1988
DOI: 10.1016/s0022-1139(00)85056-3
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New fluorosulfonyl-containing monomers/polymers

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Cited by 21 publications
(7 citation statements)
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“…In all cases these assignments are in excellent agreement with literature values(19,20,22). NMR SPECTRA The nmr chemical shifts and coupling constants for the monojbis ,8-sultones and all of their derivatives are shown in Tables VIII through XI and the spectra are reproduced in the appendix.…”
supporting
confidence: 90%
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“…In all cases these assignments are in excellent agreement with literature values(19,20,22). NMR SPECTRA The nmr chemical shifts and coupling constants for the monojbis ,8-sultones and all of their derivatives are shown in Tables VIII through XI and the spectra are reproduced in the appendix.…”
supporting
confidence: 90%
“…In the silver salt, FS02CF 2 C(O)OAg, the carbonyl frequency is found at 1708 cm-1; while in CF3COOAg, this stretching frequency is located at 1720 cm-1 ( 60) .In all sulfonyl fluoride esters, as well as the silver salt, the asymmetric and symmetric S02 stretching frequencies are assigned to the 1427-1469 cm-1 region and 1209-1259 cm-1 region, respectively. The above assignment for the S02 group agrees closely with that found for other fluorosulfuryl derivatives(19,20,22). The intense S-F absorption band is located, as expected, near the 800 cm-1 region(19,20,22).…”
supporting
confidence: 89%
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“…The J SF5-CH cis coupling values are near 0 or absent for SF 5 CH¼CH 2 [17], SF 5 CBr¼ CHCl [19], SF 5 CH¼CHCl [18], SF 5 CH¼CHOCH 3 [18], SF 5 CBr¼CHBr [20], SF 5 CCl¼CH 2 [21] and SF 5 CBr¼ CHCl [16]. Also of interest is the J SF5-CH trans interaction; for SF 5 CH¼CH 2 [17], SF 5 CH¼CHOCH 3 [18], SF 5 CBr¼ CHBr [20], and SF 5 CCl¼CH 2 [21], and trans-SF 5 CBr¼CHCl [19] the coupling values are 2.3, 3, 3.0, 3.3 and 2.2 Hz, respectively. It is clear from our data that all new compounds (1-3) have SF 5 CH¼ arrangement based on the values for the geminal coupling.…”
Section: Resultsmentioning
confidence: 96%