2015
DOI: 10.1016/j.polymer.2015.10.055
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Facile route to multigram synthesis of environmentally friendly non-isocyanate polyurethanes

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Cited by 56 publications
(94 citation statements)
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“…In recent years, numerous studies have investigated PHU synthesis with strong emphasis on the production of single-phase PHUs, crosslinked PHU networks, reaction catalysis and the synthesis of carbonate monomers . For example, Endo and coworkers [14][15][16][17][18][19][20][21][22][23], as well as others [24][25][26][27][28][29], synthesized PHUs from carbonated epoxy resins (such as Bisphenol A diglycidyl ether, hydroquinone diglycidyl ether, and butanediol diglycidyl ether) and small-molecule diamines (such as hexamethylene diamine) resulting in single-phase PHUs [14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29]. The reaction kinetics of five-, six- [17][18][19]51], seven- [20] and eight-membered ring carbonates [12], the influence of substituent on reactivity [21,52], and the effects of catalysts [22,[30][31][32] were also characterized.…”
Section: Introductionmentioning
confidence: 99%
“…In recent years, numerous studies have investigated PHU synthesis with strong emphasis on the production of single-phase PHUs, crosslinked PHU networks, reaction catalysis and the synthesis of carbonate monomers . For example, Endo and coworkers [14][15][16][17][18][19][20][21][22][23], as well as others [24][25][26][27][28][29], synthesized PHUs from carbonated epoxy resins (such as Bisphenol A diglycidyl ether, hydroquinone diglycidyl ether, and butanediol diglycidyl ether) and small-molecule diamines (such as hexamethylene diamine) resulting in single-phase PHUs [14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29]. The reaction kinetics of five-, six- [17][18][19]51], seven- [20] and eight-membered ring carbonates [12], the influence of substituent on reactivity [21,52], and the effects of catalysts [22,[30][31][32] were also characterized.…”
Section: Introductionmentioning
confidence: 99%
“…[130] A shorter chain analogue of 4f (4f')w as used for the synthesis of nanocapsules for drug delivery. [140] In this case, the authors were able to separate pure 4l from other carbonated diglycerol regioisomers. [131] 4g was preparedb yP lasseraud and co-workerss tarting from undecylenic acid (UA), at erminally unsaturated fatty acid that can be obtained from the pyrolysis of the ricinoleic acid chains of castor oil (Scheme 12, route a).…”
Section: Terminal Biscarbonatesmentioning
confidence: 99%
“…Our initial efforts focused on using diglycerol, which is a promising biorenewable tetraol monomer derived from glycerol . Glycerol, a coproduct of biodiesel production, is a relatively low cost commodity chemical formed in large excess when compared to its current demand . Previous efforts to employ diglycerol for polymer synthesis include copolymerization with an anhydride, converting to the dicarbonate, or diketal prior to copolymerization, or use as a tetraol initiator .…”
Section: Introductionmentioning
confidence: 99%
“…Glycerol, a coproduct of biodiesel production, is a relatively low cost commodity chemical formed in large excess when compared to its current demand . Previous efforts to employ diglycerol for polymer synthesis include copolymerization with an anhydride, converting to the dicarbonate, or diketal prior to copolymerization, or use as a tetraol initiator . The commercially available form of diglycerol contains three structural isomers (α,α‐, α,β‐, and β,β‐), with the α,α‐form predominating [Figure (a)] .…”
Section: Introductionmentioning
confidence: 99%
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