Two worksheets are given that walk students though visualizing and understanding solid state structure. The first worksheet focuses on metallic structure by introducing primitive, body-centered, and face-centered packing types in a cubic unit cell. Then, close packing structures are described followed by a discussion of holes in close packed or primitive packed lattices. The second worksheet introduces ionic solid structure types for the common binary salt lattices as well as perovskite and spinel structure types.

This laboratory experiment is a quick and straightforward synthesis of a MoO₂(acac)₂ complex. The ligand set allows for two possible geometric arrangements: cis and trans. Using IR spectroscopy along with group theory analysis of the Mo-O stretching modes, students can determine which isomer they formed in their synthesis. NMR spectroscopy is also employed, and confirms the geometric arrangement due to the inequivalence of the acac methyl groups.

This paper (J. Organomet. Chem. 2022, 965-966, 122317) describes the synthesis and reactivity of four-coordinate iridium compound with a tridentate ligand. This ligand is referred to in the paper as a pincer ligand which are a general class of tridentate ligands that coordinate in a mer- arrangement.

This is a really interesting paper in J. Am. Chem. Soc. (2025, 147, 34641-34646) involving a complex salt in which both the cation and anion are metallocenes. While a majority of the paper is focused on the characterization of two new compounds, it presents some excellent opportunities to practice counting electrons, one of which was a challenge to this author.

This literature discussion is in honor of Dr. Josh Figueroa, recipient of the 2026 F. Albert Cotton Award in Synthetic Inorganic Chemistry. Josh has done some tremendous work with isocyanide ligands and this paper is but a brief glimpse into this field. The complexes of interest contain carbonyl ligands and isocyanide ligands, so there are plenty of opportunities for students to use group theory to predict the number of IR-active vibrations for these ligands.