Since the discovery of buckminsterfullerene C60 (Chart 1) by Kroto, Smalley, and Curl, 1-4 a
number of reports concerning new carbon allotropes having a variety of threedimensional …

Calixarene and resorcinarene macrocycles are renowned for their ability to form inclusion
complexes or act as molecular scaffolds. The addition of chirality to these non-planar …

Macrocyclic molecules contain rings made up of seven or more atoms. They are interesting
because they provide building blocks for synthesizing precise two or three dimensional …

1, 3, 5, 7, 9-Pentakis (4-methoxyphenylthio) corannulene (3), 1, 3, 5, 7, 9-pentakis (2-
naphthylthio) corannulene (4), and 1, 3, 6, 8-tetrakis (4-methoxyphenylthio) corannulene …

AC 3-symmetric chiral concave molecule having a phosphorus atom at the center was
synthesized, and its enantiomers were resolved. The chiral concave shape and absolute …

Abstract Hexahomotrioxacalix [3] arenes, commonly called oxacalix [3] arenes, were first
reported in 1962. Since then, their chemistry has been expanded to include numerous …

Corannulene and its penta- tert -butyl derivative co-crystallize 1:1 with pristine C 60 -fullerene
- Chemical Communications (RSC Publishing) DOI:10.1039/C2CC30652B Royal Society of …

pyrroles, 1 exists (Figure1B) predominantly in the 1, 3-alternate conformation in the absence
of anions. However, in halogenated solvents 1 binds chloride anions very tightly—a binding …

This article highlights the progress made in the design, synthesis and study of
supramolecular fullerene architectures that are based upon biomimetic organization …

Molecular tweezers,(thia) calix [4] arene–porphyrin conjugates, are constructed from the
(thia) calix [4] arene unit serving as a scaffold and from two and/or four porphyrin units …