Thermal and Light-Induced Spin Transitions in 3D Hofmann-type Frameworks Built on Nonlinear 3-Substituted Pyridine and Pyrimidine Pillaring Ligands

Integration of spin crossover (SCO) properties in 3D frameworks made up of cyano-bimetallic layers connected through pillaring organic ligands, the so-called Hofmann-type coordination polymers (HCPs)- represents an important source of multifunctional advanced materials. Typically, these 3D structures are constituted by 4-substituted pyridine-based linear pillars which afford HCPs with regular <b>pcu</b> topology. Here, we have investigated the suitability of the 3-substituted pyridine and pyrimidine bis-monodentate ligands 2,5-di(pyridin-3-yl)aniline (3-dpyan) and 2,5-di(pyrimidin-5-yl)aniline (bpmdan) as alternative building blocks to explore new structural topologies and functionalities. In this context, we have prepared the compounds Fe(3-dpyan)[Ag(CN)<sub>2</sub>]<sub>2</sub>·2MeOH (<b>1</b><sup><b>Ag</b></sup><b>·2MeOH</b>), Fe(3-dpyan)[Ag(CN)<sub>2</sub>]<sub>2</sub>···0.35NO<sub>2</sub>Bz·MeOH (<b>1</b><sup><b>Ag</b></sup><b>·0.35NO</b><sub><b>2</b></sub><b>Bz·MeOH</b>), Fe(3-dpyan)[Au(CN)<sub>2</sub>]<sub>2</sub>·NO<sub>2</sub>Bz (<b>1</b><sup><b>Au</b></sup><b>·NO</b><sub><b>2</b></sub><b>Bz</b>), and Fe(bpmdan)[Ag(CN)<sub>2</sub>]<sub>2</sub>·CH<sub>3</sub>Bz (<b>2</b><sup><b>Ag</b></sup><b>·CH</b><sub><b>3</b></sub><b>Bz</b>) (MeOH = methanol, NO<sub>2</sub>Bz = nitrobenzene, CH<sub>3</sub>Bz = toluene). Our structural studies have revealed that <b>1</b><sup><b>Ag</b></sup><b>·2MeOH</b> and <b>1</b><sup><b>Ag</b></sup><b>·0.35NO</b><sub><b>2</b></sub><b>Bz·MeOH</b> exhibit isomorphous doubly interpenetrated 3D structures strongly differing from the unusual noninterpenetrated ones exhibited by <b>1</b><sup><b>Au</b></sup><b>·NO</b><sub><b>2</b></sub><b>Bz</b> and <b>2</b><sup><b>Ag</b></sup><b>·CH</b><sub><b>3</b></sub><b>Bz</b>. Temperature-dependent magnetic susceptibility measurements have shown that all the reported compounds exhibit thermal-induced SCO properties, and moreover, three of them display Light Induced Excited Spin State Trapping at low temperatures (LIESST effect). The studied compounds show a wide diversity of SCO behaviors, ranging from abrupt complete one-step SCO centered at 253 K (<b>1</b><sup><b>Au</b></sup><b>·NO</b><sub><b>2</b></sub><b>Bz</b>) to gradual and incomplete multistepped SCO centered at 120 K (<b>1</b><sup><b>Ag</b></sup><b>·0.35NO</b><sub><b>2</b></sub><b>Bz·MeOH</b>). This assorted SCO properties are discussed and correlated to the acquired chemical and structural information.

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Journal
Inorganic Chemistry
Published
2024-09-05
DOI
https://doi.org/10.1021/acs.inorgchem.4c03261
Citations
5
Primary Topic
Magnetism in coordination complexes
Type
article
Field-Weighted Citation Impact
0.59

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article

Thermal and Light-Induced Spin Transitions in 3D Hofmann-type Frameworks Built on Nonlinear 3-Substituted Pyridine and Pyrimidine Pillaring Ligands

Alejandro Orellana‐Silla, Rubén Turo‐Cortés, Manuel Meneses-Sánchez, José Antonio Real et al.
5 citations
Inorganic Chemistry
Magnetism in coordination complexes
0.59
article

Thermal and Light-Induced Spin Transitions in 3D Hofmann-type Frameworks Built on Nonlinear 3-Substituted Pyridine and Pyrimidine Pillaring Ligands

Alejandro Orellana‐Silla, Rubén Turo‐Cortés, Manuel Meneses-Sánchez, José Antonio Real, M. Carmen Muñoz, Carlos Bartual‐Murgui
article en
5 citations

Abstract

Integration of spin crossover (SCO) properties in 3D frameworks made up of cyano-bimetallic layers connected through pillaring organic ligands, the so-called Hofmann-type coordination polymers (HCPs)- represents an important source of multifunctional advanced materials. Typically, these 3D structures are constituted by 4-substituted pyridine-based linear pillars which afford HCPs with regular <b>pcu</b> topology. Here, we have investigated the suitability of the 3-substituted pyridine and pyrimidine bis-monodentate ligands 2,5-di(pyridin-3-yl)aniline (3-dpyan) and 2,5-di(pyrimidin-5-yl)aniline (bpmdan) as alternative building blocks to explore new structural topologies and functionalities. In this context, we have prepared the compounds Fe(3-dpyan)[Ag(CN)<sub>2</sub>]<sub>2</sub>·2MeOH (<b>1</b><sup><b>Ag</b></sup><b>·2MeOH</b>), Fe(3-dpyan)[Ag(CN)<sub>2</sub>]<sub>2</sub>···0.35NO<sub>2</sub>Bz·MeOH (<b>1</b><sup><b>Ag</b></sup><b>·0.35NO</b><sub><b>2</b></sub><b>Bz·MeOH</b>), Fe(3-dpyan)[Au(CN)<sub>2</sub>]<sub>2</sub>·NO<sub>2</sub>Bz (<b>1</b><sup><b>Au</b></sup><b>·NO</b><sub><b>2</b></sub><b>Bz</b>), and Fe(bpmdan)[Ag(CN)<sub>2</sub>]<sub>2</sub>·CH<sub>3</sub>Bz (<b>2</b><sup><b>Ag</b></sup><b>·CH</b><sub><b>3</b></sub><b>Bz</b>) (MeOH = methanol, NO<sub>2</sub>Bz = nitrobenzene, CH<sub>3</sub>Bz = toluene). Our structural studies have revealed that <b>1</b><sup><b>Ag</b></sup><b>·2MeOH</b> and <b>1</b><sup><b>Ag</b></sup><b>·0.35NO</b><sub><b>2</b></sub><b>Bz·MeOH</b> exhibit isomorphous doubly interpenetrated 3D structures strongly differing from the unusual noninterpenetrated ones exhibited by <b>1</b><sup><b>Au</b></sup><b>·NO</b><sub><b>2</b></sub><b>Bz</b> and <b>2</b><sup><b>Ag</b></sup><b>·CH</b><sub><b>3</b></sub><b>Bz</b>. Temperature-dependent magnetic susceptibility measurements have shown that all the reported compounds exhibit thermal-induced SCO properties, and moreover, three of them display Light Induced Excited Spin State Trapping at low temperatures (LIESST effect). The studied compounds show a wide diversity of SCO behaviors, ranging from abrupt complete one-step SCO centered at 253 K (<b>1</b><sup><b>Au</b></sup><b>·NO</b><sub><b>2</b></sub><b>Bz</b>) to gradual and incomplete multistepped SCO centered at 120 K (<b>1</b><sup><b>Ag</b></sup><b>·0.35NO</b><sub><b>2</b></sub><b>Bz·MeOH</b>). This assorted SCO properties are discussed and correlated to the acquired chemical and structural information.

Inorganic ChemistryVol. 63(37)
Universitat de València (ES), Parc Científic de la Universitat de València (ES), Universitat Politècnica de València (ES)
Ministerio de Ciencia, Innovación y Universidades, Agencia Estatal de Investigación
Openalex Percentile: Top 40%
Magnetism in coordination complexes
0.59
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