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Synthesis and Structural Aspects of Copper (II), Cobalt (II), and
Synthesis and Structural Aspects of Copper (II), Cobalt (II), and

... A similar behaviour was observed by reacting the ligand CL5 with the metal nitrate salts. This cyclic ligand is not able to coordinate any metal by itself, as AL5 do, but, also in this case, owing to the hydrolysis of the ester groups a new ligand CL6 (R = COOH; Scheme 1) was obtained that uses its ...
Dual Luminescence and Long-Lived Charge
Dual Luminescence and Long-Lived Charge

2P32 - Pilkington Group
2P32 - Pilkington Group

Transition Metals
Transition Metals

18-Electron Rule: Myth or Reality ? An NBO Perspective
18-Electron Rule: Myth or Reality ? An NBO Perspective

... Hydrogenation and Wilkinson’s Catalyst Many catalytic cycles are drawn with particular emphasis on the number of electrons but not on the relative positions of the various ligands with different stereoelectronic properties. ...
Potintiometric and Thermodynamic Studies of Some Divalent Metal
Potintiometric and Thermodynamic Studies of Some Divalent Metal

Helicene-grafted vinyl- and carbene-osmium complexes - HAL
Helicene-grafted vinyl- and carbene-osmium complexes - HAL

... (see SI for more details).8The calculated MR values of 3 were found to be overestimated as compared to the experimental result (17557 with BHLYP and 14173 with LC-PBE0) and similar to the calculated MR of 1. The trend among the set of complexes is thus correctly reproduced by the calculations. Anoth ...
IOSR Journal of Applied Chemistry (IOSR-JAC) e-ISSN: 2278-5736.
IOSR Journal of Applied Chemistry (IOSR-JAC) e-ISSN: 2278-5736.

... These compounds are worth attention because of their biological activities and clinical usage Schiff base ligand forms a stable complex with different transition metal ions and has been the subject for thorough investigation because of their extensive application in wide ranging areas from material ...
Crystal Structure of Bis(O-propyldithiocarbonato-k2S,S¢)(3,5
Crystal Structure of Bis(O-propyldithiocarbonato-k2S,S¢)(3,5

... compared to the torsion present for such bonds in related structures.11 The pyridine ring is coplanar, and held almost perpendicular to the dithiocarbonato groups. The dihedral angles between dithio-group and the pyridine ring is 87.47(6)˚. The O1–C9 bond distance [1.328(3)Å] is shorter than O1–C10 ...
UJDIPa - The Vital Chemist
UJDIPa - The Vital Chemist

Chemistry 520 - Problem Set 6
Chemistry 520 - Problem Set 6

... NO! All that  tells us is if a reaction is thermodynamically favored. It does not tell us how long the reaction will take. G ...
4550-15Lecture21
4550-15Lecture21

B. Electron Deficient (less than an octet)
B. Electron Deficient (less than an octet)

... How does one explain the linear shape? (a.) Be 1s22s2 - 2s2 is the valence shell If we promote an e- to the 2p level it is now possible to pair the two unpaired electrons with those of incoming group H or X (halide) - 2s12p1 valence state requires 323 kJ/mol (this doesn’t explain the shape, only how ...
Tuning PCP-Ir Complexes: The impact of an N
Tuning PCP-Ir Complexes: The impact of an N

08_chapter 1
08_chapter 1

... A glass whose atomic arrangement lacks regularity over a long range has higher configurational entropy and hence higher free energy, than a crystalline material of the same composition. Therefore a glass is a thermodynamically metastable material. The transformation of a glass to a crystal proceeds ...
Synthesis, Structures and Properties of Cu(II) and Mn(II) Complexes
Synthesis, Structures and Properties of Cu(II) and Mn(II) Complexes

... analysis was measured on a MOD 1106 elemental analyzer. The PXRD data were collected on a Bruker D8 diffractometer with Cu Kα radiation (λ = 1.5418Å). 3.2. Synthesis of 1-4 3.2.1. Synthesis of [Mn(phenca)2](H2O)2 (1) A solution of phenca (0.224 g, 1 mmol) and Mn(CH3COO)2 (0.172 g, 1 mmol) in water ( ...
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Understanding Heterolytic Bond Cleavage

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π bonded ligands

Academic Year 2009/2010 Semester I KTT 212/3 Inorganic
Academic Year 2009/2010 Semester I KTT 212/3 Inorganic

... An overview of the background and basic aspects related to the coordination compounds or complexes which include the definition, nomenclature based on IUPAC system, coordination number, oxidation state for central metal atom, types of ligands and complexes. Establishment of different structures owin ...
1 - inorganic reaction mechanisms and redox
1 - inorganic reaction mechanisms and redox

Nomenclature Notes
Nomenclature Notes

Resonance Enhancement of Raman Spectroscopy: Friend
Resonance Enhancement of Raman Spectroscopy: Friend

STABILITETEN AF KOORDINATIONSFORBINDELSER
STABILITETEN AF KOORDINATIONSFORBINDELSER

i PREFACE The ability of Schiff bases to form complexes with metal
i PREFACE The ability of Schiff bases to form complexes with metal

... The ability of Schiff bases to form complexes with metal ions has been well established. This is due to the presence of lone pair of electrons on the nitrogen atom and of the general electron donating character of the double bond. They also form five or, six membered stable chelates with metals, if ...
Complexometric Reactions (1)
Complexometric Reactions (1)

... (ligand) depend on the coordination no. of the metal and on the no. of complexing gps. on the ligand. ...
< 1 ... 85 86 87 88 89 90 91 92 93 ... 129 >

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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