1990
DOI: 10.1007/bf01033104
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13C NMR chemical shifts of polyisobutylene end groups and related model compounds

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Cited by 20 publications
(7 citation statements)
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“…13 C NMR spectra of samples 1 and 2 are in Figure 8. Here, the pairs of lines at 114.45 ppm (CH 2 ) and 143.8 ppm (quaternary carbon), and at 128.0 ppm (quaternary carbon) and 135.55 ppm (CH) correspond to the terminal structures A and B, respectively 33, 38, 39–41. As was shown in our previous study,33 the pair of weak lines observed in sample 1 at 122.8 ppm (CH) and 133.8 ppm (quaternary carbon) corresponds to terminal structure C. This conclusion was confirmed by other studies 39, 40.…”
Section: Resultssupporting
confidence: 88%
“…13 C NMR spectra of samples 1 and 2 are in Figure 8. Here, the pairs of lines at 114.45 ppm (CH 2 ) and 143.8 ppm (quaternary carbon), and at 128.0 ppm (quaternary carbon) and 135.55 ppm (CH) correspond to the terminal structures A and B, respectively 33, 38, 39–41. As was shown in our previous study,33 the pair of weak lines observed in sample 1 at 122.8 ppm (CH) and 133.8 ppm (quaternary carbon) corresponds to terminal structure C. This conclusion was confirmed by other studies 39, 40.…”
Section: Resultssupporting
confidence: 88%
“…As shown in Figure , resonance signals corresponding to PIB-Cl are not observed from both 1 H and 13 C NMR spectra of the PIB-DPE macromonomer. For example, the 13 C NMR spectrum of PIB-Cl exhibits characteristic resonance signals at δ = 71.9 and 35.6 ppm for the quaternary carbon attached to the terminal chloro group (−CH 2 C (CH 3 ) 2 Cl) and geminal methyl carbons of this quaternary carbon (−CH 2 C( C H 3 ) 2 Cl), respectively .…”
Section: Resultsmentioning
confidence: 99%
“…Thus difunctional tert-chloride-terminated PIB (Sample 1, M n ¼ 6700 g/mol) was nonregiospecifically dehydrochlorinated by passing through a packed bed of basic alumina. 13 C NMR confirmed the formation of a mixture of endo (1) and exo (2) olefins at the chain ends 30 (Fig. 1).…”
Section: Ozonolysis Of Mixed Exoand Endo-olefinsmentioning
confidence: 77%
“…6, inset). 30,34 It has been shown that a small amount of endo olefin is always produced when dehydrochlorination is carried out by the tert-butoxide method. 35 Both the 1 H and 13 C spectra of Sample 2 showed additional resonances in the olefinic region indicating a significant fraction of anomalous chain-end structures, primarily chain ends resulting from a cumyl initiating site that added only one IB unit (single-unit chain).…”
Section: Ozonolysis Of Pure Exo-olefin Pibmentioning
confidence: 99%