1989
DOI: 10.1016/s0277-5387(00)80328-9
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The synthesis, characterization and reaction of (propargyloxy)chlorocyclotriphosphazenes

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Cited by 7 publications
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“…All 31 P NMR spectra exhibited a clean singlet, which shifted from 20.00 ppm for HCCP to 17.87 and 17.79 ppm for ThioGlyCPZ and GlyCPZ, respectively (Figure S13), indicating that symmetrical products were obtained. 30,31 Moreover, the ESI-HR-MS with the compound's isotopic splitting fully confirmed the formation of the FRs.…”
Section: ■ Results and Discussionmentioning
confidence: 71%
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“…All 31 P NMR spectra exhibited a clean singlet, which shifted from 20.00 ppm for HCCP to 17.87 and 17.79 ppm for ThioGlyCPZ and GlyCPZ, respectively (Figure S13), indicating that symmetrical products were obtained. 30,31 Moreover, the ESI-HR-MS with the compound's isotopic splitting fully confirmed the formation of the FRs.…”
Section: ■ Results and Discussionmentioning
confidence: 71%
“…The intermediate compounds and the main products were examined by a combination of FTIR, 1 H NMR, 13 C NMR, and 31 P NMR spectroscopy; ATR-FTIR; and ESI-HR-MS (Figure S1 to Figure S16). All 31 P NMR spectra exhibited a clean singlet, which shifted from 20.00 ppm for HCCP to 17.87 and 17.79 ppm for ThioGlyCPZ and GlyCPZ, respectively (Figure S13), indicating that symmetrical products were obtained. , Moreover, the ESI-HR-MS with the compound’s isotopic splitting fully confirmed the formation of the FRs.…”
Section: Resultsmentioning
confidence: 85%