Employing 2D NMR and NOE to assign protons in an organometallic complex

Submitted by Sherzod / Northwestern University on Thu, 07/17/2014 - 20:58
Description

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 relevance of Transition Metal-Carbon Bonds in Biology and Chemistry

Submitted by Mwalimu / Russell Sage College on Tue, 07/15/2014 - 12:45
Description

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).

The Aconitase Enzyme Mechanism

Submitted by Laurel Goj Habgood / Rollins College on Mon, 07/14/2014 - 16:51
Description

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.  

Five Slides About Concurrent Tandem Catalysis

Submitted by Shirley Lin / United States Naval Academy on Thu, 07/03/2014 - 12:54
Description

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.

Protein Electrochemistry 3rd Bioinorganic Workshop

Submitted by Sheila Smith / University of Michigan- Dearborn on Tue, 06/10/2014 - 15:17
Description

This is a 90 minute talk by Fraser Armstrong of Oxford University (http://armstrong.chem.ox.ac.uk) explaining the electrochemistry of proteins immobilized on surfaces.  The talk was presented at the 3rd Bioinorganic Workshop in 2014 at Pennsylvania State University.  The talk contains an excellent basic tutorial on simple electron transfer on immobilized substrates using simple iron sulfur proteins as the primary example.

Student choice literature-based take home exam question

Submitted by Hilary Eppley / DePauw University on Fri, 01/24/2014 - 15:27
Description

During my junior/senior level inorganic course, we did several guided literature discussions over the course of the semester where the students read papers and answered a series of questions based on them (some from this site!).  As part of my take home final exam, I gave the students an open choice literature analysis question where they had the chance to integrate topics from the semester into their interpretation of a recent paper of their own choice from Inorganic Chemistry, this time with limited guidance.

Synthesis and Migratory-Insertion Reactivity of CpMo(CO)3(CH3): Small-Scale Organometallic Preparations Utilizing Modern Glove-Box Techniques

Submitted by Matt Whited / Carleton College on Mon, 08/26/2013 - 14:22
Description

This laboratory experiment spans three weeks and introduces advanced undergraduates to modern small-scale synthesis techniques involving an inert-atmosphere glove box.  The robust syntheses transform [CpMo(CO3]2 into the methylated CpMo(CO)3(CH3) and examine the phosphine-induced migratory insertion to form various Cp-supported Mo(II) acetyl complexes.  At each step in the synthesis, a combination of IR and multinuclear (1H, 13C, and 31P) NMR spectroscopies allow students to assess the purity of their products and

Literature summary through student presentation - free choice of topic.

Submitted by Cameron Gren / University of North Alabama on Wed, 06/26/2013 - 07:59
Description

(1) Student choses and reads a journal article of his/her choice that is related to a topic we have discussed during the semester. (i.e. atomic structure, MO theory, group theory, solid state structure, band theory, coordination chemistry, organometallics, catalysis). Suggested journals include, but are not limited to JACS, Inorg. Chem., Organometallics, Angew. Chem., JOMC, Chem. Comm.)

(2) Student answers the following questions regarding their chosen article:

    (a) Describe, in 1 or 2 sentences the goal of this work. 

A Visual Isotope Effect (a YouTube video)

Submitted by Dan O'Leary / Pomona College on Wed, 04/24/2013 - 17:46
Description

We have prepared a YouTube video demonstrating a visually accessible kinetic isotope effect in the Cr(VI) oxidation process, a reaction commonly encountered in introductory organic chemistry. The demo provides students with an opportunity to see an isotope effect and then understand how it can be used to provide mechanistic evidence for the identification of a rate-determining reaction step.

Online Courses Directory

Submitted by Adam Johnson / Harvey Mudd College on Mon, 04/01/2013 - 07:41
Description

This website is a free and comprehensive resource that is a collection of open college courses that spans videos, audio lectures, and notes given by professors at a variety of universities. The website is designed to be friendly and designed to be easily accessed on any mobile device.

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