1997
DOI: 10.1016/s0040-4039(97)00031-2
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Encapsulation of N,N′,N″-tricyclohexylguanidine in hydrophobic zeolite Y: Synthesis and catalytic activity

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Cited by 31 publications
(9 citation statements)
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“…The encapsulated guanidine showed a good catalytic activity in the addition reaction of benzaldehyde to acetone 71 . However, its activity in the transesterification of vegetable oils is low (14% conversion after 5 h 72 ), as the diffusion of the triglycerides through the channels of the Y zeolite is slow due to steric hindrance.…”
Section: Heterogeneously Catalyzed Processesmentioning
confidence: 99%
“…The encapsulated guanidine showed a good catalytic activity in the addition reaction of benzaldehyde to acetone 71 . However, its activity in the transesterification of vegetable oils is low (14% conversion after 5 h 72 ), as the diffusion of the triglycerides through the channels of the Y zeolite is slow due to steric hindrance.…”
Section: Heterogeneously Catalyzed Processesmentioning
confidence: 99%
“…Its alkylated molecules, alkylguanidines, are strong non-ionic organic bases with base strengths that are comparable to sodium hydroxide and the capability to catalyze liquid phase organic reactions such as methylation of phenol [109], Michael addition [110], alkylation of carboxylic acids [111] and transesterification [112][113][114][115][116][117]. Schuchardt and colleagues published several studies related to the application of alkylguanidine for the transesterification of triglyceride [112,113,116].…”
Section: Organic Solid Basesmentioning
confidence: 99%
“…The activity was slightly less than that of homogeneous system due to the hydrophobicity of the polymer support and the decreased symmetry of the alkylguanidinium cations, but the real issue was the leaching of active guanidine via nucleophilic attack of methoxide ion on the benzylic CH 2 group linking between the guanidine cation and polystyrene chain. The next strategies of heterogenizing alkylguanidine were encapsulation in the supercages of zeolite Y [114,116], entrapment in SiO 2 sol-gel matrices [116] and anchoring onto MCM-41 [116]. For the methanolysis of soybean oil, the FAME yield by these catalysts approached that of homogeneous counterparts after prolonged reaction time.…”
Section: Organic Solid Basesmentioning
confidence: 99%
“…4), afforded an active catalyst for Knoevenagel condensations, Michael additions, and Robinson annulations [27]. In an alternative approach a bulky guanidine, N,N',N"-tricyclohexylguanidine was encapsulated in the super cages of hydrophobic zeolite Y to give a ship-in-a-bottle guanidine that catalyzed the aldol reaction of acetone with benzaldehyde, affording 4-phenyl-4-hydroxybutan-2-one [28]. …”
Section: Catalysis With Solid Acids and Basesmentioning
confidence: 99%