Coordination Compounds or complex:

8.1 Double salt or lattice salts
8.2 Coordination or complex salts
8.3 Structure and terminology
8.4 Nomenclature of complex compounds
8.5 Type of ligands
8.5 Special ligands
8.6  Bonding  in complexes:
8.6.1(A) Werner's theory of coordination complexes:

8.6.1(B) Werner’s Theory and Isomerism:

8.6.1(C) Examples Based on Postulates of Werner’s Theory:

8.6.2 Sidwick theory and EAN rule

8.6.3 Valence bond theory
8.6.4 Spectrochemical series

8.6.5 Crystal field theory:

8.6.5 (A) Crystal field splitting in octahedral complexes:

8.6.5 (B) Crystal field splitting in tetrahedral complexes:

8.6.5 (C)Crystal field splitting in square planar complexes:
8.6.5 (D) Crystal field stabilisation energy (CFSE)

8.8.1 Synergic bonding:
8.9 .1 Organometallic compounds

8.10.1 Concept of colour in metal complexes :

Related Question:

(1) Although both [Mn(H2O)6]2+ and [FeF6]3- have a d5 configuration and high-spin complexes. But the dilute solutions of Mn2+ and Fe +3 complexes are therefore colorless. Why?

(2) Which of the Complex of the following pairs has the highest value of CFSE?

(3) Colour of Complexes due to charge transfer:

(4) Why violet colour of [Ti(H2O)6]Cl3 disapear (colourless) on heating heating ? 

(5) Why [Ni(CN)4]-2 is colourless while [Ni(H2O)4]-2 although both have +2 oxidation state and 3d*8 configuration ?

(6) Why [FeF6]3– is colourless whereas [CoF6]3– is coloured ?

(7) Why Fe(CO)5 is colourless while Fe(bipy)(CO)3 is intensely purple in colour ?

(8) Why all the tetrahedral Complexes are high spin Complexes ?

(9) Why transition metals and their compounds are act as catalyst?

(10) Why all the tetrahedral Complexes are high spin Complexes ?