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Mr.G.M.Dongare
(M.Sc,B.Ed,SET)
Associate Professor
Dept.of Chemistry
Shri Shivaji Colege of Arts,Commerce and
Science College, Akola.
Transitional element and
Coordination chemistry
B.Sc III Part
Academic year 2021-22
SS CI 11.5 The d block 2
The d block:
• The d block consists of three horizontal
series in periods 4, 5 & 6
– 10 elements in each series
– Chemistry is “different” from other
elements
– Special electronic configurations important
• Differences within a group in the d block are
less sharp than in s & p block
• Similarities across a period are greater
SS CI 11.5 The d block 3
Electronic Configuration
• Across the 1st row of the d block
(Sc to Zn) each element
– has 1 more electron and 1 more proton
– Each “additional” electron enters the
3d sub-shell
– The core configuration for all the
period 4 transition elements is that of
Ar
• 1s22s22p63s23p6
SS CI 11.5 The d block 4
1s
2s
3s
4s
2p
3p
3d
Energy
Ar
1s2 2s2 2p6 3s2 3p6
4p
SS CI 11.5 The d block 5
1s
2s
3s
4s
2p
3p
3d
Energy
Sc
1s2 2s2 2p6 3s2 3p6 3d1 4s2
4p
SS CI 11.5 The d block 6
Electronic Arrangement
Element Z 3d 4s
Sc 21 [Ar]  
Ti 22 [Ar]   
V 23 [Ar]    
Cr 24 [Ar]      
Mn 25 [Ar]      
Fe 26 [Ar]      
Co 27 [Ar]      
Ni 28 [Ar]      
Cu 29 [Ar]      
Zn 30 [Ar]      
SS CI 11.5 The d block 7
Chromium and Copper
• Cr and Cu don’t fit the pattern of
building up the 3d sub-shell, why?
– In the ground state electrons are always
arranged to give lowest total energy
– Electrons are negatively charged and repel
each other
– Lower total energy is obtained with e- singly
in orbitals rather than if they are paired in
an orbital
– Energies of 3d and 4s orbitals very close
together in Period 4
SS CI 11.5 The d block 8
Chromium and Copper
• At Cr
– Orbital energies such that putting one
e- into each 3d and 4s orbital gives
lower energy than having 2 e- in the
4s orbital
• At Cu
– Putting 2 e- into the 4s orbital would
give a higher energy than filling the
3d orbitals
SS CI 11.5 The d block 9
1s
2s
3s
4s
2p
3p
3d
Energy
Cr
1s2 2s2 2p6 3s2 3p6 3d5 4s1
4p
SS CI 11.5 The d block 10
1s
2s
3s
4s
2p
3p
3d
Energy
Cu
1s2 2s2 2p6 3s2 3p6 3d10 4s1
4p
SS CI 11.5 The d block 11
What is a transition metal?
• Transition metals [TM’s] have
characteristic properties
– e.g. coloured compounds, variable oxidation
states
• These are due to presence of an inner
incomplete d sub-shell
• Electrons from both inner d sub-shell
and outer s sub-shell can be involved in
compound formation
SS CI 11.5 The d block 12
What is a transition metal?
• Not all d block elements have
incomplete d sub-shells
– e.g. Zn has e.c. of [Ar]3d104s2, the
Zn2+ ion ([Ar] 3d10) is not a typical TM
ion
– Similarly Sc forms Sc3+ which has the
stable e.c of Ar. Sc3+ has no 3d
electrons
SS CI 11.5 The d block 13
What is a transition metal?
• For this reason, a transition metal
is defined as being an element
which forms at least one ion with a
partially filled sub-shell of d
electrons.
– In period 4 only Ti-Cu are TM’s!
– Note that when d block elements form
ions the s electrons are lost first
SS CI 11.5 The d block 14
What are TM’s like?
• TM’s are metals
• They are similar to each other but
different from s block metals eg Na and
Mg
• Properties of TM’s
– Dense metals
– Have high Tm and Tb
– Tend to be hard and durable
– Have high tensile strength
– Have good mechanical properties
SS CI 11.5 The d block 15
What are TM’s like?
• Properties derive from strong metallic
bonding
• TM’s can release e- into the pool of
mobile electrons from both outer and
inner shells
– Strong metallic bonds formed between the
mobile pool and the +ve metal ions
– Enables widespread use of TMs!
– Alloys very important: inhibits slip in crystal
lattice usually results in increased hardness
and reduced malleability
SS CI 11.5 The d block 16
Effect of Alloying on TM’s
SS CI 11.5 The d block 17
TM Chemical Properties
• Typical chemical properties of the
TM’s are
– Formation of compounds in a variety of
oxidation states
– Catalytic activity of the elements and
their compounds
– Strong tendency to form complexes
• See CI 11.6
– Formation of coloured compounds
• See CI 11.6
SS CI 11.5 The d block 18
Variable Oxidation States
• TM’s show a great variety of
oxidation states cf s block metals
• If compare successive ionisation
enthalpies (Hi) for Ca and V as
follows
M(g)  M+(g) + e- Hi(1)
M+(g)  M2+(g) + e- Hi(2)
M2+(g)  M3+(g) + e- Hi(3)
M3+(g)  M4+(g) + e- Hi(4)
Hi for Ca and V
Element
Ionisation Enthalpies
[kJ mol-1]
Hi(1) Hi(2) Hi(3) Hi(4)
Ca [Ar]4s2 +596 +1152 +4918 +6480
V [Ar]3d34s2 +656 +1420 +2834 +4513
SS CI 11.5 The d block 20
Hi for Ca and V
• Both Ca & V always lose the 4s electrons
• For Ca
– Hi(1) & Hi(2) relatively low as corresponds
to removing outer 4s e-
– Sharp increase in Hi(3) & Hi(4) cf Hi(2)
due to difficulty in removing 3p e-
• For Sc
– Gradual increase from Hi(1) to Hi(4) as
removing 4s then 3d e-
SS CI 11.5 The d block 21
Oxidation States of TM’s
• In the following table
– Most important OS’s in boxes
– OS = +1 only important for Cu
– In all others sum of Hi(1) + Hi(2)
low enough for 2e- to be removed
– OS = +2, where 4s e- lost shown by
all except for Sc and Ti
– OS = +3, shown by all except Zn
SS CI 11.5 The d block 22
Oxidation States of TM’s
Sc Ti V Cr Mn Fe Co Ni Cu Zn
+1
+2 +2 +2 +2 +2 +2 +2 +2
+3 +3 +3 +3 +3 +3 +3 +3 +3
+4 +4 +4
+5
+6 +6 +6
+7
SS CI 11.5 The d block 23
Oxidation States of TM’s
• No of OS’s shown by an element
increases from Sc to Mn
– In each of these elements highest OS is
equal to no. of 3d and 4s e-
• After Mn decrease in no. of OS’s shown
by an element
– Highest OS shown becomes lower and less
stable
– Seems increasing nuclear charge binds 3d e-
more strongly, hence harder to remove
SS CI 11.5 The d block 24
Oxidation States of TM’s
• In general
– Lower OS’s found in simple ionic
compounds
• E.g. compounds containing Cr3+, Mn2+,
Fe3+, Cu2+ ions
– TM’s in higher OS’s usually covalently
bound to electronegative element such
as O or F
• E.g VO3
-, vanadate(V) ion; MnO4
-,
manganate(VII) ion
• Simple ions with high OS’s such as V5+ &
Mn7+ are not formed
SS CI 11.5 The d block 25
Stability of OS’s
• Change from one OS to another is a
redox reaction
• Relative stability of different OS’s
can be predicted by looking at
Standard Electrode Potentials
– E values
SS CI 11.5 The d block 26
Stability of OS’s
• General trends
– Higher OS’s become less stable
relative to lower ones on moving from
left to right across the series
– Compounds containing TM’s in high
OS’s tend to be oxidising agents e.g
MnO4
-
– Compounds with TM’s in low OS’s are
often reducing agents e.g V2+ & Fe2+
SS CI 11.5 The d block 27
Stability of OS’s
• General trends (continued)
– Relative stability of +2 state with respect to
+3 state increases across the series
– For compounds early in the series, +2 state
highly reducing
• E.g. V2+(aq) & Cr2+(aq) strong reducing agents
– Later in series +2 stable, +3 state highly
oxidising
• E.g. Co3+ is a strong oxidising agent, Ni3+ & Cu3+
do not exist in aqueous solution.
SS CI 11.5 The d block 28
Catalytic Activity
• TM’s and their compounds effective and
important catalysts
– Industrially and biologically!!
• The “people in the know” believe
– catalysts provide reaction pathway with lower
EA than uncatalysed reaction (see CI 10.5)
• Once again,
– availability of 3d and 4s e-
– ability to change OS
– among factors which make TM’s such good
catalysts
SS CI 11.5 The d block 29
Heterogeneous Catalysis
• Catalyst in different phase from
reactants
– Usually means solid TM catalyst with
reactants in liquid or gas phases
• TM’s can
– use the 3d and 4s e- of atoms on metal
surface to from weak bonds to the
reactants.
– Once reaction has occurred on TM surface,
these bonds can break to release products
• Important example is hydrogenation of
alkenes using Ni or Pt catalyst
SS CI 11.5 The d block 30
Heterogeneous Catalysis
SS CI 11.5 The d block 31
Homogeneous Catalysis
• Catalyst in same phase as reactants
– Usually means reaction takes place in
aqueous phase
– Catalyst aqueous TM ion
• Usually involves
– TM ion forming intermediate compound
with ome or more of the reactants
– Intermediate then breaks down to
form products
SS CI 11.5 The d block 32
Homogeneous Catalysis
• Above reaction is that used in
Activity SS5.2
– 2,3-dihydroxybutanoate ion with
hydrogen peroxide
– Reaction catalysed by Co2+
O
H
C
H C
O
C
H C
O
O
O
O
H
O
H
OH
C
O
O
C
H
O
O
OH2
+ + +
3 2 2 4
SS CI 11.5 The d block 33
Suggested Mechanism
REACTANTS
H2O2 +
-O2CCH(OH)CH(OH)C02
-
Co2+ (pink)
INTERMEDIATE
containing
Co3+ (green)
Co2+ reduces
H2O2 & gets
oxidised to
Co3+
PRODUCTS
CO2, methanoate, H2O
Co2+ (pink)
Co3+
oxidises
2,3-
hydroxy-
butanoate &
gets
reduced to
Co2+
Regenerated
Catalyst

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Transition Metals and Coordination Chemistry

  • 1. Mr.G.M.Dongare (M.Sc,B.Ed,SET) Associate Professor Dept.of Chemistry Shri Shivaji Colege of Arts,Commerce and Science College, Akola. Transitional element and Coordination chemistry B.Sc III Part Academic year 2021-22
  • 2. SS CI 11.5 The d block 2 The d block: • The d block consists of three horizontal series in periods 4, 5 & 6 – 10 elements in each series – Chemistry is “different” from other elements – Special electronic configurations important • Differences within a group in the d block are less sharp than in s & p block • Similarities across a period are greater
  • 3. SS CI 11.5 The d block 3 Electronic Configuration • Across the 1st row of the d block (Sc to Zn) each element – has 1 more electron and 1 more proton – Each “additional” electron enters the 3d sub-shell – The core configuration for all the period 4 transition elements is that of Ar • 1s22s22p63s23p6
  • 4. SS CI 11.5 The d block 4 1s 2s 3s 4s 2p 3p 3d Energy Ar 1s2 2s2 2p6 3s2 3p6 4p
  • 5. SS CI 11.5 The d block 5 1s 2s 3s 4s 2p 3p 3d Energy Sc 1s2 2s2 2p6 3s2 3p6 3d1 4s2 4p
  • 6. SS CI 11.5 The d block 6 Electronic Arrangement Element Z 3d 4s Sc 21 [Ar]   Ti 22 [Ar]    V 23 [Ar]     Cr 24 [Ar]       Mn 25 [Ar]       Fe 26 [Ar]       Co 27 [Ar]       Ni 28 [Ar]       Cu 29 [Ar]       Zn 30 [Ar]      
  • 7. SS CI 11.5 The d block 7 Chromium and Copper • Cr and Cu don’t fit the pattern of building up the 3d sub-shell, why? – In the ground state electrons are always arranged to give lowest total energy – Electrons are negatively charged and repel each other – Lower total energy is obtained with e- singly in orbitals rather than if they are paired in an orbital – Energies of 3d and 4s orbitals very close together in Period 4
  • 8. SS CI 11.5 The d block 8 Chromium and Copper • At Cr – Orbital energies such that putting one e- into each 3d and 4s orbital gives lower energy than having 2 e- in the 4s orbital • At Cu – Putting 2 e- into the 4s orbital would give a higher energy than filling the 3d orbitals
  • 9. SS CI 11.5 The d block 9 1s 2s 3s 4s 2p 3p 3d Energy Cr 1s2 2s2 2p6 3s2 3p6 3d5 4s1 4p
  • 10. SS CI 11.5 The d block 10 1s 2s 3s 4s 2p 3p 3d Energy Cu 1s2 2s2 2p6 3s2 3p6 3d10 4s1 4p
  • 11. SS CI 11.5 The d block 11 What is a transition metal? • Transition metals [TM’s] have characteristic properties – e.g. coloured compounds, variable oxidation states • These are due to presence of an inner incomplete d sub-shell • Electrons from both inner d sub-shell and outer s sub-shell can be involved in compound formation
  • 12. SS CI 11.5 The d block 12 What is a transition metal? • Not all d block elements have incomplete d sub-shells – e.g. Zn has e.c. of [Ar]3d104s2, the Zn2+ ion ([Ar] 3d10) is not a typical TM ion – Similarly Sc forms Sc3+ which has the stable e.c of Ar. Sc3+ has no 3d electrons
  • 13. SS CI 11.5 The d block 13 What is a transition metal? • For this reason, a transition metal is defined as being an element which forms at least one ion with a partially filled sub-shell of d electrons. – In period 4 only Ti-Cu are TM’s! – Note that when d block elements form ions the s electrons are lost first
  • 14. SS CI 11.5 The d block 14 What are TM’s like? • TM’s are metals • They are similar to each other but different from s block metals eg Na and Mg • Properties of TM’s – Dense metals – Have high Tm and Tb – Tend to be hard and durable – Have high tensile strength – Have good mechanical properties
  • 15. SS CI 11.5 The d block 15 What are TM’s like? • Properties derive from strong metallic bonding • TM’s can release e- into the pool of mobile electrons from both outer and inner shells – Strong metallic bonds formed between the mobile pool and the +ve metal ions – Enables widespread use of TMs! – Alloys very important: inhibits slip in crystal lattice usually results in increased hardness and reduced malleability
  • 16. SS CI 11.5 The d block 16 Effect of Alloying on TM’s
  • 17. SS CI 11.5 The d block 17 TM Chemical Properties • Typical chemical properties of the TM’s are – Formation of compounds in a variety of oxidation states – Catalytic activity of the elements and their compounds – Strong tendency to form complexes • See CI 11.6 – Formation of coloured compounds • See CI 11.6
  • 18. SS CI 11.5 The d block 18 Variable Oxidation States • TM’s show a great variety of oxidation states cf s block metals • If compare successive ionisation enthalpies (Hi) for Ca and V as follows M(g)  M+(g) + e- Hi(1) M+(g)  M2+(g) + e- Hi(2) M2+(g)  M3+(g) + e- Hi(3) M3+(g)  M4+(g) + e- Hi(4)
  • 19. Hi for Ca and V Element Ionisation Enthalpies [kJ mol-1] Hi(1) Hi(2) Hi(3) Hi(4) Ca [Ar]4s2 +596 +1152 +4918 +6480 V [Ar]3d34s2 +656 +1420 +2834 +4513
  • 20. SS CI 11.5 The d block 20 Hi for Ca and V • Both Ca & V always lose the 4s electrons • For Ca – Hi(1) & Hi(2) relatively low as corresponds to removing outer 4s e- – Sharp increase in Hi(3) & Hi(4) cf Hi(2) due to difficulty in removing 3p e- • For Sc – Gradual increase from Hi(1) to Hi(4) as removing 4s then 3d e-
  • 21. SS CI 11.5 The d block 21 Oxidation States of TM’s • In the following table – Most important OS’s in boxes – OS = +1 only important for Cu – In all others sum of Hi(1) + Hi(2) low enough for 2e- to be removed – OS = +2, where 4s e- lost shown by all except for Sc and Ti – OS = +3, shown by all except Zn
  • 22. SS CI 11.5 The d block 22 Oxidation States of TM’s Sc Ti V Cr Mn Fe Co Ni Cu Zn +1 +2 +2 +2 +2 +2 +2 +2 +2 +3 +3 +3 +3 +3 +3 +3 +3 +3 +4 +4 +4 +5 +6 +6 +6 +7
  • 23. SS CI 11.5 The d block 23 Oxidation States of TM’s • No of OS’s shown by an element increases from Sc to Mn – In each of these elements highest OS is equal to no. of 3d and 4s e- • After Mn decrease in no. of OS’s shown by an element – Highest OS shown becomes lower and less stable – Seems increasing nuclear charge binds 3d e- more strongly, hence harder to remove
  • 24. SS CI 11.5 The d block 24 Oxidation States of TM’s • In general – Lower OS’s found in simple ionic compounds • E.g. compounds containing Cr3+, Mn2+, Fe3+, Cu2+ ions – TM’s in higher OS’s usually covalently bound to electronegative element such as O or F • E.g VO3 -, vanadate(V) ion; MnO4 -, manganate(VII) ion • Simple ions with high OS’s such as V5+ & Mn7+ are not formed
  • 25. SS CI 11.5 The d block 25 Stability of OS’s • Change from one OS to another is a redox reaction • Relative stability of different OS’s can be predicted by looking at Standard Electrode Potentials – E values
  • 26. SS CI 11.5 The d block 26 Stability of OS’s • General trends – Higher OS’s become less stable relative to lower ones on moving from left to right across the series – Compounds containing TM’s in high OS’s tend to be oxidising agents e.g MnO4 - – Compounds with TM’s in low OS’s are often reducing agents e.g V2+ & Fe2+
  • 27. SS CI 11.5 The d block 27 Stability of OS’s • General trends (continued) – Relative stability of +2 state with respect to +3 state increases across the series – For compounds early in the series, +2 state highly reducing • E.g. V2+(aq) & Cr2+(aq) strong reducing agents – Later in series +2 stable, +3 state highly oxidising • E.g. Co3+ is a strong oxidising agent, Ni3+ & Cu3+ do not exist in aqueous solution.
  • 28. SS CI 11.5 The d block 28 Catalytic Activity • TM’s and their compounds effective and important catalysts – Industrially and biologically!! • The “people in the know” believe – catalysts provide reaction pathway with lower EA than uncatalysed reaction (see CI 10.5) • Once again, – availability of 3d and 4s e- – ability to change OS – among factors which make TM’s such good catalysts
  • 29. SS CI 11.5 The d block 29 Heterogeneous Catalysis • Catalyst in different phase from reactants – Usually means solid TM catalyst with reactants in liquid or gas phases • TM’s can – use the 3d and 4s e- of atoms on metal surface to from weak bonds to the reactants. – Once reaction has occurred on TM surface, these bonds can break to release products • Important example is hydrogenation of alkenes using Ni or Pt catalyst
  • 30. SS CI 11.5 The d block 30 Heterogeneous Catalysis
  • 31. SS CI 11.5 The d block 31 Homogeneous Catalysis • Catalyst in same phase as reactants – Usually means reaction takes place in aqueous phase – Catalyst aqueous TM ion • Usually involves – TM ion forming intermediate compound with ome or more of the reactants – Intermediate then breaks down to form products
  • 32. SS CI 11.5 The d block 32 Homogeneous Catalysis • Above reaction is that used in Activity SS5.2 – 2,3-dihydroxybutanoate ion with hydrogen peroxide – Reaction catalysed by Co2+ O H C H C O C H C O O O O H O H OH C O O C H O O OH2 + + + 3 2 2 4
  • 33. SS CI 11.5 The d block 33 Suggested Mechanism REACTANTS H2O2 + -O2CCH(OH)CH(OH)C02 - Co2+ (pink) INTERMEDIATE containing Co3+ (green) Co2+ reduces H2O2 & gets oxidised to Co3+ PRODUCTS CO2, methanoate, H2O Co2+ (pink) Co3+ oxidises 2,3- hydroxy- butanoate & gets reduced to Co2+ Regenerated Catalyst