A greener tetraphenylporphyrin synthesis and metallation: an undergraduate teaching experiment
Summary
In this experiment, 5,10,15,20-tetraphenyl-21H,23H-porphyrin (H2TPP) is synthesized on the microscale using an optimized procedure with a research-grade microwave apparatus (CEM Discover). This experiment can also be extended to the para-substituted phenyl derivatives.
Metalloporphyrins, with an array of metals, can then be synthesized using greener routes including mechanochemical methods (with a Mixer Mill), microwave, or reflux in conjunction with the synthesized porphyrin ligand and a metal salt, such as a zinc or copper acetate. The ligand and products are analyzed using UV-Vis spectroscopy the results of which can be related to electronic structure.
This experiment was developed with students Matthew A. Nitka, Katarina E. Zerbee, and Julianne M. Dee.
Metalloporphyrins, with an array of metals, can then be synthesized using greener routes including mechanochemical methods (with a Mixer Mill), microwave, or reflux in conjunction with the synthesized porphyrin ligand and a metal salt, such as a zinc or copper acetate. The ligand and products are analyzed using UV-Vis spectroscopy the results of which can be related to electronic structure.
This experiment was developed with students Matthew A. Nitka, Katarina E. Zerbee, and Julianne M. Dee.
Keywords
Safety Precautions, Hazards, and Risk Assessment
Propionic acid is corrosive. Metal salts are inherently toxic. Ethanol is highly flammable.
Other notes/information
Iterations of this experiment have been run at both the University of Toronto and Saint Francis University.
Link to external
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