Clicking Biobased Polyphenols: A Sustainable Platform for Aromatic Polymeric Materials

被引:30
作者
Buono, Pietro [1 ]
Duval, Antoine [2 ]
Averous, Luc [2 ]
Habibi, Youssef [1 ]
机构
[1] LIST, Dept Mat Res & Technol MRT, 5 Ave Hauts Fourneaux, L-4362 Esch Sur Alzette, Luxembourg
[2] Univ Strasbourg, CNRS, UMR 7515, BioTeam ICPEES ECPM, 25 Rue Becquerel, F-67087 Strasbourg 2, France
关键词
biomass; click chemistry; green chemistry; polymers; synthesis design; PHENOLIC HYDROXYL-GROUPS; BIO-BASED POLYURETHANE; LIGNIN-BASED MATERIALS; MILLED WOOD LIGNIN; ENGINEERING PLASTICS; POLY(CARDANYL ACRYLATE); CONDENSED TANNINS; KRAFT LIGNIN; CARDANOL; DIELS;
D O I
10.1002/cssc.201800595
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lignin, tannins, and cashew nut shell liquid are considered the main sources of aromatic-based macromolecules. They represent an abundant alternative feedstock for the elaboration of aromatic chemicals and polymers, with a view to replacing some fossil-based fractions. Located in different tissues of plants, these compounds, with a large diversity and structural complexity, have, to date, been considered as byproducts derived from fractionation-separation industrial processes with low added value. In the last decade, the use of click chemistry as a tool for the synthesis of controlled macromolecular architectures has seen much development in fundamental and applied research for a wide range of applications. It could represent a valid solution to overcome the main limitations encountered in the chemical modification of natural sources of chemicals, with an environmentally friendly approach to create new substrates for the development of innovative polymers and materials. After a brief description of the main aromatic biopolymers, including the main extraction techniques, along with their structure and their properties, this Review describes chemical modifications that have mainly been focused on natural polyphenols, with the aim of introducing clickable groups, and their further use for the synthesis of biobased materials and additives. Special emphasis is given to several as-yet unexplored chemical features that could contribute to further fundamental and applied materials science research.
引用
收藏
页码:2472 / 2491
页数:20
相关论文
共 176 条
[1]   The effect of freeze-drying and its implications for botanical medicine: A review [J].
Abascal, K ;
Ganora, L ;
Yarnell, E .
PHYTOTHERAPY RESEARCH, 2005, 19 (08) :655-660
[2]   Pharmacological potential of tocotrienols: a review [J].
Ahsan, Haseeb ;
Ahad, Amjid ;
Iqbal, Jahangir ;
Siddiqui, Waseem A. .
NUTRITION & METABOLISM, 2014, 11
[3]   19F nuclear magnetic resonance spectroscopy for the quantitative detection and classification of carbonyl groups in lignins [J].
Ahvazi, BC ;
Crestini, C ;
Argyropoulos, DS .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1999, 47 (01) :190-201
[4]  
Anastas P. T., 2000, GREEN CHEM THEORY PR
[5]  
[Anonymous], 2010, Angew. Chem, DOI DOI 10.1002/ANGE.200903924
[6]  
[Anonymous], 2014, ANGEW CHEM
[7]  
Arbenz A, 2015, GREEN CHEM, V17, P2626, DOI [10.1039/C5GC00282F, 10.1039/c5gc00282f]
[8]   QUANTITATIVE P-31 NMR ANALYSIS OF LIGNINS, A NEW TOOL FOR THE LIGNIN CHEMIST [J].
ARGYROPOULOS, DS .
JOURNAL OF WOOD CHEMISTRY AND TECHNOLOGY, 1994, 14 (01) :45-63
[9]   Semiquantitative determination of quinonoid structures in isolated lignins by 31P nuclear magnetic resonance [J].
Argyropoulos, DS ;
Zhang, LM .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1998, 46 (11) :4628-4634
[10]   Production and Application of Lignosulfonates and Sulfonated Lignin [J].
Aro, Thomas ;
Fatehi, Pedram .
CHEMSUSCHEM, 2017, 10 (09) :1861-1877