2014
DOI: 10.1002/pola.27105
|View full text |Cite
|
Sign up to set email alerts
|

Side‐on main‐chain liquid crystalline polymers prepared by acyclic diene metathesis polymerization and thiol‐ene click step‐growth polymerization

Abstract: In this manuscript, we design and synthesize a series of X‐shaped mesogenic monomers, bearing two terminal‐alkene tails. Starting from these X‐shaped monomers, acyclic diene metathesis polymerization and thiol‐ene polyaddition are applied for the first time to prepare two series of side‐on main‐chain liquid crystalline polymers (LCPs), respectively. The mesomorphic behaviors and structure‐property relationships of these new polymers are studied in detail by a combination of 1H NMR, GPC, TGA, DSC, POM, and XRD … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
8
0
1

Year Published

2015
2015
2020
2020

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 16 publications
(9 citation statements)
references
References 93 publications
(151 reference statements)
0
8
0
1
Order By: Relevance
“…Thiol‐ene click chemistry reaction was carried out by UV irradiation with a UV light (365 nm, 800 W). As shown in Figure , the thiol‐ene click reaction follows a free radical addition mechanism in which a thiol group is added to a double bond and then the chain is transferred to a thiol . The thiol‐ene reaction proceeded under free radical step‐growth mechanism, as such, the thiol radicals can react with vinyl groups from different parts.…”
Section: Resultsmentioning
confidence: 99%
“…Thiol‐ene click chemistry reaction was carried out by UV irradiation with a UV light (365 nm, 800 W). As shown in Figure , the thiol‐ene click reaction follows a free radical addition mechanism in which a thiol group is added to a double bond and then the chain is transferred to a thiol . The thiol‐ene reaction proceeded under free radical step‐growth mechanism, as such, the thiol radicals can react with vinyl groups from different parts.…”
Section: Resultsmentioning
confidence: 99%
“…The importance of sulfur in modern materials science is further exemplified through the extensive usage of thiol coupling reactions. Besides the examples of thiol coupling reactions highlighted in this Review, many others exist, including dendrimer synthesis, POSS fabrication, electroluminescent networks, surface chemistry, and creative materials for reaction catalysis . Indeed, a book was recently written exploring many of these thiol coupling processes and products…”
Section: Discussionmentioning
confidence: 99%
“…The thiol‐ene radical step‐growth polymerization generates highly uniform networks, and has been used for a number of other responsive materials. This reaction has been utilized by several research groups to synthesize LCEs . Yang et al were the first group to synthesize micrometer‐sized pillars made of MC‐LCE using this synthetic route .…”
Section: Synthesis and Alignment Of Lcesmentioning
confidence: 99%