Synthesis 2018; 50(23): 4555-4568
DOI: 10.1055/s-0037-1609943
short review
© Georg Thieme Verlag Stuttgart · New York

Linear Neutral Receptors for Anions: Synthesis, Structure and Applications

Agnieszka Cholewiak
,
Pawel Stepniak
,
Janusz Jurczak*
Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warszawa, Poland   Email: [email protected]
› Author Affiliations
This work was supported by an OPUS grant (UMO-2014/15/B/ST5/05038) from the National Science Centre of Poland.
Further Information

Publication History

Received: 31 May 2018

Accepted after revision: 09 August 2018

Publication Date:
19 September 2018 (online)


Abstract

A selective digest of linear anion receptors based on different aromatic skeletons is presented. Since the structures of anions vary from one to another, different strategies have been developed over recent years in order to bind anions efficiently and selectively. Rigidity, number of hydrogen bond donors, steric hindrance, and special preorganization of linear receptors are analyzed to shed light on the rational design of anion receptors.

1 Introduction

2 1,3- and 1,2-Benzene Derivatives

3 1,3- and 5,7-Azulene Derivatives

4 1,8-Naphthalene Derivatives

5 1,8-Anthracene Derivatives

6 2,6-Pyridine Derivatives

7 2,5-Pyrrole Derivatives

8 Diamidoarenodipyrrole Derivatives

9 Carbazole Derivatives

10 DITIPIRAM Derivatives

11 Conclusion

 
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