Chemical Derivatization of Commercially Available Condensed and Hydrolyzable Tannins

被引:7
作者
Zhen, Lili [1 ,2 ]
Lange, Heiko [2 ,3 ,5 ]
Zongo, Luc [1 ]
Crestini, Claudia [2 ,4 ,5 ]
机构
[1] Univ Roma Tor Vergata, Dept Chem Sci & Technol, I-00133 Rome, Italy
[2] CSGI Ctr Colloid & Surface Sci, I-50019 Sesto Fiorentino, Italy
[3] Univ Milano Bicocca, Dept Earth & Environm Sci, I-20126 Milan, Italy
[4] Univ Venice Ca Foscari, Dept Mol Sci & Nanosyst, I-30170 Venice Mestre, Italy
[5] NAST Nanosci & Nanotechnol & Innovat Instrumentat, Rome, Italy
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2021年 / 9卷 / 30期
基金
欧盟地平线“2020”;
关键词
natural polyphenols; tannins; functional materials; copolymers; charged polymers; QUANTITATIVE P-31 NMR; STRUCTURAL ELUCIDATION; ACID; PHYTOCHEMICALS; METABOLITES; MICROBIOTA; COMPLEXES; DRUG;
D O I
10.1021/acssuschemeng.1c02114
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Novel valorization routes for tannins were opened by the development of a simple, straightforward, robust, and flexible approach to the selective functionalization of condensed and hydrolyzable tannins. Irrespective of the different degrees of polymerization, different commercial tannins were efficiently functionalized by the generation of an ether linkage bound to a short linker carrying the desired functional group. Functionalizations could be realized at varying degrees of technical loadings, i.e., amounts of introduced tannin-alien functionalities per number of phenolic hydroxyl groups. The same strategy was found suitable for the synthesis of polyethylene glycol-functionalized tannin copolymers. Condensed tannins functionalized with carboxylic acid moieties could be converted into a tannin-oligopeptide hybrid.
引用
收藏
页码:10154 / 10166
页数:13
相关论文
共 53 条
[1]  
Arbenz A, 2015, GREEN CHEM, V17, P2626, DOI [10.1039/c5gc00282f, 10.1039/C5GC00282F]
[2]  
Aresta M., 2015, BIOREFINERIES INTRO
[3]  
Argyropoulos DimitrisS., 2007, Materials, Chemicals, and Energy from Forest Biomass
[4]   Phytochemicals for human disease: An update on plant-derived compounds antibacterial activity [J].
Barbieri, Ramona ;
Coppo, Erika ;
Marchese, Anna ;
Daglia, Maria ;
Sobarzo-Sanchez, Eduardo ;
Nabavi, Seyed Fazel ;
Nabavi, Seyed Mohammad .
MICROBIOLOGICAL RESEARCH, 2017, 196 :44-68
[5]   Stimuli-Responsive Tannin-FeIII Hybrid Microcapsules Demonstrated by the Active Release of an Anti-Tuberculosis Agent [J].
Bartzoka, Elisavet D. ;
Lange, Heiko ;
Poce, Giovanna ;
Crestini, Claudia .
CHEMSUSCHEM, 2018, 11 (22) :3975-3991
[6]  
Bartzoka ED, 2017, GREEN CHEM, V19, P5074, DOI [10.1039/C7GC02009K, 10.1039/c7gc02009k]
[7]   Non-antibiotic quorum sensing inhibitors acting against N-acyl homoserine lactone synthase as druggable target [J].
Chang, Chien-Yi ;
Krishnan, Thiba ;
Wang, Hao ;
Chen, Ye ;
Yin, Wai-Fong ;
Chong, Yee-Meng ;
Tan, Li Ying ;
Chong, Teik Min ;
Chan, Kok-Gan .
SCIENTIFIC REPORTS, 2014, 4
[8]   Synthesis and characterization of tannic acid-PEG hydrogel via Mitsunobu polymerization [J].
Chen, Chen ;
Geng, Xi-wen ;
Pan, Ya-hui ;
Ma, Yu-ning ;
Ma, Yu-xia ;
Gao, Shu-zhong ;
Huang, Xiao-jun .
RSC ADVANCES, 2020, 10 (03) :1724-1732
[9]   Detailed Chemical Composition of Condensed Tannins via Quantitative 31P NMR and HSQC Analyses: Acacia catechu, Schinopsis balansae, and Acacia mearnsii [J].
Crestini, Claudia ;
Lange, Heiko ;
Bianchetti, Giulia .
JOURNAL OF NATURAL PRODUCTS, 2016, 79 (09) :2287-2295
[10]   Cyclic Carbonates as Safe and Versatile Etherifying Reagents for the Functionalization of Lignins and Tannins [J].
Duval, Antoine ;
Averous, Luc .
ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 2017, 5 (08) :7334-7343