The biobased renewable monomer 2,5-diformylfuran is polymerised using various N-heterocyclic carbene (NHC) catalysts in dimethyl sulfoxide (DMSO) affording a low molar mass polymer. It is shown that catalyst structure as well as the temperature and time the polymerization is running have a noticeable effect on its molar mass. The obtained material is characterized by nuclear magnetic resonance (NMR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and X-ray diffraction (XRD). An attempt at chain extension with diamine leads to precipitation of the polymer. This new biobased polymer material might be useful as a sustainable resin
Enzymatic polymerization provides an excellent opportunity for the conversion of renewable resources...
The functionalisation of limonene has enabled the synthesis of two renewably-sourced monomers for th...
This contribution presents a full account of experimental and theoretical/computational investigatio...
A family of monomers including 2,5-hexandiol, 2,7-octandiol, 2,5-furandicarboxylic acid (FDCA) , ter...
In recent years, considerable efforts have been made regarding the synthesis of renewable chemicals ...
Condensation of renewable resources based monomer 2,5-diformylfuran (DFF) and urea at 110 °C by melt...
Diminishing oil reserves, increasing demand, and the rising costs of petroleum-based raw materials a...
As much of the concern is being placed on metal-free polymerization, carbenes are attracting researc...
The research here deals with the conversion of 5-hydroxymethylfurfural (HMF) into a tunable polymer....
The polycondensation of diamines and dialdehydes promoted by an N-heterocyclic carbene (NHC) catalys...
The polymerisation of furan monomers and the exploitation of some of the chemical peculiarities of t...
Ring opening polymerizations of esters (ROTEP) can be used to make polymers employed in films, packa...
In this contribution, the development of a process for the synthesis of potentially highly valuable ...
Aromatic dinitriles show promise as a pivotal building block in polymer and pharmaceutical chemistry...
A designed N-heterocyclic carbene (NHC) catalyst was covalently anchored on a range of mesoporous an...
Enzymatic polymerization provides an excellent opportunity for the conversion of renewable resources...
The functionalisation of limonene has enabled the synthesis of two renewably-sourced monomers for th...
This contribution presents a full account of experimental and theoretical/computational investigatio...
A family of monomers including 2,5-hexandiol, 2,7-octandiol, 2,5-furandicarboxylic acid (FDCA) , ter...
In recent years, considerable efforts have been made regarding the synthesis of renewable chemicals ...
Condensation of renewable resources based monomer 2,5-diformylfuran (DFF) and urea at 110 °C by melt...
Diminishing oil reserves, increasing demand, and the rising costs of petroleum-based raw materials a...
As much of the concern is being placed on metal-free polymerization, carbenes are attracting researc...
The research here deals with the conversion of 5-hydroxymethylfurfural (HMF) into a tunable polymer....
The polycondensation of diamines and dialdehydes promoted by an N-heterocyclic carbene (NHC) catalys...
The polymerisation of furan monomers and the exploitation of some of the chemical peculiarities of t...
Ring opening polymerizations of esters (ROTEP) can be used to make polymers employed in films, packa...
In this contribution, the development of a process for the synthesis of potentially highly valuable ...
Aromatic dinitriles show promise as a pivotal building block in polymer and pharmaceutical chemistry...
A designed N-heterocyclic carbene (NHC) catalyst was covalently anchored on a range of mesoporous an...
Enzymatic polymerization provides an excellent opportunity for the conversion of renewable resources...
The functionalisation of limonene has enabled the synthesis of two renewably-sourced monomers for th...
This contribution presents a full account of experimental and theoretical/computational investigatio...