Francesca M. Kerton

Synthesis of cyclic carbonates from CO2 and epoxides using ionic liquids and related catalysts including choline chloride–metal halide mixtures

In this mini-review, progress made in the use of ionic liquid catalysts and related systems for cycloaddition reactions of carbon dioxide with epoxides is described with the primary focus on results from the past eight years. Catalysts described range from simple onium species including tetrabutylammonium bromide, functionalized and simple imidazolium ionic liquids, to a plethora of supported ionic liquid systems. A range of supports including alumina, silica, carbon nanotubes, magnetic nanoparticles, poly(ethyleneglycol), polystyrene, cellulose and chitosan have been used with a variety of ionic groups. These include ammonium, phosphonium and both functionalized and unfunctionalized imidazolium salts. Results have been tabulated to summarize reaction conditions and TONs for styrene oxide, propylene oxide and cyclohexene oxide conversions. It is clear that metal ions used in combination with ionic liquids, particularly ZnBr2, can enhance conversions, and hydroxyl, carboxyl and other functional groups capable of hydrogen-bonding can be incorporated to improve catalysis. Some recent results using flow reactors are highlighted. Examples of ionic catalysts used in the related processes of oxidative carboxylation of alkenes, which also yields cyclic carbonate products, and carbon dioxide–aziridine coupling reactions, which yield oxazolidinone products are described. New data on catalytic styrene carbonate production using choline chloride-transition metal chloride mixtures are presented. For 3d metals, the catalytic activity of these mixtures is Cr > Co ≈ Fe ≈ Ni > Mn ≫ Cu.

Direct conversion of chitin into a N-containing furan derivative

This paper describes the direct conversion of chitin into a nitrogen-containing (N-containing) furan derivative (3A5AF) for the first time. Under optimized conditions, the yield of 3A5AF reaches 7.5% with ca. 50% chitin conversion by using boric acid and alkaline chlorides as additives, and NMP as a solvent. A variety of other compounds, including levoglucosenone, 4-(acetylamino)-1,3-benzenediol, acetic acid and chitin–humins, have been identified as side products, based on which a plausible reaction network involved in the process is proposed. Mechanistic investigation by NMR studies and poison tests confirms the formation of a boron complex intermediate during the reaction, shedding light on the promotional effects of boric acid. Kinetic studies show that the depolymerization of the chitin crystalline region is rate-determining, and therefore disruption of the hydrogen bonding in the crystalline region of chitin, either before or during the reaction, is the key to further improving the reaction yields.

Green chemistry and the ocean-based biorefinery

Research into renewable chemicals, fuels and materials sourced from the oceans at Memorial University and elsewhere is employing green chemical technologies for the transformation of algae and food industry waste streams into useful products. A very small proportion of biomass utilization research is currently focused on these feedstocks and efforts focused in this area could reduce land space competition between food and chemical/fuel production. This perspective highlights some of the achievements and potential opportunities surrounding the use of algae and waste from shellfish and finfish processing. In particular, investigations in this field have used alternative solvents (water, supercritical carbon dioxide and methanol or ionic liquids) extensively. Supercritical Fluid Extraction (SFE) has been used to extract lipids and pigments from algae, and oils from fish-processing plant waste streams. Water can be used to isolate potentially high value biologically-active oligosaccharides from some seaweeds. Biotechnological approaches are showing promise in the separation of biopolymers from shellfish waste streams. Production of new nitrogen-containing bioplatform chemicals (e.g. 3-acetamido-5-acetylfuran) from aminocarbohydrates (chitin, chitosan and N-acetylglucosamine) is being pursued.

Hydrolysis of chitosan to yield levulinic acid and 5-hydroxymethylfurfural in water under microwave irradiation

A novel route has been developed that yields levulinic acid (4-oxopentanoic acid, LA) and 5-hydroxymethylfurfural (5-HMF) from chitosan. Hydrolysis of chitosan was performed in the presence of a range of Lewis acids with SnCl4·5H2O providing the best results. All reactions were performed in sealed vessels under microwave irradiation at 200 °C for 30 min. Typical pressures achieved were 17 to 19 bar. 23.9 wt% LA was produced from 100 mg chitosan using 0.24 mmol SnCl4·5H2O and 4 mL water. Under more dilute conditions, 10.0 wt% 5-HMF was obtained using 0.12 mmol SnCl4·5H2O and 15 mL water. We propose that under more concentrated reaction conditions the 5-HMF formed reacts further to produce LA. When chitin is treated similarly, no 5-HMF is produced but up to 12.7 wt% LA can be obtained. For comparison, 32.0 wt% LA was produced from 100 mg glucosamine hydrochloride using 0.26 mmol SnCl4·5H2O and 20 mL water. This corresponds to a yield of 59.4%. The SnCl4 forms SnO2 and HCl in solution and under similar conditions using SnO2 and HCl, chitosan formed 27.4 wt% LA.

Alkali aminoether-phenolate complexes: synthesis, structural characterization and evidence for an activated monomer ROP mechanism

Several monometallic {LO(i)}M complexes of lithium (M = Li; i = 1 (1), 2 (2), 3 (3)) or potassium (M = K, i = 3 (4)) and the heteroleptic bimetallic lithium complex {LO(3)}Li·LiN(SiMe2H)2 (5), all supported by monoanionic aminoether-phenolate {LO(i)}(-) (i = 1-3) ligands, have been synthesized and structurally characterized. A large range of coordination motifs is represented in the solid state, depending on the chelating ability of the ligand, the size of the metal and the number of metallic centres found in the complex. Pulse-gradient spin-echo NMR showed that 1-4 are monomeric in solution, irrespective of their (mono- or di)nuclearity in the solid-state. VT (7)Li and DOSY NMR measurements conducted for 5 indicated that the two Li atoms in the complex do not exchange positions even at 80 °C. Upon addition of 1-10 equiv. of BnOH, the electron-rich and sterically congested {LO(3)}Li complex (3) promotes the controlled living and immortal ring-opening polymerisation of L-lactide. The combination of polymer end-group analyses and stoichiometric model reactions unambiguously provided evidence that ROP reactions catalyzed by these two-component {LO(i)}Li/BnOH catalyst systems operate according to an activated monomer mechanism, and not via the coordination-insertion scenario frequently assumed for similar alkali phenolate-alcohol systems.

A Simple One-Pot Dehydration Process to Convert N-acetyl-d-glucosamine into a Nitrogen-Containing Compound, 3-acetamido-5-acetylfuran

An efficient process for converting N-acetyglucosamine (NAG) into 3-acetamido-5-acetylfuran (3A5AF) is reported. 3A5AF is proposed as an N-containing platform chemical, which contains renewable nitrogen. In the reported method NAG, in the presence of boric acid (B(OH)₃) and sodium chloride (NaCl), produces 58 % yield 3A5AF in dimethylacetamide under microwave irradiation (220 °C, 15 min). A maximum yield of 62 % was obtained in the presence of 4 equivalent NaCl. Performing ICP-MS analysis on NAG from different chemical suppliers highlighted the importance of Cl and B levels in this process. Trace impurities are, therefore, important considerations in biomass transformations. This solution-phase process produces approximately 30 times more 3A5AF than a pyrolysis route reported previously.

Formation of a renewable amide, 3-acetamido-5-acetylfuran, via direct conversion of N-acetyl-D-glucosamine

An effective method for transforming an amino-sugar into an N-substituted furan in an ionic liquid is reported. B(OH)3 significantly improves the yield (60%, 3 min MW heating).

A high-throughput approach to lanthanide complexes and their rapid screening in the ring opening polymerisation of caprolactone.

Libraries of lanthanide complexes supported by nitrogen and oxygen containing ligands have been synthesised using a high-throughput approach. The complexes were employed in the ring-opening polymerisation of epsilon-caprolactone, in some cases giving polycaprolactone of controlled molecular weight and narrow polydispersity. The libraries, based on twenty-one ligands and eight lanthanide reagents, were developed in order to determine the best combination of lanthanide metal and ligand. They were prepared via transamination reactions of [Ln[N(SiMe(3))(2)](3)] complexes with tetradentate dianionic ligands containing oxygen and nitrogen donors. 1H NMR spectroscopy was used to screen polymerisation activity. The steric demand of the ligand has a significant effect on the polymerisation process, as do the type of nitrogen donor and the size of the central Ln(3+) ion. Ligands containing aryl rings with bulky substituents such as tert-pentyl groups afforded species capable of performing controlled polymerisation of caprolactone, whereas less bulky groups such as methyl were not effective. Yttrium and mid-sized lanthanides such as samarium showed increased activity compared with the larger lanthanides, lanthanum and praseodymium, and the smaller lanthanides like ytterbium. X-ray crystal structures of a sterically demanding chelating amine-bis((2-hydroxyaryl)methyl) ligand and a chloride bridged dinuclear gadolinium complex are reported. The centrosymmetric molecule contains gadolinium in distorted capped trigonal prismatic environments bonded to two amine, two phenolate, one THF and two chloride donors.

Solubility of bio-sourced feedstocks in ‘green’ solvents

A group of 14 different bio-sourced, renewable feedstocks (homoserine, 1; glutamic acid, 2; aspartic acid, 3; 2,5-furandicarboxylic acid, 4; fumaric acid, 5; oxalacetic acid, 6; tartaric acid, 7; malic acid, 8; succinic acid, 9; levulinic acid, 10; γ-hydroxybutyrolactone, 11; xylitol, 12; mannitol, 13; sorbitol, 14) have been examined for their solubility/miscibility in a variety of ‘green’ solvents, including water, supercritical carbon dioxide (scCO2), and ionic liquids. Two other bio-based compounds 5-hydroxymethylfurfural, 15, and D-xylose, 16, were studied in selected solvents. Trends in solubility have been assessed so that these data may be extrapolated to help predict solubilities of other related compounds. For example, 10, 11 and 15 all demonstrated appreciable solubility in scCO2, as they possess weak intermolecular interactions. The dicarboxylic acids studied (4–9) all proved soluble in modified scCO2 (by use of MeOH as a cosolvent). While the polyols (12–14) and 1 were insoluble in scCO2 but water of various pHs and ionic liquids proved adept at their dissolution. Some of the amino acids studied (2 and 3) were only soluble in water with an adjustment of pH.

Neodymium borohydride complexes supported by diamino-bis(phenoxide) ligands : diversity of synthetic and structural chemistry, and catalytic activity in ring-opening polymerization of cyclic esters

New heterobimetallic borohydrido neodymium complexes {[OONN]1Nd(BH4)(μ-BH4)Li(THF)}2 (1) and [OONN]3Nd(BH4)(μ-BH4)Li(THF)2 (3) supported by diamino-bis(phenoxide) ligands ([OONN]1 = {CH2N(Me)CH2-3,5-Me,t-Bu-C6H2O}2; [OONN]3 = C5H4NCH2N{CH2-3,5-Me,t-Bu-C6H2O}2) were synthesized by the reactions of Nd(BH4)3(THF)2 with equimolar amounts of dilithium derivatives of diamino-bis(phenol)s Li2[OONN]n and isolated in high yields. In the case of Li2[OONN]2 ([OONN]2 = Me2NCH2CH2N{CH2-3,5-t-Bu-C6H2O}2), the same synthetic procedure afforded the heterobimetallic bis(phenoxide) complex Li{Nd[OONN2]2} (2). The structures of complexes 1–3 were established by X-ray diffraction studies. Compounds 1–3 act as single-site initiators for the ring-opening polymerization (ROP) of racemic lactide and racemic β-butyrolactone under mild conditions (20 °C), providing atactic polymers with controlled molecular weights and relatively narrow polydispersities (Mw/Mn = 1.07–1.82). While 1 and 3 initiate polymerizationvia their borohydride groups, ROP with 2 proceeds viainsertion into the Nd–O(ligand) bond.