DM bijkm: Complexes & associated colour Flashcards

1
Q

Explain in simple terms what causes colour.

A
  • When light hits a substance, it may be transmitted, reflected or absorbed
  • If frequency absorbed is in visible region, substance is coloured
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2
Q

Explain why specific elements absorb specific frequencies of light.

A
  • When light hits an atom, photons are absorbed
  • Electrons promoted to higher energy levels
  • Energy of a photon corresponds to gap between energy levels
  • Frequency of photon, ν, related to ΔE by ΔE = hν
  • Each element has unique energy levels, so absorbs unique frequencies of light
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3
Q
  • State what is meant by “complementary colours”.
  • List them.
A

Opposite frequencies of visible light on the colour wheel which, when combined, produce white light.

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4
Q
  • Give the formulae of the common ions of iron
  • Give their colours in aqueous solution
A

Fe2+, green

Fe3+, orange-brown

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5
Q
  • Give the formulae of the common ions of copper
  • Give their electronic configuration with respect to Ar
  • Give their colours in aqueous solution
A

Cu [Ar] 3d104s1

Cu+, [Ar] 3d10, unstable in solution

Cu2+, [Ar] 3d9​, blue

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6
Q

Copper(I) ions are unstable in aqueous solution. Write an equation, showing state symbols, to suggest what they break down to.

A

2Cu+(aq) → Cu(s) + Cu2+(aq)

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7
Q

What are ligands?

A

Molecules/anions which surround, and donate a lone pair of electrons to, a metal cation by coordinate (dative) bonding.

The inorganic chem equivalent of nucleophiles

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8
Q

Define the following:

  • Monodentate ligand
  • Bidentate ligand
  • Polydentate ligand
A
  • Monodentate ligand: form one coordinate bond with central metal ion
  • Bidentate ligand: form two coordinate bonds with central metal ion
  • Polydentate ligand: form several coordinate bonds with central metal ion
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9
Q

Give the corresponding prefix/suffix for naming the complex of each of the following monodentate ligands:

  • H2O:
  • :OH-
  • :CN-
  • :NH3
  • Halides, :Cl-, :Br-, :I-
  • CH3COO:
A
  • H2O aqua
  • OH- hydroxy
  • CN- cyano
  • NH3 amino
  • Cl- chloro, Br- bromo, I- iodo
  • CH3COO ethanoate
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10
Q

Explain why some transition metal solutions are coloured.

A
  • Ligands form dative bonds with central metal ion, which splits its d-orbitals
  • Creates energy gap of right magnitude to allow absorption of visible light
  • Electrons are excited to higher energy level
  • Frequency absorbed is related to energy gap by ∆E = hv
  • Colour seen is complementary colour to that absorbed (due to missing frequency)

Energies of all 5 d-orbitals in transition metals are normally equal​.

Further explanation of splitting (not on spec): d-orbitals close to ligand are repelled + pushed to higher energy levels. Those further from ligand are attracted + pushed to lower energy levels

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11
Q

On which factors does the colour of a transition metal complex depend?

A
  • Ligand
  • Ligand arrangement (affects splitting)
  • Transition metal element
  • Oxidation state (number of d-electrons)
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12
Q

Explain why the following are not coloured:

  1. Titanium(IV) oxide
  2. Compounds of Sc3+
  3. Compounds of Zn2+
  4. Compounds of Cu+
A

They have the following electronic arrangements:

  1. Ti4+ [Ar]
  2. Sc3+ [Ar]
  3. Zn2+ [Ar] 3d10
  4. Cu+ [Ar] 3d10

No incompletely filled 3d orbitals / all are either empty or full

Dative covalent bonding with ligands cannot occur

3d electron transitions / splitting not possible

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13
Q

What is a complex?

A

Central transition metal atom or ion surrounded by + bonded coordinately to several ligands.

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14
Q

How would you predict the charge of a complex?

A

Overall charge of metal atom/ion + ligands.

Charge delocalised over whole ion.

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15
Q

Define “coordination number”.

A

The number of dative bonds in a complex between the metal atom/ion and ligands.

D__oesn’t necessarily indicate the number of ligands.

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16
Q

State the possible shapes of complexes with coordination numbers 6, 4 and 2.

A

6: octahedral
4: tetrahedral or square planar
2: linear
* May be distorted, e.g. in [Cu(H2O)6]2+ 2 bonds are shorter*

17
Q

What is the general nomenclature for complexes?

A

[no. ligands][ligand prefix] [metal] [ox state] [“ion” if applicable] Ion ends in “ate” if complex is negative

18
Q
  • Name a cobalt(II) ion complexed with 6 water molecules
  • Name a copper(II) ion complexed with 4 Cl- ions
  • Name an iron(II) ion complexed with 4 Cl- ions
A
  • Hexaaqua cobalt(II) ion
  • Tetrachloro cuprate(II) ion
  • Tetrachloro ferrate(II) ion
19
Q
  • State the coordination number of the hexaqua iron(III) ion
  • State the shape of the complex ion
  • Draw its structural formula and 3D shape
A
  • 6
  • Octahedral
20
Q
  • State the coordination number of the tetrachloro nickel(II) ion
  • State its shape
  • Draw its structural formula and 3D shape
A
  • 4
  • Tetrahedral
21
Q

Draw the 3D structure of the complex which Cu2+ forms in aqueous solution.

A
22
Q
A

D

Although 3 is true for 3d elements, it doesn’t include all transition metal elements, i.e. 4d, 5d, etc

23
Q
  • The ethanedioate ion is an example of which type of ligand?
  • Draw the complex it forms with a metal ion, “M”
  • Name the ring formed
A
  • Bidentate ligand (several lone pairs but only forms 2 bonds)
  • Chelate ring (five-membered)
24
Q

Which statement(s) about ethanedioate ions is/are correct?

  1. Its formula is C2O42–
  2. It is a bidentate ligand
  3. Up to three ethanedioate ions can complex with a metal ion

A 1, 2 and 3

B Only 1 and 2

C Only 2 and 3

D Only 1

A

A

25
Q
A

B

26
Q
  • Write the equation for the reaction between hydrochloric acid and aqueous Cu(II) ions
  • What type of reaction is this?
A
  • [Cu(H2O)6]2+(aq) + 4Cl-(aq) → [CuCl4]2-(aq) + 6H2O(l)
  • Ligand exchange / substitution
27
Q

The addition of OH- (from aqueous NaOH or ammonia) to aqueous solutions of Cu2+, Fe2+ and Fe3+ results in the formation of coloured precipitates.

For each, write a simplified ionic equation to represent the interaction and state the changes which would be observed.

A

Cu2+(aq) + 2OH-(aq) → Cu(OH)2(s)

Blue solution → pale blue precipitate

Fe2+(aq) + 2OH-(aq) → Fe(OH)2(s)

Green solution → dark green precipitate

Fe3+(aq) + 3OH-(aq) → Fe(OH)3(s)

Orange-brown solution → red-brown precipitate

28
Q

The addition of OH- to aqueous solutions of Cu2+, Fe2+ and Fe3+ results in the formation of coloured precipitates.

Write full equations for each.

A

[Cu(H2O)6]2+(aq) + 2OH-(aq) → Cu(OH)2(H2O)4 + 2H2​O

[Fe(H2O)6]2+(aq) + 2OH-(aq) → Fe(OH)2(H2O)4 + 2H2​O

[Fe(H2O)6]3+(aq) + 3OH-(aq) → Fe(OH)3(H2O)3 + 3H2O

29
Q

The addition of OH- to aqueous solutions of Cu2+, Fe2+ and Fe3+ results in the formation of coloured precipitates.

Name the type of reaction which occurs.

A

Acid-base / deprotonation

Not ligand exchange; OH doesn’t replace the water, it deprotonates it

30
Q

The addition of ammonia solution to aqueous solutions of Cu2+, Fe2+ and Fe3+ results in the formation of coloured precipitates.

For which will a change be seen if excess ammonia solution is added? Describe and explain the change observed.

A
  • Cu(OH)2 re-dissolves in ammonia
  • Tetraaminodiaqua copper(II) ion is formed: [Cu(NH3)4(H2O)2]2+
  • Pale blue precipitate becomes deep blue-violet solution
31
Q
  • Write an ionic equation representing the effect of adding ammonia solution, not in excess, to a solution of Cu2+
  • Write an equation showing what happens when ammonia is in excess
  • Write an overall equation
  • Describe the changes observed throughout
A

Ammonia = weak base: NH3 + H2ONH4+ + OH-

Ammonia not in excess:

Cu(H2O)6]2+(aq) + 2OH-Cu(H2O)4(OH)2 + 2H2O(l)

Ammonia in excess:

Cu(H2O)4(OH)2 + 4NH3(aq) → [Cu(NH3)4(H2O)2]2+(aq) + 2H2O(l) + 2OH-(aq)

Overall:

[Cu(H2O)6]2+(aq) + 4NH3(aq) → [Cu(NH3)4(H2O)2]2+(aq) + 4H2O(l)

Blue solution → pale blue precipitate → dark blue-violet solution

32
Q

Adding excess ammonia solution to an aqueous solution of Cu2+ results in a colour change of blue to deep blue-purple. Which ligand, of water and ammonia, therefore has the greater splitting effect?

A
  • Blue-purple is higher frequency than blue
  • Larger gap between energy levels since ΔE = hv
  • Ammonia has greater splitting effect
33
Q

Which of the complex ions of copper(II) with water or ammonia is more stable and why?

A
  • Ammonia
  • Undergoes ligand substitution
34
Q

Explain the term complex ion, and why different complexes of d-block elements have different
colours. (6)

A

Definition of a complex ion:

  • Ligands form dative (coordinate) bonds to a central metal ion

Origin of colour:

  • Ligands split d-orbitals
  • Creates energy gap of right magnitude to allow absorption of visible light
  • Electrons are excited to higher energy level
  • Frequency absorbed is related to energy gap by ∆E = hv
  • Colour seen is complementary colour (due to
    missing frequency)

Cause of different colours:

  • Different gaps in split d-orbitals, depending on:
    • Ligand
    • Ligand arrangement (affects splitting)
    • D-block element
    • Oxidation state (number of d-electrons)
  • So different frequencies are absorbed
  • Gives different complementary colours