Based on the literature reference, this activity allows students to discover inner-sphere and outer-sphere catalytic hydrogenation mechanisms then apply their knowledge to hydroborylation. This is a guided-inquiry in-class activity that students can complete in small groups or individually with instructor support.
The article “Synthesis and Reactivity of Oxorhenium(V) Methyl, Benzyl, and Phenyl Complexes with CO; Implications for a Unique Mechanism for Migratory Insertion,” Robbins, LK; Lilly, CP; Smeltz, JL; Boyle, PD; Ison, EA;, Organometallics 2015, 34, 3152-3158 is an interesting read for students studying reaction mechanisms of organometallic complexes. The reading guide directs students to the sections of the paper that support the question posed in the Discussion Questions document.
This activity guides students into building a Molecular Orbital diagram, which focuses on metal-centered orbitals of mostly d character, for a square pyramidal complex that includes different types of ligands. Students are then asked to "fill" the resulting orbitals with metal d electrons, and examine the stability of the complex.
This literature discussion is designed for upper-level inorganic chemistry students. The article explores the motivations, design, and characterization of novel nickel(II) and nickel(IV) complexes for carbon-heteroatom bond forming reactions. Students can apply and integrate their knowledge of organic chemistry mechanisms, organometallic chemistry, and techniques for characterizing metal-ligand compounds that include NMR and CV.
This literature activity is designed to introduce students to the concept of outer-sphere hydroboration catalytic reactions. It can be used after hydrogenation and hydroboration reactions have been introduced in class (typically covered in organic chemistry). Additionally, this activity allows students to apply their understanding of redox chemistry, acid base chemistry, and physical techniques to characterize products and elucidate reactions mechanisms.
Electron counting exercise motivated by a recent paper (J. Am. Chem.
In this literature discussion, students read an Inorganic Chemistry paper (doi: 10.1021/ic503062w) about diarylamido-based PNZ pincer ligands and their Ni, Pd, and Rh complexes. Specifically, this paper uses IR and E1/2 potentials to demonstrate that the redox events occur not on the metal center but on the pincer ligands.
This is a powerpoint presentation that was developed for and used at the 2016 VIPEr workshop on Organometallic chemistry at the University of Michigan. Organometallic chemistry is a broad field, and we have divided ourselves into different classes based on what we study. For example, the reactivity of the third row metals is often quite different from that of the fourth/fifth rows. Early (high oxidation state with anionic ligands typically) and Late (low oxidation state with neutral ligands typically) metal complexes have different properties and d electron counts.
This activity introduces students to fundamental types of organometallic reactions, and directs them to examine how each of these reactions affects the total electron count for the organometallic complex and the oxidation state of the central metal. Students are then directed to use these reactions to build a sequence of steps for a catalytic cycle.
This in-class worksheet introduces students to the different ways we describe organometallic ligands – bonding, properties, spectroscopy, etc. – using carbon monoxide as an example. It is structured as an inquiry-based activity, where students work together in small groups but check in with the entire class at appropriate intervals. I plan to use this activity with my advanced inorganic students next year.