Co-Ordinate Compounds

D.A.
V PUBLIC SCHOOL
1
1. Coordination Compounds
• Coordination compounds: contain
coordinate covalent bonds formed
between metal ions with groups of anions
or polar molecules.
– Metal ion – Lewis acid
– Bonded groups – Lewis base
• Complex ion: – ion in which a metal
cation is covalently bound to one or more
molecules or ions
2
• Components of a coordination compound:
– Complex ion (enclosed in square brackets)
– Counter ions
– Some coordination compounds do not contain
a complex ion
– Most of the metals in complexes are transition

metals
3
• Properties of transition metals:
– Have incompletely filled d subshells
– Or react to form ions with incompletely
filled d subshells
• Distinctive colors
• Paramagnetism
• Catalytic activity
• Tendency to form complex ions
– Exhibit variable oxidation state
4
The Transition Metals
Transition metals shown in green box.

5
• Ligands - the molecules or ions that
surround the metal in a complex ion
– Must contain at least one unshared pair of
valence electrons
– > Donor atom – atom in the ligand directly

bonded to the metal atom
6
– > Coordination number – number of donor
atoms surrounding the central atom
• Common coordination numbers: 4 and 6
– > Classifications of ligands:
• Monodentate – 1 donor atom
• Bidentate – 2 donor atoms
• Polydentate - > 2 donor atoms
• Chelating agents – another name for bidentate or
polydentate ligands
– > Overall charge on the complex ion is
determined by:
• Oxidation state of the metal
• Charges on the ligands
7
• Nomenclature of Coordination Compounds:
– The cation is named before the anion, as in

other ionic compounds.
– Within a complex ion, the ligands are named
first, in alphabetical order, and the metal ion is
named last.
– The names of anionic ligands end with the
letter o, whereas neutral ligands are usually
called by the names of the molecules. The
exceptions are H2O (aqua), CO (carbonyl), and
NH3 (ammine).
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– When two or more of the same ligand are
present, use Greek prefixes di-, tri-, tetra-,
penta-, and hexa- to specify their number.
(Prefixes are not included in determining the
alphabetical order.) When the name of the
ligand contains a Greek prefix, a different set
of prefixes are used for the ligand: 2 = bis-, 3
= tris-, 4 = tetrakis-
– The oxidation number of the metal is indicated
in Roman numerals immediately following the
name of the metal.
– If the complex is an anion, its name ends in -
ate. (Roman numeral indicating the oxidation
state of the metal follows the suffix -ate.)
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• Give the correct name for [Cr(H2O)4Cl2]Cl:
-> tetraaquadichlorochromium(III) chloride
10
• Write the formula for:
tris(ethylenediamine)cobalt(III) sulfate
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2. Structure of Coordination
Compounds
• Molecular geometry – plays a significant
role in determining properties
– Structure is related to coordination number
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Common Geometries of Complex Ions
13
• Stereoisomers:
– Ligands arranged differently
– Distinctly different properties
• Type of complex ion stereoisomerism
– Geometric isomers – cannot be
interconverted without breaking chemical
bonds
• Designated as cis and trans
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Cis and Trans Isomers of Diamminedichloroplatinum(II)
15
– Optical isomers – nonsuperimposable mirror
images
• Termed chiral
• Rotate polarized light in different directions
–Rotation to the right – dextrorotatory (d
isomer)
–Rotation to the left – levorotatory (l
isomer)
• Enantiomers – a pair of d and l isomers
• Racemic mixture – equimolar mixture of
two enantiomers
–Net rotation of polarized light is zero
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Nonsuperimposable Mirror Images: A Common Example
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Nonsuperimposable Mirror Images: A Chemical Example
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Optical Isomers of Geometric Isomers
cis trans
rotate in any manner rotate 90o
nonsuperimposable superimposable
chiral achiral
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Operation of a Polarimeter
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21
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3. Bonding in Coordination
Compounds: Crystal Field Theory
• Crystal field theory explains the bonding in
complex ions purely in terms of
electrostatic forces.
– Attraction between the metal ion (atom) and
the ligands
– Repulsion between the lone pairs on the
ligands and the electrons in the d orbitals of
the metal
– In the absence of ligands, the d orbitals are
degenerate
23
– In the presence of ligands, electrons in d
orbitals experience different levels of
repulsion for the ligand lone pairs
– As a result (depending on the geometry)
some d orbitals attain higher energy and
others lower energy
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– In an octahedral complex :
• the electrons in the d orbitals located along
the coordinate axes experience stronger
repulsions and increase in energy
• the electrons in the d orbitals 45o from the
coordinate axes experience weaker
repulsions and decrease in energy
• The energy difference between the two
sets of orbitals is the crystal field splitting
(D)
–Depends on the nature of metal and
ligands
–Determines color and magnetic
properties
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Crystal Field Splitting with a Square Planar Geometry:
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Crystal Field Splitting with a Tetrahedral Geometry:
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Crystal Field Splitting in an Octahedral Complex:
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– Spectroscopic measurements of D allow an
ordering of ligands ability to split the d orbitals
called a spectrochemical series.
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Spectrochemical Series
increasing
weak field ligand strong field ligand
small D large D
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• Magnetic Properties:
– The magnitude of the crystal field splitting

also determines the magnetic properties of a
complex ion
– The electron configuration of the ion is a
balance between
• Energy to promote an electron to a higher
energy d orbital – related to the magnitude
of D
• Stability gained by maximum number of
unpaired spins
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– Small values of D favor maximum number of
unpaired spin
• High spin complexes
• F- is low on spectrochemical series
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– Large values of D are unfavorable for
promotion
• Low spin complexes
• CN- is high on the spectrochemical series
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Orbital Diagrams for Specific d Orbital Configurations
34
• Tetrahedral and square planar complexes:
– Proximity of the ligands to d orbitals changes

with the geometry of the complex
– d electrons in orbitals more closely associated
with the lone pairs of ligand electrons attain
higher energies
– Splitting patterns reflect this repulsion
35
THANK YOU
PRESENTED BY:
ASHWANI SINGH RAJPUT

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D.A.

– Most of the metals in complexes are transition

Transition metals shown in green box.

– > Donor atom – atom in the ligand directly

– The cation is named before the anion, as in

-> tetraaquadichlorochromium(III) chloride

weak field ligand strong field ligand

– The magnitude of the crystal field splitting

– Proximity of the ligands to d orbitals changes

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