Chatura
Goonesinghe
,
Hootan
Roshandel
,
Carlos
Diaz
,
Hyuk-Joon
Jung
,
Kudzanai
Nyamayaro
,
Maria
Ezhova
and
Parisa
Mehrkhodavandi
*
Department of Chemistry, University of British Columbia, Vancouver, BC, Canada. E-mail: mehr@chem.ubc.ca
First published on 22nd April 2020
This is a comprehensive study of the effects of rationally designed hemilabile ligands on the stability, reactivity, and change in catalytic behavior of indium complexes. We report cationic alkyl indium complexes supported by a family of hemi-salen type ligands bearing hemilabile thiophenyl (2a), furfuryl (2b) and pyridyl (2c) pendant donor arms. Shelf-life and stability of these complexes followed the trend 2a < 2b < 2c, showing direct correlation to the affinity of the pendant donor group to the indium center. Reactivity towards polymerization of epichlorohydrin and cyclohexene oxide followed the trend 2a > 2b > 2c with control of polymerization following an inverse relationship to reactivity. Surprisingly, 2c polymerized racemic lactide without an external initiator, likely through an alkyl-initiated coordination-insertion mechanism.
In contrast, there are only a handful of reports of the use of hemilabile ligands with main group metals.8 Due to their tunable Lewis acidity and oxophilic nature, complexes of group 13 elements, especially aluminum9 and indium10 have been used in a variety of reactions ranging from ring opening polymerization (ROP) of cyclic polar monomers to functionalization of small molecules.11 However, among the group 13 metals, almost all reports12 focus on aluminum complexes (Chart 1).
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Chart 1 Previously reported aluminum and indium complexes bearing hemilabile ligands (A–F) and cationic indium complexes reported by our group (G and H). |
In cationic aluminum complexes, hemilabile ligands have been used for stabilizing complexes. The first group 13 complexes bearing hemilabile ligands to show reactivity were reported by Dagorne and co-workers.13 These cationic aluminum complexes, A, bearing piperazine and morpholine pendant arms, stabilized the cationic center and showed catalytic reactivity for the ROP of propylene oxide. Kerton and co-workers reported the ROP of ε-caprolactone (ε-CL) using a cationic aluminum complex B, stabilized by a morpholinyl donor arm.14 Another cationic aluminum complex, C, proposed to be stabilized by two hemilabile furfuryl pendant arms was reported by Phomphrai and co-workers.15
Control of reactivity using hemilability was demonstrated by Shaver and co-workers by showing that the coordination of various donor arms to an aluminum center in a series of complexes, D, was key to obtaining control in the ROP of racemic lactide (rac-LA) and ε-CL.16 Finally, Kerton and co-workers reported an example of hemilabile donors altering reactivity in aluminum complexes. They showed that the displacement of an ancillary chloride ligand was facilitated by a hemilabile pendant arm in a neutral complex, E, to initiate the (co)polymerization of CO2 and cyclohexene oxide (CHO).
To the best of our knowledge, the first indium complexes bearing a hemilabile ligand architecture investigated for reactivity were described by Mountford who reported an indium alkyl complex supported by an aminophenolate ligand with a 1,4,7-triazacyclononane hemilabile pendant arm (F); their complex was unreactive towards all nucleophiles and reagents examined.17 We have reported indium catalysts supported by tridentate18 and tetradentate19 amino/imino phenolate ligands as catalysts for ROP reactions. However, due to their increased electrophilicity and coordinative unsaturation, we have recently focused on studying cationic complexes for the coupling of epoxides and ε-CL to form spiroorthoesters (G)20 and the copolymerization of cyclic ethers and lactide (H).21 However, both these complexes required solvent molecules for stabilization, and the isolated complexes suffered from rapid decomposition when the labile solvent molecules were lost. We proposed that a ligand architecture with a hemilabile pendant donor moiety could stabilize the cationic indium center, afford greater control of reactivity, and potentially change the reactivity pattern altogether.
Herein, we report the first catalytically active cationic alkyl indium complexes supported by ligands bearing hemilabile pendant donor arms with varying donor strengths. We show the pendant donor groups can be used to tune the stability of the cationic alkyl indium complexes. Furthermore, we show that these complexes can be used to control the ROP reactivity of epichlorohydrin and cyclohexene oxide. Finally, we observe that the reactivity of the cationic alkyl indium center towards ROP of rac-LA is radically altered in the presence of a strong donor group, allowing alkyl initiated polymerization. This is the first example of using rationally designed hemilabile ligands to tune the reactivity of indium complexes.
Solid-state structures of 1a–d determined by single-crystal X-ray crystallography feature distorted square pyramidal indium centers (Fig. S57–S60†). All the dialkyl species are isostructural in the solid state, with the equivalent distances between the hemilabile arm heteroatoms and the indium center in 1a–c indicating the absence of significant interactions. This is most apparent in comparison of this distance in 1c and the analogous distance to the indium center from the ortho-C of the benzyl group in 1d, where no interaction is expected (Fig. 1).
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Fig. 1 Molecular structures of complex (a) [Lc]IniBu2 (1c) and (b) [Ld]IniBu2 (1d) (depicted with thermal ellipsoids at 50% probability and H atoms, as well as solvent molecules omitted for clarity). |
To determine donor group interaction in the solution-state for complexes 1a–d, we used a modified Gutmann–Beckett method to determine relative acceptor ability (Fig. 2).23 This method involves the addition of triethylphosphine oxide (OPEt3) to form an adduct with the metal complex. Complexes 1a–d did not show a significant change in 31P{1H} chemical shifts relative to free OPEt3, indicating that the indium centers of 1a–d have electronically similar environments. This excludes the possibility of donor group interaction in the solution-state. The 1H and 13C{1H} NMR spectra obtained for 1a–d in CDCl3 agree with the solid-state structures (Fig. S17–S35†).
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Fig. 2 31P{1H} NMR spectra of OPEt3 with 1a–d show a similar acceptor ability for neutral complexes. 31P{1H} NMR (160 MHz, C6H6, 25 °C) chemical shift of free OPEt3 appears at 45 ppm. |
The reaction of complexes 1a–d with [HNMe2Ph][BArF] (BArF = tetrakis[3,5-bis(trifluoromethyl)phenyl]borate) in THF forms the cationic species 2a–d (Scheme 1). The stability of the complexes in the absence of donor solvents is related to the affinity of the heteroatom to the indium center (Table S1†). Complexes 2a–c can be synthesized in non-coordinating solvents such as dichloromethane and benzene, while 2d formed decomposition products under these conditions. Complex 2d could be synthesized at −30 °C in THF but was not isolable with high purity. After several hexane washes, residual THF can be removed from complexes 2a–c, while for complex 2d THF cannot be removed. This is reminiscent of the similar alkyl indium cationic catalyst G (Chart 1).20
The 1H NMR signals arising from the heterocyclic protons in 2a–c shift significantly upfield compared to the neutral species 1a–c, suggesting substantial shielding of these protons upon formation of the cationic complexes. Further analysis of the 1H NMR spectrum of 2c shows that the AB multiplet (υ < 10 J) arising from the diastereotopic methylene protons of the pendant arm broaden and shift downfield by ∼0.2 ppm compared to 1c. In 2a, and to a lesser extent in 2b, the Δδ for these protons increase, in relation to 1a and 1b, resembling an AX coupling (υ ≥ 10 J, Fig. 3). Based on these observations, we propose that the upfield shift of heterocyclic proton signals arise when the outer-sphere donor group approaches the cationic indium center, enhancing shielding of the heterocyclic protons. Coordination of the pendant donor groups to the cationic center would restrict the free rotation around the methylene carbon on the linker arm, thereby “locking” the methylene protons in position and increasing the Δδ of these protons.
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Fig. 3 (a) Methylene protons (![]() |
NOESY NMR spectra of 1a–c showed no through space interaction between heterocyclic protons and isobutyl protons (Fig. S21, S26 and S31†). However, heterocyclic protons on 2a–c show NOE interactions with the methyl protons of the isobutyl ligands (Fig. S40, S47 and S54†) indicating increased proximity of the pendant donor groups to the isobutyl methyl groups through the coordination of the side arms (Fig. 4).
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Fig. 4 Significant through space interactions between heterocyclic protons and methyl protons of the isobutyl ligand (NOESY NMR spectra 400 MHz, CDCl3, 25 °C). |
Variable temperature (VT) 1H NMR spectroscopy (25–125 °C, C6D5Br) of cationic complexes 2a–c show significant changes, while the neutral analogues do not change in this temperature range (Fig. S63–S65†). The thiophene complex 2a shows significant and irreversible decomposition beginning at 45 °C, while the pyridyl complex 2c was highly stable, with only minor changes in chemical shifts even at 120 °C. In contrast, the furan complex 2b shows a gradual downfield migration of the α furfuryl proton with increasing temperature, a Δδ of ∼0.6 ppm (Fig. 5). At higher temperatures (125 °C, C6D5Br) the chemical shift of the α proton approaches that of the free ligand (δ = 7.20 ppm). This change is reversible when the temperature is lowered to 30 °C.
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Fig. 5 (a–d) VT 1H NMR (400 MHz, C6D5Br, 25–125 °C) spectra showing downfield migration of the α proton of the furfuryl group (![]() |
We propose that the de-shielding of the α proton occurs as its proximity to the indium center decreases with increasing fluxional behavior of the In–Ofuran interaction at higher temperatures. This behavior of 2a–c is directly related to the donor ability of the heterocyclic pendant groups. The greater donor ability of pyridine (donor strength, DS = 38) compared to furan and thiophene (DS = 11 and 10, respectively) accounts for the unexpected stability of 2c.24 However, donor strength alone does not explain the dramatic difference in stability between 2a and 2b. The higher stability of 2b can be accounted for by the greater aromaticity of thiophene and the availability of electrons in furan for bonding.25
For these complexes to be truly hemilabile, the pendant donor arm must change its bonding in response to other coordinating ligands or solvent molecules possessing a greater donor ability.1a We studied the hemilabile behavior of furan substituted 2b in detail due to its “Goldilocks” stability and the easily observable α-proton chemical shift in the 1H NMR spectra (Fig. 6). With the addition of THF (DS = 17) to 2b, a ∼0.5 ppm downfield shift of the α-proton signal was observed in the 1H NMR spectrum (C6D6) of the mixture, indicating a loss of proximity of the furan moiety (Fig. 6b). With a weaker donor such as epichlorohydrin (ECH), only a ∼0.1 ppm downfield shift is observed, while addition of pyridine (DS = 38, donor number DN = 33.1)26 causes a ∼0.6 ppm downfield shift. Addition of OPEt3 had the greatest effect with a ∼0.9 ppm downfield shift (Fig. 6d). While, OPEt3 has a lower donor number (DN = 24) than pyridine, the predominantly anionic nature of the oxygen leads to a stronger interaction with the cationic indium center and a greater fluxionality of the In–Ofuran interaction.27
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Fig. 6
1H NMR (400 MHz, C6D6, 25 °C) downfield shift of the furfuryl α proton signal (![]() |
A single-crystal of solvated 2b·2THF suitable for single crystal X-ray crystallographic analysis was obtained through the slow evaporation of a THF/hexamethyldisiloxane solution. The structure of 2b·2THF revealed a distorted octahedral indium center with THF molecules in the axial position (Fig. 7). The bond distances and angles of 2b·2THF resemble those of cationic salen indium complex H (Chart 1).21 The de-coordination of the furfuryl pendant arm in the presence of an external donor entity confirms that 2b displays true hemilabile behavior.
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Fig. 7 Molecular structures of complex 2b·2THF (depicted with thermal ellipsoids at 50% probability and H atoms, minor disorders as well as solvent molecules and counter anion omitted for clarity). |
Although the solid-state structure of 2b·2THF shows the coordination of two THF molecules and the complete de-coordination of the pendant donor arm, the structure is different in solution. The DOSY NMR spectrum (C6D6) exhibits independent diffusion of 2b and THF (Fig. 8). These results point to a weak association of 2b with THF in solution phase. This observation held true for DOSY NMR of mixtures of 2a and 2c with THF as well (Fig. S70 and S72†). It is possible that this apparent independent diffusion of the complexes and THF is due to fast exchange occurring relative to the NMR time scale at 25 °C at 400 MHz.
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Fig. 8 DOSY NMR spectrum of 2b with excess THF (1H NMR, diffusion time (Δ) = 0.85 s, gradient length (δ) = 400 μs, 400 MHz, C6D6, 25 °C). |
Temp. (°C) | Cat. | Conv.b (%) | M n Cal (Da) | M n (Da) | Đ | i*f (%) | |
---|---|---|---|---|---|---|---|
a Reactions were performed in C6D6 for 24 h. [ECH] = 6.37 M, [cat] = 20 mM. [ECH]/[cat] = 300. b Conversion was monitored by 1H NMR spectroscopy. c M n Cal = calculated number averaged molecular weight = [ECH]/[cat] × conversion × molar mass of ECH. d M n determined using GPC in THF. e Dispersity = Mw/Mn. f Initiation efficiency = (Mn Cal/Mn) × 100. g With the addition of triphenylphosphine. h [ECH] = 2.94 M, [cat] = 10 mM, [ECH]/[cat] = 300. i Catalyst was not isolable. | |||||||
1 | 25 | 2a | 59 | 16![]() |
27![]() |
1.42 | 61 |
2 | 35 | 2a | 61 | 16![]() |
21![]() |
1.56 | 80 |
3 | 60 | 2a | 59 | 16![]() |
19![]() |
1.22 | 85 |
4g | 25 | 2a | <1 | — | — | — | — |
5h | 25 | 2a | <1 | — | — | — | — |
6 | 25 | 2b | 34 | 9400 | 24![]() |
1.23 | 39 |
7 | 35 | 2b | 61 | 16![]() |
29![]() |
1.33 | 58 |
8 | 60 | 2b | 55 | 15![]() |
21![]() |
1.30 | 72 |
9g | 25 | 2b | <1 | — | — | — | — |
10h | 25 | 2b | <1 | — | — | — | — |
11 | 25 | 2c | <1 | — | — | — | — |
12 | 60 | 2c | <1 | — | — | — | — |
13 | 80 | 2c | <1 | — | — | — | — |
14i | 25 | 2d | 73 | 20![]() |
20![]() |
1.50 | 99 |
Complexes 2a and 2b catalyze the ROP of ECH at 25 °C with 61% and 39% initiation efficiencies, respectively. The initiation efficiency of 2b approaches that of 2a at higher temperatures indicating that both complexes achieve similar reactivity at elevated temperatures. Additionally, when triphenylphosphine is added to the reaction mixture, polymerization of the epoxide halts due to the formation of a stable quaternary phosphonium species at the cationic chain end.29 This confirms the cationic nature of the polymerization mechanism (Table 1, entries 4 and 9).
The polymerization of highly reactive cyclohexene oxide (CHO)30 provides a dramatic example of the tuning of reactivity through the introduction of a hemilabile donor arm. Under neat, dilute, and even low temperature conditions, 2a and 2b polymerize CHO in an uncontrolled fashion, forming polymers with high dispersity and irreproducible molecular weights (Table 2, entries 1–6). In contrast to these species, 2c reacts slowly to produce higher molecular weight, lower dispersity poly(cyclohexene oxide) even in neat conditions. Reactions carried out at a higher temperature show greater conversions, while those carried out in solution show increased molecular weights with a significant lowering of dispersity (Table 2, entries 7–9). Although 2c is not highly controlled in general, this change in reactivity clearly shows the significant impact of the hemilabile arm.
Temp. (°C) | Cat. | Solv. | Conv.b (%) | M n Cal (Da) | M n (Da) | Đ | |
---|---|---|---|---|---|---|---|
a Reactions were performed for 24 h. In solution [CHO] = 8.0 M, [cat] = 5.6 mM. [Epoxide]/[cat] = 300, in neat conditions [epoxide]/[cat] = 2000. b Conversion was monitored by 1H NMR spectroscopy. c M n Cal = calculated number averaged molecular weight = [CHO]/[cat] × conversion × molar mass of CHO. d M n determined using GPC in THF. e Dispersity = Mw/Mn. f With the addition of triphenylphosphine. *Not determined due to uncontrolled reaction. | |||||||
1 | 25 | 2a | Neat | * | — | ∼13![]() |
∼7 |
2 | 25 | 2a | C6D6 | * | — | ∼20![]() |
∼4 |
3 | 0 | 2a | Tol. | * | — | ∼19![]() |
∼3 |
4 | 25 | 2b | Neat | * | — | ∼14![]() |
∼5 |
5 | 25 | 2b | C6D6 | * | — | ∼30![]() |
∼3 |
6 | 0 | 2b | Tole | * | — | ∼24![]() |
∼3 |
7 | 25 | 2c | Neat | 58 | 113![]() |
80![]() |
2.23 |
8 | 60 | 2c | Neat | 93 | 182![]() |
82![]() |
1.78 |
9 | 25 | 2c | C6D6 | 91 | 26![]() |
108![]() |
1.47 |
10f | 25 | 2c | Neat | — | — | — | — |
Catalyst | Conv.b (%) | M n Cal (Da) | M n (Da) | Đ | i*f (%) | |
---|---|---|---|---|---|---|
a Reactions were performed for 24 h in toluene at 100 °C. [rac-LA] = 1.6 M, [cat] = 6.4 mM. [rac-LA]/[cat] = 250. b Conversion was monitored by 1H NMR spectroscopy. c M n Cal = calculated number averaged molecular weight = [rac-LA]/[cat] × conversion × molar mass of rac-LA. d M n determined through GPC in THF. e Dispersity = Mw/Mn. f Initiation efficiency = (Mn Cal/Mn) × 100. | ||||||
1 | 2a | <1 | — | — | — | — |
2 | 2b | 20 | — | — | — | — |
3 | 2c | 94 | 34![]() |
130![]() |
1.32 | 26 |
The polymerization of rac-LA in the absence of an external initiator by 2c is unexpected. Analysis of the resultant polymer by MALDI-TOF mass spectrometry (MS) indicates that the polymerization is initiated by the In–isobutyl moiety (Fig. S74†). While there have been reports of neutral indium and rare-earth alkyl species capable of initiating ROP of rac-LA with an alkyl group,31 to the best of our knowledge, 2c is the first cationic metal complex to do so. In complex G, we found that the alkyl group attached to the cationic indium center is very stable even in the presence of trace amounts of water.20 However, in 2c and to a lesser extent in 2b, the electrophilicity of the indium center is decreased through the coordination of the hemilabile donor arm, weakening the In–C bond. We propose that with the presence of a strong hemilabile donor, the lability of the isobutyl group increases allowing it to act as an initiator in the polymerization of rac-LA.
For complex 2b, the donor arm dissociates reversibly, with more pronounced fluxional behavior of the In–Ofuran bond with increasing temperatures. This facilitates the coordination of epoxide, resulting in higher initiation efficiencies at elevated temperatures (Scheme 2a and b). At these temperatures the dissociation of the pendent arm for 2a is not reversible and it decomposes in the absence of donors (monomers or solvent).
Monomer concentration also affects initiation efficiencies. At low [ECH] the monomer coordinates to the cationic center reversibly; however, under these conditions, polymerization does not proceed (Table 1, entries 5 and 10). At higher [ECH] polymerization is initiated, and propagation ensues with the attack by a second epoxide molecule (Scheme 2c).
In contrast, we propose that rac-LA is polymerized through an alkyl-initiated coordination-insertion mechanism. This requires a highly activated In–C bond, which is not present in complexes 2a, 2b, or G. Complex 2c is active because of the greater donor ability of the pyridyl group, which decreases the electrophilicity of the indium center, polarizing the In–C bond. The difference in reactivity towards the ROP of rac-LA under the same conditions shows the clear influence the donor arm has on the reactive behavior of the complexes. This represents a rare example of changing reactivity patterns using a hemilabile donor group.
First, the complex stability and shelf life was significantly improved in hemilabile ligand bearing complexes 2a–c relative to the solvent stabilized 2d. The stability followed a trend with a direct correlation of complex stability to the donor ability of the pendant groups (2d < 2a < 2b < 2c).
Second, the reactivity could be controlled by regulating the coordination of reactants to the indium center. The reactivity is inversely related to stability with 2a and 2b, both of which are active for the ROP of epichlorohydrin. Unusually for a cationic species, 2c showed controlled reactivity towards ROP of CHO in neat conditions. The ROP of epoxides provides proof of reactivity control enforced by the hemilabile ligand system.
Third, typical reactivity of cationic alkyl indium complexes was altered by the addition of the pyridyl pendant group in 2c. Complex 2c was capable of alkyl initiated ROP of rac-LA through a coordination insertion mechanism. This provides an example of altering reactivity at the metal center by a hemilabile ligand system.
We aim to use our studies in furthering reactivity with cationic indium complexes.
Footnote |
† Electronic supplementary information (ESI) available: Experimental procedures, solution and solid-state characterization. CCDC 1987632–1987636. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/d0sc01291b |
This journal is © The Royal Society of Chemistry 2020 |