TY - JOUR
T1 - Synthesis of Biobased 1,5-Pentenediamine from the Chemical Decarboxylation of l-Lysine
T2 - A Review
AU - Qi, Jiawen
AU - Zhu, Yue
AU - Li, Xiaohong
AU - Tian, Jingqing
AU - Ma, Bing
AU - Li, Xin
AU - Zhang, Xiaoxin
AU - Zhao, Chen
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/12/23
Y1 - 2024/12/23
N2 - 1,5-Pentanediamine (1,5-PDA) is one of the important monomers for the synthesis of a variety of polyamides, polyurethanes, and other polymers. Selective decarboxylation of biomass-derived l-lysine (Lys) is one of the most promising strategies for the synthesis of 1,5-PDA. Herein, the research progress in the decarboxylation of Lys to 1,5-PDA is reviewed from both homogeneous and heterogeneous catalysis strategies. Specifically, the design of catalysts, optimization of reaction conditions, investigation of the reaction mechanism, and deactivation and regeneration of catalysts are introduced, respectively. Meanwhile, the purification of 1,5-PDA is summarized, and the current advanced strategies and bottlenecks for the process intensification are analyzed. Finally, the technical challenges and improvements toward the chemical preparation of biobased 1,5-PDA as well as the new synthetic routes are also prospected.
AB - 1,5-Pentanediamine (1,5-PDA) is one of the important monomers for the synthesis of a variety of polyamides, polyurethanes, and other polymers. Selective decarboxylation of biomass-derived l-lysine (Lys) is one of the most promising strategies for the synthesis of 1,5-PDA. Herein, the research progress in the decarboxylation of Lys to 1,5-PDA is reviewed from both homogeneous and heterogeneous catalysis strategies. Specifically, the design of catalysts, optimization of reaction conditions, investigation of the reaction mechanism, and deactivation and regeneration of catalysts are introduced, respectively. Meanwhile, the purification of 1,5-PDA is summarized, and the current advanced strategies and bottlenecks for the process intensification are analyzed. Finally, the technical challenges and improvements toward the chemical preparation of biobased 1,5-PDA as well as the new synthetic routes are also prospected.
KW - 1,5-Pentanediamine (1,5-PDA)
KW - Biobased polymer monomers
KW - Heterogeneous catalysis
KW - Homogeneous catalysis
KW - Lysine (Lys)
KW - Purification
KW - Selective decarboxylation
UR - https://www.scopus.com/pages/publications/85211567650
U2 - 10.1021/acssuschemeng.4c08683
DO - 10.1021/acssuschemeng.4c08683
M3 - 文献综述
AN - SCOPUS:85211567650
SN - 2168-0485
VL - 12
SP - 18306
EP - 18319
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 51
ER -