2020
DOI: 10.1016/j.trac.2020.116026
|View full text |Cite
|
Sign up to set email alerts
|

Recent developments for the investigation of chiral properties and applications of pillar[5]arenes in analytical chemistry

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
15
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
9

Relationship

1
8

Authors

Journals

citations
Cited by 26 publications
(15 citation statements)
references
References 91 publications
0
15
0
Order By: Relevance
“…Synthetic macrocyclic compounds, such as calixarenes, thiacalixarenes, resorcinarenes, pillararenes, and others, have excellent complexing properties and are often selective for a certain substrate [ 24 , 25 , 26 , 27 , 28 , 29 , 30 , 31 , 32 ]. The introduction of fragments of Schiff bases into the structure of (thia)calixarenes makes it possible to increase both the efficiency and selectivity with respect to metal cations.…”
Section: Introductionmentioning
confidence: 99%
“…Synthetic macrocyclic compounds, such as calixarenes, thiacalixarenes, resorcinarenes, pillararenes, and others, have excellent complexing properties and are often selective for a certain substrate [ 24 , 25 , 26 , 27 , 28 , 29 , 30 , 31 , 32 ]. The introduction of fragments of Schiff bases into the structure of (thia)calixarenes makes it possible to increase both the efficiency and selectivity with respect to metal cations.…”
Section: Introductionmentioning
confidence: 99%
“…Because of their high p-electron density induced by the electron-rich hydroquinones in the macrocycle, pillararenes are known to exhibit superb hostguest chemistry such that they can form association complexes (via chemical bonds) with electron-deficient species. [106][107][108] In the pillararene family, pillar [5]arene is the most structurally stable, and higher homologues (i.e., pillar [6][7][8][9][10][11][12][13][14][15]arenes) can be synthesized via the expansion of the pillar [5]arene ring. One of the most facile methods to synthesize pillar [5]arenes is via the condensation reaction between 1,4-dimethoxybenzene and paraformaldehyde in the presence of a suitable Lewis acid as a catalyst (refer to Table 2).…”
Section: Biomimetic and Bioinspired Channelsmentioning
confidence: 99%
“…Because of their high π-electron density induced by the electron-rich hydroquinones in the macrocycle, pillararenes are known to exhibit superb host–guest chemistry such that they can form association complexes ( via chemical bonds) with electron-deficient species. 106–108 In the pillararene family, pillar[5]arene is the most structurally stable, and higher homologues ( i.e. , pillar[6–15]arenes) can be synthesized via the expansion of the pillar[5]arene ring.…”
Section: Basic Chemistry and Intrinsic Transport Propertiesmentioning
confidence: 99%
“…We first briefly describe the discovery and the main characteristics of the par-ent pillar [5]arenes, for which several review articles have already been published. [25][26][27][28] After defining the particular features of copillararenes, we review and compare the different synthetic strategies allowing their construction. Finally, some key applications and future perspectives are described.…”
Section: Introductionmentioning
confidence: 99%