Advancements and Complexities in the Conversion of Lignocellulose Into Chemicals and Materials

This Perspective describes the challenges and objectives associated to the development of new chemical technologies for the conversion of lignocellulose (non-food or waste) into chemicals and materials; it also provides an outlook on the sources, potential products, and issues to be addresse

Synthesis of the fatty esters of solketal and glycerol-formal: biobased specialty chemicals

The caprylic, lauric, palmitic and stearic esters of solketal and glycerol formal were synthesized with high selectivity and yields by a solvent-free acid catalyzed procedure. No acetal hydrolysis was observed notwithstanding the acidic condition

One-pot tandem catalytic epoxidation – CO2 insertion of monounsaturated methyl oleate to the corresponding cyclic organic carbonate

Conversion of unsaturated fatty acids, FAMEs or triglycerides into the corresponding cyclic organic carbonates involves two reaction steps-double-bond epoxidation and CO2 insertion into the epoxide-that are generally conducted separately. We describe an assisted-tandem catalytic protocol able to carry out carbonation of unsaturated methyl oleate in one-pot without isolating the epoxide intermediate. Methyl oleate carbonate was obtained in 99% yield and high retention of cis-configuration starting from methyl oleate using hydrogen peroxide and CO2 as green reagents, in a biphasic system and in the presence of an ammonium tungstate ionic liquid catalyst with KBr as co-catalyst

Reaction of Glycerol with Trimethyl Orthoformate: Towards the Synthesis of New Glycerol Derivatives

The reactivity of glycerol with trimethyl orthoformate is here described with an emphasis on developing a reliable synthetic approach for glycerol valorization. The glycerol based orthoester 4-(dimethoxymethoxy)methyl)-2-methoxy-1,3-dioxolane (3) was synthesized, under catalytic as well as catalyst-free conditions, by taking advantage of the thermodynamically controlled equilibrium between intermediates. Both Brønsted and Lewis acid catalysts accelerated the attainment of such an equilibrium, particularly Brønsted acidic ionic liquids BSMImHSO4 and BSMImBr were the most effective compounds for this reaction. The kinetic profiles allowed the proposal of a mechanism that accounts for the selectivity of the reaction

Chitin-Derived Nanocatalysts for Reductive Amination Reactions

Chitin, the second most abundant biopolymer in the planet after cellulose, represents a renewable carbon and nitrogen source. A thrilling opportunity for the valorization of chitin is focused on the preparation of biomass-derived N-doped carbonaceous materials. In this contribution, chitin-derived N-doped carbons were successfully prepared and functionalized with palladium metal nanoparticles. The physicochemical properties of these nanocomposites were investigated following a multi-technique strategy and their catalytic activity in reductive amination reactions was explored. In particular, a biomass-derived platform molecule, namely furfural, was upgraded to valuable bi-cyclic compounds under continuous flow condition

Phosphonium salts and P-ylides

The present chapter is aimed at describing the state-of-the-art, for the period January December 2014, of two pillar classes of phosphorus-containing compounds, the phosphonium salts and ylides. Topics are organized to offer an introductory survey on the methods of preparation and characterisation of both types of compounds, followed by an analysis of the most remarkable but also curiosity driven researches for their applications. A special section is devoted to phosphonium-based ionic liquids (PILs) due to the exceptional importance of this subject

Waste-to-wealth: biowaste valorization into valuable bio(nano)materials

The waste-to-wealth concept aims to promote a future sustainable lifestyle where waste valorization is seen not only for its intrinsic benefits to the environment but also to develop new technologies, livelihoods and jobs. Based on the concept of waste valorization and circular economy, this review aims to provide an overview of present trends and future potential in the conversion of residues from different food sectors into valuable bio(nano)material

reactions of p coumaryl alcohol model compounds with dimethyl carbonate towards the upgrading of lignin building blocks

Cinnamyl alcohol 1 and 4-(3-hydroxypropyl)phenol 2, two compounds resembling the lignin building block p-coumaryl alcohol, can be selectively transformed into different products by catalytic methodologies based on dimethyl carbonate (DMC) as a green solvent/reagent. Selectivity can be tuned as a function of the reaction temperature and of the nature of the catalyst. Basic catalysts such as K2CO3, trioctylmethylphosphonium methylcarbonate ([P8881][CH3OCOO]), and CsF/αAl2O3 promote selective transesterification of the aliphatic hydroxyl group at 90 °C. However, amphoteric solids such as alkali metal-exchanged faujasites, NaX and NaY, selectively yield the corresponding alkyl ethers at higher temperatures (165–180 °C). The phenolic hydroxyl group of 2 can be methylated similarly with the faujasites at high temperatures. This preliminary screening for selectivity illustrates reactivity trends and delineates some of what might be among the most promising synthetic pathways to upgrade lignin-derived chemical building blocks

Single-Step Methylation of Chitosan Using Dimethyl Carbonate as a Green Methylating Agent

N,N,N-Trimethyl chitosan (TMC) is one chitosan derivative that, because of its improved solubility, has been studied for industrial and pharmaceutic applications. Conventional methods for the synthesis of TMC involve the use of highly toxic and harmful reagents, such as methyl iodide and dimethyl sulfate (DMS). Although the methylation of dimethylated chitosan to TMC by dimethyl carbonate (DMC, a green and benign methylating agent) was reported recently, it involved a formaldehyde-based procedure. In this paper we report the single-step synthesis of TMC from chitosan using DMC in an ionic liquid. The TMC synthesised was characterised by 1H NMR spectroscopy and a functionally meaningful degree of quaternisation of 9% was demonstrated after a 12-h reaction time

Decarboxylation of Dialkyl Carbonates to Dialkyl Ethers over Alkali Metal-exchanged Faujasites

Non-toxic DAlCs, especially lighter dimethyl- and diethyl-carbonate, are regarded as very green alkylating reagents, particularly when coupled with metal-exchanged Y- and X-faujasites as catalysts. These reactions are selective, free from wastes or byproducts, and often require no additional solvent other than the carbonate. Nonetheless, this paper demonstrates that the operating temperature and the nature of the faujasite must be carefully chosen in order to avoid DAlC decomposition. In fact, at temperatures ranging from 150 to 240 ◦ C, faujasites can promote decarboxylation of light DAlCs to the corresponding ethers CH3OCH3 and CH3CH2OCH2CH3 plus CO2. Heavier DAlCs (dipropyl- and dioctyl-carbonate) undergo a similar decomposition pathway, followed by further reactions to the corresponding alcohols (n-propanol and n-octanol) and alkenes [propylene and octene(s)]. These transformations not only consume DAlCs, but also give rise to dangerously flammable ethers, as well as undesirable alcohols, alkenes and CO2.The present work reports an original investigation of the decarboxylation of DAlCs on faujasites with the aim of providing operative boundaries to the experimental conditions to minimise unwanted decomposition. The reaction is strongly affected by the nature of the catalyst: the more basic zeolites, NaX and CsY, are by far more active systems than NaY and LiY. However, solid K2CO3 proves to be rather inefficient. The temperature also plays a crucial role: for example, the onset of the decarboxylation of DMC requires a temperature of ~30 ◦ C lower than that for DEC and DPrC. Overall, awareness that certain zeolites cause decomposition of DAlCs under conditions similar to the ones used for DAlC-promoted alkylations allows determination of the correct experimental boundaries for a safer and more productive use of DAlCs as alkylating agent