JCE Online Journal of Chemical Education
 | Subscriptions  | Software Orders  | Support  | Contributors  | Advertisers  | 

JCE Print

JCE Digital Library

JCE Software

Only@JCE Online

About JCE


  Home > JCE Print > Journal of Chemical Education > Issues > 1997  > December  >
In the Laboratory
Investigation of Atropisomerism in ortho-Substituted Tetraphenylporphyrins: An Experimental Module Involving Synthesis, Chromatography, and NMR Spectroscopy
Ruth Freitag Beeston, Shannon E. Stitzel , and Mitchell A. Rhea
Davidson College, Department of Chemistry, P.O. Box 1749, Davidson, NC 28036

Cover
December 1997
Vol. 74 No. 12
p. 1468

Abstract
An experimental module suitable for advanced undergraduates is described. This module begins with the synthesis of tetra(o-tolyl)porphyrin (T(o-Tol)P), which exists as a statistical distribution of atropisomers due to hindered rotation about the porphine-phenyl bonds. The six types of nonequivalent methyl protons in the four atropisomers (4,0; 3,1; cis 2,2; and trans 2,2) give rise to six methyl peaks in the proton NMR spectrum of T(o-Tol)P. Due to slight differences in the migration rates of the four atropisomers, samples of T(o-Tol)P which are enriched and depleted in certain atropisomers can be obtained chromatographically. NMR spectra of these samples are recorded, and an examination of the changes in relative intensities of the six methyl peaks leads to positive peak assignments. The farthest upfield methyl peak is attributed to the 4,0 isomer (in which all four methyl groups are cofacial), which has the fastest migration rate on silica gel. It is shown that as the number of cofacial methyl neighbors for a particular methyl group decreases, the chemical shift of the methyl protons increases. This experiment leads to a greater understanding of chromatography and NMR spectroscopy in addition to introducing students to porphyrin synthesis and the concepts of atropisomerism and statistical distributions.
More Information
*  Citation
Beeston, Ruth Freitag; Stitzel, Shannon E.; Rhea, Mitchell A. J. Chem. Educ. 1997 74 1468.
*  Keywords
Laboratory Instruction, Instrumental Methods, Laboratory Instruction, NMR Spectrometry, Organic Synthesis, and Stereochemistry
*  History
Created:
Last Updated:
July 20, 1999
June 23, 2005
  Home > JCE Print > Journal of Chemical Education > Issues > 1997 > December > Page 1468


Subscriptions

JCE HS CLIC

Our Secondary School editors work hard to distill all the JCE materials to produce a fraction of particular interest to high school teachers. We call it CLIC.


Contributions Welcome
JCE welcomes your submission

Advertisers
In recent years we have worked hard to better match our advertisers with our readers. When shopping for chemistry education materials, visit our advertisers' WWW sites first.

Be An Ambassador
Take JCE along on your outreach missions. Copies of the Journal, guest access to JCE Online, our publications catalog, and more are available for your participants.