Spin crossover (SCO) iron (II) 1,2,4-triazole-based coordination compounds in the form of composite SCO@SiO nanoparticles were prepared using a reverse microemulsion technique. The thickness of the silica shell and the morphology of the as obtained core@shell nanoparticles were studied by modifying the polar phase/surfactant ratio (ω), as well as the quantity and the insertion phase (organic, aqueous and micellar phases) of the tetraethylorthosilicate (TEOS) precursor, the quantity of ammonia and the reaction temperature. The morphology of the nanoparticles was monitored by transmission electron microscopy (TEM/HRTEM) while their composition probed by combined elemental analyses, thermogravimetry and EDX analyses. We report that not only the particle size can be controlled but also the size of the silica shell, allowing for interesting perspectives in post-synthetic modification of the shell. The evolution of the spin crossover properties associated with the change in morphology was investigated by variable temperature optical and magnetic measurements.
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http://dx.doi.org/10.3390/nano11123169 | DOI Listing |
Symmetry-breaking spin-state transitions in two of three isostructural salts of MnIII spin-crossover cations, [MnIII(3-OMe-5-NO2-sal2323)]+, with heavy anions are reported. The ReO4- salt undergoes two-step spin crossover which is coupled with a re-entrant symmetry-breaking structural phase transition between a high temperature phase (S = 2, C2/c), an intermediate ordered phase (S = 1/S = 2, P21/c), and a low temperature phase (S = 1, C2/c). The AsF6- complex undergoes an abrupt transition between a high temperature phase (S = 2, C2/c) and a low temperature ordered phase (S = 1/S = 2, P-1).
View Article and Find Full Text PDFDalton Trans
January 2025
State Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, School of Chemical Engineering, Dalian University of Technology, No. 2 Linggong Road, Dalian 116024, P. R. China.
Molecular materials that exhibit synergistic coupling between luminescence and spin-crossover (SCO) behaviors hold significant promise for applications in molecular sensors and memory devices. However, the rational design and underlying coupling mechanisms remain substantial challenges in this field. In this study, we utilized a luminescent complementary ligand pair as an intramolecular luminophore to construct a new Fe-based SCO complex, namely [FeLL](BF)·HO (1-Fe, L is a 2,2':6',2''-terpyridine (TPY) derivative ligand and L is 2,6-di-1-pyrazol-1-yl-4-pyridinecarboxylic acid), and two isomorphic analogs (2-Co, [CoLL](BF)·HO and 3-Zn, [ZnLL](BF)·HO).
View Article and Find Full Text PDFInorg Chem
January 2025
Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 10617, Taiwan.
Transition metal carbonyl and transition metal dinitrogen are fundamental chemical complexes in many important biological and catalytic processes. Interestingly, binding between a transition metal (TM) atom and carbonyl or dinitrogen results in spin state change. However, no study has evaluated the spin-orbit (SO) effect along the association pathway of any TM-CO or TM-N bond.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Key Laboratory of Cluster Science of Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, People's Republic of China.
The integration of spin crossover (SCO) magnetic switching and electric polarization properties can engender intriguing correlated magnetic and electric phenomena. However, achieving substantial SCO-induced polarization change through rational molecular design remains a formidable challenge. Herein, we present a polar Fe(II) compound that exhibits substantial polarization change in response to a thermally regulated low-spin ↔ high-spin transition.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
IISER Kolkata: Indian Institute of Science Education and Research Kolkata, Department of Chemical Sciences, Mohanpur, 741246, Nadia, INDIA.
Chiral allyl amines are important structural components in natural products, pharmaceuticals, and chiral catalysts. Herein, we report a cobalt-catalyzed enantioselective reductive coupling of imines with internal alkynes to synthesize chiral allyl amines. The reaction is catalyzed by a cobalt complex derived from commercially available bisphosphine ligand utilizing zinc as the electron donor.
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