2007
DOI: 10.1134/s0965545x07080056
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Study of isocyanate group opening initiated by potassium polyoxyethylene glycolate

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Cited by 6 publications
(4 citation statements)
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“…[60] Potassium polyoxyethylene glycolates (PEGÀ K, 37) catalyzed linear polymerization of phenyl isocyanate via an anionic pathway at 30 °C in carbon tetrachloride while formation of isocyanurate from back-biting of isocyanate polymer was only observed with a very low rate constant. [61] Alkali metal cyanates (MOCN, M=Li, Na, K, 38) reacted with organic isocyanates and provided the metal isocyanuric acid salts in dipolar aprotic solvents, during which the isocyanurate was formed as a side product. [62] Alkyl isocyanates formed more isocyanurate (> 50 %) than aryl isocyanates (< 50 %), and the formation of isocyanurate increased with higher isocyanate concentration as well as addition of electrolyte.…”
Section: Lewis Basic Catalystsmentioning
confidence: 99%
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“…[60] Potassium polyoxyethylene glycolates (PEGÀ K, 37) catalyzed linear polymerization of phenyl isocyanate via an anionic pathway at 30 °C in carbon tetrachloride while formation of isocyanurate from back-biting of isocyanate polymer was only observed with a very low rate constant. [61] Alkali metal cyanates (MOCN, M=Li, Na, K, 38) reacted with organic isocyanates and provided the metal isocyanuric acid salts in dipolar aprotic solvents, during which the isocyanurate was formed as a side product. [62] Alkyl isocyanates formed more isocyanurate (> 50 %) than aryl isocyanates (< 50 %), and the formation of isocyanurate increased with higher isocyanate concentration as well as addition of electrolyte.…”
Section: Lewis Basic Catalystsmentioning
confidence: 99%
“…Certain acyl aminimides with hydroxyl groups ( 36 ) are active cyclotrimerization catalysts; primary hydroxy groups are more active than secondary hydroxy groups [60] . Potassium polyoxyethylene glycolates (PEG−K, 37 ) catalyzed linear polymerization of phenyl isocyanate via an anionic pathway at 30 °C in carbon tetrachloride while formation of isocyanurate from back‐biting of isocyanate polymer was only observed with a very low rate constant [61] . Alkali metal cyanates (MOCN, M=Li, Na, K, 38 ) reacted with organic isocyanates and provided the metal isocyanuric acid salts in dipolar aprotic solvents, during which the isocyanurate was formed as a side product [62] .…”
Section: Catalysts Operating Via Lewis Basic Cyclotrimerization Mecha...mentioning
confidence: 99%
“…In [12,13] it was established that the open chain analogs of crown ethers, which are block copolymers of ethylene oxide and propylene oxide containing terminal and potassium alcoholate groups, are effective initiators of opening the isocyanate groups along the thermodynamically more stable carbonyl group. It was assumed that the capture of the metal cation by polyester fragment acting as a linear podand promotes the preferential localization of the negative charge on the oxygen atom of the growing chain in anionic polymerization.…”
Section: Fundamentals Of Synthesis Of Mesoporous Polymers Based On Armentioning
confidence: 99%
“…[14][15][16] It was assumed [15,16] that the capture of a metal cation by a polyether fragment, performing the role of a linear podand, promoted the preferred localization of a negative charge on an oxygen atom of the growing chain during the anionic polymerization ( Figure 1). …”
Section: Introductionmentioning
confidence: 99%