scholarly journals Amphiphilic Polymer Nanoreactors for Multiple Step, One-Pot Reactions and Spontaneous Product Separation

Polymers ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 1992
Author(s):  
Andrew Harrison ◽  
Christina Tang

Performing multiple reaction steps in “one pot” to avoid the need to isolate intermediates is a promising approach for reducing solvent waste associated with liquid phase chemical processing. In this work, we incorporated gold nanoparticle catalysts into polymer nanoreactors via amphiphilic block copolymer directed self-assembly. With the polymer nanoreactors dispersed in water as the bulk solvent, we demonstrated the ability to facilitate two reaction steps in one pot with spontaneous precipitation of the product from the reaction mixture. Specifically, we achieved imide synthesis from 4-nitrophenol and benzaldehyde as a model reaction. The reaction occured in water at ambient conditions; the desired 4-benzylideneaminophenol product spontaneously precipitated from the reaction mixture while the nanoreactors remained stable in dispersion. A 65% isolated yield was achieved. In contrast, PEGylated gold nanoparticles and citrate stabilized gold nanoparticles precipitated with the reaction product, which would complicate both the isolation of the product as well as reuse of the catalyst. Thus, amphiphilic nanoreactors dispersed in water are a promising approach for reducing solvent waste associated with liquid phase chemical processing by using water as the bulk solvent, eliminating the need to isolate intermediates, achieving spontaneous product separation to facilitate the recycling of the reaction mixture, and simplifying the isolation of the desired product.

2004 ◽  
Vol 108 (35) ◽  
pp. 13280-13286 ◽  
Author(s):  
Jadab Sharma ◽  
S. Mahima ◽  
Bhalchandra A. Kakade ◽  
Renu Pasricha ◽  
A. B. Mandale ◽  
...  

2015 ◽  
Vol 51 (31) ◽  
pp. 6730-6733 ◽  
Author(s):  
Guillaume Rousseau ◽  
Christophe Lavenn ◽  
Luis Cardenas ◽  
Stéphane Loridant ◽  
Yanhui Wang ◽  
...  

Self-assembly of homogeneous ultra-small gold nanoparticles thanks to the design of a new hexaadduct fullerene bearing 12 thiocyanate functions.


Author(s):  
A Nimrodh Ananth ◽  
Goutam Ghosh ◽  
S Umapathy ◽  
M A Jothi Rajan

2010 ◽  
Vol 21 (30) ◽  
pp. 305601 ◽  
Author(s):  
Yi Wang ◽  
Li Qiang Chen ◽  
Yuan Fang Li ◽  
Xi Juan Zhao ◽  
Li Peng ◽  
...  

ChemSusChem ◽  
2010 ◽  
Vol 3 (5) ◽  
pp. 541-549 ◽  
Author(s):  
Hai-Long Jiang ◽  
Sanjay Kumar Singh ◽  
Jun-Min Yan ◽  
Xin-Bo Zhang ◽  
Qiang Xu

2013 ◽  
Vol 49 (17) ◽  
pp. 1732 ◽  
Author(s):  
María González-Béjar ◽  
Kate Peters ◽  
Geniece L. Hallett-Tapley ◽  
Michel Grenier ◽  
Juan C. Scaiano

2015 ◽  
Vol 441 ◽  
pp. 10-16 ◽  
Author(s):  
Dhruvinkumar Patel ◽  
Kurtis T. James ◽  
Martin O’Toole ◽  
Guandong Zhang ◽  
Robert S. Keynton ◽  
...  

2019 ◽  
Author(s):  
Liman Hou ◽  
Marta Dueñas-Diez ◽  
Rohit Srivastava ◽  
Juan Perez-Mercader

<p></p><p>Belousov-Zhabotinsky (B-Z) reaction driven polymerization-induced self-assembly (PISA), or B-Z PISA, is a novel method for the autonomous one-pot synthesis of polymer vesicles from a macroCTA (macro chain transfer agent) and monomer solution (“soup”) containing the above and the BZ reaction components. In it, the polymerization is driven (and controlled) by periodically generated radicals generated in the oscillations of the B-Z reaction. These are inhibitor/activator radicals for the polymerization. Until now B-Z PISA has only been carried out in batch reactors. In this manuscript we present the results of running the system using a continuously stirred tank reactor (CSTR) configuration which offers some interesting advantages.Indeed, by controlling the CSTR parameters we achieve reproducible and simultaneous control of the PISA process and of the properties of the oscillatory cargo encapsulated in the resulting vesicles. Furthermore, the use of flow chemistry enables a more precise morphology control and chemical cargo tuning. Finally, in the context of biomimetic applications a CSTR operation mimics more closely the open non-equilibrium conditions of living systems and their surrounding environments.</p><p></p>


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