The complex dielectric permittivity of a series of spin crossover complexes, with variable ligand stoichiometry [Fe(Htrz) (trz) (NHtrz) ](BF) ·nHO, has been investigated as a function of temperature in a wide frequency range. In each compound, a substantial drop of the conductivity and permittivity is evidenced when going from the low spin to the high spin state, albeit with decreasing amplitude for increasing ligand substitution (i.e. for increasing x). The deconvolution of the dielectric spectra using the Havriliak-Negami equation allowed to extract the dipole and conductivity relaxation times, their distributions as well as the dielectric strengths in both spin states. Remarkably, no clear correlation appears between the conductivity changes and the lattice properties (Debye temperature) in the dilution series. We rationalize these results by considering the dimensionality of the system (1D), wherein the charge transport occurs most likely by hopping along the [Fe(Rtrz)] chains.
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http://dx.doi.org/10.1088/1361-648X/ab7ba2 | DOI Listing |
Angew 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.
View Article and Find Full Text PDFMini Rev Med Chem
January 2025
Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, Johor Bahru 81310, Johor, Malaysia.
Indole, a ubiquitous structural motif in bioactive compounds, has played a pivotal role in drug discovery. Among indole derivatives, indole-3-carboxaldehyde (I3A) has emerged as a particularly promising scaffold for the development of therapeutic agents. This review delves into the recent advancements in the chemical modification of I3A and its derivatives, highlighting their potential applications in various therapeutic areas.
View Article and Find Full Text PDFAnticancer Agents Med Chem
January 2025
Department of Chemistry, Andhra University, Vishakapatnam, Andra Pradesh, India.
Background: Cancer presents a significant global health challenge, necessitating effective treatment strategies. While chemotherapy is widely employed, its non-specific nature can induce adverse effects on normal cells, prompting the exploration of targeted therapies. The 1,2,4-triazole scaffold has emerged as a promising element in anticancer drug development due to its structural diversity and potential to target cancer cells.
View Article and Find Full Text PDFChemistry
January 2025
University of Regensburg, Inorganic Chemistry, Universitätsstrasse 31, D-93040, Regensburg, GERMANY.
The systematic nucleophilic functionalization of the cationic pentaphosphole ligand complex [Cp*Fe(η4-P5Me)][OTf] (A) with group 16/17 nucleophiles is reported. This method represents a highly reliable and versatile strategy for the design of novel transition-metal complexes featuring twofold substituted end-deck cyclo-P5 ligands, bearing unprecedented hetero-element substituents. By the reaction of A with classical group 16 nucleophiles, complexes of the type [Cp*Fe(η4-P5MeE)] (E = OEt (1), OtBu (2), SPh (3), SePh (4)) are obtained.
View Article and Find Full Text PDFDalton Trans
January 2025
Department of Chemistry, Babeş-Bolyai University, Str. Arany Janos Nr. 11, RO-400028 Cluj-Napoca, Romania.
The synthesis and characterization of novel platinum(II) and platinum(IV) complexes derived from unsymmetrical ethylene or propylenediamine derivatives are presented. IR spectroscopy and ESI mass spectrometry techniques were employed to characterize the complexes, revealing distinctive absorption bands and isotope patterns. Furthermore, the complexes were characterized by H and C NMR spectroscopy.
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