Effect of 4-position pyridine ring substitution on Zn(II) complexes of 4-substituted Py<sub>2</sub>N<sub>2</sub> pyridinophane macrocycles

The metal binding properties of macrocyclic small molecules are a key property that drives the applications for which these ligands can be used. Pyridine-modified Py<sub>2</sub>N<sub>2</sub> pyridinophane small molecules are a new class of macrocyclic small molecules, whose properties have not been explored. As a result, Zn(II) metal binding of a library of six pyridine-modified Py<sub>2</sub>N<sub>2</sub> complexes is reported here. These results include <sup>1</sup>H NMR, log <i>β</i><sub>Zn(II)</sub>, and X-ray diffraction, which are compared to PyN<sub>3</sub> congeners to show that the differences in each scaffold yield markedly different metal binding properties that can be exploited in future applications.

Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28341187.v2
Primary Topic
Organometallic Complex Synthesis and Catalysis
Type
article
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article

Effect of 4-position pyridine ring substitution on Zn(II) complexes of 4-substituted Py2N2 pyridinophane macrocycles

Figshare
Organometallic Complex Synthesis and Catalysis
article

Effect of 4-position pyridine ring substitution on Zn(II) complexes of 4-substituted Py2N2 pyridinophane macrocycles

article en

Abstract

The metal binding properties of macrocyclic small molecules are a key property that drives the applications for which these ligands can be used. Pyridine-modified Py<sub>2</sub>N<sub>2</sub> pyridinophane small molecules are a new class of macrocyclic small molecules, whose properties have not been explored. As a result, Zn(II) metal binding of a library of six pyridine-modified Py<sub>2</sub>N<sub>2</sub> complexes is reported here. These results include <sup>1</sup>H NMR, log <i>β</i><sub>Zn(II)</sub>, and X-ray diffraction, which are compared to PyN<sub>3</sub> congeners to show that the differences in each scaffold yield markedly different metal binding properties that can be exploited in future applications.

Figshare
Openalex Percentile: Top 54%
Organometallic Complex Synthesis and Catalysis
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