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... to a longer distance than standard becausenickel of the scattering phase the material. Figure 4b displays the XANES spectra of CoO, Co3O4, and Cry-Co. The cobalt atoms in Extended X-ray absorption fine structure (EXAFS) spectroscopy [22] is one of the most powerful Cry-Co have similar features to Co ...
... to a longer distance than standard becausenickel of the scattering phase the material. Figure 4b displays the XANES spectra of CoO, Co3O4, and Cry-Co. The cobalt atoms in Extended X-ray absorption fine structure (EXAFS) spectroscopy [22] is one of the most powerful Cry-Co have similar features to Co ...
DNA-Mediated Photoelectron Transfer Reactions
... These results open the exciting possibility of investigating diffusion to ruthenium ratio and are curved downward and reach a plateau at higher quencher concentration; (ii) the quenching slopes for Ia as donor and various Co(II1) complexes as quenchers in the (12) The native DNA was sonicated and th ...
... These results open the exciting possibility of investigating diffusion to ruthenium ratio and are curved downward and reach a plateau at higher quencher concentration; (ii) the quenching slopes for Ia as donor and various Co(II1) complexes as quenchers in the (12) The native DNA was sonicated and th ...
Molecular Structures of M2(CO)9 and M3(CO)12
... the formal electron counting does not change (two electrons per CO) despite the presence of pairwise equivalent metalcarbon σ bonds. In agreement with the lower CO stretching frequencies, the electron density received by the bridging ligand in only one π* level is greater than that received in two o ...
... the formal electron counting does not change (two electrons per CO) despite the presence of pairwise equivalent metalcarbon σ bonds. In agreement with the lower CO stretching frequencies, the electron density received by the bridging ligand in only one π* level is greater than that received in two o ...
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... The precise nature of the complex between the zirconium and the propylene is complicated. This compexation stabilizes the zirconium but not for long. When this complex forms, it rearrange itself into a new form. The electrons in the zirconium-methyl carbon bond shift to form a bond between the meth ...
... The precise nature of the complex between the zirconium and the propylene is complicated. This compexation stabilizes the zirconium but not for long. When this complex forms, it rearrange itself into a new form. The electrons in the zirconium-methyl carbon bond shift to form a bond between the meth ...
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... – type Brönsted acid-Lewis acid doping. In this case, the PANI base is first doped to saturation with HCl (a Brönsted acid). Such doping results in the protonation of the imine sites, which constitute 50% of nitrogen atoms in the polymer. Then, a Lewis acid complexation is carried out on the remaini ...
... – type Brönsted acid-Lewis acid doping. In this case, the PANI base is first doped to saturation with HCl (a Brönsted acid). Such doping results in the protonation of the imine sites, which constitute 50% of nitrogen atoms in the polymer. Then, a Lewis acid complexation is carried out on the remaini ...
Nanostructured Transition Metal Chalcogenides as - KIT
... materials.[2] In the 70s some researcher realized that layered phases like TiS2 and MoS2 were also candidates as positive electrode materials for rechargeable lithium batteries.[3,4] Whittingham was the first to demonstrate fast, reversible Li insertion into TiS2 over the solidsolution range 0 ≤ x ≤ ...
... materials.[2] In the 70s some researcher realized that layered phases like TiS2 and MoS2 were also candidates as positive electrode materials for rechargeable lithium batteries.[3,4] Whittingham was the first to demonstrate fast, reversible Li insertion into TiS2 over the solidsolution range 0 ≤ x ≤ ...
Post-Transition Metals
... - 10 least in some of the heavy post-transition metals, there is a large sp gap meaning, that for certain combinations of metal and ligand, the p-orbitals may be a little high in energy to get involved in covalent bonding, given that the heavier post-transition elements from rather weak M-X bonds. ...
... - 10 least in some of the heavy post-transition metals, there is a large sp gap meaning, that for certain combinations of metal and ligand, the p-orbitals may be a little high in energy to get involved in covalent bonding, given that the heavier post-transition elements from rather weak M-X bonds. ...
Oxidative Additions of Aryl Halides to Palladium Proceed through
... there is no direct experimental evidence to support the calculations. Kinetic studies suggest the identity of the halide is critical, with iodo- and bromobenzenes reacting with PdL2 and chlorobenzenes with PdL.[25] However, it is difficult if not impossible to unambiguously isolate the highly reacti ...
... there is no direct experimental evidence to support the calculations. Kinetic studies suggest the identity of the halide is critical, with iodo- and bromobenzenes reacting with PdL2 and chlorobenzenes with PdL.[25] However, it is difficult if not impossible to unambiguously isolate the highly reacti ...
University of Groningen Importance of interatomic hole screening in
... CI 共NOCI兲 method26 –28 has been used with a NiO6 cluster to study the 3s level XPS spectra.13,14 With this approach, optimized orbital representations for the CT configurations were obtained, improving the description of the final states. However, the interpretation of the character of the XPS peaks ...
... CI 共NOCI兲 method26 –28 has been used with a NiO6 cluster to study the 3s level XPS spectra.13,14 With this approach, optimized orbital representations for the CT configurations were obtained, improving the description of the final states. However, the interpretation of the character of the XPS peaks ...
Chapter 7 - Brian Tissue Home
... (a) KMnO4(s): Mn(VII) in a covalent oxyanion, MnO4−. (b) MnCl63−(aq): Mn(III), Cl has a −1 oxidation state, and the overall complex charge is −3. (c) Mn(H2O)62+(aq): Mn(II), water is neutral, and the overall charge of this ion is +2. (d) Mn(H2O)67+(aq): Mn(VII), this complex as written does not exis ...
... (a) KMnO4(s): Mn(VII) in a covalent oxyanion, MnO4−. (b) MnCl63−(aq): Mn(III), Cl has a −1 oxidation state, and the overall complex charge is −3. (c) Mn(H2O)62+(aq): Mn(II), water is neutral, and the overall charge of this ion is +2. (d) Mn(H2O)67+(aq): Mn(VII), this complex as written does not exis ...
Complexometric Titration of Zinc
... The criteria needed to allow a reaction to be used for titrimetric analysis are: 1. goes to completion, 2. is stoichiometric, 3. proceeds rapidly, and 4. allows for easy end-point detection. EDTA satisfies the first three of these very well, but an indicator must also be sought. Another complexing a ...
... The criteria needed to allow a reaction to be used for titrimetric analysis are: 1. goes to completion, 2. is stoichiometric, 3. proceeds rapidly, and 4. allows for easy end-point detection. EDTA satisfies the first three of these very well, but an indicator must also be sought. Another complexing a ...
Mono- and Trinuclear Nickel(II) Complexes with Sulfur-Containing Oxime Ligands:
... as NiDtoxH+ or NiDtoxClO4+ were not immediately apparent in the FABS mass spectra (Figure 2) of either the lilac or the purple-black nickel chelates of the dioxime ligand. The lilac complex, however, displays an intense peak at m/e ) 475, corresponding to 35ClO4--adduced [58Ni{(Dtox)(CH3CNH)2}]2+, t ...
... as NiDtoxH+ or NiDtoxClO4+ were not immediately apparent in the FABS mass spectra (Figure 2) of either the lilac or the purple-black nickel chelates of the dioxime ligand. The lilac complex, however, displays an intense peak at m/e ) 475, corresponding to 35ClO4--adduced [58Ni{(Dtox)(CH3CNH)2}]2+, t ...
surface structural model for ferrihydrite
... 0.50, leading to a magnitude for the whole magnetite prepeak of ~0.075 • 1.5 = 0.112, notably lower than the experimental one (0.141). The underestimation of the new prepeak intensity comes from a 2nd source of error, that is, the ratio of oscillator strengths between ViFe(I[I) and IVFe(I/I) species ...
... 0.50, leading to a magnitude for the whole magnetite prepeak of ~0.075 • 1.5 = 0.112, notably lower than the experimental one (0.141). The underestimation of the new prepeak intensity comes from a 2nd source of error, that is, the ratio of oscillator strengths between ViFe(I[I) and IVFe(I/I) species ...
Structural Evaluation and Solution Integrity of Alkali Metal Salt
... multifunctional hydroxamic acid (e.g., salicylhydroxamic acid) or oxime is used to stabilize the metallacrown ring. Incorporation of transition metals into the metallacrowns affords properties not found in the simple organic crowns, such as redox activity, strong absorption spectra, and paramagnetis ...
... multifunctional hydroxamic acid (e.g., salicylhydroxamic acid) or oxime is used to stabilize the metallacrown ring. Incorporation of transition metals into the metallacrowns affords properties not found in the simple organic crowns, such as redox activity, strong absorption spectra, and paramagnetis ...
Absorption of Flue-Gas Components by Ionic Liquids
... by absorption and desorption of SO2 up to 10 times in the dry gas without any significant changes in the absorption capacity as shown in our previous work (5). Based on a X-ray investigation of crystals obtained of the SO2 adduct [TMGH]ClSO2, we previously suggested strong interaction between Lewis ...
... by absorption and desorption of SO2 up to 10 times in the dry gas without any significant changes in the absorption capacity as shown in our previous work (5). Based on a X-ray investigation of crystals obtained of the SO2 adduct [TMGH]ClSO2, we previously suggested strong interaction between Lewis ...
1 - Max Planck Institut für Festkörperforschung
... substrate provides the possibility for ionic O‚‚‚H-C hydrogen bond interactions21 between neighboring TPA molecules. This ionic hydrogen bonding is facilitated by deprotonation of the TPA carboxylate groups. Core level spectra indicate that upon deposition at room temperature, the majority (>80%) of ...
... substrate provides the possibility for ionic O‚‚‚H-C hydrogen bond interactions21 between neighboring TPA molecules. This ionic hydrogen bonding is facilitated by deprotonation of the TPA carboxylate groups. Core level spectra indicate that upon deposition at room temperature, the majority (>80%) of ...
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).