2022
DOI: 10.1039/d2py00850e
|View full text |Cite
|
Sign up to set email alerts
|

Polymers fromS-vinyl monomers: reactivities and properties

Abstract: The large variety of available functional groups, their versatility, and the various polymerization technique have made vinyl monomers the prevalent source for preparation of polymers. Interestingly, among this wide variety...

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
5
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 11 publications
(5 citation statements)
references
References 212 publications
(369 reference statements)
0
5
0
Order By: Relevance
“…This is because polymer chains could have an excess content of hydrophobic NAT beyond what the system can accommodate, leading to nanoparticle aggregation and reduced stabilization. 22,23 To further understand the resulting morphologies, we analyzed the nanostructures using dynamic light scattering (DLS) and transmission electron microscopy (TEM) measurements (Fig. 2).…”
Section: Polymer Chemistry Papermentioning
confidence: 99%
“…This is because polymer chains could have an excess content of hydrophobic NAT beyond what the system can accommodate, leading to nanoparticle aggregation and reduced stabilization. 22,23 To further understand the resulting morphologies, we analyzed the nanostructures using dynamic light scattering (DLS) and transmission electron microscopy (TEM) measurements (Fig. 2).…”
Section: Polymer Chemistry Papermentioning
confidence: 99%
“…The use of divinyl sulfone allows the formation of poly(ether-sulfone)s. Aliphatic polymers with polar sulfone groups might, e.g. be interesting in flameretardant materials due to good chemical and heat resistance [73], in optical elements because of high refractive indices [74,75] or in electrochemistry due to a wide electrochemical window [76]. By using diacrylates and dialcohols poly(ether-ester)s can be obtained [33,53].…”
Section: Oxa-michael Polymerizationmentioning
confidence: 99%
“…The use of divinyl sulfone allows the formation of poly(ethersulfone)s. Polymers with polar sulfone groups might e.g. be interesting in flame retardant materials due to good chemical and heat resistance, [72] in optical elements because of high refractive indices [73,74] or in electrochemistry due to a wide electrochemical window. [75] By using diacrylates and dialcohols poly(ether-ester)s can be obtained.…”
Section: Oxa-michael Polymerizationmentioning
confidence: 99%