Chapter 1--Stanley Organometallics

Submitted by George Stanley / Louisiana State University on Fri, 06/10/2016 - 14:45
Description

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.


Ligand effects in titration calorimetry from the Angelici lab

Submitted by Chip Nataro / Lafayette College on Mon, 05/23/2016 - 21:08
Description

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.

Mix and Match Ligand Group Orbitals and Metal Orbitals

Submitted by samuelson / Indian Institute of Science on Thu, 03/31/2016 - 00:34
Description

Students are often presented with the finished MO correlation diagrams of molecules like bis benzene chromium or ferrocene in classes and in organometallic chemistry text books. This activity helps them match the ligand group orbitals of the two benzene rings with the metal valence orbitals. Their understanding and appreciation of such diagrams is significantly enhanced when they find out how only some matches have the appropriate symmetry requirements.

Working with Catalytic Cycles

Submitted by Matt Whited / Carleton College on Mon, 09/28/2015 - 14:05
Description

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.

Iron Cross-Coupling Catalysis

Submitted by Laurel Goj Habgood / Rollins College on Wed, 09/16/2015 - 13:08
Description

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).

Kinetics of electrocatalytic reduction of carbon dioxide by Mn catalysts containing bulky bipyridine ligands

Submitted by Kathleen Field / WGU on Thu, 07/02/2015 - 17:23
Description

This question set has students examine the kinetics of the electrocatalytic reduction of CO2 to CO described in Sampson, D.L.; Nguygen, D., Grice, K.A.; Moore, C.E.; Rheingold, A.L.; Kubiak, C.P. Manganese Catalysts with Bulky Bipyridine Ligands for the Electrocatalytic Reduction of Carbon Dioxide:  Eliminating Dimerization and Altering Catalysis.  J. Am. Chem. Soc. 2014, 136, 5460-5471. 

Ir(III) Catalyst Regeneration Using Molecular Oxygen: Addressing Key Challenges that Hinder Alkane Dehydrogenation Catalysis. A Literature Discussion

Submitted by Vanessa / Albion College on Thu, 07/02/2015 - 15:56
Description

This Learning Object involves reading a recent scientific journal article, answering questions relating to the content, and participating in a classroom discussion. The paper under review is “Regeneration of an Iridium (III) Complex Active for Alkane Dehydrogenation Using Molecular Oxygen,” Organometallics, 33, 1337-1340. DOI: /10.1021/om401241e).

Advanced Inorganic Chemistry Course Videos

Submitted by Kathryn Haas / Saint Mary's College, Notre Dame, IN on Wed, 07/01/2015 - 12:02
Description

At this website, you will find a link to the syllabus and all lecture videos for a "flipped" version of an Advanced Inorganic Chemistry Course taught at Saint Mary's College (Notre Dame, IN).  I used Shiver & Atkins for this course, and the format is based off of Dr. Franz's course at Duke.  If anyone is interested in the problem sets, I will be happy to share, although much of the material I used is from VIPEr.  

Synthesis of Aspirin- A Lewis Acid Approach

Submitted by Kathleen Field / WGU on Mon, 06/29/2015 - 21:29
Description

This is the procedure for a Fe(III) catalyzed synthesis of aspirin, an alternative to the traditionally sulfuric acid catalyzed synthesis of aspirin.  The prep compares and contrasts the Bronsted acid catalyzed esterification reaction with a Lewis acid iron (III) catalyzed pathway.  This can be used in different courses at different levels, but is it written for a general/intro level chemistry course.    

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