CN100336870C - 酞菁染料及其制法 - Google Patents
酞菁染料及其制法 Download PDFInfo
- Publication number
- CN100336870C CN100336870C CNB031105149A CN03110514A CN100336870C CN 100336870 C CN100336870 C CN 100336870C CN B031105149 A CNB031105149 A CN B031105149A CN 03110514 A CN03110514 A CN 03110514A CN 100336870 C CN100336870 C CN 100336870C
- Authority
- CN
- China
- Prior art keywords
- phthalocyanine
- dimethyl
- bromination
- pentyloxy
- copper
- 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.)
- Expired - Lifetime
Links
- 239000001007 phthalocyanine dye Substances 0.000 title abstract 4
- 238000002360 preparation method Methods 0.000 title description 4
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims abstract description 52
- 238000000034 method Methods 0.000 claims abstract description 33
- 230000031709 bromination Effects 0.000 claims abstract description 29
- 238000005893 bromination reaction Methods 0.000 claims abstract description 29
- -1 amido pyridine Chemical compound 0.000 claims abstract description 17
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 claims abstract description 13
- GPRSOIDYHMXAGW-UHFFFAOYSA-N cyclopenta-1,3-diene cyclopentanecarboxylic acid iron Chemical compound [CH-]1[CH-][CH-][C-]([CH-]1)C(=O)O.[CH-]1C=CC=C1.[Fe] GPRSOIDYHMXAGW-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052751 metal Inorganic materials 0.000 claims abstract description 7
- 239000002184 metal Substances 0.000 claims abstract description 7
- 238000003763 carbonization Methods 0.000 claims abstract description 5
- 239000000049 pigment Substances 0.000 claims description 36
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 32
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 24
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 18
- 238000004519 manufacturing process Methods 0.000 claims description 16
- HWKYVLAXTYPDHE-UHFFFAOYSA-N CC(C)C(C(C)C)O[Cu] Chemical compound CC(C)C(C(C)C)O[Cu] HWKYVLAXTYPDHE-UHFFFAOYSA-N 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 11
- 238000001914 filtration Methods 0.000 claims description 11
- 229910001507 metal halide Inorganic materials 0.000 claims description 11
- 150000005309 metal halides Chemical class 0.000 claims description 11
- 239000011541 reaction mixture Substances 0.000 claims description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 5
- 150000003222 pyridines Chemical class 0.000 claims description 5
- 239000000741 silica gel Substances 0.000 claims description 5
- 229910002027 silica gel Inorganic materials 0.000 claims description 5
- 239000000725 suspension Substances 0.000 claims description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 4
- 150000003949 imides Chemical class 0.000 claims description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 239000011572 manganese Substances 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- 239000011701 zinc Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 10
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 abstract 1
- 229910000071 diazene Inorganic materials 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- 230000026030 halogenation Effects 0.000 abstract 1
- 238000005658 halogenation reaction Methods 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 10
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 10
- VIKNJXKGJWUCNN-XGXHKTLJSA-N norethisterone Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 VIKNJXKGJWUCNN-XGXHKTLJSA-N 0.000 description 8
- 239000000975 dye Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000470 constituent Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000002310 reflectometry Methods 0.000 description 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000001376 precipitating effect Effects 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 231100000331 toxic Toxicity 0.000 description 4
- 230000002588 toxic effect Effects 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 239000003643 water by type Substances 0.000 description 4
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 210000003739 neck Anatomy 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 238000004528 spin coating Methods 0.000 description 3
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 3
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 2
- 230000010748 Photoabsorption Effects 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- HXQQJHHWWNVMJS-UHFFFAOYSA-N 2,4-dimethylpentan-3-yl hydrogen carbonate Chemical compound CC(C)C(C(C)C)OC(O)=O HXQQJHHWWNVMJS-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- WMSWDJFQLBDFLN-UHFFFAOYSA-N CC(C)C(C(C)C)O[Cu](OC(C(C)C)C(C)C)(OC(C(C)C)C(C)C)OC(C(C)C)C(C)C Chemical class CC(C)C(C(C)C)O[Cu](OC(C(C)C)C(C)C)(OC(C(C)C)C(C)C)OC(C(C)C)C(C)C WMSWDJFQLBDFLN-UHFFFAOYSA-N 0.000 description 1
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 1
- XZPIASHAFVMKCF-UHFFFAOYSA-N OC[Cu](OC(C(C)C)C(C)C)(OC(C(C)C)C(C)C)(OC(C(C)C)C(C)C)(OC(C(C)C)C(C)C)CO Chemical class OC[Cu](OC(C(C)C)C(C)C)(OC(C(C)C)C(C)C)(OC(C(C)C)C(C)C)(OC(C(C)C)C(C)C)CO XZPIASHAFVMKCF-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 1
- ZBOGUDPFEVIZIQ-UHFFFAOYSA-N toluene;dihydrochloride Chemical compound Cl.Cl.CC1=CC=CC=C1 ZBOGUDPFEVIZIQ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Description
盘片 | BLER | I3R | I11R | REF | Jitter | Beta | ||||||
最大 | 平均 | L-3T | P-3T | L-11T | P-11T | 最小 | 最大 | 平均 | ||||
比较例2 | 100* | 24.1* | 0.35 | 0.63 | 59.1 | 28 | 29 | 33 | 26 | -11.8* | 5.5 | -1.62 |
实例2 | 20 | 3.3 | 0.33 | 0.60 | 64.0 | 29 | 27 | 27 | 25 | -9.5 | 1.2 | -5.31 |
实例3 | 24 | 2.7 | 0.36 | 0.64 | 65.0 | 24 | 23 | 24 | 22 | -10.7 | -1.5 | -6.55 |
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB031105149A CN100336870C (zh) | 2003-04-07 | 2003-04-07 | 酞菁染料及其制法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB031105149A CN100336870C (zh) | 2003-04-07 | 2003-04-07 | 酞菁染料及其制法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1446858A CN1446858A (zh) | 2003-10-08 |
CN100336870C true CN100336870C (zh) | 2007-09-12 |
Family
ID=28050266
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB031105149A Expired - Lifetime CN100336870C (zh) | 2003-04-07 | 2003-04-07 | 酞菁染料及其制法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN100336870C (zh) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109100313B (zh) * | 2018-07-30 | 2020-04-28 | 四川大学 | 检测Pb离子和Ni离子的试剂盒、检测方法及浓度测定方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1232480A (zh) * | 1996-10-03 | 1999-10-20 | 西巴特殊化学品控股有限公司 | 取代的酞菁类化合物及其应用 |
CN1312816A (zh) * | 1998-08-11 | 2001-09-12 | 西巴特殊化学品控股有限公司 | 金属茂基-酞青染料 |
CN1394864A (zh) * | 2002-08-20 | 2003-02-05 | 天津青迈信息材料有限公司 | 金属苯茂基酞菁衍生物及其制备方法和用途 |
-
2003
- 2003-04-07 CN CNB031105149A patent/CN100336870C/zh not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1232480A (zh) * | 1996-10-03 | 1999-10-20 | 西巴特殊化学品控股有限公司 | 取代的酞菁类化合物及其应用 |
CN1312816A (zh) * | 1998-08-11 | 2001-09-12 | 西巴特殊化学品控股有限公司 | 金属茂基-酞青染料 |
CN1394864A (zh) * | 2002-08-20 | 2003-02-05 | 天津青迈信息材料有限公司 | 金属苯茂基酞菁衍生物及其制备方法和用途 |
Also Published As
Publication number | Publication date |
---|---|
CN1446858A (zh) | 2003-10-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR101709800B1 (ko) | 근적외선 흡수 색소 및 근적외선 차단 필터 | |
Feng et al. | Controlling the columnar orientation of C3-symmetric" superbenzenes" through alternating polar/apolar substitutents | |
CN1145678C (zh) | 取代的酞菁类化合物及其制备方法 | |
CN1144227A (zh) | 芳香含硫聚合物的合成工艺 | |
CN100336870C (zh) | 酞菁染料及其制法 | |
CN1760235A (zh) | 一种聚三苯胺聚合物的合成方法 | |
CN1364829A (zh) | 水溶性3h-吲哚菁染料 | |
JPH0119693B2 (zh) | ||
CN1753953A (zh) | 水溶性、荧光性苝四羧酸双二酰亚胺 | |
CN1873396A (zh) | 用于检测水的组合物以及用于检测水的指示剂 | |
CN1101929A (zh) | 一种具有双发色团的荧光染料及其制备方法 | |
CN109265473B (zh) | 一种含混合配体锌(ⅱ)金属有机配合物及其制备方法和应用 | |
WO2007026609A1 (ja) | 高分子固定化パラジウム触媒及びその製法 | |
CN109776329B (zh) | 一种可光致手性翻转的多元丙烯酸酯类化合物、制备方法和器件 | |
CN1119369C (zh) | 交联型酞菁聚合物及其均匀透明薄膜的制备 | |
CN87100853A (zh) | 卤代酰亚胺的制备方法含有它们的配方及其作为防火处理剂的应用 | |
CN115873137A (zh) | 一种纤维素氨羧衍生物及其制备方法 | |
CN1148368C (zh) | Dvd-r光盘用不对称菁染料的制备方法 | |
CN110105406B (zh) | 一种基于邻羧基苯乙酸配体的[CdNa2]异金属荧光材料及其制备方法 | |
US20210018662A1 (en) | Polymer-Based Nanocomposite and Optical Filter Based Thereon | |
CN111039879B (zh) | 一种含砜基三唑类化合物/聚合物及其制备方法和应用 | |
CN1063739C (zh) | 纯化氟锁草醚的方法 | |
US20070155962A1 (en) | Process for preparing titanyl phthalocyanine | |
CN1837294A (zh) | ε晶形铜酞菁的制造方法 | |
CN114702953B (zh) | 一种基于镧系离子杂化共价有机框架材料的荧光探针及制备方法及应用 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
ASS | Succession or assignment of patent right |
Owner name: TAIFU TECHNOLOGY CO., LTD. Free format text: FORMER OWNER: ZHONGHUA YANSHENG SCIENCE AND TECHNOLOGY CO., LTD. Effective date: 20051125 |
|
C41 | Transfer of patent application or patent right or utility model | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20051125 Address after: Taiwan, China Applicant after: TAIWAN FLUORO TECHNOLOGY Co.,Ltd. Address before: Taoyuan County of Taiwan Province Applicant before: Exon Science, Inc. |
|
ASS | Succession or assignment of patent right |
Owner name: FENGSHENG TECHNOLOGY INDUSTRIAL STOCK CO., LTD. Free format text: FORMER OWNER: TAIFU TECHNOLOGY CO., LTD. Effective date: 20070316 |
|
C41 | Transfer of patent application or patent right or utility model | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20070316 Address after: Taiwan, China Applicant after: Tube Smith Technology Co.,Ltd. Address before: Taiwan, China Applicant before: TAIWAN FLUORO TECHNOLOGY Co.,Ltd. |
|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C56 | Change in the name or address of the patentee |
Owner name: TAIWAN FLUORO TECHNOLOGY CO., LTD. Free format text: FORMER NAME: FENGSHENG TECHNOLOGY INDUSTRIAL CO., LTD. |
|
CP03 | Change of name, title or address |
Address after: Taiwan, China Patentee after: TAIWAN FLUORO TECHNOLOGY Co.,Ltd. Address before: 000000 Taiwan, China Patentee before: Tube Smith Technology Co.,Ltd. |
|
CX01 | Expiry of patent term |
Granted publication date: 20070912 |
|
CX01 | Expiry of patent term |