CN107090299A - 一种含甲基取代基多氟取代化合物的液晶组合物及其应用 - Google Patents
一种含甲基取代基多氟取代化合物的液晶组合物及其应用 Download PDFInfo
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- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 75
- 239000000203 mixture Substances 0.000 title claims abstract description 39
- 150000001875 compounds Chemical class 0.000 title claims abstract description 32
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 title claims abstract description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 76
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 74
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 229910052731 fluorine Inorganic materials 0.000 claims description 20
- 125000003545 alkoxy group Chemical group 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- 239000011737 fluorine Substances 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 125000003342 alkenyl group Chemical group 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000001188 haloalkyl group Chemical group 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 6
- 150000001336 alkenes Chemical class 0.000 claims 2
- 150000002118 epoxides Chemical class 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 230000014759 maintenance of location Effects 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract description 2
- 238000012360 testing method Methods 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 6
- 0 *c1cc(*)c(*)c(I)c1 Chemical compound *c1cc(*)c(*)c(I)c1 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 230000004044 response Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- UWCWUCKPEYNDNV-LBPRGKRZSA-N 2,6-dimethyl-n-[[(2s)-pyrrolidin-2-yl]methyl]aniline Chemical compound CC1=CC=CC(C)=C1NC[C@H]1NCCC1 UWCWUCKPEYNDNV-LBPRGKRZSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000012769 display material Substances 0.000 description 2
- 125000005291 haloalkenyloxy group Chemical group 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000001471 micro-filtration Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- WOMWYTFHBFYIMC-UHFFFAOYSA-N CC1CC[I](C)CC1 Chemical compound CC1CC[I](C)CC1 WOMWYTFHBFYIMC-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000003044 adaptive effect Effects 0.000 description 1
- 150000001345 alkine derivatives Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 230000009514 concussion Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
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- C09K19/10—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
- C09K19/12—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
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- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
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- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
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- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
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- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
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- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
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- Optics & Photonics (AREA)
- Liquid Crystal Substances (AREA)
Abstract
Description
项目 | S-N(℃) | Cp(℃) | △n | ne | △ε | ε⊥ | γ1 |
数值 | ≤-40 | 88 | 0.110 | 1.598 | 5.0 | 3.3 | 63 |
项目 | S-N(℃) | Cp(℃) | △n | ne | △ε | ε⊥ | γ1 |
数值 | ≤-30 | 100 | 0.110 | 1.586 | 7.6 | 3.4 | 105 |
项目 | S-N(℃) | Cp(℃) | △n | ne | △ε | ε⊥ | γ1 |
数值 | ≤-40 | 93 | 0.117 | 1.598 | 8.5 | 3.6 | 70 |
项目 | S-N(℃) | Cp(℃) | △n | ne | △ε | ε⊥ | γ1 |
数值 | ≤-40 | 88 | 0.120 | 1.601 | 12.5 | 3.8 | 63 |
项目 | S-N(℃) | Cp(℃) | △n | ne | △ε | ε⊥ | γ1 |
数值 | ≤-40 | 96 | 0.101 | 1.599 | 8.9 | 3.5 | 78 |
项目 | S-N(℃) | Cp(℃) | △n | ne | △ε | ε⊥ | γ1(mpa.s) |
数值 | ≤-40 | 98 | 0.110 | 1.605 | 15.9 | 3.5 | 85 |
项目 | S-N(℃) | Cp(℃) | △n | ne | △ε | ε⊥ | γ1(mpa.s) |
数值 | ≤-40 | 92 | 0.100 | 1.597 | 8.6 | 3.4 | 92 |
Claims (9)
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107760316A (zh) * | 2017-09-30 | 2018-03-06 | 烟台显华化工科技有限公司 | 含有3‑氟5‑甲基取代基苯与二氟亚甲氧基连接基团的液晶化合物及其制备方法与应用 |
CN108048113A (zh) * | 2017-12-08 | 2018-05-18 | 烟台显华化工科技有限公司 | 一种液晶组合物及其应用 |
CN108148602A (zh) * | 2018-02-09 | 2018-06-12 | 烟台显华化工科技有限公司 | 一种液晶组合物及其应用 |
CN108192641A (zh) * | 2018-01-22 | 2018-06-22 | 烟台显华化工科技有限公司 | 一种液晶组合物及其应用 |
CN108531197A (zh) * | 2018-05-31 | 2018-09-14 | 烟台显华化工科技有限公司 | 一种液晶组合物及其应用 |
CN109749755A (zh) * | 2018-12-20 | 2019-05-14 | 西安近代化学研究所 | 一种提高液晶材料环境适应性的液晶化合物及组合物 |
CN110760311A (zh) * | 2019-10-31 | 2020-02-07 | 武汉轻工大学 | 一种侧甲基多联苯类液晶化合物和液晶组合物及其应用 |
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CN104513665A (zh) * | 2014-12-31 | 2015-04-15 | 石家庄诚志永华显示材料有限公司 | 一种含三联苯类化合物的液晶介质及其应用 |
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JP2013216848A (ja) * | 2012-03-13 | 2013-10-24 | Dainippon Printing Co Ltd | 強誘電性液晶組成物および液晶表示素子 |
JP2013241536A (ja) * | 2012-05-22 | 2013-12-05 | Dainippon Printing Co Ltd | 強誘電性液晶組成物および液晶表示素子 |
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JP2016011346A (ja) * | 2014-06-27 | 2016-01-21 | Jnc株式会社 | 重合性化合物、重合性組成物および液晶表示素子 |
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Publication number | Priority date | Publication date | Assignee | Title |
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CN107760316A (zh) * | 2017-09-30 | 2018-03-06 | 烟台显华化工科技有限公司 | 含有3‑氟5‑甲基取代基苯与二氟亚甲氧基连接基团的液晶化合物及其制备方法与应用 |
CN108048113A (zh) * | 2017-12-08 | 2018-05-18 | 烟台显华化工科技有限公司 | 一种液晶组合物及其应用 |
CN108192641A (zh) * | 2018-01-22 | 2018-06-22 | 烟台显华化工科技有限公司 | 一种液晶组合物及其应用 |
CN108148602A (zh) * | 2018-02-09 | 2018-06-12 | 烟台显华化工科技有限公司 | 一种液晶组合物及其应用 |
CN108531197A (zh) * | 2018-05-31 | 2018-09-14 | 烟台显华化工科技有限公司 | 一种液晶组合物及其应用 |
CN109749755A (zh) * | 2018-12-20 | 2019-05-14 | 西安近代化学研究所 | 一种提高液晶材料环境适应性的液晶化合物及组合物 |
CN109749755B (zh) * | 2018-12-20 | 2022-03-15 | 西安近代化学研究所 | 一种提高液晶材料环境适应性的液晶化合物及组合物 |
CN110760311A (zh) * | 2019-10-31 | 2020-02-07 | 武汉轻工大学 | 一种侧甲基多联苯类液晶化合物和液晶组合物及其应用 |
CN110760311B (zh) * | 2019-10-31 | 2021-06-29 | 武汉轻工大学 | 一种侧甲基多联苯类液晶化合物和液晶组合物及其应用 |
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