We have shown that some phenylethynylsilicon compounds are good cure crosslinkersof heat-curable silicone rubber(HCSR). In this paper the effects of 1, 1, 3, 3-tetramethyl-1, 3-diphenylethynyldisiloxane (TMDPDS) as a ...We have shown that some phenylethynylsilicon compounds are good cure crosslinkersof heat-curable silicone rubber(HCSR). In this paper the effects of 1, 1, 3, 3-tetramethyl-1, 3-diphenylethynyldisiloxane (TMDPDS) as a crosslinker on HCSR were studied. Thevulcanizates with fine mechanical properties could be obtained with suitable amounts ofTMDPDS. Sol fractions, and crosslinking density of vulcanizates and vulcanizationretardation effect of TMDPDS on hydrosilation curing silicone rubber were also discussed.展开更多
Vapor-liquid equilibrium data of hexamethyl disiloxane+vinyl acetate system at 101.3kPa were measured by using double circulating vapor-liquid equilibrium still.The thermodynamic consistency of the VLE data was examin...Vapor-liquid equilibrium data of hexamethyl disiloxane+vinyl acetate system at 101.3kPa were measured by using double circulating vapor-liquid equilibrium still.The thermodynamic consistency of the VLE data was examined by Herrington method.Experimental data was correlated by non-random two-liquid(NRTL),Wilson and universal quasichemical(UNIQUAC)parameter models.All the models satisfactorily correlated with the VLE data.The result showed that the NRTL model was the most suitable one to represent experimental data satisfactorily.The system had a minimum temperature azeotrope at 345.71 K and the mole azeotropic composition was 0.0541.展开更多
MQ silicone resins were prepared through hydrolytic condensation of ethyl polysilicate or tetraethoxysilane and hexamethyl disiloxane. The unit ratio of the MQ resins was determined by Si-29-NMR. The relationship of t...MQ silicone resins were prepared through hydrolytic condensation of ethyl polysilicate or tetraethoxysilane and hexamethyl disiloxane. The unit ratio of the MQ resins was determined by Si-29-NMR. The relationship of the unit ratio of the product resins with that in the feed was studied. When the reaction was catalyzed by aqueous hydrochloric acid, and the unit ratio of M to Q in the feed was more than 1, the unit ratio of the product was usually lower than that of the feed. The MQ silicon with an unit ratio of M/Q > 2 could not be obtained. However, if the reaction was catalyzed by concentrated sulfuric acid and the reverse hydrolysis process was employed, MQ silicone resin with very high M/Q ratio was successfully prepared.展开更多
A series of Si-containing polyester-polyether multiblock copolymers were synthesizedby transesterification and melt copolycondensation of organosilicon monomers [1, 1, 3, 3-tetramethyl-1, 3-bis （p-carbomethoxyphenyl...A series of Si-containing polyester-polyether multiblock copolymers were synthesizedby transesterification and melt copolycondensation of organosilicon monomers [1, 1, 3, 3-tetramethyl-1, 3-bis （p-carbomethoxyphenyl） disiloxane] （I ） or dimethyl bis （p-carbometh-oxyphenyl） silane] （II） and dimethyl terephthalate （DMT）, with 1, 4-butanediol, poly-tetramethylene glycol （PTMG） respectively. The organosilicon monomers were preparedby Grinard reaction, oxidation and esterification. The structures of the above monomers（I）, （II） and the copolymers were characterized by MS anal. and;H-NMR.展开更多
Developing method for strong Si–F σ bond activation is a very important tool in organosilicon transformation chemistry, only few examples of Si–F bond activation are precedent in the literature. Herein, we develope...Developing method for strong Si–F σ bond activation is a very important tool in organosilicon transformation chemistry, only few examples of Si–F bond activation are precedent in the literature. Herein, we developed a new and efficient method to activate strong Si–F bond by transition-metal-free Si–F/Si–H cross coupling reaction catalyzed with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) catalytic system under mild conditions. Various disiloxanes bearing tolerated functional groups were successfully synthesized in moderate to excellent yields from fluorosilanes and hydrosilanes. Moreover, H_(2)O was found to be the oxygen donor in this catalytic system. Density functional theory calculations were performed to verify the mechanism of DBU promoted Si–F/Si–H cross-coupling reactions.展开更多
文摘We have shown that some phenylethynylsilicon compounds are good cure crosslinkersof heat-curable silicone rubber(HCSR). In this paper the effects of 1, 1, 3, 3-tetramethyl-1, 3-diphenylethynyldisiloxane (TMDPDS) as a crosslinker on HCSR were studied. Thevulcanizates with fine mechanical properties could be obtained with suitable amounts ofTMDPDS. Sol fractions, and crosslinking density of vulcanizates and vulcanizationretardation effect of TMDPDS on hydrosilation curing silicone rubber were also discussed.
文摘Vapor-liquid equilibrium data of hexamethyl disiloxane+vinyl acetate system at 101.3kPa were measured by using double circulating vapor-liquid equilibrium still.The thermodynamic consistency of the VLE data was examined by Herrington method.Experimental data was correlated by non-random two-liquid(NRTL),Wilson and universal quasichemical(UNIQUAC)parameter models.All the models satisfactorily correlated with the VLE data.The result showed that the NRTL model was the most suitable one to represent experimental data satisfactorily.The system had a minimum temperature azeotrope at 345.71 K and the mole azeotropic composition was 0.0541.
文摘MQ silicone resins were prepared through hydrolytic condensation of ethyl polysilicate or tetraethoxysilane and hexamethyl disiloxane. The unit ratio of the MQ resins was determined by Si-29-NMR. The relationship of the unit ratio of the product resins with that in the feed was studied. When the reaction was catalyzed by aqueous hydrochloric acid, and the unit ratio of M to Q in the feed was more than 1, the unit ratio of the product was usually lower than that of the feed. The MQ silicon with an unit ratio of M/Q > 2 could not be obtained. However, if the reaction was catalyzed by concentrated sulfuric acid and the reverse hydrolysis process was employed, MQ silicone resin with very high M/Q ratio was successfully prepared.
文摘A series of Si-containing polyester-polyether multiblock copolymers were synthesizedby transesterification and melt copolycondensation of organosilicon monomers [1, 1, 3, 3-tetramethyl-1, 3-bis （p-carbomethoxyphenyl） disiloxane] （I ） or dimethyl bis （p-carbometh-oxyphenyl） silane] （II） and dimethyl terephthalate （DMT）, with 1, 4-butanediol, poly-tetramethylene glycol （PTMG） respectively. The organosilicon monomers were preparedby Grinard reaction, oxidation and esterification. The structures of the above monomers（I）, （II） and the copolymers were characterized by MS anal. and;H-NMR.
基金the support of the Foundation of Department of Education of Guangdong Province(Nos.2021ZDZX2045,2024KTSCX040)the Wuyi University Innovation and Entrepreneurship Project(2023CX07,S202411349118)+1 种基金the National Natural Science Foundation of China(22163007)Guizhou Provincial Key Technology R&D Program(ZZSG[2024]002).
文摘Developing method for strong Si–F σ bond activation is a very important tool in organosilicon transformation chemistry, only few examples of Si–F bond activation are precedent in the literature. Herein, we developed a new and efficient method to activate strong Si–F bond by transition-metal-free Si–F/Si–H cross coupling reaction catalyzed with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) catalytic system under mild conditions. Various disiloxanes bearing tolerated functional groups were successfully synthesized in moderate to excellent yields from fluorosilanes and hydrosilanes. Moreover, H_(2)O was found to be the oxygen donor in this catalytic system. Density functional theory calculations were performed to verify the mechanism of DBU promoted Si–F/Si–H cross-coupling reactions.
