Abstract:
:The UV spectra of 29 chlorobiphenyls have been examined. With increasing chloro substitution in which there are less than two chlorine groups ortho to the Ph-Ph bond the lambdamax values for the K band (attributed to the conjugation between the two phenyl rings) are shifted to longer wavelengths and for the more highly substituted chlorobiphenyls there is also a bathochromic shift of the main band (due to the benzenoid skeleton). Introduction of two or more chlorine atoms ortho to the Ph-Ph bond results in a hipsochromic shift of K band and diminished xi value due to steric inhibition of resonance between the two phenyl rings. The sterically hindered chlorobiphenyls and the more highly chlorinated Aroclors also exhibit a series of low-intensity fine-structured absorption maxima between 268-302 nm. The UV spectra of chlor-biphenyls are particularly diagnostic with respect to the degree of substitution at the 2, 2', 6 and 6' positions and can be used in the structural analysis of separated chlorobiphenyls. The data may also aid in correlating the photochemical reactivities.
journal_name
Bull Environ Contam Toxicoljournal_title
Bulletin of environmental contamination and toxicologyauthors
MacNeil JD,Safe S,Hutzinger Odoi
10.1007/BF01686197subject
Has Abstractpub_date
1976-01-01 00:00:00pages
66-77issue
1eissn
0007-4861issn
1432-0800journal_volume
15pub_type
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