Aza-Michael Reaction as a Greener, Safer, and More Sustainable Approach to Biobased Polyurethane Thermosets

被引:33
|
作者
Peyrton, Julien [1 ]
Averous, Luc [1 ]
机构
[1] Univ Strasbourg, BioTeam, ICPEES, ECPM,UMR CNRS 7515, F-67087 Strasbourg, France
来源
关键词
Green chemistry; Oleochemistry; Amine; Itaconic acid; Gel formation; Rheology; Aza-Michael;
D O I
10.1021/acssuschemeng.1c00312
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polyurethanes (PUs) such as foams or coatings are generally obtained by polyaddition between polyols and toxic polyisocyanates. In the frame of green chemistry principles, which claims, for example, that the reduction of hazardous derivatives and the design of safer chemicals, aza-Michael addition has been recently explored to substitute, for instance, the usual PUs in a safer way. Aza-Michael reaction is based on the addition between a primary or secondary amine (Michael donor) and an activated double bond (Michael acceptor). In this study, polymer network formations from biobased soybean and olive oil derivatives were largely investigated via aza-Michael addition. First, on a reactional model, the impact of the Michael donor structure on the aza-Michael reaction was demonstrated by deep NMR kinetics. Second, the model results were confirmed by monitoring of the aza-Michael polyaddition by multiwave rheology experiments. The effect of several factors, i.e., Michael donors, Michael acceptors, catalysts, and stoichiometry, on the gelation has been largely investigated. Controlling these parameters, the aza-Michael polyaddition was evaluated as a substitute for green and safer thermosets.
引用
收藏
页码:4872 / 4884
页数:13
相关论文
共 50 条
  • [21] Asymmetric Synthesis of (-)-Lentiginosine by Double Aza-Michael Reaction
    Liu, Sin-Wei
    Hsu, He-Chu
    Chang, Chiao-Hsin
    Tsai, Hui-Hsu Gavin
    Hou, Duen-Ren
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2010, 2010 (25) : 4771 - 4773
  • [22] Aza-Michael Reaction for an Undergraduate Organic Chemistry Laboratory
    Nigam, Manisha
    Rush, Brittney
    Patel, Jay
    Castillo, Raul
    Dhar, Preeti
    JOURNAL OF CHEMICAL EDUCATION, 2016, 93 (04) : 753 - 756
  • [23] Amphoteric Amino Aldehydes Reroute the Aza-Michael Reaction
    Hili, Ryan
    Yudin, Andrei K.
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (45) : 16404 - +
  • [24] Ionic amino acids: Application as organocatalysts in the aza-Michael reaction
    Morimoto, Naoki
    Takeuchi, Yasuo
    Nishina, Yuta
    JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2013, 368 : 31 - 37
  • [25] Addition of azoles to methyl vinyl ketone by the Aza-Michael reaction
    S. S. Hayotsyan
    A. N. Khachatryan
    A. O. Baltayan
    H. S. Attaryan
    G. V. Hasratyan
    Russian Journal of General Chemistry, 2015, 85 : 993 - 995
  • [26] Lipase-Catalyzed Aza-Michael Reaction on Acrylate Derivatives
    Steunenberg, Peter
    Sijm, Maarten
    Zuilhof, Han
    Sanders, Johan P. M.
    Scott, Elinor L.
    Franssen, Maurice C. R.
    JOURNAL OF ORGANIC CHEMISTRY, 2013, 78 (08): : 3802 - 3813
  • [27] Functionalization of polydopamine via the Aza-Michael reaction for antimicrobial interfaces
    Phuong Anh Ha
    Huang, Chun Jen
    Liu, Chia Yu
    Huang, Yung Chi
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2017, 253
  • [28] Supramolecular Assemblies in Ionic Liquid Catalysis for Aza-Michael Reaction
    Roy, Sudipta Raha
    Chakraborti, Asit K.
    ORGANIC LETTERS, 2010, 12 (17) : 3866 - 3869
  • [29] Aza-Michael reaction promoted by aqueous sodium carbonate solution
    Tang, Xiao-Ji
    Yan, Zhao-Lei
    Chen, Wen-Liang
    Gao, Ya-Ru
    Mao, Shuai
    Zhang, Yan-Lei
    Wang, Yong-Qiang
    TETRAHEDRON LETTERS, 2013, 54 (21) : 2669 - 2673
  • [30] Vinylacidic Acid in the Reaction of Aza-Michael with 1-Ethylpyrazole
    H. N. Khachatryan
    A. G. Shahkhatuni
    A. M. Arzumanyan
    G. G. Danagulyan
    H. S. Attaryan
    Russian Journal of Organic Chemistry, 2020, 56 : 1488 - 1490