LanthanideMolecular Clusters and Metal–OrganicLayers Constructed by Manipulation of Substituents

Usually, complexes with different connections and shapes are constructed by regulating the substituents. However, it is extremely challenging to construct two lanthanide complexes with different dimensions by only fine-tuning the substituents of the ligands, especially the substituents (−CH<sub>3</sub> and −CH<sub>2</sub>CH<sub>3</sub>) with almost similar physical and chemical properties. Herein, by only regulating the substituents of the multidentate chelating ligands, two lanthanide complexes with different dimensions and connection modes were successfully constructed using a multicomponent “one-pot method” under the guidance of the multidentate chelating coordination method (MCC). They are the 11-nuclear lanthanide molecular cluster (<b>Dy</b><sub><b>11</b></sub>) and the metal–organic layer (<b>2D-Dy</b>). Specifically, when the selected ligand is an imidazole-2-carboxaldehyde derivative and its substituent is −CH<sub>3</sub>, a layered <b>2D-Dy</b> is obtained. The linker [Dy­(HL<sup>1</sup>)<sub>3</sub>] with a propeller configuration is formed by chelating the Dy­(III) ion with an acylhydrazone ligand (HL<sup>1</sup>) formed by the condensation of three salicylhydrazides and 1-methyl-1H-imidazole-2-carboxaldehyde. The above linkers were further linked alternately with propeller-shaped [Dy­(NO<sub>3</sub>)<sub>3</sub>] as a secondary building unit (SBU) to form <b>2D-Dy</b>. In addition, by changing the −CH<sub>3</sub> on the ligand to −CH<sub>2</sub>CH<sub>3</sub>, we obtained an example of <b>Dy</b><sub><b>11</b></sub> formed by epitaxial assembly of two Dy­(III) ions with an hourglass-shaped Dy<sub>9</sub> as the core, and its molecular formula is [Dy<sub>11</sub>(HL<sup>2</sup>)<sub>8</sub>(μ<sub>3</sub>–OH)<sub>8</sub>(μ<sub>4</sub>-O)<sub>2</sub>(CH<sub>3</sub>O)<sub>4</sub>(NO<sub>3</sub>)<sub>4</sub>]­(NO<sub>3</sub>)<sub>5</sub> 18CH<sub>3</sub>OH. The cluster <b>Dy</b><sub><b>11</b></sub> was bombarded using high-resolution electrospray ionization mass spectrometry (HRESI-MS) and the molecular ion peaks of various fragments formed were captured. Based on the above molecular ion peaks, the possible fragmentation mechanisms of <b>Dy</b><sub><b>11</b></sub> were inferred to be Dy<sub>11</sub> → Dy<sub>4</sub>(HL<sup>2</sup>)<sub>4</sub> → Dy<sub>3</sub>(HL<sup>2</sup>)<sub>2</sub> → Dy<sub>2</sub>(HL<sup>2</sup>)<sub>2</sub> → Dy­(HL<sup>2</sup>)<sub>2</sub> and Dy<sub>11</sub> → Dy­(HL<sup>2</sup>)<sub>2</sub>/Dy<sub>2</sub>(HL<sup>2</sup>)<sub>2</sub>/Dy<sub>3</sub>(HL<sup>2</sup>)<sub>2</sub>/Dy<sub>4</sub>(HL<sup>2</sup>)<sub>4</sub>. This work is one of the rare examples where fine-tuning of ligand substituents leads to the formation of complexes of different dimensions, which promotes the progress of crystal engineering of lanthanide complexes.

Publication Details

Journal
Figshare
Published
2025-02-05
DOI
https://doi.org/10.1021/acs.inorgchem.4c04885.s001
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Metal-Organic Frameworks: Synthesis and Applications
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article
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article

LanthanideMolecular Clusters and Metal–OrganicLayers Constructed by Manipulation of Substituents

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Metal-Organic Frameworks: Synthesis and Applications
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LanthanideMolecular Clusters and Metal–OrganicLayers Constructed by Manipulation of Substituents

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Abstract

Usually, complexes with different connections and shapes are constructed by regulating the substituents. However, it is extremely challenging to construct two lanthanide complexes with different dimensions by only fine-tuning the substituents of the ligands, especially the substituents (−CH<sub>3</sub> and −CH<sub>2</sub>CH<sub>3</sub>) with almost similar physical and chemical properties. Herein, by only regulating the substituents of the multidentate chelating ligands, two lanthanide complexes with different dimensions and connection modes were successfully constructed using a multicomponent “one-pot method” under the guidance of the multidentate chelating coordination method (MCC). They are the 11-nuclear lanthanide molecular cluster (<b>Dy</b><sub><b>11</b></sub>) and the metal–organic layer (<b>2D-Dy</b>). Specifically, when the selected ligand is an imidazole-2-carboxaldehyde derivative and its substituent is −CH<sub>3</sub>, a layered <b>2D-Dy</b> is obtained. The linker [Dy­(HL<sup>1</sup>)<sub>3</sub>] with a propeller configuration is formed by chelating the Dy­(III) ion with an acylhydrazone ligand (HL<sup>1</sup>) formed by the condensation of three salicylhydrazides and 1-methyl-1H-imidazole-2-carboxaldehyde. The above linkers were further linked alternately with propeller-shaped [Dy­(NO<sub>3</sub>)<sub>3</sub>] as a secondary building unit (SBU) to form <b>2D-Dy</b>. In addition, by changing the −CH<sub>3</sub> on the ligand to −CH<sub>2</sub>CH<sub>3</sub>, we obtained an example of <b>Dy</b><sub><b>11</b></sub> formed by epitaxial assembly of two Dy­(III) ions with an hourglass-shaped Dy<sub>9</sub> as the core, and its molecular formula is [Dy<sub>11</sub>(HL<sup>2</sup>)<sub>8</sub>(μ<sub>3</sub>–OH)<sub>8</sub>(μ<sub>4</sub>-O)<sub>2</sub>(CH<sub>3</sub>O)<sub>4</sub>(NO<sub>3</sub>)<sub>4</sub>]­(NO<sub>3</sub>)<sub>5</sub> 18CH<sub>3</sub>OH. The cluster <b>Dy</b><sub><b>11</b></sub> was bombarded using high-resolution electrospray ionization mass spectrometry (HRESI-MS) and the molecular ion peaks of various fragments formed were captured. Based on the above molecular ion peaks, the possible fragmentation mechanisms of <b>Dy</b><sub><b>11</b></sub> were inferred to be Dy<sub>11</sub> → Dy<sub>4</sub>(HL<sup>2</sup>)<sub>4</sub> → Dy<sub>3</sub>(HL<sup>2</sup>)<sub>2</sub> → Dy<sub>2</sub>(HL<sup>2</sup>)<sub>2</sub> → Dy­(HL<sup>2</sup>)<sub>2</sub> and Dy<sub>11</sub> → Dy­(HL<sup>2</sup>)<sub>2</sub>/Dy<sub>2</sub>(HL<sup>2</sup>)<sub>2</sub>/Dy<sub>3</sub>(HL<sup>2</sup>)<sub>2</sub>/Dy<sub>4</sub>(HL<sup>2</sup>)<sub>4</sub>. This work is one of the rare examples where fine-tuning of ligand substituents leads to the formation of complexes of different dimensions, which promotes the progress of crystal engineering of lanthanide complexes.

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