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tutorial-sheets - Chem.iitb
tutorial-sheets - Chem.iitb

... processes/phenomena that could not be explained by classical physics. 2. In photoelectric effect phenomenon, how do the following parameters vary with increasing frequency of incident radiation: (a) Photocurrent and (b) Kinetic energy of photoelectrons. 3. What are the postulates of Bohr’s theory fo ...
the second and third row metals
the second and third row metals

013-IC-2008-47-11228..
013-IC-2008-47-11228..

... Syntheses and Structure of Square-Pyramidal [FeIIMe2 + I((tame-N3)S2 )] (1), [FeIII(Et-N2S2Me2)]22- (2), [FeIII(EtN2S2Me2)(py)]1- (3), and [FeIII((tame-N2S)S2Me2)]2- (15). Imine-ligated [FeIII ((tame-N3)S2Me2)] (PF6) · PhCN (1) was synthesized under anaerobic conditions via an Fe2+templated, Schiff- ...
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... What will happen to the system if the temperature of the system is increased and the volume is kept constant? The reaction will shift to the (right / left) ...
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... due to the reactivity that is intrinsic to metal centers and ligand variability leads to several geometries.1, 2 Cisplatin, PtCl2(NH3)2, and related platinum based drugs have been extensively used as anti-cancer treatments and are highly effective, but suffer from several problems: some cancer lines ...
Microsoft Word
Microsoft Word

TRANSITION METAL COMPLEXES AS
TRANSITION METAL COMPLEXES AS

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Studies on nickel(II) and palladium(II) complexes with some
Studies on nickel(II) and palladium(II) complexes with some

... vibrations.18,25,26 The above observation strongly suggests18,22,25,26 that the proposed macrocyclic framework was formed. The formation of a tellurium-containing macrocyclic ring is supported by appearance of new weak intensity bands around 420–410 cm–1 due to Te–N.18,27 Evidence for the formation ...
Introduction to Auto-Docking
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... lowers the time and energy necessary to plan a major combinatorial study. One approach to auto-docking is to use molecular mechanics techniques to minimize the energy of a ligand in a binding pocket starting from a series of random positions and orientations within the binding site. Finding the low ...
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... – First to a viscous sol (particles of colloidal dimensions, ~1-1000 nm) – Finally to a transparent, homogeneous, amorphous solid known as a gel – Without precipitation of any crystalline phases The gel is then heated at high temperatures to remove volatile components trapped in the pores of the gel ...
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CHAPTER 3 Overview to the Theoretical Studies on Polyoxometalates

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Rules and Clues for Determining Oxidation Number

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Q>K → delGK → delG >0 → Reverse

... Crystal field splitting does not change the total energy of the d orbitals. The largest crystal field splittin energies are rd found in complexes of metal ions from the 3 row of the transition metals, that have charges of at least +3 and ligands that have localized lone pairs of e-. Octahedral d3 an ...
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Exercises to the Textbook “Physical Chemistry from

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Synthesis, Spectral and Pharmacological Study of Cu(II)

... suggests octahedral geometry around Co(II)17. The ν3 band is seen quite sharp while ν2 band is very weak. The octahedral geometry of these complexes is further supported by the value of ν2 / ν1 which comes out to be 2.12 and 2.11, respectively. The values of β obtained in the case of both the comple ...
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... • A unidentate ligand is a ligand that can bind through only one atom. • A polydentate ligand is a ligand that can bind through more than one donor atom. • There are known examples of bidentate, tridentate, quadridentate, quinquedentate, and sexidentate ligands. • Chelate complexes are complexes tha ...
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... Ni(Ⅲ) ( ) ((d7) low-spin Co(Ⅱ) (d7) - low-spin Cr(Ⅱ): distorted from Oh → to D4h : 2 absorption bands one in Vis one in near IR : if pure Oh → only one d-d transition (Chapter 11) Inorganic Chemistry 2 ...
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... protons, which assigned to the CH3 protons in the benzopyran-4one ring in position two[11]. The proton of CHO appears at 10.2 ppm for all the ligands. The OH signal of the benzopyran-4-one ring appears at 11.90-12.8 ppm. The NH signal of the sulfa drug moiety appears at10.4-11.9. The multiple signal ...
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... 10b. (3 pts) How many absorbance bands would you expect to see? 10c. (2 pts) The complex MnO4-2 is a very pretty green. Given that there is only one absorbance band in the visible region, what is the approximate wavelength of the absorbance band? Circle one: 400 nm 500 nm 600 nm 700 nm 11. In class ...
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Forming Ligand in Homo-and Heterometallic Complexes - Hal-CEA

Chapter 24 Chemistry of Coordination Compounds • Transition
Chapter 24 Chemistry of Coordination Compounds • Transition

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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).
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