JP2009155490A5 - - Google Patents
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- Publication number
- JP2009155490A5 JP2009155490A5 JP2007335697A JP2007335697A JP2009155490A5 JP 2009155490 A5 JP2009155490 A5 JP 2009155490A5 JP 2007335697 A JP2007335697 A JP 2007335697A JP 2007335697 A JP2007335697 A JP 2007335697A JP 2009155490 A5 JP2009155490 A5 JP 2009155490A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- aromatic
- unit
- dendritic polyester
- represented
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 229920000728 polyester Polymers 0.000 claims description 23
- 125000003118 aryl group Chemical group 0.000 claims description 18
- 125000000524 functional group Chemical group 0.000 claims description 8
- 229920005992 thermoplastic resin Polymers 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000005843 halogen group Chemical group 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 6
- 241000790917 Dioxys <bee> Species 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 239000011342 resin composition Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000003700 epoxy group Chemical group 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 4
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 description 7
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 6
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 6
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 4
- 150000001491 aromatic compounds Chemical group 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229940074391 gallic acid Drugs 0.000 description 3
- 235000004515 gallic acid Nutrition 0.000 description 3
- RDJUHLUBPADHNP-UHFFFAOYSA-N 1,2,3,5-tetrahydroxybenzene Chemical compound OC1=CC(O)=C(O)C(O)=C1 RDJUHLUBPADHNP-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- VERMEZLHWFHDLK-UHFFFAOYSA-N benzene-1,2,3,4-tetrol Chemical compound OC1=CC=C(O)C(O)=C1O VERMEZLHWFHDLK-UHFFFAOYSA-N 0.000 description 2
- UYQMSQMCIYSXOW-UHFFFAOYSA-N benzene-1,2,4,5-tetrol Chemical compound OC1=CC(O)=C(O)C=C1O UYQMSQMCIYSXOW-UHFFFAOYSA-N 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- OVALYCIUDYJCCC-UHFFFAOYSA-N naphthalene-1,4,5,8-tetrol Chemical compound C1=CC(O)=C2C(O)=CC=C(O)C2=C1O OVALYCIUDYJCCC-UHFFFAOYSA-N 0.000 description 2
- ZJASMNZFUUBMRG-UHFFFAOYSA-N naphthalene-2,3,6,7-tetrol Chemical compound OC1=C(O)C=C2C=C(O)C(O)=CC2=C1 ZJASMNZFUUBMRG-UHFFFAOYSA-N 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-UHFFFAOYSA-N 0.000 description 1
- FWZONMFJTUSBCW-UHFFFAOYSA-N 2,3,5-triaminophenol Chemical compound NC1=CC(N)=C(N)C(O)=C1 FWZONMFJTUSBCW-UHFFFAOYSA-N 0.000 description 1
- KKTUQAYCCLMNOA-UHFFFAOYSA-N 2,3-diaminobenzoic acid Chemical compound NC1=CC=CC(C(O)=O)=C1N KKTUQAYCCLMNOA-UHFFFAOYSA-N 0.000 description 1
- WZPLEIAOQJXZJX-UHFFFAOYSA-N 2,3-dihydroxynaphthalene-1-carboxylic acid Chemical compound C1=CC=C2C(C(=O)O)=C(O)C(O)=CC2=C1 WZPLEIAOQJXZJX-UHFFFAOYSA-N 0.000 description 1
- GPNNOCMCNFXRAO-UHFFFAOYSA-N 2-aminoterephthalic acid Chemical compound NC1=CC(C(O)=O)=CC=C1C(O)=O GPNNOCMCNFXRAO-UHFFFAOYSA-N 0.000 description 1
- JOSLTWKGYSUVOL-UHFFFAOYSA-N 3,4,5-triaminobenzoic acid Chemical compound NC1=CC(C(O)=O)=CC(N)=C1N JOSLTWKGYSUVOL-UHFFFAOYSA-N 0.000 description 1
- RVMIFSMOZZSLNK-UHFFFAOYSA-N 3,4,5-triaminophenol Chemical compound NC1=CC(O)=CC(N)=C1N RVMIFSMOZZSLNK-UHFFFAOYSA-N 0.000 description 1
- WGLQHUKCXBXUDV-UHFFFAOYSA-N 3-aminophthalic acid Chemical compound NC1=CC=CC(C(O)=O)=C1C(O)=O WGLQHUKCXBXUDV-UHFFFAOYSA-N 0.000 description 1
- MAQQETDJGIXPQI-UHFFFAOYSA-N 4-(2,4-dicarboxyphenyl)benzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC(C(=O)O)=CC=C1C1=CC=C(C(O)=O)C=C1C(O)=O MAQQETDJGIXPQI-UHFFFAOYSA-N 0.000 description 1
- CFGDTWRKBRQUFB-UHFFFAOYSA-N 4-(2,4-dihydroxyphenyl)benzene-1,3-diol Chemical group OC1=CC(O)=CC=C1C1=CC=C(O)C=C1O CFGDTWRKBRQUFB-UHFFFAOYSA-N 0.000 description 1
- LFBALUPVVFCEPA-UHFFFAOYSA-N 4-(3,4-dicarboxyphenyl)phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)C(C(O)=O)=C1 LFBALUPVVFCEPA-UHFFFAOYSA-N 0.000 description 1
- MZEFNGQKJROKHS-UHFFFAOYSA-N 4-(3,4-dihydroxyphenyl)benzene-1,2-diol Chemical group C1=C(O)C(O)=CC=C1C1=CC=C(O)C(O)=C1 MZEFNGQKJROKHS-UHFFFAOYSA-N 0.000 description 1
- QURGMSIQFRADOZ-UHFFFAOYSA-N 5-(3,5-dicarboxyphenyl)benzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C=2C=C(C=C(C=2)C(O)=O)C(O)=O)=C1 QURGMSIQFRADOZ-UHFFFAOYSA-N 0.000 description 1
- VZLUGGCFYPMLMI-UHFFFAOYSA-N 5-(3,5-dihydroxyphenyl)benzene-1,3-diol Chemical group OC1=CC(O)=CC(C=2C=C(O)C=C(O)C=2)=C1 VZLUGGCFYPMLMI-UHFFFAOYSA-N 0.000 description 1
- KBZFDRWPMZESDI-UHFFFAOYSA-N 5-aminobenzene-1,3-dicarboxylic acid Chemical compound NC1=CC(C(O)=O)=CC(C(O)=O)=C1 KBZFDRWPMZESDI-UHFFFAOYSA-N 0.000 description 1
- RQEYORYAAMKFBL-UHFFFAOYSA-N CC(C)(c1ccc(C)cc1)c1ccc(C)c(C)c1 Chemical compound CC(C)(c1ccc(C)cc1)c1ccc(C)c(C)c1 RQEYORYAAMKFBL-UHFFFAOYSA-N 0.000 description 1
- 0 Cc1cc(*)c(*c2c(*)cc(C)cc2)cc1 Chemical compound Cc1cc(*)c(*c2c(*)cc(C)cc2)cc1 0.000 description 1
- JQDKLRDTPXELAB-UHFFFAOYSA-N Cc1cc(-c2cc(C)c(C)c(C)c2)cc(C)c1C Chemical compound Cc1cc(-c2cc(C)c(C)c(C)c2)cc(C)c1C JQDKLRDTPXELAB-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- -1 aromatic organic compound Chemical class 0.000 description 1
- KAMGOKSXKBHPHL-UHFFFAOYSA-N benzene-1,2,3,4-tetramine Chemical compound NC1=CC=C(N)C(N)=C1N KAMGOKSXKBHPHL-UHFFFAOYSA-N 0.000 description 1
- VVWINCXZUPKZBK-UHFFFAOYSA-N benzene-1,2,3,5-tetramine Chemical compound NC1=CC(N)=C(N)C(N)=C1 VVWINCXZUPKZBK-UHFFFAOYSA-N 0.000 description 1
- ANUAIBBBDSEVKN-UHFFFAOYSA-N benzene-1,2,4,5-tetramine Chemical compound NC1=CC(N)=C(N)C=C1N ANUAIBBBDSEVKN-UHFFFAOYSA-N 0.000 description 1
- AIEZFWSIZQLXEG-UHFFFAOYSA-N biphenyl-2,2',3,3'-tetraol Chemical group OC1=CC=CC(C=2C(=C(O)C=CC=2)O)=C1O AIEZFWSIZQLXEG-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- CXUCHQYVHFUANW-UHFFFAOYSA-N naphthalene-1,2,4,5,6,8-hexacarboxylic acid Chemical compound OC(=O)C1=C(C(O)=O)C=C(C(O)=O)C2=C(C(O)=O)C(C(=O)O)=CC(C(O)=O)=C21 CXUCHQYVHFUANW-UHFFFAOYSA-N 0.000 description 1
- KWAZCDCEGNCKII-UHFFFAOYSA-N naphthalene-1,2,4,5,6,8-hexol Chemical compound OC1=C(O)C=C(O)C2=C(O)C(O)=CC(O)=C21 KWAZCDCEGNCKII-UHFFFAOYSA-N 0.000 description 1
- OLAPPGSPBNVTRF-UHFFFAOYSA-N naphthalene-1,4,5,8-tetracarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=C(C(O)=O)C2=C1C(O)=O OLAPPGSPBNVTRF-UHFFFAOYSA-N 0.000 description 1
- DOBFTMLCEYUAQC-UHFFFAOYSA-N naphthalene-2,3,6,7-tetracarboxylic acid Chemical compound OC(=O)C1=C(C(O)=O)C=C2C=C(C(O)=O)C(C(=O)O)=CC2=C1 DOBFTMLCEYUAQC-UHFFFAOYSA-N 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007335697A JP5256729B2 (ja) | 2007-12-27 | 2007-12-27 | 樹状ポリエステル、その製造方法および熱可塑性樹脂組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007335697A JP5256729B2 (ja) | 2007-12-27 | 2007-12-27 | 樹状ポリエステル、その製造方法および熱可塑性樹脂組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009155490A JP2009155490A (ja) | 2009-07-16 |
| JP2009155490A5 true JP2009155490A5 (enrdf_load_stackoverflow) | 2011-02-10 |
| JP5256729B2 JP5256729B2 (ja) | 2013-08-07 |
Family
ID=40959843
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007335697A Expired - Fee Related JP5256729B2 (ja) | 2007-12-27 | 2007-12-27 | 樹状ポリエステル、その製造方法および熱可塑性樹脂組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP5256729B2 (enrdf_load_stackoverflow) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6179361B2 (ja) * | 2012-11-29 | 2017-08-16 | 東レ株式会社 | 末端変性ポリマーを含む熱可塑性樹脂 |
| JP6263456B2 (ja) * | 2014-08-27 | 2018-01-17 | 住化ポリカーボネート株式会社 | 帯電防止性ポリカーボネート樹脂組成物及びそれからなる成形品 |
| JP6263457B2 (ja) * | 2014-08-27 | 2018-01-17 | 住化ポリカーボネート株式会社 | 帯電防止性ポリカーボネート樹脂組成物及びそれからなる成形品 |
| TWI711668B (zh) | 2019-01-30 | 2020-12-01 | 南亞塑膠工業股份有限公司 | 一種低比重ｐｅｔ複合材料之用途 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5211293A (en) * | 1975-07-16 | 1977-01-28 | Nippon Ester Co Ltd | Preparation of polyester resin |
| JP2517568B2 (ja) * | 1986-11-13 | 1996-07-24 | ポリプラスチックス株式会社 | 分子鎖末端が封止された液晶性コポリエステル |
| JP3098074B2 (ja) * | 1991-10-01 | 2000-10-10 | ポリプラスチックス株式会社 | 電子部品封止用樹脂組成物及び電子部品 |
| JP2000143947A (ja) * | 1998-11-05 | 2000-05-26 | Toray Ind Inc | 液晶性ポリエステル樹脂組成物およびその射出成形品 |
| MY167262A (en) * | 2006-03-30 | 2018-08-14 | Toray Industries | Hyperbranched-polyester, method for producing the same, and thermoplastic resin composition |
-
2007
- 2007-12-27 JP JP2007335697A patent/JP5256729B2/ja not_active Expired - Fee Related
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