2003
DOI: 10.1016/s0032-3861(03)00410-5
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Macrocycles 25. Cyclic poly(ether sulfone)s derived from 4-tert-butylcatechol

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Cited by 40 publications
(44 citation statements)
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“…No linear chains were observed in this mass range. 20 Polycondensations of free or silylated bisphenol-A with 4,4 0 -difluorodiphenyl sulfone gave similar results, 39 but the mass range of the MT mass spectra was limited to 13 kDa. With less reactive 4,4 0 -dichlorodiphenyl sulfone, conversions above 99.9% are difficult to achieve with the consequence that the extent of cyclization is lower.…”
Section: Figure 1 Number Fraction Of Rings (N R ) Versus Conversion (P)mentioning
confidence: 88%
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“…No linear chains were observed in this mass range. 20 Polycondensations of free or silylated bisphenol-A with 4,4 0 -difluorodiphenyl sulfone gave similar results, 39 but the mass range of the MT mass spectra was limited to 13 kDa. With less reactive 4,4 0 -dichlorodiphenyl sulfone, conversions above 99.9% are difficult to achieve with the consequence that the extent of cyclization is lower.…”
Section: Figure 1 Number Fraction Of Rings (N R ) Versus Conversion (P)mentioning
confidence: 88%
“…Unfavorable cases MT mass spectra of virgin reaction products may cover the mass range up to 20 kDa. [20][21][22] However, a polycondensate with a M n of 10-25 kDa, as it is typical for several technical products, contains a small fraction of chains having masses above 50 kDa, which escape from any mass-spectroscopy identification at this time.…”
Section: Figure 1 Number Fraction Of Rings (N R ) Versus Conversion (P)mentioning
confidence: 99%
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