CN102459155B - 酰肼化合物及其制造方法、以及使用它的固化剂、树脂组合物及固化体 - Google Patents
酰肼化合物及其制造方法、以及使用它的固化剂、树脂组合物及固化体 Download PDFInfo
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- CN102459155B CN102459155B CN201080025073.6A CN201080025073A CN102459155B CN 102459155 B CN102459155 B CN 102459155B CN 201080025073 A CN201080025073 A CN 201080025073A CN 102459155 B CN102459155 B CN 102459155B
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- hydrazide compound
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- solidifying agent
- hydrazide
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- HCOMFAYPHBFMKU-UHFFFAOYSA-N butanedihydrazide Chemical compound NNC(=O)CCC(=O)NN HCOMFAYPHBFMKU-UHFFFAOYSA-N 0.000 description 1
- 125000006226 butoxyethyl group Chemical group 0.000 description 1
- XEVRDFDBXJMZFG-UHFFFAOYSA-N carbonyl dihydrazine Chemical compound NNC(=O)NN XEVRDFDBXJMZFG-UHFFFAOYSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- ASKVAEGIVYSGNY-UHFFFAOYSA-L cobalt(ii) hydroxide Chemical compound [OH-].[OH-].[Co+2] ASKVAEGIVYSGNY-UHFFFAOYSA-L 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 150000007973 cyanuric acids Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- HUYREUUJFLHEDE-UHFFFAOYSA-N cyclohexanecarbohydrazide Chemical compound NNC(=O)C1CCCCC1 HUYREUUJFLHEDE-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000012933 diacyl peroxide Substances 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- QQHJDPROMQRDLA-UHFFFAOYSA-N hexadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCC(O)=O QQHJDPROMQRDLA-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 125000005439 maleimidyl group Chemical class C1(C=CC(N1*)=O)=O 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000001455 metallic ions Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- VMFUMDXVTKTZQY-UHFFFAOYSA-N naphthalene-1-carbohydrazide Chemical compound C1=CC=C2C(C(=O)NN)=CC=CC2=C1 VMFUMDXVTKTZQY-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- BFDHFSHZJLFAMC-UHFFFAOYSA-L nickel(ii) hydroxide Chemical compound [OH-].[OH-].[Ni+2] BFDHFSHZJLFAMC-UHFFFAOYSA-L 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- AFEQENGXSMURHA-UHFFFAOYSA-N oxiran-2-ylmethanamine Chemical compound NCC1CO1 AFEQENGXSMURHA-UHFFFAOYSA-N 0.000 description 1
- 125000004043 oxo group Chemical group O=* 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- PJBQYCIDGYKEMN-UHFFFAOYSA-N pentanehydrazide Chemical compound CCCCC(=O)NN PJBQYCIDGYKEMN-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 150000004978 peroxycarbonates Chemical class 0.000 description 1
- 125000005562 phenanthrylene group Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- DXGIRFAFSFKYCF-UHFFFAOYSA-N propanehydrazide Chemical compound CCC(=O)NN DXGIRFAFSFKYCF-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/06—Cobalt compounds
- C07F15/065—Cobalt compounds without a metal-carbon linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic Table
- C07F3/003—Compounds containing elements of Groups 2 or 12 of the Periodic Table without C-Metal linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/069—Aluminium compounds without C-aluminium linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/003—Compounds containing elements of Groups 4 or 14 of the Periodic Table without C-Metal linkages
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4014—Nitrogen containing compounds
- C08G59/4035—Hydrazines; Hydrazides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
- C08K5/24—Derivatives of hydrazine
- C08K5/25—Carboxylic acid hydrazides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Liquid Crystal (AREA)
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JP2009-139569 | 2009-06-10 | ||
JP2009139569A JP4961458B2 (ja) | 2009-06-10 | 2009-06-10 | ヒドラジド化合物及びその製造方法、並びにそれを用いた硬化剤、樹脂組成物及び硬化体 |
PCT/JP2010/059034 WO2010143540A1 (ja) | 2009-06-10 | 2010-05-27 | ヒドラジド化合物及びその製造方法、並びにそれを用いた硬化剤、樹脂組成物及び硬化体 |
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CN102459155B true CN102459155B (zh) | 2015-03-25 |
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JP (1) | JP4961458B2 (ko) |
KR (1) | KR101712687B1 (ko) |
CN (1) | CN102459155B (ko) |
TW (1) | TWI482750B (ko) |
WO (1) | WO2010143540A1 (ko) |
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WO2012077720A1 (ja) * | 2010-12-09 | 2012-06-14 | 協立化学産業株式会社 | 光重合開始剤に適した化合物、光重合開始剤及び光硬化性樹脂組成物 |
JP5796890B2 (ja) * | 2011-09-21 | 2015-10-21 | 日本化薬株式会社 | 新規ヒドラジド化合物及びそれを用いた樹脂組成物 |
JP6290599B2 (ja) * | 2012-11-13 | 2018-03-07 | 積水化学工業株式会社 | 液晶表示素子用シール剤、上下導通材料、液晶表示素子、及び、ヒドラジド系熱硬化剤 |
CN103193959B (zh) * | 2013-04-18 | 2014-07-30 | 艾达索高新材料无锡有限公司 | 可降解酰肼类潜伏型环氧树脂固化剂及其应用 |
CN105734177B (zh) | 2016-03-11 | 2020-08-11 | 广西叶茂食品有限责任公司 | 一种全营养纯净粉糖和液体糖浆的工业化生产工艺及设备 |
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JP2007297492A (ja) * | 2006-04-28 | 2007-11-15 | Kansai Paint Co Ltd | 硬化型樹脂組成物 |
CN101356241A (zh) * | 2006-08-08 | 2009-01-28 | 三菱化学株式会社 | 酰肼螯形配位化合物和使用了该化合物的光学记录介质及其记录方法 |
CN101416104A (zh) * | 2006-03-29 | 2009-04-22 | 积水化学工业株式会社 | 液晶滴下技术用密封剂、上下导通材料及液晶显示元件 |
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JPS4730154U (ko) * | 1971-05-04 | 1972-12-05 | ||
JPH05222296A (ja) * | 1992-02-14 | 1993-08-31 | Mitsubishi Yuka Badische Co Ltd | 水性架橋性樹脂組成物 |
JPH09104687A (ja) * | 1995-10-06 | 1997-04-22 | Daicel Chem Ind Ltd | トリス(カルボヒドラジド−o,n)マグネシウム(ii)硝酸塩錯体とその製造方法及びガス発生剤組成物 |
AU7890898A (en) * | 1996-12-26 | 1998-07-31 | Otsuka Kagaku Kabushiki Kaisha | Carbohydrazine/manganese complex and gas-generating agent for air bag |
JP3030499B2 (ja) * | 1997-02-19 | 2000-04-10 | 大塚化学株式会社 | エポキシ樹脂用硬化剤 |
JPH11152288A (ja) * | 1997-11-19 | 1999-06-08 | Daicel Chem Ind Ltd | ジ(カルボヒドラジド−o,n)カルシウム(ii)硝酸塩一水和物及びその脱水錯体とそれらの製造方法及びガス発生剤組成物 |
JP2006058466A (ja) | 2004-08-18 | 2006-03-02 | Sekisui Chem Co Ltd | 液晶表示素子用光硬化性樹脂組成物、液晶表示素子用シール剤、上下導通材料及び液晶表示素子 |
JP4783602B2 (ja) * | 2005-08-25 | 2011-09-28 | 株式会社シナネンゼオミック | 消臭剤および消臭性樹脂組成物 |
JP4483802B2 (ja) * | 2006-02-27 | 2010-06-16 | 三菱化学株式会社 | 光学記録媒体の記録層形成用色素、及びそれを用いた光学記録媒体、その光学記録媒体の記録方法 |
CN101454713B (zh) * | 2006-05-26 | 2011-03-09 | 日本化药株式会社 | 液晶密封剂以及使用该密封剂的液晶显示单元 |
JP4974344B2 (ja) * | 2006-06-19 | 2012-07-11 | 日本化薬株式会社 | 液晶シール剤及びそれを用いた液晶表示セル |
WO2008016122A1 (fr) * | 2006-08-04 | 2008-02-07 | Mitsui Chemicals, Inc. | Matière d'étanchéité pour cristaux liquides, procédé pour la production d'écrans à cristaux liquides avec celle-ci et écrans à cristaux liquides |
US20090252013A1 (en) * | 2006-08-08 | 2009-10-08 | Mitsubishi Chemical Corporation | Hydrazide chelate complex compound, optical recording medium using the compound and recording method thereof |
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- 2010-05-27 CN CN201080025073.6A patent/CN102459155B/zh active Active
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CN101416104A (zh) * | 2006-03-29 | 2009-04-22 | 积水化学工业株式会社 | 液晶滴下技术用密封剂、上下导通材料及液晶显示元件 |
JP2007297492A (ja) * | 2006-04-28 | 2007-11-15 | Kansai Paint Co Ltd | 硬化型樹脂組成物 |
CN101356241A (zh) * | 2006-08-08 | 2009-01-28 | 三菱化学株式会社 | 酰肼螯形配位化合物和使用了该化合物的光学记录介质及其记录方法 |
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JP2010285370A (ja) | 2010-12-24 |
KR20120032522A (ko) | 2012-04-05 |
CN102459155A (zh) | 2012-05-16 |
TW201113241A (en) | 2011-04-16 |
KR101712687B1 (ko) | 2017-03-06 |
TWI482750B (zh) | 2015-05-01 |
JP4961458B2 (ja) | 2012-06-27 |
WO2010143540A1 (ja) | 2010-12-16 |
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