Purely covalent molecular cages and containers for guest encapsulation

G Montà-González, F Sancenón… - Chemical …, 2022 - ACS Publications
Cage compounds offer unique binding pockets similar to enzyme-binding sites, which can
be customized in terms of size, shape, and functional groups to point toward the cavity and …

Development of ion chemosensors based on porphyrin analogues

Y Ding, WH Zhu, Y Xie - Chemical Reviews, 2017 - ACS Publications
Sensing of metal ions and anions is of great importance because of their widespread
distribution in environmental systems and biological processes. Colorimetric and fluorescent …

Calix [4] pyrroles: versatile molecular containers with ion transport, recognition, and molecular switching functions

DS Kim, JL Sessler - Chemical Society Reviews, 2015 - pubs.rsc.org
Over the last two decades, calix [4] pyrroles have attracted considerable attention as
molecular containers. Used in this capacity, they have been exploited as strong and …

[图书][B] Encyclopedia of Supramolecular Chemistry-Two-Volume Set (Print)

JL Atwood - 2013 - books.google.com
The two-volume Encyclopedia of Supramolecular Chemistry offers authoritative, centralized
information on a rapidly expanding interdisciplinary field. User-friendly and high-quality …

Syntheses of copillar [5] arenes by co-oligomerization of different monomers

Z Zhang, B Xia, C Han, Y Yu, F Huang - Organic Letters, 2010 - ACS Publications
Three copillar [5] arenes, pillar [5] arenes containing different repeating units, were
successfully prepared by co-oligomerization of different monomers. It was demonstrated that …

Aryl-Extended and Super Aryl-Extended Calix [4] pyrroles: Design, Synthesis, and Applications

L Escobar, Q Sun, P Ballester - Accounts of Chemical Research, 2023 - ACS Publications
Conspectus Proteins exhibit high-binding affinity and selectivity, as well as remarkable
catalytic performance. Their binding pockets are hydrophobic but also contain polar and …

Molecular engineering of free‐base porphyrins as ligands—the N− H⋅⋅⋅ X binding motif in tetrapyrroles

M Kielmann, MO Senge - Angewandte Chemie International …, 2019 - Wiley Online Library
The core N− H units of planar porphyrins are often inaccessible to forming hydrogen‐
bonding complexes with acceptor molecules. This is due to the fact that the amine moieties …

Urea derivatives as functional molecules: supramolecular capsules, supramolecular polymers, supramolecular gels, artificial hosts, and catalysts

M Yokoya, S Kimura… - Chemistry–A European …, 2021 - Wiley Online Library
Urea, which has both hydrogen bond acceptor and donor moieties, is an ideal structure for a
supramolecular synthon. Various supramolecules having ureido group (s) have been widely …

Hydrogen bonded supramolecular capsules with functionalized interiors: the controlled orientation of included guests

L Adriaenssens, P Ballester - Chemical Society Reviews, 2013 - pubs.rsc.org
This tutorial review aims to present and describe selected examples of still quite rare endo-
functionalized supramolecular capsules. Only capsules assembled through the use of …

Binding hydrated anions with hydrophobic pockets

P Sokkalingam, J Shraberg, SW Rick… - Journal of the American …, 2016 - ACS Publications
Using a combination of isothermal titration calorimetry and quantum and molecular
dynamics calculations, we demonstrate that relatively soft anions have an affinity for …