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 is a key property that drives what 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 are reported here. These results include <sup>1</sup>H NMR, log β<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.

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Journal
Journal of Coordination Chemistry
Published
2025-02-03
DOI
https://doi.org/10.1080/00958972.2025.2453062
Primary Topic
Metal complexes synthesis and properties
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Timothy M. Schwartz, Katherine J. Smith, Hannah M. Johnston, Kristof Pota et al.
Journal of Coordination Chemistry
Metal complexes synthesis and properties
article

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

Timothy M. Schwartz, Katherine J. Smith, Hannah M. Johnston, Kristof Pota, Kayla N. Green, David M. Freire
article en

Abstract

The metal binding properties of macrocyclic small molecules is a key property that drives what 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 are reported here. These results include <sup>1</sup>H NMR, log β<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.

Journal of Coordination ChemistryVol. 78(1-3)
Texas Christian University (US)
Welch Foundation, National Institute of General Medical Sciences
Openalex Percentile: Top 97%
Metal complexes synthesis and properties
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