
Influence of Substituents on the Energy and Nature of the Lowest
... Table 1 shows that fluorine atoms (complexes 1 and 2) are stronger electron-withdrawing substituents than trifluoromethyl groups (complexes 3 and 4). However, one must keep in mind that the fluorine substituents exert both inductive and mesomeric effects. In all complexes, the frontier MOs are local ...
... Table 1 shows that fluorine atoms (complexes 1 and 2) are stronger electron-withdrawing substituents than trifluoromethyl groups (complexes 3 and 4). However, one must keep in mind that the fluorine substituents exert both inductive and mesomeric effects. In all complexes, the frontier MOs are local ...
Amidine: Structure, Reactivity and Complexation Behaviour
... synthesized and characterized by various spectral techniques with thermal studies and forms tetrahedral geometry[46]. The manganese complex(figure 10) show intense absorption at >25000 cm-1 assigned to ligand centered transition while two weak transitions are observed at 22472 cm-1 & 21413 cm-1 may ...
... synthesized and characterized by various spectral techniques with thermal studies and forms tetrahedral geometry[46]. The manganese complex(figure 10) show intense absorption at >25000 cm-1 assigned to ligand centered transition while two weak transitions are observed at 22472 cm-1 & 21413 cm-1 may ...
STUDIES ON MERCURY(II), NICKEL(II) AND LEAD(II)
... decrease in coordinating tendency of ligand with higher state of aggregation17, 18. High stability constant values of the mercury(II) α-aminobutyric acid complexes indicate strong bonding between the mercury(II) cation and the α-aminobutyric acid anion. Whilst low stability constant values of lead(I ...
... decrease in coordinating tendency of ligand with higher state of aggregation17, 18. High stability constant values of the mercury(II) α-aminobutyric acid complexes indicate strong bonding between the mercury(II) cation and the α-aminobutyric acid anion. Whilst low stability constant values of lead(I ...
A Density Functional Theory and Quantum Theory of
... insignificant relativistic effects.36 DFT methods reproduce geometries quite well, and are reasonably good for vibrational frequencies and total energies.36 Among the ligands we are interested in are the amino-alcohols. They are used in the pharmaceutical industry38-40 and as chiral reagents in orga ...
... insignificant relativistic effects.36 DFT methods reproduce geometries quite well, and are reasonably good for vibrational frequencies and total energies.36 Among the ligands we are interested in are the amino-alcohols. They are used in the pharmaceutical industry38-40 and as chiral reagents in orga ...
SYNTHESIS, CHARACTERIZATION, ANTIMICROBIAL ACTIVITY AND CYTOTOXICITY STUDIES - METAL COMPLEXES
... nitrogen in the range of temperature upto (1000oC) is carried out. The correlations between the decomposition steps of the complex with the corresponding weight loss are discussed in terms of the proposed formula of the complex. The TGA curve obtained for Cu (II) -2-Mbtye (1:1) complex showed decomp ...
... nitrogen in the range of temperature upto (1000oC) is carried out. The correlations between the decomposition steps of the complex with the corresponding weight loss are discussed in terms of the proposed formula of the complex. The TGA curve obtained for Cu (II) -2-Mbtye (1:1) complex showed decomp ...
Characterization of Photo-Induced Charge Transfer
... The pump beam is generated by frequency-doubling to 400 nm (fwhm ≈ 11 nm, refer to Figure S3, Supporting Information) the rest of the split near-IR pulse energy in a 100 μm thick type-I β-BaB2O4 (BBO) crystal. A variable neutral density filter controls the pump beam power, which is focused to a spot ...
... The pump beam is generated by frequency-doubling to 400 nm (fwhm ≈ 11 nm, refer to Figure S3, Supporting Information) the rest of the split near-IR pulse energy in a 100 μm thick type-I β-BaB2O4 (BBO) crystal. A variable neutral density filter controls the pump beam power, which is focused to a spot ...
Solubility of alkali metals in non
... agent are introduced into the receiver under ultrasonic mixing. The resulting metal blue solution is filtered off through the glass frit to the NMR and ESR tubes for analysis and desired applications. Another technique is based on a K-Na alloy dissolution. A similar apparatus is used, however withou ...
... agent are introduced into the receiver under ultrasonic mixing. The resulting metal blue solution is filtered off through the glass frit to the NMR and ESR tubes for analysis and desired applications. Another technique is based on a K-Na alloy dissolution. A similar apparatus is used, however withou ...
Topic 14-Chemical Bonding-Structure
... bond (π) is formed by the sideways overlap of atomic orbitals, resulting in electron density above and below the plane of the nuclei of the bonding atoms. ...
... bond (π) is formed by the sideways overlap of atomic orbitals, resulting in electron density above and below the plane of the nuclei of the bonding atoms. ...
View/Open - Minerva Access
... trap.19 Typical ESI, CID and IMR conditions used are given in the Supporting Information. DFT calculations: Gaussian 09 20 was used to fully optimize all the structures reported in this paper at the B3LYP-D3BJ level of theory. The effective-core potential of Hay and Wadt with a double-ξ valence bas ...
... trap.19 Typical ESI, CID and IMR conditions used are given in the Supporting Information. DFT calculations: Gaussian 09 20 was used to fully optimize all the structures reported in this paper at the B3LYP-D3BJ level of theory. The effective-core potential of Hay and Wadt with a double-ξ valence bas ...
REEL IA - OSU Chemistry
... Generally the increase in splitting is due to an increase in the bonding interactions between the ligand and the metal. For example, you can see that going from fluorine (F–) to oxygen (H2O) to nitrogen (NH3, en, NO2–) the electronegativity of the anion bonding to the cation decreases. Because anion ...
... Generally the increase in splitting is due to an increase in the bonding interactions between the ligand and the metal. For example, you can see that going from fluorine (F–) to oxygen (H2O) to nitrogen (NH3, en, NO2–) the electronegativity of the anion bonding to the cation decreases. Because anion ...
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).