

Table 1

Comparative Selected Bond Lengths (Å) for the Two Independent Complexes Present in the Crystals of 2b

bond length	2b-A	2b-B	bond length	2b-A	2b-B
Ga(1)–N(1)	2.1274(15)	2.1232(15)	Ga(1)–O(29)	1.8881(12)	1.8863(13)
Ga(1)–O(9)	1.8871(13)	1.8868(13)	Ga(1)–O(40)	1.7904(13)	1.7844(15)
Ga(1)–N(21)	2.1310(16)	2.1493(16)

The molecular structure of the C2-symmetric complex 2a. Selected bond lengths (Å): Ga–Cl(1) 2.1915(6), n class="Chemical">Ga–N(1) 2.1073(10), Ga–O(12) 1.8680(10).

Polymerization of rac-LA

Compounds 1c, 2b–d were tested as initiators in the ROP of rac-LA (Table 2). Polymerizations were conducted under a standard set of conditions: using a 1 M solution of n class="Chemical">lactide in toluene, at 348 K with an initiator concentration of 10 mM. In the case of compounds 1c and 2c, an equivalent (vs initiator) of isopropyl alcohol was added so as to enable generation of the active gallium alkoxide species in situ. The polymerizations were monitored by taking aliquots at regular time intervals, which were analyzed using 1H NMR spectroscopy, to determine the LA conversion, and by GPC-MALLS (gel permeation chromatography-multiangle laser light scattering), to determine the number average molecular weight, Mn, and the polydispersity index, PDI. In each case, the polymerization rate was compared by determination of the pseudo-first-order rate constant, kobs, which is the gradient of the linear plots of ln([LA]0/[LA]) versus time. The tacticity of the PLA obtained using compound 2b was determined by integration of the methyne region of the homonuclear decoupled NMR spectrum. The normalized integrals were compared against the values predicted using Bernoullian statistics to give the probability of isotactic linkages, Pi.[13] The polymerization results are summarized in Table 2.

Table 2

Polymerization Data Using Initiators 1c, 2b–d

initiator (I)	[LA]0/[iPrOH]/[I]a	time (h)	conversion (%)b	kobs × 105 (s–1)c	Mn (exp) (g mol–1)d	Mn (calcd) (g mol–1)	PDId	Pie
1c	1/1/100	45	92	1.8	11 300	13 200	1.24	0.5
2b	1/0/100	51	91	1.3	14 600	13 100	1.25	0.70
2c	1/1/100	38	96	2.6	15 200	13 800	1.19	0.5
2d	1/1/100		0
AlL2Et(11) R1=R2=Cl	1/1/100	137	91	0.5	9900	13 100	1.11	0.72

Polymerization conditions: toluene, 348 K, 1:1:100 [I]:[iPrOH]:[LA], 1 M [LA].

Determined by integration of the methine region of the 1H NMR spectrum (LA 4.98–5.04 ppm; PLA 5.08–5.22 ppm).

Determined from the gradients of the plots of ln{[LA]0/[LA]} versus time, where the average errors = 9–10% (determined using initiator 1c).

Determined by GPC in THF, using multiangle laser light scattering (GPC-MALLS).

Determined by analysis of all of the tetrad signals in the methine region of the homonuclear decoupled 1H NMR spectrum.

Polymerization conditions: n class="Chemical">toluene, 348 K, 1:1:100 [I]:[iPrOH]:[LA], 1 M [LA].

Determined by GPC in THF, using multiangle laser light scattering (GPC-Mn class="Chemical">ALLS).

Determined by analysis of n class="Chemical">all of the tetrad signals in the methine region of the homonuclear decoupled 1H NMR spectrum.

Because of the previously discussed problems with the isolation of compound 2b, the compound was synthesized in situ at a known concentration in toluene. The n class="Chemical">potassium chloride salt was removed by centrifugation, and the stock solution was added to the polymerization mixture. At this point, it is worth highlighting that the stoichiometric salt metathesis reaction proceeds to full conversion, as observed in the 1H NMR experiments. We can therefore eliminate the possibility of any excess potassium tert-butoxide salt, a known active initiator for the ROP reaction, initiating the polymerization. The initiator, 2b, was moderately active in the ROP of rac-lactide, with the polymerization proceeding to high conversion in excess of 50 h. Such rates are typical for discrete group 13 initiators, and indeed the polymerization occurs at a rate similar to that of the previously reported bis(8-quinolinolato) aluminum ethyl initiators.[9a,10,11] The initiator gives rise to PLA with a moderate degree of isotactic enchainment, with a Pi value of 0.70 consistent with a bias toward a stereoblock microstructure (Supporting Information Figure S8). There are only two other examples of iso-selective gallium initiators: compound D (Figure 2, Pi = 0.70) and a dimethyl gallium N-heterocyclic carbene complex, reported by Horeglad and co-workers, where a Pi value of up to 0.78 was claimed.[9b,10]

The initiator bis(5,7-dichloro-2-methyl-8-quinolinolato) gallium tert-butoxide, 2b, is ann class="Chemical">alogous to the bis(5,7-dichloro-2-methyl-8-quinolinolato) aluminum ethyl initiator, where the active alkoxide initiator is formed in situ by reaction with isopropyl alcohol during the course of the ROP reaction.[11] Initiator 2b is significantly faster than its aluminum analogue, with around a 3 times higher kobs value (1.3 × 10–5 s–1 for 2b vs 5.0 × 10–6 s–1 for the Al analogue) (Figure 8). This finding is in line with the only other comparison between Ga and Al complexes, in that case using κ3-N,O,N-{(C6F5N–C6H4)2O}MNMe2-type complexes.[10] The increased activity of the gallium compounds is tentatively attributed to the reduced Lewis acidity of Ga resulting in a weaker or more labile gallium alkoxide bond. In addition to the beneficial increase in rates, the Ga complex also shows high iso-selectivity and good polymerization control (equaling those observed with the Al analogue). This is particularly relevant as studies comparing Al and In catalysts have been hampered by a reduction in stereocontrol for the indium congeners.[7a]

Figure 8

Plot of ln([LA]0/[LA]) versus time of initiator 2b. Conditions: [LA]0 1 M, 1:100 [I]:[LA], toluene, 348 K.

Initiator 2d has the same ancillary ligand as bis(5,7-dichloro-2-methyl-n class="Chemical">8-quinolinolato) aluminum ethyl. The proposed active alkoxide complex is formed in situ during the polymerizations by reaction between 2d and the equivalent of alcohol. It was therefore somewhat surprising that complex 2d completely failed to polymerize rac-LA, even in the presence of an equivalent of isopropyl alcohol. Dagorne et al. used a κ3-N,O,N-{(C6F5N–C6H4)2O}GaMe initiator, in the presence of an equivalent of alcohol; this system was also completely inactive toward the ROP of rac-LA.[10] This was in contrast to the analogous aluminum complex, which showed moderate activity under the same conditions. The lack of reactivity of compound 2d, in the presence of iso-propyl alcohol, can be attributed to the failure to form the active alkoxide initiating species. An NMR scale experiment between 2d and a slight excess of iso-propyl alcohol, heated at 348 K for 24 h in toluene-d8, showed no conversion to the desired alkoxide product.

In contrast, monoligated compounds, 1c and 2c, were active initiators for the ROP of LA, in the presence of 1 equiv of n class="Chemical">isopropyl alcohol. The polymerizations using 1c and 2c are marginally faster than those using initiator 2b, with kobs values of 1.8 and 2.6 × 10–5 s–1, respectively (Figure 9). Thus, the halide ligand substituents increase the rate of polymerization, in line with previous structure–activity studies using Al complexes.[11] In both systems, an initiation period of approximately 2–3 h was observed (note such initiation periods are not observed using the gallium alkoxide complex 2b). Once again, the alcoholysis reaction was studied using compound 2c, which was heated at 348 K in toluene with 1–10 equiv of iso-propyl alcohol for 72 h. This experiment failed to result in any formation of a gallium alkoxide complex, leaving only compound 2c unreacted. The lack of reactivity of compound 2c toward alcoholysis indicates that the ring-opening polymerization may be likely to proceed via a different mechanism to the usual coordination insertion route. A possible reaction pathway could be via an activated monomer mechanism; such a mechanism does not require any formation of a gallium alkoxide species. Instead, the Lewis acidic gallium metal center acts as a nucleophile, activating the lactide monomer unit to attack by uncoordinated iso-propyl alcohol. Such a mechanism has been previously proposed for a series of (phenoxy-imine)indium complexes, which were also shown to be inert to alcoholysis reactions.[6e] Furthermore, invoking this mechanistic pathway could rationalize the lack of polymerization activity observed with compound 2d, which would be expected to have a lower Lewis acidity than 1c/2c due to its higher coordination number (penta- vs tetracoordinate Ga). Thus, 2c might be insufficiently Lewis acidic to activate the lactide, a key step in the activated monomer polymerization pathway.

Figure 9

Plot of ln([LA]0/[LA]) versus time of initiator 1c and 2c. Conditions: [LA]0 1 M, 1:1:100 [I]:[iPrOH]:[LA], toluene, 348 K.

Analysis of the homonuclear decoupled n class="Chemical">1H{1H} NMR spectrum showed the formation of atactic PLA for 1c and 2c, consistent with the reduced steric influence of the hydroxyl-quinoline ligands in monoligated complexes. All of the initiators display a high degree of polymerization control, showing a linear evolution of the Mn with % conversion (Supporting Information Figures S9 and S10) and Mn values that are close to those predicted on the basis of the initiator concentration (Table 2). The monomodal molecular weight distribution, observed with all initiators, is especially relevant for 2b as it provides further support for the lack of any additional initiating species, such as KOtBu, in the polymerization system. All of the PDIs are also narrow throughout the course of the polymerizations, below 1.25 in all cases, indicative of limited transesterification side reactions. The end groups of the polymers formed by initiators 1c and 2c were analyzed by MALDI-ToF mass spectrometry, which confirmed that the chains were end-capped with iso-propyl ester groups (Supporting Information Figure S11). The peaks were separated by 144 amu. However, there is also a series of low molecular weight peaks that correspond to the formation of cyclic PLA (Supporting Information Figure S12).

Plot of ln([LA]0/[LA]) versus time of initiator 1c and 2c. Conditions: [LA]0 1 M, 1:1:100 [I]:[iPrOH]:[LA], n class="Chemical">toluene, 348 K.

Conclusions

A series of gallium complexes featuring one or two n class="Chemical">8-quinolinolato ligands have been synthesized with either chloride, tert-butyl alkoxide, or methyl coligands. The new complexes were fully characterized, and in two cases X-ray crystallographic data were obtained. Some of the complexes were tested as initiators (2b) or as part of initiating systems, with exogenous alcohol (1c, 2c) for the polymerization of rac-LA. Both the initiator and the initiating systems displayed moderate rates and excellent polymerization control. It is tentatively proposed that compounds 1c and 2c operate by an activated monomer mechanism, due to their lack of reactivity with exogenous alcohol. The complexes were all more active than the aluminum counterparts.

Interestingly, initiator 2b yielded stereoblock PLA, with a Pi value of 0.70, from rac-LA. This is an unusun class="Chemical">al example of a gallium complex capable of exerting iso-selectivity and yielding the higher value stereoblock PLA. Of particular note is that the complex exhibits equivalent good stereocontrol to an aluminum analogue but operates at approximately 3 times the rate. It is clear that further improvements to the rate and stereocontrol are desirable and could be achieved by rational ligand design.

Experimental Section

Materials and Methods

All reactions were conducted under an inert n class="Chemical">nitrogen atmosphere, using a nitrogen-filled glovebox or standard Schlenk techniques. All solvents and reagents were obtained from commercial sources, and triethyl aluminum was obtained from Strem. Toluene was distilled from sodium, degassed, and stored under nitrogen. Isopropyl alcohol was heated to reflux over CaH2, distilled onto fresh CaH2 and further refluxed, then distilled, degassed, and stored under nitrogen. Benzene-d6 was distilled from sodium, and toluene-d8 and CDCl3 were dried over CaH2; all of the NMR solvents were degassed and stored under nitrogen. rac-Lactide was obtained from Purac Plc. and was purified by recrystallization (dry toluene) and sublimation (three times).

Nuclear magnetic resonance (NMR) spectra were recorded on a Bruker Av400 spectrometer operating at 400 MHz for 1H, and 100 MHz for n class="Chemical">13C{1H} spectra. Solvent peaks were used as internal references for 1H and 13C chemical shifts (ppm). Higher resolution 1H{1H} NMR (homodecoupled spectroscopy) experiments were performed on a Bruker Av500 spectrometer and also a DRX 400 spectrometer. Spectra were processed and analyzed using Mestrenova software. Elemental analyses were determined by Mr. Stephen Boyer at London Metropolitan University, Science Centre, 29 Hornsey Road, London N7 7DD, UK. GPC-MALLS measurements were conducted on a Polymer Laboratories PL GPC-50 instrument at 35 °C, using two Polymer Laboratories Mixed D columns in series and THF as the eluent, at a flow rate of 1 mL min–1. The light scattering detector was a Dawn 8, Wyatt Technology, and data were analyzed using Astra V version 5.3.4.18. The refractive angle increment for polylactide (dn/dc) in THF was 0.042 mL g–1.[14]

Bis(2-methyl-8-quinolinolato)gallium Chloride 1a

8-Hydroxy-2-methylquinoline (0.45 g, 2.8 mmol) in n class="Chemical">toluene (10 mL) was added dropwise, with stirring, to a solution of gallium(III)chloride, in toluene (0.25 g, 4.4 mmol) at 273 K. The reaction was stirred for 12 h, after which time a pale green solid precipitated from the reaction. The precipitate was filtered and dried in vacuo. The solid was then crystallized from THF, at low temperature, to yield a pale yellow, microcrystalline, air-stable solid (0.30 mg, 0.71 mmol, 51%).

1H NMR (400 MHz, n class="Chemical">CDCl3) δ (ppm): 3.24 (s, 6H, CH3), 7.15 (dd, 2H, CH, 3JHH = 8.0 Hz, 4JHH = 1.0 Hz), 7.22 (dd, 2H, CH, 3JHH = 8.0 Hz, 4JHH = 1.0 Hz), 7.50 (m, 4H, CH), 8.31 (d, 2H, CH, 3JHH = 8.0 Hz). 13C{1H} NMR (100 MHz, CDCl3) δ (ppm): 23.3 (CH), 112.8 (CH), 114.2 (CH), 124.3 (CIV), 127.0 (CH), 129.0 (CH), 136.9 (CIV), 139.8 (CH), 155.6 (CIV), 156.9 (CIV). Anal. Calcd (GaC10H16N2O2Cl): C, 56.99; H, 3.83; N, 6.65. Found: C, 56.89; H, 3.9; N, 6.58. m/z (LSIMS): 422 (M+, 15%), 385 (M+ – Cl, 45%).

Bis(5,7-dichloro-2-methyl-8-quinolinolato)gallium Chloride 2a

5,7-Dichloro-8-hydroxy-2-methylquinoline (0.65 g, 2.8 mmol) in n class="Chemical">toluene (15 mL) was added dropwise with stirring to a solution of gallium(III)chloride (0.25 g, 1.4 mmol) in toluene (10 mL) at 273 K. The reaction was left to stir for 12 h at 298 K, after which time the solvent was removed in vacuo. The yellow solid was then recrystallized from toluene to yield yellow crystals (391 mg, 0.70 mmol, 53%).

1H NMR (400 MHz, n class="Chemical">CDCl3) δ (ppm): 3.25 (s, 6H), 7.59 (s, 2H), 7.60 (d, 2H, 3JHH = 8.4 Hz), 8.59 (d, 2H, 3JHH = 8.4 Hz). 13C{1H} NMR (100 MHz, CDCl3) δ (ppm): 23.3 (CH), 117.1 (CIV), 118.0 (CIV), 123.6 (CIV), 125.1 (CH), 128.2 (CIV), 129.2 (CH), 137.5 (CH), 150.7 (CIV), 159.4 (CIV). Anal. Calcd (GaC20H12O2N2Cl5): C, 42.95; H, 2.16; N, 5.01. Found: C, 43.09; H, 2.08; N, 4.92. m/z (LSIMS): 560 (M+, 40%), 523 (M+ – Cl, 25%).

Bis(5,7-dichloro-2-methyl-8-quinolinolato)gallium tert-Butoxide 2b

Bis(5,7-dichloro-2-methylquinolinato)gallium n class="Chemical">chloride (0.10 g, 0.18 mmol) was added portion-wise over 30 min to a suspension of potassium tert-butoxide (20 mg, 0.18 mmol) in benzene-d6 (4 mL). The reaction was allowed to stir at 298 K for 24 h. The orange precipitate was removed by centrifugation, and 1H NMR spectroscopy of the solution revealed complete conversion to the product.

1H NMR (400 MHz, n class="Chemical">benzene-d6) δ (ppm): 1.17 (s, 9H, OC(CH3)3), 3.16 (s, 6H, CH3), 6.50 (d, 2H, CH, 3JHH = 8.8 Hz), 7.41 (s, 2H, CH), 7.79 (d, 2H, CH, 3JHH = 8.8 Hz).

1H NMR Data of the Degradation Product of 2b

1H NMR (400 MHz, n class="Chemical">toluene-d8) δ (ppm): 3.23 (s, 6H, CH3), 6.10 (d, 2H, CH, 3JHH = 8.6 Hz), 7.26 (s, 2H, CH), 7.49 (d, 2H, CH, 3JHH = 8.6 Hz).

(2-Methyl-8-quinolinolato)dimethyl Gallium 1c

Trimethylgallium (108 mg, 0.94 mmol) in n class="Chemical">toluene (3 mL) was added dropwise to a solution of 5,7-dichloro-8-hydroxy-2-methylquinoline (0.15 g, 0.94 mmol) in toluene (10 mL). The solution was stirred at 298 K for 16 h, after which time a yellow precipitate had formed. The solid was isolated by filtration and dried in vacuo to yield a yellow solid. The volume of the filtrate was reduced, and further product was isolated (0.18 g, 0.70 mmol, 74%).

1H NMR (400 MHz, n class="Chemical">benzene-d6) δ (ppm): 0.10 (s, 6H, CH3), 1.97 (s, 3H, CH3), 6.27 (d, 1H, CH, 3JHH = 8.4 Hz), 6.73 (dd, 1H, CH, 3JHH = 8.0 Hz, 4JHH = 1.2 Hz), 7.29 (t, 1H, CH, 3JHH = 7.8 Hz), 7.34 (dd, 1H, CH, 3JHH = 7.8 Hz, 4JHH = 1.2 Hz), 7.38 (d, 1H, CH, 3JHH = 8.4 Hz). 13C{1H} NMR (100 MHz, CDCl3) δ (ppm): −6.0 (CH3), 22.4 (CH3), 110.3 (CIV), 111.6 (CH), 114.7 (CH), 122.2 (CH), 130.6 (CH), 139.0 (CIV), 139.8 (CH), 153.6 (CIV), 162.0 (CIV). Anal. Calcd (GaC12H14NO): C, 55.87; H, 5.47; N, 5.43. Found: C, 55.96; H, 5.51; N, 5.57.

(5,7-Dichloro-2-methyl-8-quinolinolato)dimethyl Gallium 2c

Trimethylgallium (0.20 g, 1.8 mmol) in n class="Chemical">toluene (3 mL) was added dropwise to a solution of 5,7-dichloro-8-hydroxy-2-methylquinoline (0.40 g, 1.8 mmol) in toluene (15 mL). The solution was stirred at 298 K for 16 h, after which time the solvent was removed in vacuo to yield a yellow solid (0.50 g, 1.53 mmol, 87%).

1H NMR (400 MHz, n class="Chemical">benzene-d6) δ (ppm): 0.00 (s, 6H, CH3), 1.82 (s, 3H, CH3), 6.15 (d, 1H, CH, 3JHH = 8.4 Hz), 7.47 (s, 1H, CH), 7.82 (d, 1H, CH, 3JHH = 8.4 Hz). 13C{1H} NMR (100 MHz, CDCl3) δ (ppm): −6.1 (CH3), 22.3 (CH3), 113.9 (CIV), 119.1 (CIV), 122.7 (CH), 124.4 (CIV), 130.6 (CH), 137.1 (CH), 138.9 (CIV), 155.3 (CIV), 156.9 (CIV). Anal. Calcd (GaC12H12NOCl2): C, 44.10; H, 3.70; N, 4.29. Found: C, 44.13; H, 3.74; N, 4.35.

Bis(5,7-dichloro-2-methyl-8-quinolinolato)methyl Gallium 2d

Trimethylgallium (50.8 mg, 0.44 mmol) in n class="Chemical">toluene (3 mL) was added dropwise to a solution of 5,7-dichloro-8-hydroxy-2-methylquinoline (0.20 g, 0.88 mmol) in toluene (15 mL). The solution was heated at reflux for 24 h, after which time the solvent was removed in vacuo to yield a yellow solid. The product was isolated by washing with hot hexane to remove the side products, yielding a pale yellow solid (60 mg, 0.11 mmol, 25%).

1H NMR (400 MHz, n class="Chemical">benzene-d6) δ (ppm): 0.16 (s, 3H, Ga–CH3), 2.83 (s, 6H, CH3), 6.45 (d, 2H, CH, 3JHH = 8.8 Hz), 7.44 (s, 2H, CH), 7.82 (s, 2H, CH, 3JHH = 8.8 Hz). 13C{1H} NMR (100 MHz, CDCl3) δ (ppm): −4.9 (Ga–CH3), 22.9 (CH3), 115.5 (CIV), 117.5 (CIV), 124.0 (CH), 124.0 (CIV), 129.2 (CH), 135.9 (CH), 138.8 (CIV),153.9 (CIV), 157.5 (CIV). Anal. Calcd (GaC21H15N2O2Cl4): C, 46.80; H, 2.81; N, 5.20. Found: C, 46.72; H, 2.87; N, 5.15.

General Polymerization Procedure

In a glovebox, a Young’s tap ampule was loaded with rac-lactide (432 mg, 3 mmol) and n class="Chemical">(2-methyl-8-quinolinolato) 1c (7.7 mg, 0.03 mmol). Toluene (2.9 mL) and iso-propyl alcohol (0.03 mmol) were injected into the reaction, such that the overall concentration of lactide was 1 M and of initiator was 10 mM. The ampule was removed from the glovebox and placed in an oil bath at 348 K. Aliquots were taken from the reaction, under an nitrogen atmosphere. Aliquots were quenched with hexane (1–2 mL), and the solvent was allowed to evaporate. The crude product was analyzed by 1H NMR and homonuclear decoupled 1H NMR spectroscopy and GPC-MALLS. The conversion of LA to PLA was determined by integration of the methine proton peaks of the 1H NMR spectra, δ 5.00–5.30. The Pi value was determined by integration of the methine region of the homonuclear decoupled 1H NMR spectrum, δ 5.1–5.24.[13] The PLA number-averaged molecular weight, Mn, and polydispersity index (Mw/Mn; PDI) were determined using gel permeation chromatography equipped with multiangle laser light scattering (GPC-MALLS).