2016
DOI: 10.1039/c6gc01096b
|View full text |Cite
|
Sign up to set email alerts
|

Non-isocyanate poly(amide-hydroxyurethane)s from sustainable resources

Abstract: A one-pot melt polymerization of plant oil-based monomers and diamines afforded film-forming, isocyanate-free poly(amide-hydroxyurethane)s with processability and mechanical integrity.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

5
85
0

Year Published

2017
2017
2022
2022

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 81 publications
(90 citation statements)
references
References 42 publications
5
85
0
Order By: Relevance
“…FT‐IR analyses were carried out to observe the hydrogen bond cleavage in the self‐healing polymer with water when it is exposed to moisture at different relative humidities. Variable temperature FT‐IR spectroscopy is described as a method of choice to study hydrogen bonding events in polymers and oligomers based on (NH) and (CO) frequency shifts in their hydrogen bonded and free state . That method was used for polyurethanes and polyureas proving the dissociation of hydrogen bonds as a function of temperature.…”
Section: Resultsmentioning
confidence: 99%
“…FT‐IR analyses were carried out to observe the hydrogen bond cleavage in the self‐healing polymer with water when it is exposed to moisture at different relative humidities. Variable temperature FT‐IR spectroscopy is described as a method of choice to study hydrogen bonding events in polymers and oligomers based on (NH) and (CO) frequency shifts in their hydrogen bonded and free state . That method was used for polyurethanes and polyureas proving the dissociation of hydrogen bonds as a function of temperature.…”
Section: Resultsmentioning
confidence: 99%
“…[10a, 103] Methyl 9-decenoate (9-DAME)i sap roduct of the ethenolysis of methyl oleate (MO). [105] 3f reacted with diaminesl eadingt op oly(amide-hydroxyurethane)s through 5CC ring openinga nd amidation of the ester functionality. [105] 3f reacted with diaminesl eadingt op oly(amide-hydroxyurethane)s through 5CC ring openinga nd amidation of the ester functionality.…”
Section: Other Functionalized Monocarbonatesmentioning
confidence: 99%
“…Comparison of nonsustainable (top) and sustainable (bottom) strategies for:a ,b)The glycidylation of building blocksdisplaying multiple hydroxy groups; c, d) the esterification of building blocks with multiple carboxylic acids with GD;e,f)the epoxidation of building blocksw ith multiple olefins. Finally,w hereas using sacrificial peroxyacids such as m-CPBA is convenienta tt he laboratory scalef or the epoxidation of olefinic groups (Scheme23e), [105,106,175] this strategy is not regarded as sustainable. Reviews moieties (Scheme23c).…”
Section: Synthesis Of Sustainable 5cc Monomersmentioning
confidence: 99%
See 1 more Smart Citation
“…This reaction is quite fast and very intense, so polyurethane materials are easy to make from the chemical point of view. In addition, recently environmental and safety concerns motivated the design of polyurethane materials from other kinds of monomers and macromonomers [10]. Elastomeric polyurethanes consist of the so-called soft segments, typically an OH terminated flexible polyether or polyester, and the hard segments, typically a sequence of a diisocyanate and a short diol.…”
Section: Introductionmentioning
confidence: 99%