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Module TRANSITION METAL CHEMISTRY

Module code: CH311
Credits: 5
Semester: 2
Department: CHEMISTRY
International: Yes
Overview Overview
 

Introduction to crystal field theory to understand the optical and magnetic properties of d-block transition metal co-ordination complexes. Use of group theory to look at the effects of high symmetry crystal fields on the incomplete d-orbitals. Construction of Orgel diagrams to predict the ground and excited electronic states and by applying Selection rules, predict the absorption transitions of co-ordination complexes.

Organometallic Chemistry: Meaning of Organometallic complexes, electron counting, oxidation state and electronic configuration of organo-transition metal complexes. General overview of the CFT (Crystal Field Theory) and MO (Molecular Orbital) theory applied to organometallic complexes. ¿pi-acceptor and ¿pi-donor ligands. Back bonding.

Ligands: Carbon Monoxide (CO): MO of CO, coordination to a metal centre. Carbonyl complexes, synthesis and applications. Carbenes: coordination to a metal centre. Fischer and Schrock carbenes, synthesis and applications. pi-ligands: back bonding and hapticity. Cyclopentadienyl ring.

Ferrocene. Synthesis and reactivity of ferrocene. MO of ferrocene.

Chemistry of the f-Block elements and compounds: Material covered includes: Lanthanoids (lanthanides) - electronic configuration; oxidation states; M3+, M4+ and M2+ ions; the lanthanoid contraction, coordination and organometallic complexes; UV-vis spectra, luminescent and magnetic properties. Actinoids (actinides) - electronic configuration; oxidation states; coordination and organometallic complexes; UV-vis spectra and magnetic properties. The ground state term symbol for f-block metal ions. Trends in the elements, ions or compounds of the f-block, and comparisons with the chemical/physical properties of those of the s- and d-blocks.

Open Learning Outcomes
 
Open Teaching & Learning methods
 
Open Assessment
 
Open Autumn Supplementals/Resits
 
Open Pre-Requisites
 
Open Timetable
 
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