JP2007506827A

JP2007506827A - 重縮合物の分子量増加及び変性

重縮合物の分子量増加及び変性 Download PDF

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Publication number: JP2007506827A
Authority: JP; Japan
Prior art keywords: group; carbon atoms; alkyl; alkyl group; substituted
Prior art date: 2003-09-25
Legal status : Pending

Application number

JP2006527402A

Other languages

English (en)

Japanese (ja)

Other versions

JP2007506827A5 (cg-RX-API-DMAC7.html

Inventor

サイモン，ディルク

プフェンドナー，ルドルフ

Current Assignee

BASF Schweiz AG

Original Assignee

Ciba Spezialitaetenchemie Holding AG

Priority date

2003-09-25

Filing date

2004-09-15

Publication date

2007-03-22

2004-09-15 Application filed by Ciba Spezialitaetenchemie Holding AG filed Critical Ciba Spezialitaetenchemie Holding AG

2007-03-22 Publication of JP2007506827A publication Critical patent/JP2007506827A/ja

2007-10-25 Publication of JP2007506827A5 publication Critical patent/JP2007506827A5/ja

Status Pending legal-status Critical Current

Links

230000004048 modification Effects 0.000 title claims abstract description 5
238000012986 modification Methods 0.000 title claims abstract description 5
238000000034 method Methods 0.000 claims abstract description 54
239000000203 mixture Substances 0.000 claims abstract description 50
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims abstract description 32
ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical class C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 claims abstract description 30
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims abstract description 29
ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims abstract description 23
150000001875 compounds Chemical class 0.000 claims abstract description 20
-1 polyethylene terephthalate Polymers 0.000 claims description 514
125000004432 carbon atom Chemical group C* 0.000 claims description 394
125000000217 alkyl group Chemical group 0.000 claims description 189
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 62
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 58
125000004430 oxygen atom Chemical group O* 0.000 claims description 38
229910052717 sulfur Inorganic materials 0.000 claims description 36
125000004434 sulfur atom Chemical group 0.000 claims description 36
229920000728 polyester Polymers 0.000 claims description 26
229920000139 polyethylene terephthalate Polymers 0.000 claims description 24
239000005020 polyethylene terephthalate Substances 0.000 claims description 24
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 23
229920001707 polybutylene terephthalate Polymers 0.000 claims description 23
229920000515 polycarbonate Polymers 0.000 claims description 23
239000004417 polycarbonate Substances 0.000 claims description 23
125000003545 alkoxy group Chemical group 0.000 claims description 22
125000002947 alkylene group Chemical group 0.000 claims description 21
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 18
125000001544 thienyl group Chemical group 0.000 claims description 18
125000002252 acyl group Chemical group 0.000 claims description 17
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 17
125000001624 naphthyl group Chemical group 0.000 claims description 17
125000000753 cycloalkyl group Chemical group 0.000 claims description 15
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 14
125000005843 halogen group Chemical group 0.000 claims description 12
125000003884 phenylalkyl group Chemical group 0.000 claims description 12
125000004423 acyloxy group Chemical group 0.000 claims description 11
125000001931 aliphatic group Chemical group 0.000 claims description 11
229920001577 copolymer Polymers 0.000 claims description 11
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150000002148 esters Chemical class 0.000 claims description 10
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239000002184 metal Substances 0.000 claims description 9
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125000004429 atom Chemical group 0.000 claims description 8
PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 claims description 8
150000001768 cations Chemical class 0.000 claims description 8
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125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 8
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 8
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125000001309 chloro group Chemical group Cl* 0.000 claims description 7
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125000004450 alkenylene group Chemical group 0.000 claims description 6
125000001118 alkylidene group Chemical group 0.000 claims description 6
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
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125000004957 naphthylene group Chemical group 0.000 claims description 6
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125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 claims description 5
125000002993 cycloalkylene group Chemical group 0.000 claims description 5
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 5
YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
125000003302 alkenyloxy group Chemical group 0.000 claims description 4
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 claims description 4
125000005605 benzo group Chemical group 0.000 claims description 4
239000004305 biphenyl Substances 0.000 claims description 4
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125000004230 chromenyl group Chemical group O1C(C=CC2=CC=CC=C12)* 0.000 claims description 4
125000004987 dibenzofuryl group Chemical group C1(=CC=CC=2OC3=C(C21)C=CC=C3)* 0.000 claims description 4
125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 4
125000001041 indolyl group Chemical group 0.000 claims description 4
125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims description 4
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239000000155 melt Substances 0.000 claims description 4
125000005561 phenanthryl group Chemical group 0.000 claims description 4
125000005954 phenoxathiinyl group Chemical group 0.000 claims description 4
125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 claims description 4
125000000168 pyrrolyl group Chemical group 0.000 claims description 4
125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 claims description 4
239000004953 Aliphatic polyamide Substances 0.000 claims description 3
SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 claims description 3
229920001634 Copolyester Polymers 0.000 claims description 3
125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 claims description 3
229920003231 aliphatic polyamide Polymers 0.000 claims description 3
150000001340 alkali metals Chemical class 0.000 claims description 3
239000004760 aramid Substances 0.000 claims description 3
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235000010290 biphenyl Nutrition 0.000 claims description 3
125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 3
125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 claims description 3
125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims description 3
125000002883 imidazolyl group Chemical group 0.000 claims description 3
125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 3
125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 claims description 3
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125000005327 perimidinyl group Chemical group N1C(=NC2=CC=CC3=CC=CC1=C23)* 0.000 claims description 3
125000004934 phenanthridinyl group Chemical group C1(=CC=CC2=NC=C3C=CC=CC3=C12)* 0.000 claims description 3
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239000011112 polyethylene naphthalate Substances 0.000 claims description 3
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125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 claims description 3
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