The biphenyl-monitored effective size of unsaturated functional or fluorinated ortho substituents

• Published in: Organic & biomolecular chemistry Vol. 8; no. 19; pp. 4463 - 4471
• Main Authors: Ruzziconi, Renzo, Spizzichino, Sara, Mazzanti, Andrea, Lunazzi, Lodovico, Schlosser, Manfred
• Format: Journal Article
• Language: English
• Published: CAMBRIDGE Royal Soc Chemistry 07.10.2010
• Subjects: Chemistry; Chemistry, Organic; Physical Sciences; Science & Technology; ENERGY; ETHERS; TORSIONAL BARRIERS; STEREODYNAMICS; MOLECULAR-STRUCTURE; INTERNAL-ROTATION; ELECTRON-DIFFRACTION; CONFORMATIONAL-ANALYSIS; GASEOUS STATE; DERIVATIVES
• ISSN: 1477-0520; 1477-0539
• DOI: 10.1039/c0ob00136h

The size of a series of typical substituents has been probed by dynamic NMR measurements of the barriers to aryl-aryl rotation of the corresponding biphenyls. The resulting B values are meaningful because only mono-ortho substituted compounds were investigated and thus the results are not compromised by the non-additivity of multiple steric effects. On the basis of the chosen model system ethynyl and cyano groups were found to be slightly smaller than a phenyl ring. In contrast, vinyl and, in particular, formyl groups proved to be larger than phenyl. The latter difference is due to the loss of conjugation forces at the planar transition state. alpha-Hydroxyhexafluoroisopropyl is slightly more bulky than tert-butyl. Pentafluorophenyl and trifluoromethoxy exhibit nearly the same effective size as phenyl and methoxy, respectively Trifluoromethyl is somewhat smaller than isopropyl.