2013
DOI: 10.1016/j.tetlet.2013.07.098
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Interfacial synthesis of bisphenol A tetrachlorocyclotriphosphazene from bisphenol A and hexachlorocyclotriphosphazene

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Cited by 4 publications
(4 citation statements)
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“…[19][20][21] Interestingly, IP has been successfully employed in the preparation of several HCCP-based molecules. Thompson et al 22 achieved selective di-substitution of HCCP with bisphenol A, yielding di(bisphenol A)-tetrachlorocyclotriphosphazene. Chen-Yang et al 23 prepared mono-through hexa-substituted ( phenoxy)cyclotriphosphazenes by interfacial condensation of HCCP with phenol.…”
Section: Introductionmentioning
confidence: 99%
“…[19][20][21] Interestingly, IP has been successfully employed in the preparation of several HCCP-based molecules. Thompson et al 22 achieved selective di-substitution of HCCP with bisphenol A, yielding di(bisphenol A)-tetrachlorocyclotriphosphazene. Chen-Yang et al 23 prepared mono-through hexa-substituted ( phenoxy)cyclotriphosphazenes by interfacial condensation of HCCP with phenol.…”
Section: Introductionmentioning
confidence: 99%
“…30,31 Another chemical shift at around 27 ppm was caused by the different spatial configuration of DOPO. The results from 31 P NMR confirmed that the Cl atom was substituted by the DOPO conjugated structure.…”
Section: Materials Advances Papermentioning
confidence: 99%
“…28,29 Different from the 31 P NMR spectrum of HCCP with only chemical shift at À0.4 ppm, there were two obvious signals at 25.0 ppm and 6.3 ppm in the 31 P NMR spectrum of EHP, which were assigned to the phosphaphenanthrene and cyclotriphosphazene structure, respectively. 30,31 Another chemical shift at around 27 ppm was caused by the different spatial configuration of DOPO. The results from 31 P NMR confirmed that the Cl atom was substituted by the DOPO conjugated structure.…”
Section: Characterization Of Ehpmentioning
confidence: 99%
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