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Alkylammonium Cation Complexation into the Narrow Cavity of Dihomooxacalix[4]arene Macrocycle

The Journal of Organic Chemistry, 2012
How big should a calixarene macrocycle be for endo-cavity complexation to occur or to allow through-the-annulus threading? To answer these questions, a complete study on the complexation of primary and secondary (di)alkylammonium cations by 18-membered p-tert-butyldihomooxacalix[4]arene macroring has been performed in the presence of the "superweak ...
GAETA, CARMINE   +6 more
openaire   +2 more sources

Giant Cavity Macrocycle: Synthesis, Structure, and Its Complexation with Pagoda[5]arene

Organic Letters, 2023
A novel stretched hexagon structure naphthalene diimides-extended-pillar[6]arene 1 with a giant cavity size of 18.769 Å in width and 17.109 Å in height is reported. 1 exhibits highly selective binding of pagoda[5]arene compared to pillar[5]arene and prism[5]arene.
Fei Zeng   +3 more
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Size Complementarity of Macrocyclic Cavities and Stoppers in Amide-Rotaxanes

Helvetica Chimica Acta, 1999
New [2]rotaxanes were prepared by the threading and the slipping procedure, the latter having the advantage of not needing templating interactions. As a consequence, the first [2]rotaxane consisting of a tetraamide macrocycle and a pure hydrocarbon thread was synthesized (see 12a in Scheme 2).
Christiane Heim   +3 more
openaire   +1 more source

Study on Molecular Cavity of Oligoamide Macrocycles by Using Scanning Tunneling Microscopy

ChemPhysChem, 2012
The molecular structures and assembly structures of aromatic oligoamide macrocycles are identified by using scanning tunneling microscopy at liquid/solid interface, which shows persistent shapes, tunable cavity sizes, and binding of water molecules.
Yibing, Wang   +10 more
openaire   +2 more sources

Synthesis and characterization of the novel shape-persistent nanosized cavity macrocycle

Synthetic Metals, 2011
Abstract The Friedel–Crafts reaction was employed to prepare the shape-persistent macrocycle (TPAP)3 with direct cyclization from three monomers of 2-(4′-(Phenyl(4″-methylphenyl)amino) phenyl)-propan-2-ol (TPAP), which contains two reactive groups of the t-hydroxyl and the p-proton on the triphenylamine. Under a very low monomer concentration (ca. 1%)
Qinggang Kong   +8 more
openaire   +1 more source

A shape-persistent arylene ethynylene macrocycle with a multiple acetamide modified cavity: synthesis and gelation

Soft Matter, 2021
Strong H-bonds suppress π–π stacking leading to an AIEE gel from a planar conjugated macrocycle.
Yang Ruan   +3 more
openaire   +2 more sources

Synthesis and conformation of macrocyclic porphyrin dimers with potentially spacious cavities

Journal of the Chemical Society, Chemical Communications, 1988
The importance of π–π donor–acceptor interactions is demonstrated in the synthesis and conformation of macrocyclic porphyrin dimers covalently linked by biphenyl or pyromellitimide bridges.
Christopher A. Hunter   +2 more
openaire   +1 more source

ChemInform Abstract: Studies in the Flexibility of Macrocycle Ligands. Calculation of Macrocycle Cavity Size by Force‐field Methods.

Chemischer Informationsdienst, 1986
AbstractDer Co‐Komplex kristallisiert in der RG P212121 mit Z=4 und ist oktaedrisch koordiniert.
M. G. B. DREW, S. HOLLIS, P. C. YATES
openaire   +1 more source

Closing the cavity: reactive and light switchable dienone-ether macrocycles

CrystEngComm, 2010
Dienone-ether macrocycles may be reversibly switched from the thermodynamically stable E,E,E,E-isomers, with an open central cavity, to globular, cavity-closed E,E,Z,Z-isomers by the action of sunlight. They are restored to their open forms by gentle heating, but more intense heating may result in an intramolecular reaction, closing the cavity in a ...
Luke T. Higham   +2 more
openaire   +1 more source

Synthesis and Evaluation of Chiral Selectors with Multiple Hydrogen-Bonding Sites in the Macrocyclic Cavities

The Journal of Organic Chemistry, 2010
Chiral macrocycles with the hydrogen bond donor/acceptor sites in the cavity were synthesized and covalently bonded to silica gel to give chiral stationary phases (CSPs), which showed excellent abilities to resolve various chiral compounds including ketones, esters, carboxylic acids, sulfoxides, amines, amino acid derivatives, and metal complexes.
Tadashi, Ema   +5 more
openaire   +2 more sources

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