Coherences of Photoinduced Electron Spin Qubit Pair States in Photosystem I.

This publication presents the first comprehensive experimental study of electron spin coherences in photosynthetic reaction center proteins, specifically focusing on photosystem I (PSI). The ultrafast electron transfer in PSI generates spin-correlated radical pairs (SCRPs), which are entangled spin pairs formed in well-defined spin states (Bell states). Since their discovery in our group in the 1980s, SCRPs have been extensively used to enhance our understanding of structure-function relationships in photosynthetic proteins. More recently, SCRPs have been utilized as tools for quantum sensing. Electron spin decoherence poses a significant challenge in realizing practical applications of electron spin qubits, particularly the creation of quantum entanglement between multiple electron spins. This work is focused on the systematic characterization of decoherence in SCRPs of PSI. These decoherence times were measured as electron spin echo decay times, termed phase memory times (TM), at various temperatures. Decoherence was recorded on both transient SCRP states P700+A1- and thermalized states. Our study reveals that TM exhibits minimal dependence on the biological species, biochemical treatment, and paramagnetic species. The analysis indicates that nuclear spin diffusion and instantaneous diffusion mechanisms alone cannot explain the observed decoherence. As a plausible explanation we discuss the assumption that the low-temperature dynamics of methyl groups in the protein surrounding the unpaired electron spin centers is the main factor governing the loss of the spin coherence in PSI.

Host-Guest Chemistry in Discrete Polyoxo-12-Palladate(II) Cubes [MO8Pd12L8]n- (M = ScIII, CoII, CuII, L = AsO43 -; M = CdII, HgII, L = PhAsO32-): Structure, Magnetism, and Catalytic Hydrogenation.

A family of five host-guest assemblies comprising different metal ions inside a cuboid 12-palladium-oxo cage, [MO8Pd12L8]n- (MPd12L8, M = ScIII, CoII, CuII, L = AsO43-; M = CdII, HgII, L = PhAsO32-), was synthesized and structurally characterized in the solid state by single-crystal X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and thermogravimetric analysis, and their solution and gas-phase stability were validated by multinuclear NMR spectroscopy and electrospray-ionization mass spectrometry (ESI-MS). The polyoxopalladates (POPs) ScPd12As8, CoPd12As8, and CuPd12As8 represent the first three examples of the MPd12As8 archetype. The unique cubic ligand field of {MO8} allows for collecting the speciation profiles of the POPs in solution using 45Sc and 113Cd NMR techniques. Detailed magnetic and electron paramagnetic resonance (EPR) studies were performed on CuPd12As8. Catalytic studies on MPd12As8 (M = CuII and CoII) supported on SBA-15 unveiled a guest metal-dependent structure-function relationship, with CuPd12As8 being the more efficient precatalyst for the hydroconversion of o-xylene in a fixed-bed reactor.

Arsenic(III)-Capped 12-Tungsto-2-Arsenates(III) [M2(AsIIIW6O25)2(AsIIIOH)x]n- (M = CrIII, FeIII, ScIII, InIII, TiIV, MnII) and Their Magnetic Properties.

Six arsenic(III)-capped 12-tungsto-2-arsenates(III) of the type [M2(AsIIIW6O25)2(AsIIIOH)x]n- (M = CrIII, 1; FeIII, 2; ScIII, 3; InIII, 4; TiIV, 5; MnII, 6) have been synthesized in aqueous medium by direct reaction of the elements using a one-pot strategy and structurally characterized by FT-IR spectroscopy, single-crystal XRD, and elemental analysis. Polyanions 1-6 are comprised of two octahedrally coordinated guest metal ions M sandwiched between two {AsW6} units, resulting in a structure with C2h point-group symmetry. Polyanions 1-5 contain tri- and tetravalent metal ion guests M (M = CrIII, FeIII, ScIII, InIII, and TiIV, respectively), and they have one {AsIIIOH} group grafted on each {AsW6} unit, whereas the divalent MnII-containing derivative 6 has two such {AsIIIOH} groups grafted on each {AsW6} unit. Magnetic studies on polyanions 3-5 over the temperature range 1.8-295 K and magnetic fields of 0-7 T confirmed that they are diamagnetic. On the other hand, polyanions 1, 2, and 6 are strongly magnetic and follow the Curie-Weiss law above 30 K. The susceptibility plots of 1 and 6 exhibit broad peaks suggesting short-range antiferromagnetic ordering, while the very weak antiferromagnetic ordering of 2 is overshadowed by traces of a paramagnetic impurity. The magnetization data of 1, 2, and 6 at 1.8 K over 0-7 T were analyzed by using the Heisenberg exchange procedure. Small (negative) values of the obtained J values help in understanding the absence of long-range antiferromagnetic ordering.

Synthesis, structure, electrochemistry and magnetism of cobalt-, nickel- and zinc-containing [M4(OH)3(H2O)2(α-SiW10O36.5)2]13- (M = Co2+, Ni2+, and Zn2+).

Interaction of the trilacunary 9-tungstosilicate [A-α-SiW9O34]10- with cobalt(ii), nickel(ii) and zinc(ii) ions in pH 9 aqueous medium at room temperature led to the formation of the respective M4-containing heteropolytungstates [M4(OH)3(H2O)2(α-SiW10O36.5)2]13- (M = Co2+ (1), Ni2+ (2), and Zn2+ (3)). Polyanions 1-3 were characterized in the solid state by single-crystal XRD, FT-IR spectroscopy, and thermogravimetric and elemental analyses. Electrochemical studies showed that the Co2+ ions in 1 can be oxidized to Co3+ and the CVs of the WVI centers of the polyanions feature well-defined and chemically reversible reduction waves. Magnetic measurements on 1 and 2 showed paramagnetism with complex ferromagnetic and antiferromagnetic interactions. A model was presented for extracting the exchange constants for the magnetic exchange interaction.

FeIII 48 -Containing 96-Tungsto-16-Phosphate: Synthesis, Structure, Magnetism and Electrochemistry.

The 48-FeIII -containing 96-tungsto-16-phosphate, [FeIII 48 (OH)76 (H2 O)16 (HP2 W12 O48 )8 ]36- (Fe48 ), has been synthesized and structurally characterized. This polyanion comprises eight equivalent {FeIII 6 P2 W12 } units that are linked in an end-on fashion forming a macrocyclic assembly that contains more iron centers than any other polyoxometalate (POM) known to date. The novel Fe48 was synthesized by a simple one-pot reaction of an {Fe22 } coordination complex with the hexalacunary {P2 W12 } POM precursor in water. The title polyanion was characterized by single-crystal XRD, FTIR, TGA, magnetic and electrochemical studies.

Tetra-MnIII-Containing 30-Tungsto-4-phosphate, [MnIII4(H2O)2(P2W15O56)2]12-: Synthesis, Structure, XPS, Magnetism, and Electrochemical Study.

Reaction of the mixed-valent Mn12-acetato complex [MnIII8MnIV4O12(CH3COO)16(H2O)4] with the trilacunary Wells-Dawson-type heteropolytungstate [P2W15O56]12- in acidic acetate solution (pH 1.1) resulted in the tetra-MnIII-containing polyanion [MnIII4(H2O)2(P2W15O56)2]12- (1). Single-crystal XRD on Na12[MnIII4(H2O)2(P2W15O56)2]·84H2O (1a) revealed that four MnIII ions form a rhombic Mn4O16 core encapsulated by two [P2W15O56]12- units. X-ray photoelectron spectroscopy (XPS) data confirm the +3 oxidation state of the four manganese ions in 1. Magnetic measurements from 1.8-300 K in a 100 Oe magnetic field allowed for the extraction of full fitting parameters from the susceptibility data for 1. The negative Ja value (Ja = -2.16 ± 0.08 K, Jb = 3.24 ± 1.73 K, g = 2.35 ± 0.040, and ρ = 0.34 ± 0.03) suggests a dominant antiferromagnetic spin exchange interaction between the four MnIII ions, with the positive Jb being an accompanying result of Ja. Electrochemical studies revealed a reversible MnIV/MnIII redox couple in 1 at the +0.80 to +1.1 V potential region with E1/2 = +0.907 V.

15-Copper(ii)-containing 36-tungsto-4-silicates(iv) [Cu15O2(OH)10X(A-α-SiW9O34)4]25- (X = Cl, Br): synthesis, structure, magnetic properties, and electrocatalytic CO2 reduction.

The 15-copper(ii)-containing 36-tungsto-4-silicates [Cu15O2(OH)10X(A-α-SiW9O34)4]25- (X = Cl, 1; Br, 2) have been prepared in 70% yield by reaction of the trilacunary 9-tungstosilicate precursor [A-α-SiW9O34]10- with Cu2+ ions in aqueous pH 8 medium. Both polyanions 1 and 2 were isolated as hydrated mixed potassium/sodium salts and characterized in the solid state by FT-IR, TGA, single-crystal XRD, and elemental analysis. DC magnetic susceptibility measurements from 1.8-300 K established the ground state to be paramagnetic with a magnetic moment corresponding to 15 uncoupled Cu2+ (S = 1/2) ions. EPR measurements and simulations were consistent with this analysis. Electrochemical studies were performed for polyanions 1 and 2 dissolved in solution to elucidate the electroactivity of both copper and tungstate sites. Using 2 as a representative example, the electrocatalytic activity towards CO2 reduction upon deposition on a glassy carbon electrode surface, while retaining selectivity relative to hydrogen evolution, was demonstrated.

Enhancing the Magnetic Anisotropy of Linear Cr(II) Chain Compounds Using Heavy Metal Substitutions.

Magnetic properties of the series of three linear, trimetallic chain compounds Cr2Cr(dpa)4Cl2, 1, Mo2Cr(dpa)4Cl2, 2, and W2Cr(dpa)4Cl2, 3 (dpa = 2,2'-dipyridylamido), have been studied using variable-temperature dc and ac magnetometry and high-frequency EPR spectroscopy. All three compounds possess an S = 2 electronic ground state arising from the terminal Cr(2+) ion, which exhibits slow magnetic relaxation under an applied magnetic field, as evidenced by ac magnetic susceptibility and magnetization measurements. The slow relaxation stems from the existence of an easy-axis magnetic anisotropy, which is bolstered by the axial symmetry of the compounds and has been quantified through rigorous high-frequency EPR measurements. The magnitude of D in these compounds increases when heavier ions are substituted into the trimetallic chain; thus D = -1.640, -2.187, and -3.617 cm(-1) for Cr2Cr(dpa)4Cl2, Mo2Cr(dpa)4Cl2, and W2Cr(dpa)4Cl2, respectively. Additionally, the D value measured for W2Cr(dpa)4Cl2 is the largest yet reported for a high-spin Cr(2+) system. While earlier studies have demonstrated that ligands containing heavy atoms can enhance magnetic anisotropy, this is the first report of this phenomenon using heavy metal atoms as "ligands".

Cr(i)Cl as well as Cr+ are stabilised between two cyclic alkyl amino carbenes.

Cr(i)Cl is a very unstable species. The present work describes the stabilisation of Cr(i)Cl in the low coordinate environment of cyclic alkyl(amino) carbene ligands and its synthetic application to yield an unprecedented cationic complex with a two coordinate Cr(i). One electron reduction of (cAAC)2CrCl2 (1) with equivalent amount of KC8 results in the formation of (cAAC)2CrCl (2), with a distorted trigonal planar configuration at the metal centre. SQUID, EPR and theoretical studies reveal a Cr(i) centre with S = 5/2 spin ground state for 2. It represents the first example of a mononuclear Cr complex showing slow relaxation of magnetisation under an applied magnetic field. The chlorine atom in 2 is expected to be prone to further reactions with appropriate reagents. This qualifies 2 as a promising precursor for the preparation of various interesting complexes with Cr(i) in a low coordinate environment. The first example of this metathesis reaction is observed when 2 is treated with Na[B(C6H3(CF3)2)4] resulting in [(cAAC)2Cr]+[B(C6H3(CF3)2)4]-, a linear cationic complex with two coordinate Cr(i) and an S = 5/2 spin ground state.