Deep Eutectic Solvents in Polymerizations: A Greener Alternative to Conventional Syntheses

被引:205
作者
del Monte, Francisco [1 ]
Carriazo, Daniel [1 ]
Serrano, Maria C. [1 ]
Gutierrez, Maria C. [1 ]
Luisa Ferrer, M. [1 ]
机构
[1] CSIC, ICMM, Madrid 28049, Spain
关键词
eutectic solvents; green chemistry; ionic liquids; materials science; polymerization; UREA-SALT MIXTURES; CHOLINE CHLORIDE/UREA; ASSISTED SYNTHESIS; IONIC LIQUIDS; IONOTHERMAL SYNTHESIS; FRONTAL POLYMERIZATION; CARBON MONOLITHS; TRAVELING FRONTS; LACTIC-ACID; EXTRACTION;
D O I
10.1002/cssc.201300864
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The use of deep eutectic solvents (DESs) that act as all-in-one solvent-template-reactant systems offers an interesting green alternative to conventional syntheses in materials science. This Review aims to provide a comprehensive overview to emphasize the similarities and discrepancies between DES-assisted and conventional syntheses and rationalize certain green features that are common for the three DES-assisted syntheses described herein: one case of radical polymerization and two cases of polycondensations. For instance, DESs contain the precursor itself and some additional components that either provide certain functionality (e.g., drug delivery and controlled release, or electrical conductivity) to the resulting materials or direct their formation with a particular structure (e.g., hierarchical-type). Moreover, DESs provide a reaction medium, so polymerizations are ultimately carried out in a solventless fashion. This means that DES-assisted syntheses match green chemistry principles2 and 5 because of the economy of reagents and solvents, whereas the functionality incorporated by the second component allows the need for any post-synthesis derivatization to be minimized or even fully avoided (principle8). DESs also provide new precursors that favor more efficient polymerization (principle6) by decreasing the energy input required for reaction progress. Finally, the use of mild reaction conditions in combination with the compositional versatility of DESs, which allows low-toxic components to be selected, is also of interest from the viewpoint of green chemistry because it opens up the way to design biocompatible and/or eco-friendly synthetic methods (principle3).
引用
收藏
页码:999 / 1009
页数:11
相关论文
共 97 条
[1]   Extraction of glycerol from biodiesel into a eutectic based ionic liquid [J].
Abbott, Andrew P. ;
Cullis, Paul M. ;
Gibson, Manda J. ;
Harris, Robert C. ;
Raven, Emma .
GREEN CHEMISTRY, 2007, 9 (08) :868-872
[2]   Eutectic-based ionic liquids with metal-containing anions and cations [J].
Abbott, Andrew P. ;
Barron, John C. ;
Ryder, Karl S. ;
Wilson, David .
CHEMISTRY-A EUROPEAN JOURNAL, 2007, 13 (22) :6495-6501
[3]   Application of hole theory to define ionic liquids by their transport properties [J].
Abbott, Andrew P. ;
Harris, Robert C. ;
Ryder, Karl S. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2007, 111 (18) :4910-4913
[4]   Electrodeposition of zinc-tin alloys from deep eutectic solvents based on choline chloride [J].
Abbott, Andrew P. ;
Capper, Glen ;
McKenzie, Katy J. ;
Ryder, Karl S. .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2007, 599 (02) :288-294
[5]   Cationic functionalisation of cellulose using a choline based ionic liquid analogue [J].
Abbott, Andrew P. ;
Bell, Thomas J. ;
Handa, Sandeep ;
Stoddart, Barry .
GREEN CHEMISTRY, 2006, 8 (09) :784-786
[6]   Salt modified starch: sustainable, recyclable plastics [J].
Abbott, Andrew P. ;
Ballantyne, Andrew D. ;
Conde, Jesus Palenzuela ;
Ryder, Karl S. ;
Wise, William R. .
GREEN CHEMISTRY, 2012, 14 (05) :1302-1307
[7]   Electrodeposition of copper composites from deep eutectic solvents based on choline chloride [J].
Abbott, Andrew P. ;
El Ttaib, Khalid ;
Frisch, Gero ;
McKenzie, Katy J. ;
Ryder, Karl S. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2009, 11 (21) :4269-4277
[8]   Selective extraction of metals from mixed oxide matrixes using choline-based ionic liquids [J].
Abbott, AP ;
Capper, G ;
Davies, DL ;
Rasheed, RK ;
Shikotra, P .
INORGANIC CHEMISTRY, 2005, 44 (19) :6497-6499
[9]   Deep eutectic solvents formed between choline chloride and carboxylic acids: Versatile alternatives to ionic liquids [J].
Abbott, AP ;
Boothby, D ;
Capper, G ;
Davies, DL ;
Rasheed, RK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (29) :9142-9147
[10]   Novel solvent properties of choline chloride/urea mixtures [J].
Abbott, AP ;
Capper, G ;
Davies, DL ;
Rasheed, RK ;
Tambyrajah, V .
CHEMICAL COMMUNICATIONS, 2003, (01) :70-71