氰尿酸三烯丙酯的合成研究进展
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摘要
介绍了氰尿酸三烯丙酯(TAC)的理化性质及其应用领域。综述了TAC国内外的合成研究进展情况,指出了今后的改进方向。
Physicochemical properties and application of triallyl cyanurate were introduced. Research progress situation in synthesis of triallyl cyanurate at home and abroad were summarized and the modification trends were pointed out.
Physicochemical properties and application of triallyl cyanurate were introduced. Research progress situation in synthesis of triallyl cyanurate at home and abroad were summarized and the modification trends were pointed out.
引文
[1]北京化学试剂公司编.化学试剂·精细化学品手册[M].北京:化学工业出版社,2002:1129
[2]Kirk-Othmer.Encyclopedia of Chemical Technology(Fourth Edition Volume 2)[M].John Wiley&Sons,1992:176-179
[3]Bert H Clampitt,Dale E German,Joseph R Galli.Polymerization of Triallyl Cyanurate[J].J.Polymer Sci.,1958,(27):515-522
[4]Balitskaya L G,Khomenkova K K,Laptii S V.Isomerization of Cyanurates in the Presence of Copper[J].Ukr.Khim.Zh.,1974,40(8):881-882(Russ)
[5]Werle Peter,Krimmer Hans-Peter,Schmidt,Manfred,et al.Preparation of Triallyl Isocyanurate:DE102006032167[P].2007-02-22
[6]Weiler Peter,Kerimo Hans Peter,Semite Manfered,et al.Process for Preparation of Triallyl Isocyanurate:CN101125832A[P].2008-02-20
[7]赢创德固赛有限责任公司.制备异氰尿酸三烯丙酯(TAIC)的方法:CN 101490019 A[P].2009-07-22
[8]赢创德固赛有限责任公司.制备异氰尿酸三烯丙酯(TAIC)的方法:CN 101490019 B[P].2012-03-09
[9]张育川.氰尿酸三烯丙酯[J].精细与专用化学品,2001(12):21
[10]赵小平,樊真.过氧化物交联剂和烯丙基系列助交联剂[J].精细与专用化学品,2003,11(17):13-15
[11]James R.Dudley.Insecticidal Compositions:US 2,510,564[P].1950-06-06
[12]James R Dudley.Unsaturated Triazine Esters:US 2,537,816[P].1951-01-09
[13]Hans Gysin,Enrico Knüsli.s-Triazine Plant-growth in Hibitors:US 2,909,421[P].1959-10-20
[14]Yamada,Isao.Triallyl Cyanurate:JP 71 36,633[P].1971-10-27
[15]James R Dudley,Jack T Thurston,Frederic C Schaefer,et al.Cyanuric Acid Derivatives.ⅢAlkoxys-triazines[J].J.Am.Chem.Soc.,1951(73):2986-2990
[16]Robert G.Nelb.Triallyl Cyanurate:US 2631,148[P].1953-03-10
[17]Horst Schulze.Triallyl-and Trimethallyl Cyanurate:Ger:1064071[P].1959-08-27
[18]Horst Schulze.Unsaturated Esters of Cyanuric Acid:Ger.,18104[P].1960-01-19
[19]Khomenkova K K,Balitskaya L G,Zukhawa E I,et al.Triallyl Cyanurate for Transparent Material.[J].Plast.Massy,1970(10):17-18
[20]Gregg Harry D Jr,Lemaster Howard V.Triallyl Cyanurate:US 3644410[P].1972-02-27
[21]Musashino Chemical Research Institute,Ltd..Triallyl Cyanurate:Brit.,1,283,313[P].1972-07-26
[22]Kucharski Mieczyslaw,Mazurkiewicz Witold.Preparation of Triallyl Cyanurate by Condensation of Cyanuric chloride with Allyl Alcohol[J].Chem.Stosow.,1976,20(1):115-123(Pol)
[23]Kucharski,Mieczyslaw;Mazurkiewicz,Witold.Triallyl Cyanurate:Pol.89,571[P].1977-07-30
[24]张亨.三聚氰酸三烯酯的合成[J].塑料助剂,2003(4):16-18
[25]Haefner Volker,Suchsland Helmut,Werle,Peter.Process for Production of Triallyl Cyanurate:WO2008009540[P].2008-01-24
[26]Billy E.Lloyd,Fred L Kelly.Triallyl Isocyanurate:US2,894,950[P].1959-07-14
[27]Kenichi Fukui,Hisao Kitano.Isocyanuric Acid Derivatives:Brit.858,810[P].1961-01-18
[28]Thomas C Frazier,Edwin D Little,Billy E Lloyd.Isocyanurates.I.Condensation Reaction of Cyanuric Acid[J].J.Org.Chem.,1960,(25):1944-1946
[29]Z N Pazenko,T N Lebedeva,L I Chovnik,et al.The Synthesis of Monomers Containing the S-triazine Ring[J].Sintez I Svoistva Monomerov,Akad.Nauk SSSR,Inst.Neftekhim.Sinteza,Sb.Rabot 12-oi[Dvenadtsatoi]Konf.Po Vysokomolekul.Soedin.,1962:287-291
[30]黄勇.三聚氰酸三烯丙酯的生产工艺:CN102491951A[P].2012-06-13
[31]Donald W Kaiser.Aliphatic cyanurates:US 2,682,541[P].1954-06-29
[2]Kirk-Othmer.Encyclopedia of Chemical Technology(Fourth Edition Volume 2)[M].John Wiley&Sons,1992:176-179
[3]Bert H Clampitt,Dale E German,Joseph R Galli.Polymerization of Triallyl Cyanurate[J].J.Polymer Sci.,1958,(27):515-522
[4]Balitskaya L G,Khomenkova K K,Laptii S V.Isomerization of Cyanurates in the Presence of Copper[J].Ukr.Khim.Zh.,1974,40(8):881-882(Russ)
[5]Werle Peter,Krimmer Hans-Peter,Schmidt,Manfred,et al.Preparation of Triallyl Isocyanurate:DE102006032167[P].2007-02-22
[6]Weiler Peter,Kerimo Hans Peter,Semite Manfered,et al.Process for Preparation of Triallyl Isocyanurate:CN101125832A[P].2008-02-20
[7]赢创德固赛有限责任公司.制备异氰尿酸三烯丙酯(TAIC)的方法:CN 101490019 A[P].2009-07-22
[8]赢创德固赛有限责任公司.制备异氰尿酸三烯丙酯(TAIC)的方法:CN 101490019 B[P].2012-03-09
[9]张育川.氰尿酸三烯丙酯[J].精细与专用化学品,2001(12):21
[10]赵小平,樊真.过氧化物交联剂和烯丙基系列助交联剂[J].精细与专用化学品,2003,11(17):13-15
[11]James R.Dudley.Insecticidal Compositions:US 2,510,564[P].1950-06-06
[12]James R Dudley.Unsaturated Triazine Esters:US 2,537,816[P].1951-01-09
[13]Hans Gysin,Enrico Knüsli.s-Triazine Plant-growth in Hibitors:US 2,909,421[P].1959-10-20
[14]Yamada,Isao.Triallyl Cyanurate:JP 71 36,633[P].1971-10-27
[15]James R Dudley,Jack T Thurston,Frederic C Schaefer,et al.Cyanuric Acid Derivatives.ⅢAlkoxys-triazines[J].J.Am.Chem.Soc.,1951(73):2986-2990
[16]Robert G.Nelb.Triallyl Cyanurate:US 2631,148[P].1953-03-10
[17]Horst Schulze.Triallyl-and Trimethallyl Cyanurate:Ger:1064071[P].1959-08-27
[18]Horst Schulze.Unsaturated Esters of Cyanuric Acid:Ger.,18104[P].1960-01-19
[19]Khomenkova K K,Balitskaya L G,Zukhawa E I,et al.Triallyl Cyanurate for Transparent Material.[J].Plast.Massy,1970(10):17-18
[20]Gregg Harry D Jr,Lemaster Howard V.Triallyl Cyanurate:US 3644410[P].1972-02-27
[21]Musashino Chemical Research Institute,Ltd..Triallyl Cyanurate:Brit.,1,283,313[P].1972-07-26
[22]Kucharski Mieczyslaw,Mazurkiewicz Witold.Preparation of Triallyl Cyanurate by Condensation of Cyanuric chloride with Allyl Alcohol[J].Chem.Stosow.,1976,20(1):115-123(Pol)
[23]Kucharski,Mieczyslaw;Mazurkiewicz,Witold.Triallyl Cyanurate:Pol.89,571[P].1977-07-30
[24]张亨.三聚氰酸三烯酯的合成[J].塑料助剂,2003(4):16-18
[25]Haefner Volker,Suchsland Helmut,Werle,Peter.Process for Production of Triallyl Cyanurate:WO2008009540[P].2008-01-24
[26]Billy E.Lloyd,Fred L Kelly.Triallyl Isocyanurate:US2,894,950[P].1959-07-14
[27]Kenichi Fukui,Hisao Kitano.Isocyanuric Acid Derivatives:Brit.858,810[P].1961-01-18
[28]Thomas C Frazier,Edwin D Little,Billy E Lloyd.Isocyanurates.I.Condensation Reaction of Cyanuric Acid[J].J.Org.Chem.,1960,(25):1944-1946
[29]Z N Pazenko,T N Lebedeva,L I Chovnik,et al.The Synthesis of Monomers Containing the S-triazine Ring[J].Sintez I Svoistva Monomerov,Akad.Nauk SSSR,Inst.Neftekhim.Sinteza,Sb.Rabot 12-oi[Dvenadtsatoi]Konf.Po Vysokomolekul.Soedin.,1962:287-291
[30]黄勇.三聚氰酸三烯丙酯的生产工艺:CN102491951A[P].2012-06-13
[31]Donald W Kaiser.Aliphatic cyanurates:US 2,682,541[P].1954-06-29