Strapped calix[4]pyrroles: from syntheses to applications

• Published in: Chemical Society reviews Vol. 49; no. 3; p. 865
• Main Authors: Peng, Sangshan, He, Qing, Vargas-Zúñiga, Gabriela I, Qin, Lei, Hwang, Inhong, Kim, Sung Kuk, Heo, Nam Jung, Lee, Chang-Hee, Dutta, Ranjan, Sessler, Jonathan L
• Format: Journal Article
• Language: English
• Published: England 07-02-2020
• Subjects: Anions - chemistry; Apoptosis; Calixarenes - chemistry; Calixarenes - metabolism; Cations - chemistry; Cell Membrane Permeability; Crystallization; Models, Molecular; Molecular Structure; Organic Chemicals - chemistry; Porphyrins - chemistry; Porphyrins - metabolism; Structure-Activity Relationship; Thermodynamics
• ISSN: 1460-4744
• DOI: 10.1039/c9cs00528e

Supramolecular chemistry is a central topic in modern chemistry. It touches on many traditional disciplines, such as organic chemistry, inorganic chemistry, physical chemistry, materials chemistry, environmental chemistry, and biological chemistry. Supramolecular hosts, inter alia macrocyclic hosts, play critical roles in supramolecular chemistry. Calix[4]pyrroles, non-aromatic tetrapyrrolic macrocycles defined by sp
hybridized meso bridges, have proved to be versatile receptors for neutral species, anions, and cations, as well as ion pairs. Compared to the parent system, octamethylcalix[4]pyrrole and its derivatives bearing simple appended functionalities, strapped calix[4]pyrroles typically display enhanced binding affinities and selectivities. In this review, we summarize advances in the design and synthesis of strapped calix[4]pyrroles, as well as their broad utility in molecular recognition, supramolecular extraction, separation technology, ion transport, and as agents capable of inhibiting cancer cell proliferation. Future challenges within this sub-field are also discussed.