Isomerism in coordination compounds.pptx
Examples of Coordination Compounds
[(NH3)5Cr Cr(NH3)5] Cl5: µ-hydroxo-bis-pentaamine Chromium(III)
[(NH3)4Co Co(NH3)4]4+: µ-amido µ-hydroxo octaminedicobalt(III)
[Zn(OH)4]2-: Tetra hydroxo Zincate(II)
[Co(NO2)3(NH3)3]: Triammine trinitrocobalt(III)
[Co(NH3)6][Cr(C2O4)3]: Hexamminecobalt(III) trioxalatochromate(III)
NH4[Cr(SCN)4(NH3)2]: Ammonium diamine tetrathiocyanato chromate(III)
Isomerism in Coordination Compounds
Isomerism Defined: Compounds with the same formula but different structures (isomers).
Types of Isomerism:
Stereoisomerism
Structural Isomerism:
Geometrical
Optical
Linkage
Ionization
Coordination
Solvate (Hydrate)
Coordination Isomerism: Isomerism from ligand interchange between cation and anion. Example: [Co(NH3)6][Cr(CN)6] vs [Cr(NH3)6][Co(CN)6].
Linkage Isomerism: Ligands with multiple donor atoms can create scenarios like in NO2-.
Ionization Isomerism: Group exchange between the complex and external ions. Example: [Co(NH3)5Br]SO4 vs [Co(NH3)5SO4]Br.
Hydrate Isomerism: Varying amounts of H2O inside vs. outside the coordination sphere. Example: [Cr(H2O)6]Cl3 and its variants.
Geometrical Isomerism: Arrangements can be cis or trans. Example: cis- and trans- Pt(NH3)2Cl2.
Optical Isomers: Non-superimposable mirror images (enantiomers) that are chiral. Significant in pharmaceuticals due to differing effects.
Optical Activity: Dextrorotatory (d-isomer) rotates light right; Levorotatory (l-isomer) left. Racemic mixtures show no optical activity due to equal parts of both isomers.