Answer: Dr. Blom: The picoSpin has been integrated into the physical chemistry and organic chemistry curriculum thus far. In organic chemistry, students perform multi-step syntheses as individual investigations. They select procedures from various sources, including the Journal of Chemical Education, and tailor them to fit the available equipment and reagents available within the laboratory. They use various methods, including NMR spectroscopy, to characterize products along the steps within the synthesis. Projects this year included synthesis of fragrant esters, methone, phenacetin and others. The picoSpin was used extensively by students in this course to confirm successful production of the desired substances.
In physical chemistry, students have used the picoSpin in multiple laboratories. In one laboratory they are given unknowns and are asked to characterize them spectroscopically using the various methods available in the lab including NMR and FTIR. Students then interpret their spectra to determine the structure of their unknown. Another laboratory has students looking for evidence of hydrogen bonding. They are allowed to use any method desired (UV/Vis, FTIR, NMR, GC, HPLC) that they think will help them find evidence of hydrogen bonding. One particular project where the picoSpin was useful was the keto-enol tautomerization of acetylacetone. The student was able to definitively show the difference in the two tautomers in different solvents and the intramolecular hydrogen bond present in the enol form was clearly observed.