Homework 8 solution
... a. Consider the storage of video information (FM signal) on a video tape. Suppose that the maximum signal frequency to be recorded as a spatial magnetic pattern is 10 MHz. The heads helically scan the tape, and the relative velocity of the tape to head is about 10 m s-1. What is the minimum spatial ...
... a. Consider the storage of video information (FM signal) on a video tape. Suppose that the maximum signal frequency to be recorded as a spatial magnetic pattern is 10 MHz. The heads helically scan the tape, and the relative velocity of the tape to head is about 10 m s-1. What is the minimum spatial ...
Electronic spectroscopy • Lecture 5: π
... transferred through protein structure to the next deoxygenated haem group decreasing its activation energy for O2 attachment ...
... transferred through protein structure to the next deoxygenated haem group decreasing its activation energy for O2 attachment ...
Alfred Werner
... Found in compounds in which both cations and anions are complexes, complexes through the exchange of some ligands from the cationic part to the anionic part [Co(NH3)6] [Cr(C2O4)3] and [Co(C2O4)3] [Cr(NH3)6] [Zn (NH3)4] [CuCl4] and [ZnCl4] [Cu(NH3)4] ...
... Found in compounds in which both cations and anions are complexes, complexes through the exchange of some ligands from the cationic part to the anionic part [Co(NH3)6] [Cr(C2O4)3] and [Co(C2O4)3] [Cr(NH3)6] [Zn (NH3)4] [CuCl4] and [ZnCl4] [Cu(NH3)4] ...
streszczenie po angielsku
... semiconductor alloys of group III-V diluted by bismuth, which can be applied in optoelectronics devices operating in the near and mid infrared spectral region. Due to the above mentioned aim the dissertation was focused mainly on these three issues: i) influence of bismuth on electronic band structu ...
... semiconductor alloys of group III-V diluted by bismuth, which can be applied in optoelectronics devices operating in the near and mid infrared spectral region. Due to the above mentioned aim the dissertation was focused mainly on these three issues: i) influence of bismuth on electronic band structu ...
How binding oxygen triggers changes in haemoglobin
... The repulsive force between the ligand electrons and the electrons in d orbitals causes their energy to be raised, but it will be raised more for electrons in the orbitals which point directly at the ligands, the ...
... The repulsive force between the ligand electrons and the electrons in d orbitals causes their energy to be raised, but it will be raised more for electrons in the orbitals which point directly at the ligands, the ...
spin and electron density redistribution upon binding of non
... a seemingly simple property (a well isolated bond between two subsystems) but difficult to treat with sufficient accuracy by QC methods. The quality of the metal–ligand bond description depends critically on the electronic processes accompanying the bond formation which, in turn, rely on a proper descri ...
... a seemingly simple property (a well isolated bond between two subsystems) but difficult to treat with sufficient accuracy by QC methods. The quality of the metal–ligand bond description depends critically on the electronic processes accompanying the bond formation which, in turn, rely on a proper descri ...
(Phosphines) - Bite angles for bidentate ligands
... Phosphines :PR3 - very important ligands - -donors - p-acceptors For years, it was assumed that p-backdonation occurred from the metal into empty d-orbitals on phosphorus. Actually: p-backdonation occurs into MOs formed by combination of two d-orbitals on phosphorus and the * orbitals involved ...
... Phosphines :PR3 - very important ligands - -donors - p-acceptors For years, it was assumed that p-backdonation occurred from the metal into empty d-orbitals on phosphorus. Actually: p-backdonation occurs into MOs formed by combination of two d-orbitals on phosphorus and the * orbitals involved ...
Introduction to Crystal Field Theory
... CFT focuses on the interaction of the five (n − 1)d orbitals with ligands arranged in a regular array around a transitionmetal ion. We will focus on the application of CFT to octahedral complexes, which are by far the most common and the easiest to visualize. Other common structures, such as square ...
... CFT focuses on the interaction of the five (n − 1)d orbitals with ligands arranged in a regular array around a transitionmetal ion. We will focus on the application of CFT to octahedral complexes, which are by far the most common and the easiest to visualize. Other common structures, such as square ...
Problems - UCI Chemistry
... consistent with these observations. 10.21 a. Explain the effect on the d-orbital energies when an octahedral complex is compressed along the z axis. b. Explain the effect on the d-orbital energies when an octahedral complex is stretched along the z axis. In the limit, this results in a square-planar ...
... consistent with these observations. 10.21 a. Explain the effect on the d-orbital energies when an octahedral complex is compressed along the z axis. b. Explain the effect on the d-orbital energies when an octahedral complex is stretched along the z axis. In the limit, this results in a square-planar ...
Dinitrogen Cleavage by a Molybdenum(III) Complex
... No appreciable dissociation at 3000 ºC and ordinary pressure2 bp 77.3 K N2(g) = 2N(g) ∆H = 944.7 kJ mol-1 Study Questions: What is the electronic configuration of N (what orbitals are the electrons in)? In its ground state, is the nitrogen atom a singlet, doublet, triplet, quartet, etc.? Draw the Le ...
... No appreciable dissociation at 3000 ºC and ordinary pressure2 bp 77.3 K N2(g) = 2N(g) ∆H = 944.7 kJ mol-1 Study Questions: What is the electronic configuration of N (what orbitals are the electrons in)? In its ground state, is the nitrogen atom a singlet, doublet, triplet, quartet, etc.? Draw the Le ...
Slide 1
... While H2 complexes can be isolated, stable alkane complexes are unknown. Nevertheless, stable complexes with agostic (from Greek “to hold onto oneself”) CH bond are multiple. PMe2 ...
... While H2 complexes can be isolated, stable alkane complexes are unknown. Nevertheless, stable complexes with agostic (from Greek “to hold onto oneself”) CH bond are multiple. PMe2 ...
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).