Organometallics course F 2014
This is a collection of LOs that I used to teach a junior-senior seminar course on organometallics during Fall 2014 at Harvey Mudd College.
This is a collection of LOs that I used to teach a junior-senior seminar course on organometallics during Fall 2014 at Harvey Mudd College.
This set of questions was used to promote discussion within small groups (3 to 4 students) on how changing ligand properties can have dramatic effects on the product distributions in Pd-catalyzed cross coupling reactions. The questions are pretty difficult and not always straightforward, partly because they are derived from the primary literature and thus inherently "messy".
In this activity, students apply knowledge of the trans effect to the synthesis of planar Pt(II) complexes that contain cis-amine/ammine motifs. These complexes are of interest as both potential novel chemotherapeutic Pt(II) complexes and as intermediates for promising chemotherapeutic drugs such as satraplatin. The questions in this LO are based on recent research described in the paper “Improvements in the synthesis and understanding of the iodo-bridged intermediate en route to the Pt(IV) prodrug satraplatin,” by Timothy C. Johnstone and Stephen C.
Over the past several years, I've been doing this in-class exercise shortly after discussing mechanisms of ligand exchange. The exercise expands on the lecture material by having the students think about metal ions, rather than ligands, exchanging from a coordination complex. The students are encouraged to work in groups of 3-5 and actively discuss the material amongst themselves before we go over it as a class. I do not provide the students with the article ahead of time, so that they may come up with their own conclusions, as opposed to simply repeating those of the authors.
The following paper will be given to the students to study at home along with the questions in the attached document. Students will be allowed to discuss their answers in small groups and refine their answers, before the corresct answer is revealed.
The students will not need to see the actual spectra that are in the SI to be able to address the given questions, the spectra can be projected to the class when the answers of the student groups are discussed
Origins of Enantioselectivity during Allylic Substitution Reactions Catalyzed by Metallacyclic Iridium Complexes.
The students will write a paper in which they analyze the Vitamin B12 co-enzyme from biological, chemical and biochemical perspectives, and will use the guided questions to help show the relevance of an organometallic chemistry experiment to real biochemical systems. This activity is based on a synthetic lab experiment that students would have performed on transition metal-carbon bonds in biology and chemistry (The lab experiment was adapted from third edition of “Inorganic Experiments” by Derek Woollins).
This learning objective focuses on the enzyme aconitase. The iron-sulfur cluster is used to regulate iron in the cell and isomerize citrate for energy – two very different mechanisms. The activity consists of an introduction to the enzyme and a student discussion on the mechanism of the isomerization of citrate to isocitrate; starting in a small group setting followed by a class debriefing.
This set of slides is adapted from a presentation given at the ACS National Meeting in New Orleans Spring 2013 in the symposium "Undergraduate Research at the Frontiers of Inorganic Chemistry" organized by members of the VIPEr leadership council. The slides are from the introduction to the presentation that takes the audience through how catalytic cycles are depicted and then to the concept of concurrent tandem catalysis (CTC). At the end, there is a slide with references that gives an example of how CTC can be applied to aryl halide substrates to form new C-C and C-H bonds.