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Determination of the structural configuration of cresol–novolak resins by 13C NMR spectroscopy

✍ Scribed by J. A. Carothers; E. Gipstein; W. W. Fleming; T. Tompkins


Publisher
John Wiley and Sons
Year
1982
Tongue
English
Weight
310 KB
Volume
27
Category
Article
ISSN
0021-8995

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✦ Synopsis


Abstract

^13^C NMR spectroscopy was used to investigate the structures of a series of pure isomeric cresylic novolak resins. Chemical shifts were measured and assigned, and end groups were distinguished from the central repeat units of the chains. Based on these measurements, the number average molecular weight of the para‐cresylic oligomer was determined. A comparison of the ^13^C decoupled and coupled spectra of the three isomeric resins indicates that the para isomer has a linear, ordered structure in which the aromatic rings are linked only by ortho–ortho′ methylene‐bridging groups. The structures of the ortho and meta isomers are more complex and contain ortho–ortho′, ortho–para′, and para–para′ methylene bridges.


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