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.
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.
In this literature discussion, students are asked to read an article describing a type of dual catalytic system in which the synergistic combination of photoredox catalysis and nickel catalysis provides a general method that would exploit naturally abundant, inexpensive organic molecules as coupling partners. This paper addresses several green chemistry principles and serves as a great literature example for teaching organometallic chemistry or green chemistry course.
Examples taken from the literature for the six palladium-catalyzed coupling reactions used in organic chemistry.
In the 2013 Inorganic Curriculum Survey, respondents were asked about the resources they used when they teach inorganic chemistry. About 20% of respondents selected "other" and provided information about these resources. A number of people mentioned specific websites. This collection consists of the websites submitted in the survey.
It is the classic game of telephone (or whatever local varient name you might use). Put a bunch of people in a line. Start by whispering something to the first person and then have them whisper it to the next. This process continues until the last person states out loud what they heard. Usually the starting and ending statements are quite different. When students are reading a paper, it is fairly likely that they feel anything the paper they are reading says about a reference is correct.
This in-class group activity provides several examples of varying difficulty for students to assign MLXZ classifications and electron counts to organometallic complexes. Though some of the problems are straightforward, some are really ambiguous, and the intent is for student groups to grapple with the issues raised by each one and present their findings to the class to spark further discussion.
The slides provide review questions for a senior-level treatment of the spectroscopy and reactivity of metal carbonyl complexes. These are intended to be dispersed through one to three class periods.
The first slide is a review of electron counting and the 18-electron rule.
The second slide quizzes the students on the relationship between the electron-density of the metal center and the strength of the C-O bonds in the carbonyl ligands. It is intended to be given after a discussion of how IR can be used to assess the strength of M-C and C-O bonds in the compounds.
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.