Functionalized Calix[4]Nanocones

A Anika Haidisch (Organisch‐Chemisches Insitut Ruprecht‐Karls‐Universität Heidelberg Im Neuenheimer Feld 270 69120 Heidelberg Germany) F Frank Rominger (Institute of Organic Chemistry) M Michael Mastalerz (Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 272, Heidelberg 69120, Germany)

Abstract

Abstract The interest in synthesizing conjugated nanobelts (CNBs) and nanocones has increased recently. Although a number of various structures have been achieved, almost none have additional functional groups at the peripheral rims. Based on a calix[4]arene, a functionalized calix[4]nanocone was synthesized. Due to its rigid structure in combination with methoxy groups on both the upper and the lower rim, the nanocone was tested for the binding of alkaline ions in solution by NMR measurements. The nanocone shows a high selectivity for binding Na + in favor of Li + and K + in CDCl 3 . By comparing the nanocone with a related but structurally flexible methoxy calix[4]arene, the impact of structural rigidity on selectivity is clearly demonstrated.

Article Details

Volume / Issue Vol. 64, Issue 37
Published September 08, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (3)

A

Anika Haidisch

Organisch‐Chemisches Insitut Ruprecht‐Karls‐Universität Heidelberg Im Neuenheimer Feld 270 69120 Heidelberg Germany

F

Frank Rominger

Institute of Organic Chemistry

M

Michael Mastalerz

Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 272, Heidelberg 69120, Germany