
view - The Long Group - University of California, Berkeley
... clusters.11 The effective magnetic moment of 1.74 µB calculated from C indicates that one unpaired electron is delocalized over the cluster. The EPR spectra of a solution of 1 in acetonitrile were recorded over the temperature range 4–50 K. As the temperature is lowered, the intensity of an isotropic ...
... clusters.11 The effective magnetic moment of 1.74 µB calculated from C indicates that one unpaired electron is delocalized over the cluster. The EPR spectra of a solution of 1 in acetonitrile were recorded over the temperature range 4–50 K. As the temperature is lowered, the intensity of an isotropic ...
5276-10.pdf
... isolated as perchlorate salt\ ðRuIII"bpy#"L8#1ŁClO3[ Although dithiocarbonate "L0Ð6# and dithi! ophosphate "L7# ligands stabilize the ruthenium ion in the complexes 0Ð7 in bivalent Ru"II# state\ the cor! responding dithiocarbamate complex 8 stabilizes the trivalent Ru"III# state[ The chemically and ...
... isolated as perchlorate salt\ ðRuIII"bpy#"L8#1ŁClO3[ Although dithiocarbonate "L0Ð6# and dithi! ophosphate "L7# ligands stabilize the ruthenium ion in the complexes 0Ð7 in bivalent Ru"II# state\ the cor! responding dithiocarbamate complex 8 stabilizes the trivalent Ru"III# state[ The chemically and ...
The Bio-Organometallic Chemistry of Technetium and Rhenium
... most widely used element in diagnostic medicine, is so diverse. Compounds of technetium exist in oxidation states from -I to +VII consisting of ligands that are as simple as hydride (H-) to more complex multidentate chelates. The diversity of the chemistry of technetium is both a dilemma and an oppo ...
... most widely used element in diagnostic medicine, is so diverse. Compounds of technetium exist in oxidation states from -I to +VII consisting of ligands that are as simple as hydride (H-) to more complex multidentate chelates. The diversity of the chemistry of technetium is both a dilemma and an oppo ...
Magnetism of Metal Phthalocyanines, Juan
... D/kB = 53.2 K, with S = 1, in other words the ground state corresponds to Sz = 0 while the excited state is Sz = ±1. Therefore, the ground state is non-magnetic, and the observed paramagnetism corresponds to the thermal population of the excited doublet [27]. In the α-phase, on the other hand, the i ...
... D/kB = 53.2 K, with S = 1, in other words the ground state corresponds to Sz = 0 while the excited state is Sz = ±1. Therefore, the ground state is non-magnetic, and the observed paramagnetism corresponds to the thermal population of the excited doublet [27]. In the α-phase, on the other hand, the i ...
Controlling Aggregation of Copper(II)
... modes (e.g., copper(II)) are less predictable.13,14 In this case, the directing and templating effects of the ligands are weaker, and other variables, most notably the coordination or hydrogen bonding abilities of the solvent or counterion, can cause changes as significant as a different cluster nuc ...
... modes (e.g., copper(II)) are less predictable.13,14 In this case, the directing and templating effects of the ligands are weaker, and other variables, most notably the coordination or hydrogen bonding abilities of the solvent or counterion, can cause changes as significant as a different cluster nuc ...
Accurate Spin-State Energies for Iron Complexes
... one (TZP) or two (TZ2P) sets of polarization functions. Core electrons (1s for second period, 1s2s2p for third-fourth period) were not treated explicitly during the geometry optimizations (frozen core approximation46), as it was shown49 to have a negligible effect on the obtained geometries. An auxi ...
... one (TZP) or two (TZ2P) sets of polarization functions. Core electrons (1s for second period, 1s2s2p for third-fourth period) were not treated explicitly during the geometry optimizations (frozen core approximation46), as it was shown49 to have a negligible effect on the obtained geometries. An auxi ...
Understanding d0-Olefin Metathesis Catalysts: Which Metal, Which
... the square-based pyramidal metallacycle isomers (SP) have also been included in the study because these intermediates correspond to potential resting states (Figures S21-S23, Supporting Information). The coordination of ethene (I f II via TSI) requires a change of coordination from a tetrahedron to ...
... the square-based pyramidal metallacycle isomers (SP) have also been included in the study because these intermediates correspond to potential resting states (Figures S21-S23, Supporting Information). The coordination of ethene (I f II via TSI) requires a change of coordination from a tetrahedron to ...
Sedimentary brines in ore deposits and basement rocks
... In addition to Br-enrichment, they commonly show evidence for extensive fluid-rock interaction with elevated levels of Ca and transition metals relative to evaporated seawater. Brines formed in the sub-surface may be more saline, reflecting the higher temperature at which saltsaturation was attained ...
... In addition to Br-enrichment, they commonly show evidence for extensive fluid-rock interaction with elevated levels of Ca and transition metals relative to evaporated seawater. Brines formed in the sub-surface may be more saline, reflecting the higher temperature at which saltsaturation was attained ...
An introduction to the virtual issue on Coordination
... The past two decades have witnessed a veritable explosion of reports detailing the solid-state structures of coordination compounds consisting of conceptually infinite one-dimensional chains, two-dimensional nets and three-dimensional frameworks. The obvious common feature shared by these different ...
... The past two decades have witnessed a veritable explosion of reports detailing the solid-state structures of coordination compounds consisting of conceptually infinite one-dimensional chains, two-dimensional nets and three-dimensional frameworks. The obvious common feature shared by these different ...
XAS and DFT Investigation of Mononuclear Cobalt(III) Peroxo
... with changes in the macrocycle ring size.17 In a recent crystal structure of [(12-TMC)CoO2]þ (1), we have shown a side-on binding mode of the O2 moiety to the Co center (Scheme 1) and showed that 1 is electron paramagnetic resonance (EPR) silent. Resonance Raman (rR) data revealed an O-O stretching ...
... with changes in the macrocycle ring size.17 In a recent crystal structure of [(12-TMC)CoO2]þ (1), we have shown a side-on binding mode of the O2 moiety to the Co center (Scheme 1) and showed that 1 is electron paramagnetic resonance (EPR) silent. Resonance Raman (rR) data revealed an O-O stretching ...
Chapter 19 C-H Bond Activation with Neutral Platinum Methyl
... Shilov et al. first demonstrated Pt(II)-catalyzed oxidation of alkanes to alcohols and alkyl chlorides some 30 years ago with simple platinum salts(1). In spite of the limitations imposed by the Pt(IV) stoichiometric oxidant and poor catalyst lifetime due to Pt metal precipitation, this mild (120°C) ...
... Shilov et al. first demonstrated Pt(II)-catalyzed oxidation of alkanes to alcohols and alkyl chlorides some 30 years ago with simple platinum salts(1). In spite of the limitations imposed by the Pt(IV) stoichiometric oxidant and poor catalyst lifetime due to Pt metal precipitation, this mild (120°C) ...
Transition Metals and their reactions
... • Most transition metal colours are due to d-d electron transitions. The energy gap between the split d-orbitals corresponds to visible light (E=hf). • Some of the really strong colours are due to charge transfer (such as in MnO4-). ...
... • Most transition metal colours are due to d-d electron transitions. The energy gap between the split d-orbitals corresponds to visible light (E=hf). • Some of the really strong colours are due to charge transfer (such as in MnO4-). ...
Spin crossover

Spin Crossover (SCO), sometimes referred to as spin transition or spin equilibrium behavior, is a phenomenon that occurs in some metal complexes wherein the spin state of the complex changes due to external stimuli such as a variation of temperature, pressure, light irradiation or an influence of a magnetic field.With regard to a ligand field and ligand field theory, the change in spin state is a transition from a low spin (LS) ground state electron configuration to a high spin (HS) ground state electron configuration of the metal’s d atomic orbitals (AOs), or vice versa. The magnitude of the ligand field splitting along with the pairing energy of the complex determines whether it will have a LS or HS electron configuration. A LS state occurs because the ligand field splitting (Δ) is greater than the pairing energy of the complex (which is an unfavorable process).Figure 1 is a simplified illustration of the metal’s d orbital splitting in the presence of an octahedral ligand field. A large splitting between the t2g and eg AOs requires a substantial amount of energy for the electrons to overcome the energy gap (Δ) to comply with Hund’s Rule. Therefore, electrons will fill the lower energy t2g orbitals completely before populating the higher energy eg orbitals. Conversely, a HS state occurs with weaker ligand fields and smaller orbital splitting. In this case the energy required to populate the higher levels is substantially less than the pairing energy and the electrons fill the orbitals according to Hund’s Rule by populating the higher energy orbitals before pairing with electrons in the lower lying orbitals. An example of a metal ion that can exist in either a LS or HS state is Fe3+ in an octahedral ligand field. Depending on the ligands that are coordinated to this complex the Fe3+ can attain a LS or a HS state, as in Figure 1.Spin crossover refers to the transitions between high to low, or low to high, spin states. This phenomenon is commonly observed with some first row transition metal complexes with a d4 through d7 electron configuration in an octahedral ligand geometry. Spin transition curves are a common representation of SCO phenomenon with the most commonly observed types depicted in Figure 2 in which γHS (the high-spin molar fraction) is plotted vs. T. The figure shows a gradual spin transition (left), an abrupt transition with hysteresis (middle) and a two-step transition (right). For a transition to be considered gradual, it typically takes place over a large temperature range, even up to several hundred K, whereas for a transition to be considered abrupt, it should take place within 10 K or less.These curves indicate that a spin transition has occurred in a metal complex as temperature changed. The gradual transition curve is an indication that not all metal centers within the complex are undergoing the transition at the same temperature. The abrupt spin change with hysteresis indicates a strong cooperativity, or “communication”, between neighboring metal complexes. In the latter case, the material is bistable and can exist in the two different spin states with a different range of external stimuli (temperature in this case) for the two phenomena, namely LS → HS and HS → LS. The two-step transition is relatively rare but is observed, for example, with dinuclear SCO complexes for which the spin transition in one metal center renders the transition in the second metal center less favorable.There are several types of spin crossover that can occur in a complex; some of them are light induced excited state spin trapping (LIESST), ligand-driven light induced spin change (LD-LISC), and charge transfer induced spin transition (CTIST).