• Bulletin of the Korean Chemical Society
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• v.34 no.1
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• pp.133-138
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• 2013

An efficient synthesis of phospha-Morita-Baylis-Hillman adducts was carried out in good yields via the Michaelis-Arbuzov reaction of the DABCO salts of MBH bromides. Instead of a DABCO salt, a phosphonium salt could be effectively used for some substrates which showed some problems in the presence of DABCO.

• Elastomers and Composites
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• v.53 no.2
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• pp.86-94
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• 2018

The effect of the NCO index and catalyst type on the thermal stability of poly(urethane-isocyanurate) (PUIR) foams was investigated to identify a method for enhancing the flame resistance of PUIR. PUIR foams were prepared using 4,4-diphenylmethane diisocyanate (MDI) and [(diethylene glycol)adipate]diol, which were synthesized by esterification of adipic acid and diethylene glycol. Dabco K-15, Dabco TMR-30, and Toyocat RX-5 were used as the catalysts for trimerization and gelation. The amount of urea and isocyanurate groups in PUIR was semi-quantitatively determined by normalizing their absorbance with the phenyl absorbance measured by FT-IR. The normalization data showed that Dabco TMR-30 effectively generated isocyanurate groups in PUIR. As a result, Dabco TMR-30 effectively raised the decomposition temperature and increased the 800 K and 900 K residues of the PUIR foam synthesized with an NCO index of 200.

• Bulletin of the Korean Chemical Society
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• v.23 no.6
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• pp.789-791
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• 2002

• Applied Chemistry for Engineering
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• v.8 no.2
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• pp.308-314
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• 1997

The effects of catalyst and blocking reagents(BR) on the blocking reactions of TDI and MDI in the preparation of polyurethane varnishes have been studied. It was found that certain types of catalysts, such as 1,4-diazabicyclo[2.2.2]octane(DABCO) and tetramethyl guanidine(TMG), were necessary to complete the NCO blocking reactions. Blocking rate of TMG was shown much faster than that of DABCO. Reactivity increased with the increase of TMG concentration, at least to the concentration of 1%. In case of DABCO, the 0.25% concentration of catalyst showed the highest reactivity. In order to study the steric effects of BR on the blocking reactions, phenol, p-cresol, m-cresol, o-cresol, 2,4-xylenol were used as blocking reagents. As expected, BR which has less steric hindrance showed higher reactivity. The increase in BR concentration and reaction temperature increased the productivity of polyurethanes in this reaction system.

• Journal of the Korean Chemical Society
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• v.57 no.2
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• pp.252-259
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• 2013

A green and simple method to synthesize of 1,4-diketones via aldol reaction of arylglyoxals and ketones such as 1-(4-methoxyphenyl)-2-propanone, deoxybenzoin and substituted acetophenones in the presence of a catalytic amount of DABCO in water at room temperature has been reported. Corresponding 2-hydroxy-1,4-diones were obtained in moderate to high yields with simple separation of obtained solid from reaction mixture and recrystallization.

• Bulletin of the Korean Chemical Society
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• v.33 no.4
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• pp.1154-1158
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• 2012

A room-temperature ionic liquid (RTIL) derived from 1,4-diazabicyclo[2.2.2]octane (DABCO) consisting of tetrafluoroborate anion, 1-butyl-4-(4-sulfonylbutyl)-1,4-diazoniabicyclo[2.2.2]octane hydrogen sulfate tetrafluoroborate ($[C_4DABCOC_4SO_3H][BF_4][HSO_4]$) was synthesized and catalytically evaluated in the synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes by cyclocondensation reaction of ${\beta}$-naphthol and aryl aldehydes. This novel RTIL with an acidic $SO_3H$ group showed high catalytic activity with good to excellent yields of the desired products in short reaction times. Moreover, the catalyst could be recovered and reused at least three times with only slight reduction in its catalytic activity.

• Journal of the Korean Chemical Society
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• v.49 no.6
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• pp.603-608
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• 2005

• Bulletin of the Korean Chemical Society
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• v.21 no.11
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• pp.1111-1114
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• 2000

The kinetic study of the enaryloxynitriles via the nucleophilic vinylic substitution reaction of various phenol derivatives with 1-chloro-1-phenyl-2,2-dicyanoethene (1) was conducted in the presence of 1,4-diazabicyclo[2,2,2]octane (DABCO). Nucleo philic vinylic substitution of phenol derivatives with electrophilic olefins carrying sluggish leaving group involves a third-order reaction. The reaction was applied to solution polymerization of diphenol derivatives with p-bis(1-chrolo-2,2-dicyanovinyl)benzene (2), which yielded various polyenaryloxynitriles with moderate molecular weight.

• Applied Biological Chemistry
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• v.38 no.3
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• pp.259-262
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• 1995

Oxidative stabilities of fat in DHA(cis-4,7,10,13,16,19-docosahexaenoic acid)-added dry milk and ordinary dry milk during storage were studied by determining thiobarbituric acid values of samples. Two kinds of milk powder samples were purchased in the local supermarket and $2{\pm}0.05\;g$ of samples were transferred into serum bottles, which were stored under the light or under dark The oxidation of fat in DHA-added milk powder was higher than that of fat in ordinary milk powder and the acceleration was more evident in the presence of light Light and unsaturated fats accelerated synergistically oxidation of milk fat Addition of DABCO(diazabicyclooctane), which is an efficient singlet oxygen quencher, significantly decreased the photooxidation of milk fat This result clearly suggested that singlet oxygen oxidation (Type II reaction) was involved in the system. Deceleration of milk fat oxidation by DABCO was higher in the DHA-added milk powder.

• Bulletin of the Korean Chemical Society
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• v.31 no.3
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• pp.742-745
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• 2010