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A main goal of molecular electronics is to relate the performance of devices to the structure and electronic state of molecules. Among the variety of possibilities that organic, organometallic and coordination chemistries offer to tune the energy levels of molecular components, spin crossover phenomenon is a perfect candidate for elaboration of molecular switches. The reorganization of the electronic state population of the molecules associated to the spin crossover can indeed lead to a significant change in conductivity. However, molecular spin crossover is very sensitive to the environment and can disappear once the molecules are integrated into devices. Here, we show that the association of ultra-small 1.2 nm platinum nanoparticles with Fe triazole-based spin crossover coordination polymers leads to self-assemblies, extremely well organized at the sub-3 nm scale. The quasi-perfect alignment of nanoparticles observed by transmission electron microscopy, in addition to specific signature in infrared spectroscopy, demonstrates the coordination of the long-chain molecules with the nanoparticles. Spin crossover is confirmed in such assemblies by X-ray absorption spectroscopic measurements and shows unambiguous characteristics both in magnetic and charge transport measurements. Coordinating polymers are therefore ideal candidates for the elaboration of robust, well-organized, hybrid self-assemblies with metallic nanoparticles, while maintaining sensitive functional properties, such as spin crossover.
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http://dx.doi.org/10.1039/d0nr02154g | DOI Listing |
J Phys Condens Matter
December 2024
Department of Physics and Astronomy, University of Nebraska-Lincoln, Jorgenesen Hall, 855 North 16th Street, Lincoln, Nebraska, 68588-0299, UNITED STATES.
Evidence of chirality was observed at the Fe metal center in Fe(III) spin crossover coordination salts [Fe(qsal)Ni(dmit)] and [Fe(qsal)(TCNQ)] from X-ray absorption spectroscopy at the Fe 2pcore threshold. Based on the circularly polarized X-ray absorption data, the X-ray natural circular dichroism seen [Fe(qsal)Ni(dmit)] and [Fe(qsal)(TCNQ)] is far stronger than seen for [Fe(qsal)Cl] suggesting this natural circular dichroism signature is a ligand effect rather than a result of just a loss of octahedral symmetry on the Fe core. The larger the chiral effects in the Fe 2p core to bound X-ray absorption, the greater the perturbation of the Fe 2pto 2pspin-orbit splitting seen in the X-ray absorption spectra.
View Article and Find Full Text PDFChemphyschem
December 2024
Laboratoire de Chimie Quantique, Universit� de Strasbourg, Department of Chemistry, 4 rue Blaise Pascal, 67000, Strasbourg, FRANCE.
Recent, theoretical studies have shown that placing a spin-crossover ion in a field of radical ligands can induce local superpositions of local spin states (see Ref.[1,2]). This phenomenon, termed spinmerism, raises questions about its stability when spin-orbit coupling is included.
View Article and Find Full Text PDFInorg Chem
December 2024
Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
Transition metal mechanophores exhibiting force-activated spin-crossover are attractive design targets, yet large-scale discovery of them has not been pursued due in large part to the time-consuming nature of trial-and-error experiments. Instead, we leverage density functional theory (DFT) and external force explicitly included (EFEI) modeling to study a set of 395 feasible Fe and Co mechanophore candidates with tridentate ligands that we curate from the Cambridge Structural Database. Among nitrogen-coordinating low-spin complexes, we observe the prevalence of spin crossover at moderate force, and we identify 155 Fe and Co spin-crossover mechanophores and derive their threshold force for low-spin to high-spin transition ().
View Article and Find Full Text PDFChemistry
December 2024
RWTH Aachen University: Rheinisch-Westfalische Technische Hochschule Aachen, Institute of Inorganic Chemistry, Landoltweg 1a, 52074, Aachen, GERMANY.
In this study, we present the first experimental determination of the spin state of transition metal complexes by using Hirshfeld Atom Refinement. For the demonstration, the two iron(II) complexes, (NH4)2Fe(SO4)2*6H2O and [Fe(pic)3]Cl2*EtOH were investigated. The method involves the refinement using wavefunctions of different spin multiplicity and comparison against experimental diffraction data by means of refinement indicators and residual electron density.
View Article and Find Full Text PDFPhys Chem Chem Phys
December 2024
Post Industry Technology Research and Development Center of the State Posts Bureau (Internet of Things Technology), Nanjing University of Posts and Telecommunications, Nanjing 210023, P.R. China.
This paper introduces a novel butterfly optimization algorithm, called the spiral search and dynamic crossover based butterfly optimization algorithm (SCBO), for parameter estimation in proton exchange membrane fuel cell (PEMFC) models. To enhance the global performance of the butterfly algorithm, a spin-search strategy is incorporated to expand its exploration range, while an adaptive factor is introduced to strike a balance between exploration and exploitation. Additionally, a dynamic crossover operation is integrated to enhance solution diversity, addressing the algorithm's tendency to converge to local optima.
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