Furanic compounds, such as furfural (FUR) and 5-hydroxymethylfurfural (HMF), are promising platform chemicals, which can be derived from hemicellulose (FUR) and cellulose (HMF) contained in residual biomass. These compounds can be coupled with epichlorohydrin (derived from renewable-based glycerol), forming the corresponding mono- and bis-oxirane, which, upon CO2 insertion, are selectively transformed in cyclic organic carbonates (COCs). Although up to now, there are relatively few examples of COCs derived from furanics present in literature, and these compounds are suitable for a wide range of synthetic and materials’ applications. Interestingly, the furan moiety can be further functionalized via Diels–Alder reactions, amplifying the range of applications of the resulting functional molecules and/or polymers while decreasing their toxicity.
Cyclic organic carbonates from furanics: Opportunities and challenges
Bragato N.Writing – Original Draft Preparation
;Fiorani G.
2021-01-01
Abstract
Furanic compounds, such as furfural (FUR) and 5-hydroxymethylfurfural (HMF), are promising platform chemicals, which can be derived from hemicellulose (FUR) and cellulose (HMF) contained in residual biomass. These compounds can be coupled with epichlorohydrin (derived from renewable-based glycerol), forming the corresponding mono- and bis-oxirane, which, upon CO2 insertion, are selectively transformed in cyclic organic carbonates (COCs). Although up to now, there are relatively few examples of COCs derived from furanics present in literature, and these compounds are suitable for a wide range of synthetic and materials’ applications. Interestingly, the furan moiety can be further functionalized via Diels–Alder reactions, amplifying the range of applications of the resulting functional molecules and/or polymers while decreasing their toxicity.File | Dimensione | Formato | |
---|---|---|---|
Curr. Opin. Green Sustainable Chem. 2021, 30, 1000479.pdf
non disponibili
Descrizione: Published Article
Tipologia:
Versione dell'editore
Licenza:
Accesso chiuso-personale
Dimensione
861.79 kB
Formato
Adobe PDF
|
861.79 kB | Adobe PDF | Visualizza/Apri |
I documenti in ARCA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.