2014
DOI: 10.1039/c3py01194a
|View full text |Cite
|
Sign up to set email alerts
|

Functionalization of cardanol: towards biobased polymers and additives

Abstract: Among the renewable resource materials, cashew nut shell liquid (CNSL) is considered as an important starting material due to its unique structural features, abundant availability and low cost. A large number of chemicals and products have been developed starting from CNSL by taking advantage of the three reactive sites, namely, phenolic hydroxyl, aromatic ring and unsaturation(s) in the alkenyl side chain. This comprehensive review deals with general information on CNSL, its purification and separation method… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

4
253
0
3

Year Published

2016
2016
2023
2023

Publication Types

Select...
5
4

Relationship

1
8

Authors

Journals

citations
Cited by 388 publications
(260 citation statements)
references
References 217 publications
(242 reference statements)
4
253
0
3
Order By: Relevance
“…Our team published a comprehensive review on the functionalization of cardanol for the synthesis of monomers, polymers and additives (Voirin et al, 2014). Moreover, we synthesized new building blocks from cardanol 1 in one or two step synthesis by various reactions (Jaillet et al, 2015), such as thiol-ene coupling, allylation, epoxidation, carbonation or acrylation (Scheme 1).…”
Section: Building Blocks Synthesismentioning
confidence: 99%
“…Our team published a comprehensive review on the functionalization of cardanol for the synthesis of monomers, polymers and additives (Voirin et al, 2014). Moreover, we synthesized new building blocks from cardanol 1 in one or two step synthesis by various reactions (Jaillet et al, 2015), such as thiol-ene coupling, allylation, epoxidation, carbonation or acrylation (Scheme 1).…”
Section: Building Blocks Synthesismentioning
confidence: 99%
“…The lower exotherm peak may be due to the reaction took place through unsaturation of side chain, both from internal double bond (monoene, diene) and vinyl bond (triene). This reaction could lead to the increase in viscosity of the benzoxazine monomer [3]. According to Rodrigues et al cardanol could be thermal oligomerized at 140 °C and the dimer was the main oligomer formed.…”
Section: Structural Characterization Of Cardanol Based Benzoxazinementioning
confidence: 99%
“…20,21 More derivatives have been given in a recent review. 1 Despite the voluminous literature, there seems to be no prior report on the use of ene reaction to derivatize the olefins on the alkenyl moieties of cardanol. In the ene reaction, an electron-deficient olefin forms a bond with an olefin that contains an allylic hydrogen.…”
Section: Introductionmentioning
confidence: 99%
“…Cardanol, obtained by double vacuum distillation of CNSL, is not only cheap but biodegradable and abundantly available, especially in India. 1,2 It is an alkyl/alkenyl phenol where the non-aromatic chain contains 15 carbon atoms, which may be a saturated hydrocarbon (5-8%), a mono-ene (48-49%), a diene (16-17%), or a triene (29-30%) as shown in Figure 1.…”
Section: Introductionmentioning
confidence: 99%