Key spring semester Flashcards

1
Q

Transition element

A

D-block metals that have the ability to form compounds and ions with partially filled d-block orbitals.

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2
Q

ligands

A

Lewis bases that donate a pair of electrons to the d-block metal to form dative covalent bonds in complexes

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3
Q

Denticity

A

the number of donor atoms coordinated to the metal ion

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4
Q

Charges on
en
dppe
biby
ox
pn
phen
dien

A

charges are
0
0
0
2-
0
0
0

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5
Q

ambiente ligands

A

can bind to metal ligands in several different locations

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6
Q

structural isomerism

A

same molecular but different structural formula
solute > position of water either on complex or as water of crystallisation
linkage > mordent ligands that have different location for dative bonds (nitro and nitrito)
coordination > different ligands attached to metals when two complexes
ionisation > ligands swap places with uncoordinated ligands

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7
Q

Stereoisomerism

A

atoms arranged in different elocution in space
geometrical > cis and trans
optical > chiral complete with are mirror images of each other

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8
Q

Crystal field stabilisation theory

A

This is when the degenerate d orbital split into two groups in tetrahedral (t2 and e) and in octahedral (t2g and eg``0 due to repulsion between the electron field around the complex from the ligands and d electrons creating repulsion. This mean the d-orbital pointing directly at he ligands increases in energy whereas the ones between decrease in energy. This theory lower the energy of the complex increasing its stability.
Δt = 4/9Δo

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9
Q

Calculating CFSE

A

Each electron in the lower energy level is multiplied by -0.4 and each electron in the higher is multiplied by +0.6 this is then added together. The number of paired electrons is written after as +xP

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10
Q

Interpreting CFSE

A
  • The lower/more negative the Δo is the more stable the ligand is
  • a very low Δo will cause high spin ligands (CN- and CO) as it is strong enough to overcome pairing energies
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11
Q

Determining square planar

A
  • needs to be very low Δo
  • d8 electrons
  • large metal ions e.g. Pt
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12
Q

Jhan-teller

A

If a group state electronic configuration of a complex is orbitally degenerate the geometry of the complex will distort to remove the degeneracy and achieve a lower energy.
If the degrrancy is in a t2g or t is T-state if it in eg or e its e-state if it has no degeneracy its A-state.
It will distort by elongating the two orbitals along the Z axis

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13
Q

Magnitude of Jhan-teller

A

The magnitude of dengeracy depends on which set of orbital the degeneracy lies in
- If its in the t2g the orbitals point between the ligands do than Tyler effect is small
-if degeneracy is on eg which point at ligands the distortion will be large

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14
Q

Irving William series

A

The general stability sequence of high spin octahedral metal complexes M(II) for the replacement of water by other ligands

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15
Q

What affects M(II0 stability in Irving Williams series

A
  • Zeff charge increases. the decrease in atomic radii thus increases nuclear attraction to ligands increasing stabilit, lack of electrons shielding (d-block contraction)
  • All metal complexes are high spin so they will all gain extra stability form CFSE (Mn will have all electrons with parallel spins so increases stability)
  • Cu is very stable has contains Jhanteller effect
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16
Q
A
17
Q
A