This is a worksheet for students to complete in class to practice nomenclature of coordination compounds. It may alternatively be assigned as homework after a lesson on nomenclature. Includes examples of Ewing-Bassett system as well as Stock system.
Chapter 2 from George Stanley's organometallics course, Lewis Base ligands
this chapter covers halides, oxygen and nitrogen donor ligands
The powerpoint slides contain answers to some of the in-class exercises, so those are behind the "faculty only" wall. I share these with students after the class, but not before.
Everyone is more than welcome to edit the materials to suit their own uses, and I would appreciate being notified of any mistakes that are found.
This is an LO for the collection of organometallics LOs by George Stanley. Adam Johnson is curating the material that was written by George.
For many years, George hosted his organometallics lecture notes, powerpoint slides, and handouts, on his personal website at LSU. He always wanted that material available to the public. Recently, they moved to a CMS and that material is no longer available. Adam is working with George to get the 2016-2017 version of his materials up on VIPEr for everyone to use.
The lecture notes are freely available to all.
chapter 1 of George Stanley's Organometallics course: Introduction, Orbitals, Electron counting
This chapter is an overview of the field, with an emphasis on electron counting
The powerpoint slides contain answers to some of the in-class exercises, so those are behind the "faculty only" wall. I shares these with students after the class, but not before.
everyone is more than welcome to edit the materials to suit their own uses, and I would appreciate being notified of any mistakes that are found.
This literature discussion focuses on a paper from the Angelici lab that examines the heat of protonation of [CpʹIr(PR3)(CO)] compounds. The compounds presented in the paper provide good introductory examples for electron counting in organometallic compounds. The single carbonyl ligand in these compounds provide an excellent probe to monitor the electron richness at the metal center which is impacted by the electron donor ability of the ligands.
Students work in groups to derive the ligand-field diagram for a square-pyramidal vanadium(III) oxo complex using octahedral V(III) as a starting point. The activity helps students to correlate changes in orbital energies as a function of changing ligands and geometry as well as rationalizing why certain geometries can be particularly good (or bad) for particular complexes. The activity also helps students see why oxo complexes of early metals are frequently best described as triple bonds.
I used this as an in class activity but it may work better as a problem set for your class. I had the students read the pertinent chapters of the textbook which go through symmetry and molecular vibrations, including using both stretches and cartesian axes as bases. In class, I divided the students up into four groups. Each group did one of the problems for 30 minutes and during the last 20 minutes of class, they reported out their solution. The students had not seen the Hooke’s law in the textbook so I included it as part of the activity.
In this experiment, students will synthesize and characterize a series of Ru(II) p-cymene piano-stool complexes.
Students work in groups to identify relevant steps and intermediates in 3 catalytic cycles, all the while considering bonding (and electron counting) factors. Following assignment of these steps and intermediate species, the students consider several questions related to catalysis more broadly, particularly the role of each reagent, how to speed up or slow down specific steps, and the importance of regiospecificity in certain steps.
In this experiment, students will synthesize and characterize an iron complex followed by completion of two series of catalytic cross-coupling reactions mimicking the methodology utilized by organometallic chemists to balance catalyst efficacy and substrate scope. Initially the complex Fe(acac)3 [acac = acetylacetone] is prepared. Two sets of catalytic reactions are completed: one comparing different iron catalysts (Fe(acac)3, FeCl2, FeCl3) while the other compares substrates (4-chlorotoluene, 4-chlorobenzonitrile, 4-chlorotrifluorotoluene).