Student Led Point Group Determinations

Submitted by John Lee / University of Tennessee Chattanooga on Tue, 06/18/2013 - 09:43
Description

All chemistry is learned best by "doing," and I believe this is especially true for determining molecular symmetry.  This activity was designed to end a three-part lecture/activity on symmetry and point groups for my advanced inorganic class.  I call this unit on symmetry a lecture/activity series because it was designed to be student-guided learning and requires the students to teach each other how to determine a molecular point group.  I only gave one formal lecture on symmetry and point groups, which was followed by the symmetry scavenger hunt activity LO.  Finally this assignment was do

A DFT Study of Metal Pentacarbonyls

Submitted by Sibrina Collins / College of Arts and Sciences at Lawrence Technological University on Thu, 05/09/2013 - 16:57
Description

Metal carbonyls are the most widely studied organometallic complexes.  This exercise uses Gaussian with the GaussView interface to investigate the role of the metal centers on backbonding to the CO ligand. Density Functional Theory (DFT) methods were used to evaluate two classic metal pentacarbonyls, namely Fe(CO)5 and Ru(CO)5.

 

MO Theory for Organometallic Compounds: Pentalene

Submitted by Zachary Tonzetich / University of Texas at San Antonio on Thu, 04/11/2013 - 16:54
Description

This is an in-class exercise for upper level inorganic students designed to highlight aspects of symmetry, group theory, MO theory, and Hückel theory. The exercise is an expansion of a Problem Set question I give to my Advanced Inorganic Chemistry class. In this activity, students will develop the MO diagram for the π system of the pentalene dianion using the Hückel approach. They will then consider the effect of folding the ring system using a Walsh diagram.

Voices of Inorganic Chemistry

Submitted by Sibrina Collins / College of Arts and Sciences at Lawrence Technological University on Sun, 01/27/2013 - 17:08
Description

This learning object focuses on the new video series, “Voices in Inorganic Chemistry,” established to commemorate the 50th anniversary of the American Chemical Society journal, Inorganic Chemistry. The are currently 12 videos celebrating pioneers in the field of inorganic chemistry.  This activity consists of two components, namely the students watching one interview and writing an essay about their chosen inorganic chemist.

(mu-NO)2[CoCp]2 is not paramagnetic

Submitted by Joanne Stewart / Hope College on Fri, 10/26/2012 - 02:05
Description

In this paper by Andersen and Berg (J. Am. Chem. Soc., 1988, 110 (14), pp 4849–4850) the authors present magnetic measurements that refute the calculated ground state of an organometallic cobalt nitrosyl dimer. Students will learn about two physical techniques for measuring magnetism and will learn how magnetic measurements can be used to indicate paramagnetism versus diamagnetism.

Metal-Ligand Multiple Bonds and Frustrated Lewis Pairs

Submitted by Matt Whited / Carleton College on Wed, 10/10/2012 - 14:40
Description

This is a literature-based activity that focuses on a review I recently published as part of a thematic series on C-H activation.

The review highlights similarities between the newly discovered frustrated Lewis pairs and polarized metal-ligand multiple bonds.  There are many ways to use the review, but the attached set of questions focuses on drawing analogies among seemingly diverse types of reactivity using frontier-molecular-orbital considerations.

Identifying Organometallic Reaction Classes in a Catalytic Cycle

Submitted by Nancy Williams / Scripps College, Pitzer College, Claremont McKenna College on Tue, 08/28/2012 - 19:01
Description

This contains three parts: A "Pre-Read" section for students to read before coming to class, an in-class worksheet to be worked in groups, and instructor keys for the worksheet.

The purpose of this exercise is to familiarize and give practice with identifying major classes of reaction (oxidative addition, etc.) in an organometallic catalytic cycle. After this exercise, students should be able to do the same for a new catalytic cycle provided by the instructor on a homework set or exam.

Alkyne Semihydrogenation with Niobium(II) Imido Complexes: Exploring An Unconventional Hydrogenation Mechanism

Submitted by Matt Whited / Carleton College on Thu, 08/09/2012 - 11:30
Description

This is a literature discussion based on an interesting Bergman/Arnold paper utilizing d2 niobium imido complexes for the semihydrogenation of arylalkynes to Z-alkenes.  The mechanism is quite unusual, and I found it to be an interesting paper to discuss after we had talked about the classical hydrogenation mechanisms (typically observed for late transition metals).  The students should come into the discussion understanding fundamental reaction mechanisms (including σ-bond metathesis), and it's helpful if they are somewhat familiar with mono- and dihydride mech

Exploration of Nitrosyl Complexes

Submitted by Brad Kraft / St. John Fisher College on Mon, 07/30/2012 - 15:33
Description

This in-class activity and the related problem set allows students to discover the linear and bent bonding modes of NO to metals based on VSEPR theory through guided inquiry.  Two examples follow which illustrate how the electrons are counted in NO complexes depending on the coordination mode/formal charge of NO. Students must have had prior practice in counting electrons of complexes to complete the problems.   

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