Reduction of terbium(III) double-decker phthalocyanine, TbPc (1), by sodium fluorenone ketyl in the presence of bis(triphenylphosphoranylidene)ammonium cations yields one-electron-reduced (PPN){Tb(Pc)}·2.5CHCl (2) containing the dianionic Pc macrocycles, whereas a stronger NaCpCo(CO) reductant in the presence of an excess of cryptand yields two-electron-reduced {Cryptand(Na)}{(Pc)Tb(Pc)} (3) containing the Pc radical trianionic macrocycle. Isolated pairs of the {Tb(Pc)} anions are formed in 2, whereas compound 3 has unique 3D packing of the macrocycles with weak π-orbitals overlapping in all three directions. This is the first example of the two-electron-reduced lanthanide double-decker containing Pc radical trianion studied in solid state. Compound 2 manifests single-ion magnet (SIM) behavior with a large effective spin-reversal energy barrier of U = 538 cm in comparison with previously studied (BuN){Tb(Pc)} ( U = 230 cm). Thus, changes in cation size and shape affect the molecular packing of {Tb(Pc)} and increase the spin-reversal energy barrier. At the same time, two-electron-reduced species 3 containing Tb and Pc show no signs of SIM such as hysteresis loop at 1.9 K, and no peaks are observed on the temperature dependencies of in-phase (χ') and out-of-phase (χ″) signals. In contrast to EPR silent 2, both compounds 1 and 3 manifest broad signals from paramagnetic Tb ions. Narrower signals attributed to Pc are of high intensity only in 3. In addition to the absorption bands of Pc in the UV and visible spectral range, compound 3 manifests the lowest energy absorption band in solid-state spectra even in the near IR range at 4700 cm (2130 nm), whereas such bands are not observed in the spectrum of 2. These data show that the reduction of the Pc macrocycles in the lanthanide double-deckers leads to the appearance of new very low-energy new transitions associated with Pc whose energy is the lowest among known reduced metal phthalocyanines.
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http://dx.doi.org/10.1021/acs.inorgchem.9b00131 | DOI Listing |
Molecules
October 2022
Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Leninsky pr., 31, Bldg. 4, 119071 Moscow, Russia.
Double- and triple-decker lanthanide phthalocyaninates exhibit unique physical-chemical properties, particularly single-molecule magnetism. Among other factors, the magnetic properties of these sandwiches depend on their conformational state, which is determined via the skew angle of the phthalocyanine ligands. Thus, in the present work we report the comprehensive conformational study of substituted terbium(III) and yttrium(III) trisphthalocyaninates in solution depending on the substituents at the periphery of molecules, redox-states and nature of solvents.
View Article and Find Full Text PDFSmall
January 2022
Frumkin Institute of Physical Chemistry and Electrochemistry of Russian Academy of Sciences, Leninsky pr. 31-4, Moscow, 119071, Russia.
Achievement of information storage at molecular level remains a pressing task in miniaturization of computing technology. One of the promising approaches for its practical realization is development of nanoscale molecular switching materials including redox-active systems. The present work demonstrates a concept of expansion of a number of available redox-states of self-assembled monolayers through supramolecular approach.
View Article and Find Full Text PDFDalton Trans
September 2021
Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, Akad. Lavrentieva ave 3, Novosibirsk 630090, Russia.
Two series of highly luminescent yttrium(iii), europium(iii) and terbium(iii) metal-organic frameworks containing diimine aromatic ligands and the dicarboxylate linker trans-1,4-cyclohexanedicarboxylate (chdc) which can be described by the general formulas [M(bpy)(chdc)], where M = Y (1), Eu (2), and Tb (3) and bpy = 2,2'-bipyridyl, and [M(phen)(chdc)], where M = Y (4), Eu (5), and Tb (6) and phen = 1,10-phenanthroline, were synthesized and characterized. All compounds are based on the same dinuclear {M(L)(OOCR)} building blocks and possess a similar topology of the 3D framework with narrow pores. The chelate aromatic ligands act as efficient light-harvesting antennas for subsequent energy transfer to the emitting metal center (M = Eu, Tb) or intraligand photoemission (M = Y).
View Article and Find Full Text PDFFree Radic Biol Med
May 2020
Department of Chemistry and Biochemistry, University of Delaware, Newark, DE, 19716, United States. Electronic address:
Cysteine sulfinic acid (Cys-SO) is a protein post-translational modification that is formed reversibly under oxidative conditions. A short, encodable peptide was developed whose metal binding and terbium luminescence are dependent on cysteine (Cys) oxidation to the sulfinic acid. The protein design is based on the modification of a key metal-binding aspartate (Asp) in a canonical EF-Hand motif (DKDADGWISPAEAK) to Cys.
View Article and Find Full Text PDFInorg Chem
April 2019
Institute of Problems of Chemical Physics RAS, Chernogolovka , Moscow Region , 142432 Russia.
Reduction of terbium(III) double-decker phthalocyanine, TbPc (1), by sodium fluorenone ketyl in the presence of bis(triphenylphosphoranylidene)ammonium cations yields one-electron-reduced (PPN){Tb(Pc)}·2.5CHCl (2) containing the dianionic Pc macrocycles, whereas a stronger NaCpCo(CO) reductant in the presence of an excess of cryptand yields two-electron-reduced {Cryptand(Na)}{(Pc)Tb(Pc)} (3) containing the Pc radical trianionic macrocycle. Isolated pairs of the {Tb(Pc)} anions are formed in 2, whereas compound 3 has unique 3D packing of the macrocycles with weak π-orbitals overlapping in all three directions.
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