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Hard and Soft Acid and Bases

Lewis Acids & Bases


A base is an electron-pair donor, and an acid is an electron-pair acceptor. The
two combine to form an adduct.
A + :B  A-B
In complexes metals are electron acceptors hence they are acids and Ligands
give lone pair of electrons and are bases. Metals were divided into two
categories

Class A/Type I Class B/Type II


1.Alkali and alkaline earths Transition metals lower OS
2. TM in higher OS Large size
3. Small size Less electropositive
4. Highly electropositive
Hard and Soft Acids
R.G. Pearson (1963) categorized acids and bases as either hard or soft (using Kf
values).

Hard acids
1. Alkali and alkaline earths

2. TM in higher OS

3. Highly electropositive and very few electrons

4. They are not very polarisable and prefer less polarisable ligands.

5. Prefer complexes with ligands having donor atoms like N, O, F

6. high charge density

7. Their d orbitals are often unavailable to engage in π bonding.

8. Hard Acids prefer to bond with Hard Bases


Hard and Soft Acids
Hard Bases
1. Ligands having highly electronegative donor atoms – F, O, N
2. They prefer complexes with hard acids.
3. Less polarisable
4. Small size
5. Strength of hard bases –
F>Cl> Br >O > S> Se>N> P>

Soft Bases
1. Donor atom is less electronegative – P,As,
2. Large size
3. High polarisability
4. They prefer complexes with soft acids
Acids
Hard Acids Borderline Soft Acids
H+, Li+, Na+, K+ BBr3,B(CH3)3 Cu+,Ag+, Au+,

Be2+, Mg2+, Ca2+ Cd2+,Hg22+,

BF3, BCl3, B(OR)3 BH3,Tl+, Tl(CH3)3 Hg2+, Pd2+,Pt2+,

Al3+, AlCl3,AlH3 Pt4+


Cr3+,Mn2+, Fe3+, Co3+ Fe2+,Co2+,Ni2+
Cu2+,Zn2+,Rh3+
Ir3+, Ru3+, Os2+
Bases
Hard Bases Borderline Soft Bases
F-, Cl- Br- H-, I-
H2O, OH-,O2- NO2-, N3- , N2 H2S, HS-, S2-
ROH, RO-, R2O, CH3CO2- SO32- RSH, RS-, R2S
NO3-, ClO4- SCN-, CN-, CO
CO32-,SO42-, PO43- S2O32-
NH3, RNH2 C6H5NH2 R3P, C6H6
HSAB principle

•Hard Acids prefer to bond with Hard Bases


•Soft Acids prefer to bond with Soft Bases.
•HA and HB are not polarisable so the bond is mostly ionic.
•SA and SB is highly polarisable so the bond is covalent.
Applications of Hard/Soft Theory
1. Stability of a complex –
A complex would be more stable if metal and ligand, both are hard or soft.

eg – 1. AgI2- is stable but AgF2- is not.

Ag+ + 2I-  AgI2-

SA SB Stable complex

Ag+ + 2F-  AgF2-

SA HB Unstable

2. [CoF6] 3- is more stable than [CoI6] 3-

HA-HB HA-SB
2. Feasibility of a reaction

A reaction is favourable if the product follows HSAB rule, like combinations.


Eg.
LiI + CsF  LiF + CsI
HA-SB SA-HB HA-HB SA-SB

CaS + H 2O  CaO + H 2S
HA-SB HB HA-HB SB

3. The Qual Scheme, a series of chemical reactions used to separate


and identify the presence of dozens of metal ions, is based largely on the
hard and soft properties of the metal ions.
The softer metals are precipitated out as chlorides or sulfides,
with the harder ions formed as carbonates.
4.Thiocyanate, an ambidentate ligand:

SCN- vs. NCS- Thiocyanate (SCN-) is a particularly interesting ligand. It is


ambidentate, and can bind to metal ions either through the S or the N.
Obviously, it prefers to bind to soft metal ions through the S, and to hard
metal ions through the N. This can be seen in the structures of [Au(SCN)2]-
and [Fe(NCS)6]3- in the Figure below:
Thiocyanate
Complexes showing
a) N-bonding in the
[Fe(NCS)6]3-
complex with the hard
Fe(III) ion, and

b) S-bonding in the
[Au(SCN)2]- complex
(CSD: AREKOX) with
the soft Au(I) ion
5. Evidence in Nature
The chalcophile elements are typically found as sulfides or bonded
to Se2- or Te2-. They include: Cd2+, Pb2+, Sb3+, and Bi3+. These are soft Lewis
acids.
6.
Hard-soft considerations allow us to make reasonable predictions

Hard acids tend to react better with hard bases and soft acids with soft
bases, in order to produce hard-hard or soft-soft combinations

In general, hard-hard combinations are energetically


more favorable than soft-soft

But there is more to it…

An acid or a base may be hard or soft


and at the same time it may be strong or weak

Both characteristics must always be taken into account

e.g. If two bases equally soft compete for the same acid,
the one with greater basicity will be preferred
but if they are not equally soft, the preference may be inverted

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