TWI769857B - 一種包含二苯並衍生物的液晶組合物及液晶顯示器件 - Google Patents
一種包含二苯並衍生物的液晶組合物及液晶顯示器件 Download PDFInfo
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- TWI769857B TWI769857B TW110121509A TW110121509A TWI769857B TW I769857 B TWI769857 B TW I769857B TW 110121509 A TW110121509 A TW 110121509A TW 110121509 A TW110121509 A TW 110121509A TW I769857 B TWI769857 B TW I769857B
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- liquid crystal
- crystal composition
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- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 170
- 239000000203 mixture Substances 0.000 title claims abstract description 118
- 150000001875 compounds Chemical class 0.000 claims abstract description 54
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 63
- 125000000217 alkyl group Chemical group 0.000 claims description 50
- 125000004429 atom Chemical group 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 4
- 238000006467 substitution reaction Methods 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 238000002834 transmittance Methods 0.000 abstract description 12
- 230000000694 effects Effects 0.000 abstract description 10
- 230000003287 optical effect Effects 0.000 abstract description 10
- 125000003545 alkoxy group Chemical group 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- -1 4,6-Difluoro-dibenzo[b,d]furan-3,7-diyl Chemical group 0.000 description 8
- 125000003342 alkenyl group Chemical group 0.000 description 7
- 239000000463 material Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 239000003381 stabilizer Substances 0.000 description 5
- 210000004027 cell Anatomy 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000004044 response Effects 0.000 description 4
- OCCXSCMDIKCVAV-UHFFFAOYSA-N 4,6-difluorodibenzofuran Chemical class O1C2=C(F)C=CC=C2C2=C1C(F)=CC=C2 OCCXSCMDIKCVAV-UHFFFAOYSA-N 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 description 2
- 125000005449 2-fluoro-1,4-phenylene group Chemical group [H]C1=C([*:2])C([H])=C(F)C([*:1])=C1[H] 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
- 125000005450 2,3-difluoro-1,4-phenylene group Chemical group [H]C1=C([*:2])C(F)=C(F)C([*:1])=C1[H] 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 101100208473 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) lcm-2 gene Proteins 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000003302 alkenyloxy group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 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
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000012769 display material Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000005699 methyleneoxy group Chemical group [H]C([H])([*:1])O[*:2] 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000004192 tetrahydrofuran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
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- C—CHEMISTRY; METALLURGY
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- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
- C09K19/44—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40 containing compounds with benzene rings directly linked
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- C09K19/06—Non-steroidal liquid crystal compounds
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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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- C09K19/3491—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having sulfur as hetero atom
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- C09K19/3066—Cyclohexane rings in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers
- C09K19/3068—Cyclohexane rings in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers chain containing -COO- or -OCO- groups
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- C09K19/06—Non-steroidal liquid crystal compounds
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—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
- 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
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
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- C09K2019/121—Compounds containing phenylene-1,4-diyl (-Ph-)
- C09K2019/122—Ph-Ph
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- C09K2019/121—Compounds containing phenylene-1,4-diyl (-Ph-)
- C09K2019/123—Ph-Ph-Ph
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- C09K2019/181—Ph-C≡C-Ph
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- C09K19/2007—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters or ethers the chain containing -COO- or -OCO- groups
- C09K2019/2035—Ph-COO-Ph
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- 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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Abstract
本發明提供一種包含二苯並衍生物的液晶組合物及液晶顯示器件。所述液晶組合物包含至少一種通式I的化合物,以及至少一種通式II的化合物。本發明的液晶組合物均具有高的清亮點、大的光學各向異性、大的介電各向異性、較高的垂直於分子軸的介電常數ε⊥
、較高的垂直介電與介電絕對值的比值ε⊥
/|Δε|及較高的平均彈性常數Kave
,包含該些液晶組合物的液晶顯示器件均具備穿透率佳、對比度高的效果。本發明的液晶組合物可滿足液晶顯示器件對功耗低、顯示效果好的要求,在IPS模式、FFS模式及VA模式的液晶顯示器中具有較高的應用價值。
Description
本發明屬於液晶顯示材料技術領域,具體涉及一種包含二苯並衍生物的液晶組合物及液晶顯示器件。
液晶顯示器(Liquid Crystal Display,LCD)因其體積小、重量輕、功耗低且顯示品質優異而獲得了飛速發展,特別是在可擕式電子資訊產品中獲得廣泛的應用。根據顯示模式的類型,可將液晶顯示器分為PC(phase change,相變)、TN(twist nematic,扭曲向列)、STN(super twisted nematic,超扭曲向列)、ECB(electrically controlled birefringence,電控雙折射)、OCB(optically compensated bend,光學補償彎曲)、IPS(in-plane switching,共面轉變)、FFS(fringe field switching,邊緣場切換)、VA(vertical alignment,垂直配向)及PSA(polymer stable alignment,聚合物穩定配向)等類型。
這些模式中,已知IPS模式、FFS模式及VA模式可改善TN模式、STN模式等動作模式視角窄的缺點。這些顯示模式的液晶顯示器主要使用具有負介電各向異性的液晶組合物。為進一步提高液晶顯示器的特性,所述組合物優選有下述(1)~(8)的物性:
(1) 對熱、光等的高穩定性;
(2) 高清亮點;
(3) 液晶相的下限溫度低;
(4) 低的黏度;
(5) 適當的光學各向異性;
(6) 負值大的介電各向異性;
(7) 適當的彈性常數;
(8) 液晶化合物的相容性良好。
液晶組合物的物性對液晶顯示器的顯示效果有重要影響。如,對熱、光等穩定性高的液晶組合物可增大液晶顯示器的電壓保持率,進而延長液晶顯示器的使用壽命;清亮點高、液晶相的下限溫度低的液晶組合物可擴大液晶顯示器的可使用的溫度範圍;黏度低的液晶組合物可縮短液晶顯示器的回應時間;具有適當的光學各向異性的液晶組合物可提高液晶顯示器的對比度,在液晶顯示器逐步向更薄的趨勢發展時,比較合適的是具有較大光學各向異性的液晶組合物;具有負值大的介電各向異性的液晶組合物可降低液晶顯示元件的閾值電壓,由此可降低電力消耗;彈性常數大的液晶組合物可縮短液晶顯示器的回應時間,彈性常數小的液晶組合物可降低液晶顯示器的閾值電壓;液晶化合物的相容性良好有利於將物性不同的液晶化合物混合來調節液晶組合物的物性。
另外,提升液晶顯示器的對比度也是業內不斷研究的目標之一。研究表明,影響液晶顯示元件的對比度的最主要因素為液晶材料的漏光,而影響漏光的主要因素是液晶材料的光散射(LC Scattering),而LC Scattering與平均彈性常數Kave
的關係式如下:
LC Scattering ∝,
其中,d表示液晶盒的間距,ne
表示非尋常光折射率,no
表示尋常光折射率。由該關係式可知,LC Scattering與Kave
成反比例,在提高Kave
的情況下,可以降低液晶材料的漏光。
此外,對比度(CR)與亮度(L)的關係式如下:
CR=L255
/L0
×100%,
其中,L255
為開態亮度,L0
為關態亮度。可以看出,顯著影響CR的應該是L0
的變化。關態下,L0
與液晶分子的介電無關,與液晶材料本身的LC Scattering相關,LC Scattering愈小,L0
也愈小,CR從而也就會顯著提高。
另外,目前的液晶顯示器件還存在功耗高的問題,這是因為只有大約5%左右的背光能夠穿透顯示器件而被人眼捕獲,絕大部分光是被“浪費”了的。如果能夠開發出光穿透率高的液晶,即能夠降低背光強度,從而實現節省能耗的目的,延長設備的使用時間。
中國公開專利CN104926765A公開了一種4,6-二氟二苯並呋喃衍生物,其具有類似如下結構:。
上述化合物具有負介電各向異性,且其具有介電各向異性絕對值大、光學各向異性大的特點,但與其他液晶化合物的互溶性較差。
公開號為CN110300746A的中國專利申請公開了一種具有環狀端基的4,6-二氟二苯並呋喃衍生物(具有類似如下的結構):。
該類具有環端基的4,6-二氟二苯並呋喃衍生物與其他液晶化合物相容性有所提高,但包含該化合物的液晶組合物的穿透率及對比度往往無法滿足液晶顯示器日益更新的需求。
因此,在現有技術的基礎上,期待開發一種具有更高穿透率、更高對比的液晶組合物,從而能夠滿足液晶顯示器越來越高的視覺效果及低功耗的需求。
針對現有技術中存在的缺陷,本發明的目的在於提供一種包含二苯並衍生物的液晶組合物及包含其的液晶顯示器件,所述液晶組合物具有高的清亮點、大的光學各向異性、大的介電各向異性、較高的垂直於分子軸的介電常數ε⊥
、較高的垂直介電與介電絕對值的比值ε⊥
/|Δε|及較高的平均彈性常數Kave
。
為了實現上述發明目的,本發明採用以下技術方案:
第一方面,本發明提供了一種包含二苯並衍生物的液晶組合物,所述液晶組合物包含至少一種通式I的化合物,以及至少一種通式II的化合物:
其中,
R表示-H、鹵素、-CN、含有1-12個碳原子的直鏈或支鏈烷基、、或,所述含有1-12個碳原子的直鏈或支鏈烷基、、或中的一個或不相鄰的至少兩個-CH2
-可分別獨立地被-CH=CH-、-C≡C-、-O-、-S-、-CO-、-CO-O-或-O-CO-替代,所述含有1-12個碳原子的直鏈或支鏈烷基、、或中的一個或至少兩個-H可分別獨立地被-F或-Cl取代;
Rx
表示-H、含有1-12個碳原子的直鏈或支鏈的烷基,所述含有1-12個碳原子的直鏈或支鏈的烷基中的一個或不相鄰的至少兩個-CH2
-可分別獨立地被-CH=CH-、-C≡C-、-O-、-S-、-CO-、-CO-O-或-O-CO-替代,所述含有1-12個碳原子的直鏈或支鏈的烷基中的一個或至少兩個-H可分別獨立地被-F或-Cl取代,所述Rx
與環中任意碳原子相連接;
R1
和R2
各自獨立地表示含有1-12個碳原子的直鏈或支鏈的烷基、、或,所述含有1-12個碳原子的直鏈或支鏈的烷基中的一個或不相鄰的至少兩個-CH2
-可分別獨立地被-CH=CH-、-C≡C-、-O-、-S-、-CO-、-CO-O-或-O-CO-替代,所述含有1-12個碳原子的直鏈或支鏈的烷基中的一個或至少兩個-H可分別獨立地被-F或-Cl取代,所述R1
和R2
與通式II中氧原子相連的原子均為碳原子;
環表示、、、或,前述基團中的一個或至少兩個環中單鍵可被雙鍵替代;
環表示、或;所述、中的一個或至少兩個-CH2
-可被-O-替代,一個或至多兩個環中單鍵可被雙鍵替代;所述中的一個或至少兩個-H可被-F或-Cl取代,一個或至少兩個環中-CH=可被-N=替代;“一個或至少兩個環中的-CH=可被-N=替代”中“一個或至少兩個”指的是被-N=替代的-CH=的數量,本發明涉及到相同的表達方式,均具有同樣的意義;
環表示,所述中的一個或至少兩個-H可被-F或-Cl取代,一個或至少兩個環中-CH=可被-N=替代;
Z1
表示-(CH2
)a
O-或-(CH2
)a
S-,其中a表示0至7的整數;例如a可以為0、1、2、3、4、5、6或7;
Z2
表示-O-、-S-、-CO-O-、-O-CO-、-CF2
O-、-OCF2
-、-CH2
O-、-CH2
S-、-OCH2
-、-SCH2
-、-CH2
-、-CH2
CH2
-、-(CH2
)4
-、-CH=CH-CH2
O-、-C2
F4
-、-CH2
CF2
-、-CF2
CH2
-、-CF=CF-、-CH=CF-、-CF=CH-、-CH=CH-、-C≡C-或單鍵;
L1
和L2
各自獨立地表示-F、-Cl、-CF3
或-CHF2
;
X表示-CO-、-S-或-O-;
n表示0、1或2,其中當n表示2時,環相同或不同,Z2
相同或不同;
m表示0、1或2,當m表示2時,環相同或不同。
| I; | |
| II; |
本發明中,“可分別獨立地被……替代”指的是可以被替代,也可以不被替代,即,替代或不被替代,均屬於本發明的保護範圍之內,“可分別獨立地被……取代”同理,且“替代”和“取代”的位置可以是任意的。
本發明中,所述鹵素包括氟、氯、溴或碘等。
本發明中,所述1-12個碳原子可以為1、2、3、4、5、6、7、8、9、10、11或12個碳原子。
本發明的通式I的化合物和通式II的化合物均對液晶組合物的垂直於分子軸的介電常數ε⊥
、垂直介電與介電絕對值的比值ε⊥
/|Δε|及平均彈性常數Kave
有提升作用,協同作用後,可產生更加明顯的改善效果。
在本發明的優選實施方案中,所述n表示0或1。
在本發明的優選實施方案中,所述L1
和L2
均表示-F。
在本發明的優選實施方案中,所述X表示-O-或-S-。
在本發明的優選實施方案中,所述液晶組合物中含有至少一種X表示-O-的通式I的化合物;進一步優選地,所述液晶組合物中含有至少一種X表示-O-的通式I的化合物,以及至少一種X表示-S-的通式I的化合物。
在本發明的優選實施方案中,所述a表示0至3的整數,例如0、1、2或3;進一步優選地,a表示1至3的整數,再進一步優選地,a表示1。
在本發明的優選實施方案中,所述R表示-H、含有1-12(例如1、2、3、4、5、6、8、10或11等)個碳原子的直鏈或支鏈烷基、、或,所述含有1-12個碳原子的直鏈或支鏈烷基、、或中的一個或不相鄰的至少兩個-CH2
-可分別獨立地被-CH=CH-、-O-或-S-替代,所述含有1-12個碳原子的直鏈或支鏈烷基、、或中的一個或至少兩個-H可分別獨立地被-F取代。
進一步優選地,所述R表示含有1-12個碳原子的直鏈烷基或含有1-11個碳原子的烷氧基。
在本發明的優選實施方案中,所述Rx
表示-H、含有1-12(例如1、2、3、4、5、6、8、10或11等)個碳原子的直鏈或支鏈的烷基;進一步優選地,所述Rx
表示-H或含有1-6個碳原子的直鏈烷基。
在本發明的優選實施方案中,所述通式I的化合物占液晶組合物總重量的0.1-40%,例如0.2%、0.5%、0.8%、1%、3%、5%、8%、10%、12%、15%、18%、20%、22%、25%、28%、30%、32%、35%、37%或39%等;進一步優選地,所述通式I的化合物占液晶組合物總重量的1-30%。
在本發明的優選實施方案中,所述m表示0或1。
在本發明的優選實施方案中,所述R1
、R2
各自獨立地表示含有1-12(例如1、2、3、4、5、6、8、10或11等)個碳原子的直鏈或支鏈的烷基,或所述含有1-12個碳原子的直鏈或支鏈的烷基中的一個或不相鄰的至少兩個-CH2
-被-O-替代。
在本發明的優選實施方案中,所述液晶組合物中含有至少一種m=0的通式II的化合物。
在本發明的優選實施方案中,所述液晶組合物中含有至少一種m=1的通式II的化合物。
在本發明的優選實施方案中,所述液晶組合物中含有至少一種m=0的通式II的化合物,以及至少一種m=1的通式II的化合物。
在本發明的優選實施方案中,所述液晶組合物中含有至少一種R2
表示含有2-11個碳原子的烷氧烷基的通式II的化合物。所述烷氧烷基是指烷基中非位於兩端的-CH2
-被-O-替代後的基團,如-CH2
OCH3
、-CH2
CH2
CH2
OCH2
CH2
CH2
CH3
等。
在本發明的優選實施方案中,所述通式II的化合物占液晶組合物總重量的0.1-30%,例如0.2%、0.5%、0.8%、1%、3%、5%、8%、10%、12%、15%、18%、20%、21%、23%、25%、27%或29%等;進一步優選地,所述通式II的化合物占液晶組合物總重量的1-25%,再進一步優選地,所述通式II的化合物占液晶組合物總重量的1-20%。
在本發明的優選實施方案中,所述液晶組合物中還包含一種或至少兩種通式M的化合物M;
其中,
RM1
和RM2
各自獨立地表示含有1-12(例如1、2、3、4、5、6、8、10或11等)個碳原子的直鏈或支鏈的烷基、、或,所述含有1-12個碳原子的直鏈或支鏈的烷基中的一個或不相鄰的至少兩個-CH2
-可分別獨立地被-CH=CH-、-C≡C-、-O-、-CO-、-CO-O-或-O-CO-替代;
環、環和環各自獨立地表示或,所述中的一個或至少兩個-CH2
-可被-O-替代,所述中的至多一個-H可被鹵素取代;
ZM1
和ZM2
各自獨立地表示單鍵、-CO-O-、-O-CO-、-CH2
O-、-OCH2
-、-CH=CH-、-C≡C-、-CH2
CH2
-、-(CH2
)4
-、-CF2
O-、-OCF2
-或-CF2
CF2
-;
nM1
表示0、1、2或3,其中當nM1
=2或3時,環相同或不同,ZM2
相同或不同。
在本發明的優選實施方案中,所述RM1
和RM2
各自獨立地表示含有1-10(例如1、2、3、4、5、6、8、9或10)個碳原子的直鏈的烷基、含有1-9(例如1、2、3、4、5、6、8或9)個碳原子的直鏈的烷氧基或含有2-10(例如2、3、4、5、6、8、9或10)個碳原子的直鏈的烯基。
進一步優選地,所述RM1
和RM2
各自獨立地表示含有1-8個碳原子的直鏈的烷基、含有1-7個碳原子的直鏈的烷氧基或含有2-8個碳原子的直鏈的烯基。
再進一步優選地,RM1
和RM2
各自獨立地表示含有1-5個碳原子的直鏈的烷基、含有1-4個碳原子的直鏈的烷氧基或含有2-5個碳原子的直鏈的烯基。
在本發明的優選實施方案中,所述RM1
和RM2
中的任意一者為含有2-5個碳原子的直鏈的烯基,而另一者為含有1-5個碳原子的直鏈的烷基。
本發明中的烯基優選為式(V1)至式(V9)中的任意一者所表示的基團,特別優選為式(V1)、式(V2)、式(V8)或(V9)。式(V1)至式(V9)所表示的基團如下所示: ,
其中,*表示上述基團與化合物的連接位點。
本發明中的烯氧基優選為式(OV1)至式(OV9)中的任意一者所表示的基團,特別優選為式(OV1)、式(OV2)、式(OV8)或(OV9)。式(OV1)至式(OV9)所表示的基團如下所示: ,
其中,*表示所鍵結的環結構中的碳原子。
在本發明的優選實施方案中,所述RM1
和RM2
中的任意一者為含有1-5個碳原子的直鏈的烷基,而另一者為含有1-5個碳原子的直鏈的烷基或含有1-4個碳原子的直鏈的烷氧基;進一步優選地,所述RM1
和RM2
兩者均各自獨立地為含有1-5個碳原子的直鏈的烷基。
在本發明的優選實施方案中,所述通式M的化合物選自由如下化合物組成的組:
其中,RM1
和RM2
各自獨立地表示含有1-12個碳原子的直鏈或支鏈的烷基,或所述含有1-12個碳原子的直鏈或支鏈的烷基中的一個或不相鄰的至少兩個-CH2
-可分別獨立地被-CH=CH-或-O-替代。
| M1; | |
| M2; | |
| M3; | |
| M4; | |
| M5; | |
| M6; | |
| M7; | |
| M8; | |
| M9; | |
| M10 | |
| M11; | |
| M12; | |
| M13; | |
| M14; | |
| M15; | |
| M16; | |
| M17; | |
| M18; | |
| M19; | |
| M20; | |
| M21; | |
| M22; | |
| M23; | |
| M24; | |
| M25; | |
| M26; | |
| M27; | |
| M28; | |
| M29; | |
| M30; | |
| M31;以及 | |
| M32。 |
優選地,所述通式M的化合物占液晶組合物總重量的10-70%,例如11%、13%、15%、18%、20%、22%、25%、28%、30%、33%、35%、38%、40%、43%、45%、48%、50%、52%、55%、58%、60%、62%、65%、67%或69%等。
為了調節液晶組合物的清亮點、粘度及低溫存儲穩定性等方面的性能,以使獲得的液晶顯示器件除了在透過率和色彩表現方面表現優異外,還具有更好的應用價值,需要調節液晶組合物的組分構成;具體地,相對於本發明的液晶組合物的總重量,其中環表示的通式M的化合物的含量為10-50%;優選地,其中環表示的通式M的化合物的含量為20-45%。
關於通式M的化合物的含量,在需要保持本發明的液晶組合物粘度較低且回應時間較短時,優選其下限值較高且上限值較高;進一步地,在需要保持本發明的液晶組合物的清亮點較高且溫度穩定性良好時,優選其下限值較高且上限值較高;在為了將驅動電壓保持為較低且介電各向異性的絕對值變大時,優選使其下限值變低且上限值變低。
在重視可靠性的情形時,優選RM1
和RM2
均各自獨立地為烷基;在重視降低化合物的揮發性的情形時,優選RM1
和RM2
均各自獨立地為烷氧基;在重視粘度降低的情形時,優選RM1
和RM2
中至少一者為烯基。
在本發明的優選實施方案中,為了進一步降低液晶組合物的黏度,所述液晶組合物中包含一種或至少兩種其中RM1
和/或RM2
為正丙基的通式M1的化合物
在本發明的優選實施方案中,所述液晶組合物還包含一種或至少兩種通式N的化合物
其中,
RN1
和RN2
各自獨立地表示含有1-12(例如1、2、3、4、5、6、8、10或11等)個碳原子的直鏈或支鏈的烷基、、或,所述含有1-12個碳原子的直鏈或支鏈的烷基中的一個或不相鄰的至少兩個-CH2
-可分別獨立地被-O-、-CO-、-CO-O-或-O-CO-替代,所述含有1-12個碳原子的直鏈或支鏈的烷基、、或中的一個或至少兩個-H可分別獨立地被-F或-Cl取代,所述RN1
、RN2
中的至少一個與通式N中環結構相連的原子為碳原子,即RN1
和RN2
與通式N中的環結構相連的原子不可同時為氧;
環和環各自獨立地表示或,所述中的一個或至少兩個-CH2
-可被-O-替代,所述中的一個或至少兩個-H可被-F或-Cl取代,一個或至少兩個環中-CH=可被-N=替代;
ZN1
和ZN2
各自獨立地表示單鍵、-CO-O-、-O-CO-、-CH2
O-、-OCH2
-、-CH2
CH2
-、-(CH2
)4
-、-CF2
O-、-OCF2
-或-CF2
CF2
-;
LN1
和LN2
各自獨立地表示-H或甲基;
nN1
表示0、1、2或3,nN2
表示0或1,且0≤nN1
+nN2
≤3,其中當nN1
=2或3時,環相同或不同,ZN1
相同或不同。
| M1。 |
| N; |
在本發明的優選實施方案中,所述RN1
和RN2
各自獨立地表示含有1-8(例如1、2、3、4、5、6、7或8)個碳原子的直鏈或支鏈的烷基或烷氧基,進一步優選地,所述RN1
和RN2
各自獨立地為含有1-5個碳原子的直鏈或支鏈的烷基或烷氧基。
在本發明的優選實施方案中,所述通式N的化合物選自由如下化合物組成的組:
其中,
RN1
表示含有1-5個碳原子的直鏈或支鏈的烷基,RN2
表示含有1-4個碳原子的直鏈或支鏈的烷氧基。
| N1; | |
| N2; | |
| N3; | |
| N4; | |
| N5; | |
| N6; | |
| N7; | |
| N8; | |
| N9; | |
| N10; | |
| N11; | |
| N12; | |
| N13; | |
| N14; | |
| N15; | |
| N16; | |
| N17; | |
| N18; | |
| N19; | |
| N20; | |
| N21;以及 | |
| N22, |
優選地,所述通式N的化合物占液晶組合物總重量的1-75%,例如2%、4%、6%、8%、10%、13%、15%、18%、20%、22%、25%、28%、30%、33%、35%、38%、40%、43%、45%、48%、50%、52%、55%、58%、60%、62%、65%、67%、70%、72%或74%等。
關於通式N的化合物含量,在需要保持本發明的液晶顯示器件回應時間較短時,優選其下限值較低且上限值較低;進一步地,在需要保持本發明的液晶顯示器件工作溫度範圍更寬時,優選其下限值較低且上限值較低;另外,在為了將液晶組合物的驅動電壓保持為較低而使介電各向異性的絕對值變大時,優選使其下限值變高且上限值較高。
在本發明的優選實施方案中,可以向液晶組合物中添加本領域技術人員已知和文獻中描述的一種或更多種其他添加劑。
優選地,穩定劑選自如下所示的穩定劑。
在本發明的優選實施方案中,穩定劑占液晶組合物總重量的0-5%;優選地,穩定劑占液晶組合物總重量的0-1%;更優選地,穩定劑占液晶組合物總重量的0.01-0.1%。
| 。 |
另一方面,本發明提供一種包含如上所述的液晶組合物的液晶顯示器件。
優選地,所述液晶顯示器件為IPS模式型液晶顯示器件、FFS模式型液晶顯示器件或VA模式型液晶顯示器件。
相對於現有技術,本發明具有以下有益效果:
本發明提供的液晶組合物均具有高的清亮點、大的光學各向異性、大的介電各向異性、較高的垂直於分子軸的介電常數ε⊥
、較高的垂直介電與介電絕對值的比值ε⊥
/|Δε|及較高的平均彈性常數Kave
,包含該些液晶組合物的液晶顯示器件均具備穿透率佳、對比度高的效果。本發明的液晶組合物可滿足液晶顯示器件對功耗低、顯示效果好的要求,在IPS模式、FFS模式及VA模式型液晶顯示器中具有較高的應用價值。
以下將結合具體實施方式來說明本發明的技術方案。本領域技術人員應該明瞭,以下實施例為本發明的示例,僅用來說明和幫助理解本發明,不應視為對本發明的限制。在不偏離本發明主旨或範圍的情況下,可進行本發明構思內的其他組合和各種改良。
在本發明中如無特殊說明,本發明中提及的比例均為重量比,所有溫度均為攝氏溫度。
為便於表達,以下各實施例中,液晶化合物的基團結構用表1所列的代碼表示:
表1 液晶化合物的基團結構代碼
以如下結構式的化合物為例:
該結構式如用表1所列代碼表示,則可表達為:nCCGF,代碼中的n表示左端烷基的C原子數,例如n為“3”,即表示該烷基為-C3
H7
;代碼中的C代表1,4-亞環己基,G代表2-氟-1,4-亞苯基,F代表氟取代基。
| 基團的單元結構 | 代碼 | 基團名稱 |
| C | 1,4-亞環己基 | |
| P | 1,4-亞苯基 | |
| G | 2-氟-1,4-亞苯基 | |
| W | 2,3-二氟-1,4-亞苯基 | |
| B(O) | 4,6-二氟-二苯並[b,d]呋喃-3,7-二基 | |
| B(S) | 4,6-二氟-二苯並[b,d]噻吩-3,7-二基 | |
| THF(2,5) | 四氫呋喃-2,5-二基 | |
| THT(2,5) | 四氫噻吩-2,5-二基 | |
| C(5) | 環戊烷基 | |
| THF | 四氫呋喃-2-基 | |
| THF(3) | 四氫呋喃-3-基 | |
| DHF(1) | 4,5-二氫呋喃-2-基 | |
| THT | 四氫噻吩-2-基 | |
| THT(3) | 四氫噻吩-3-基 | |
| -CH2 CH2 - | 2 | 乙基橋鍵 |
| -CH2 CH2 CH2 - | 3 | 丙基橋鍵 |
| -CH2 O- | 1O | 亞甲氧基 |
| -F | F | 氟取代基 |
| -O- | O | 氧橋基 |
| -S- | S | 硫橋基 |
| -Cn H2n+1 | n(n表示1-12的正整數) | 烷基 |
| -CH=CH-或-CH=CH2 | V | 乙烯基 |
以下實施例中測試專案的簡寫代號如下:
其中,
Cp:通過熔點儀量法測試獲得;
Δε:Δε=ε‖
-ε⊥
,其中,ε‖
為平行於分子軸的介電常數,ε⊥
為垂直於分子軸的介電常數,測試條件:25℃、1 KHz、盒厚7 μm的TN90型測試盒;
Δn:使用阿貝折光儀在鈉光燈(589 nm)光源下、25℃測試得到;
γ1
:使用LCM-2型液晶物性評價系統測試得到;測試條件:25℃、240 V、測試盒厚20 μm;
Kave
=(K11
+K22
+K33
),K11
、K22
、K33
是使用LCR儀和反平行摩擦盒,測試液晶的C-V曲線計算所得,測試條件:7 μm反平行摩擦盒,V=0.1~20V。
穿透率的測試條件:利用DMS 505光電綜合測試儀測試調光器件的V-T曲線,V-T曲線中Tmax
值即為液晶材料的穿透率,所述調光器件為負性IPS型測試盒,盒厚3.5μm。
| Cp | 清亮點(向列相-各向同性相轉變溫度,℃) |
| Δε | 介電各向異性(1 KHz,25℃) |
| ε⊥ | 垂直於分子軸的介電常數(1 KHz,25℃) |
| ε⊥ /|Δε| | 垂直介電與介電絕對值的比值 |
| Δn | 光學各向異性(光照波長589 nm,25℃) |
| γ1 | 旋轉黏度(mPa·s,25℃) |
| Kave | 平均彈性常數 |
| T(%) | 穿透率(DMS-505,盒厚3.5μm) |
在以下的實施例中所採用的各成分,均可以通過公知的方法進行合成,或者通過商業途徑獲得。這些合成技術是常規的,所得到各液晶組合物經測試符合電子類化合物標準。
按照以下實施例規定的各液晶組合物的配比製備液晶組合物。液晶組合物的製備是按照本領域的常規方法進行的,如採取加熱、超聲波、懸浮等方式按照規定比例混合制得。
對比例
1
一種液晶組合物,組分及性能參數如表2所示:
表2液晶組合物的組成及性能參數
| 組分代碼 | 重量百分數 | 通式代碼 | 性能參數 | |
| 3CCWO2 | 8 | N5 | Cp | 77 |
| 2CCWO2 | 8 | N5 | Δn | 0.096 |
| 3CPWO2 | 8 | N11 | Δε | -3.6 |
| 4CPWO2 | 6 | N11 | ε⊥ | 6.4 |
| 5OPWO2 | 3 | II | ε⊥ /|Δε| | 1.78 |
| 3OPWO2 | 6 | II | γ1 | 95 |
| 3CWO2 | 6 | N2 | Kave | 12.6 |
| 1PP2V | 2 | M6 | T | 13.1% |
| 3CPP2 | 1.5 | M16 | ||
| 3CCV | 33.5 | M1 | ||
| 3CCV1 | 10 | M1 | ||
| 2OB(O)O3 | 2 | |||
| 3OB(O)O4 | 3 | |||
| 3OB(S)O5 | 3 | |||
| 合計 | 100 |
實施例
1
一種液晶組合物,組分及性能參數如表3所示:
表3液晶組合物的組成及性能參數
| 組分代碼 | 重量百分數 | 通式代碼 | 性能參數 | |
| 3CCWO2 | 8 | N5 | Cp | 81 |
| 2CCWO2 | 8 | N5 | Δn | 0.099 |
| 3CPWO2 | 8 | N11 | Δε | -3.8 |
| 4CPWO2 | 6 | N11 | ε⊥ | 6.9 |
| 5OPWO2 | 3 | II | ε⊥ /|Δε| | 1.82 |
| 3OPWO2 | 6 | II | γ1 | 94 |
| 3CWO2 | 6 | N2 | Kave | 13.5 |
| 1PP2V | 2 | M6 | T | 14.0% |
| 3CPP2 | 1.5 | M16 | ||
| 3CCV | 33.5 | M1 | ||
| 3CCV1 | 10 | M1 | ||
| THF1OB(O)O4 | 2 | I | ||
| THF1OB(O)O5 | 3 | I | ||
| THF1OB(O)O3 | 3 | I | ||
| 合計 | 100 |
對比例
2
一種液晶組合物,組分及性能參數如表4所示:
表4液晶組合物的組成及性能參數
| 組分代碼 | 重量百分數 | 通式代碼 | 性能參數 | |
| 3C1OWO2 | 6 | N3 | Cp | 76 |
| 2CC1OWO2 | 10.5 | N6 | Δn | 0.101 |
| 3CC1OWO2 | 10 | N6 | Δε | -3.6 |
| 4CC1OWO2 | 6 | N6 | ε⊥ | 6.1 |
| 5PWO2 | 7 | N10 | ε⊥ /|Δε| | 1.69 |
| 3PWO2 | 3 | N10 | γ1 | 103 |
| 3CPWO2 | 6 | N11 | Kave | 13.5 |
| 4CPWO2 | 1.5 | N11 | T | 13.5% |
| 3CPP2 | 1.5 | M16 | ||
| 3CCV | 38.5 | M1 | ||
| 3CCV1 | 5 | M1 | ||
| C(5)OB(O)O5 | 2 | |||
| C(5)OB(S)O3 | 3 | |||
| 合計 | 100 |
實施例
2
一種液晶組合物,組分及性能參數如表5所示:
表5液晶組合物的組成及性能參數
| 組分代碼 | 重量百分數 | 通式代碼 | 性能參數 | |
| 3C1OWO2 | 6 | N3 | Cp | 78 |
| 2CC1OWO2 | 10.5 | N6 | Δn | 0.104 |
| 3CC1OWO2 | 10 | N6 | Δε | -3.7 |
| 4CC1OWO2 | 6 | N6 | ε⊥ | 6.9 |
| 5OPWO2 | 7 | II | ε⊥ /|Δε| | 1.86 |
| 3OPWO2 | 3 | II | γ1 | 100 |
| 3CPWO2 | 6 | N11 | Kave | 13.9 |
| 4CPWO2 | 1.5 | N11 | T | 14.2% |
| 3CPP2 | 1.5 | M16 | ||
| 3CCV | 38.5 | M1 | ||
| 3CCV1 | 5 | M1 | ||
| C(5)OB(O)O5 | 2 | I | ||
| C(5)OB(S)O3 | 3 | I | ||
| 合計 | 100 |
實施例
3
一種液晶組合物,組分及性能參數如表6所示:
表6液晶組合物的組成及性能參數
| 組分代碼 | 重量百分數 | 通式代碼 | 性能參數 | |
| 3C1OWO2 | 11.5 | N3 | Cp | 83 |
| 2CC1OWO2 | 2 | N6 | Δn | 0.109 |
| 3CC1OWO2 | 12.5 | N6 | Δε | -3.5 |
| 2OPWO2 | 6.5 | II | ε⊥ | 7.5 |
| 3CCV | 37 | M1 | ε⊥ /|Δε| | 2.14 |
| 3CCV1 | 3 | M2 | γ1 | 89 |
| 3PPWO4 | 2 | N12 | Kave | 14.3 |
| 3PPWO2 | 2 | N12 | T | 14.8% |
| 5PPWO2 | 1 | N12 | ||
| 4PPWO2 | 2 | N12 | ||
| 3CPP2V | 2 | M16 | ||
| 3CPP2V1 | 3 | M16 | ||
| 3CPWO2 | 9 | N11 | ||
| 5OWO3 | 1.5 | II | ||
| THF1OB(O)O4 | 2.5 | I | ||
| THF1OB(O)O5 | 2.5 | I | ||
| 合計 | 100 |
實施例
4
一種液晶組合物,組分及性能參數如表7所示:
表7液晶組合物的組成及性能參數
| 組分代碼 | 重量百分數 | 通式代碼 | 性能參數 | |
| 3PWO2 | 11.5 | N10 | Cp | 78 |
| 2CC1OWO2 | 4.5 | N6 | Δn | 0.11 |
| 3CC1OWO2 | 10 | N6 | Δε | -3.8 |
| 2OPWO2 | 6.5 | II | ε⊥ | 7.8 |
| 3CCV | 38 | M1 | ε⊥ /|Δε| | 2.05 |
| 3CCWO4 | 3 | N5 | γ1 | 87 |
| 3PPWO2 | 2 | N12 | Kave | 14.8 |
| 4PPWO2 | 2 | N12 | T | 14.5% |
| 3CPWO2 | 9 | N11 | ||
| 5OWO3O4 | 1.5 | II | ||
| C(5)OB(O)O1THF | 2.5 | I | ||
| C(5)OB(S)O1THF | 2.5 | I | ||
| THF1OB(S)O4 | 2 | I | ||
| THF1OB(S)O3 | 3 | I | ||
| 1PP2V | 2 | M6 | ||
| 合計 | 100 |
實施例
5
一種液晶組合物,組分及性能參數如表8所示:
表8液晶組合物的組成及性能參數
| 組分代碼 | 重量百分數 | 通式代碼 | 性能參數 | |
| 3PWO2 | 10.5 | N10 | Cp | 80 |
| 2CC1OWO2 | 4.5 | N6 | Δn | 0.11 |
| 3CC1OWO2 | 4 | N6 | Δε | -4.2 |
| 2OPWO2 | 10.5 | II | ε⊥ | 7.9 |
| 3CCV | 35 | M1 | ε⊥ /|Δε| | 1.88 |
| 3CCWO4 | 3 | N5 | γ1 | 82 |
| 3CPWO2 | 7 | N11 | Kave | 15.1 |
| 3OWO3O4 | 3.5 | II | T | 15.3% |
| THF1OB(O)O4 | 2.5 | I | ||
| THF1OB(O)O5 | 2.5 | I | ||
| 2THF(2,5)1OB(S)O4 | 2 | I | ||
| THF1OB(S)O3 | 3 | I | ||
| C(5)1OB(S)O3 | 3 | I | ||
| C(5)1OB(O)O3 | 3 | I | ||
| C(5)1OB(O)O4 | 3 | I | ||
| C(5)1OB(S)O4 | 3 | I | ||
| 合計 | 100 |
實施例
6
一種液晶組合物,組分及性能參數如表9所示:
表9液晶組合物的組成及性能參數
| 組分代碼 | 重量百分數 | 通式代碼 | 性能參數 | |
| 4CC1OWO2 | 8 | N6 | Cp | 76 |
| 3CC1OWO2 | 12.5 | N6 | Δn | 0.11 |
| 2OPWO2 | 7 | II | Δε | -4.1 |
| 3PWO2 | 5.5 | N10 | ε⊥ | 7.5 |
| 3PPWO4 | 2 | N12 | ε⊥ /|Δε| | 1.83 |
| 3PPWO2 | 2 | N12 | γ1 | 90 |
| 3CPWO2 | 5 | N11 | Kave | 14.1 |
| 4OWO3 | 1.5 | II | T | 14.9% |
| 3CCV | 40.5 | M1 | ||
| 3CPP2V | 1.5 | M16 | ||
| 3CPP2V1 | 1.5 | M16 | ||
| THF2OB(O)O4 | 2.5 | I | ||
| THF2OB(O)O5 | 2.5 | I | ||
| THF1OB(S)O4 | 2 | I | ||
| THF1OB(S)O3 | 3 | I | ||
| C(5)1OB(S)O3 | 3 | I | ||
| 合計 | 100 |
實施例
7
一種液晶組合物,組分及性能參數如表10所示:
表10液晶組合物的組成及性能參數
| 組分代碼 | 重量百分數 | 通式代碼 | 性能參數 | |
| 3OPWO3O4 | 3 | II | Cp | 91 |
| 2CC1OWO2 | 2.5 | N6 | Δn | 0.107 |
| 3CC1OWO2 | 11 | N6 | Δε | -4.1 |
| 2OPWO2 | 6 | II | ε⊥ | 7.4 |
| 3CCV | 39 | M1 | ε⊥ /|Δε| | 1.80 |
| 3CCWO4 | 2 | N5 | γ1 | 89 |
| 3CCWO2 | 2 | N5 | Kave | 15 |
| 3CPWO2 | 4 | N11 | T | 15.1% |
| 3CPP2V | 2 | M16 | ||
| 3CPP2V1 | 3 | M16 | ||
| 3CPWO2 | 8 | N11 | ||
| 3OWO2 | 4.5 | II | ||
| THF1OB(O)O4 | 2.5 | I | ||
| THF1OB(O)O5 | 2.5 | I | ||
| 2THF(2,5)1OB(S)O4 | 4 | I | ||
| THF1OB(S)O4 | 4 | I | ||
| 合計 | 100 |
實施例
8
一種液晶組合物,組分及性能參數如表11所示:
表11液晶組合物的組成及性能參數
| 組分代碼 | 重量百分數 | 通式代碼 | 性能參數 | |
| 3OPWO3O4 | 3 | II | Cp | 90 |
| 2CC1OWO2 | 2.5 | N6 | Δn | 0.106 |
| 3CC1OWO2 | 12 | N6 | Δε | -4 |
| 2OPWO2 | 6 | II | ε⊥ | 7.3 |
| 3CCV | 36 | M1 | ε⊥ /|Δε| | 1.83 |
| 3CCV1 | 4 | M1 | γ1 | 87 |
| 3CCWO4 | 2 | N5 | Kave | 15.1 |
| 3CCWO2 | 2 | N5 | T | 15.3% |
| 3CPWO2 | 4 | N11 | ||
| 3CPP2V | 2 | M16 | ||
| 3CPP2V1 | 3 | M16 | ||
| 3CPWO2 | 9 | N11 | ||
| 2OWO3 | 1.5 | II | ||
| THF(3)1OB(O)O4 | 2.5 | I | ||
| THF(3)1OB(O)O5 | 2.5 | I | ||
| DHF(1)1OB(O)O4 | 4 | I | ||
| DHF(1)1OB(O)O5 | 4 | I | ||
| 合計 | 100 |
由上述對比例1與實施例1對比可以看出,本發明的通式I的化合物更有利於提升液晶組合物的垂直於分子軸的介電常數ε⊥
、垂直介電與介電絕對值的比值ε⊥
/|Δε|及平均彈性常數Kave
,使得液晶組合物在維持基本相當的清亮點、光學各向異性及介電各向異性的前提下,具有更高的垂直於分子軸的介電常數ε⊥
、更高的垂直介電與介電絕對值的比值ε⊥
/|Δε|及更高的平均彈性常數Kave
,從而使包含該液晶組合物的液晶顯示器件具備更高的穿透率及更高的對比度。
由上述對比例2與實施例2對比可以看出,本發明的通式II的化合物同樣非常有利於提升液晶組合物的垂直於分子軸的介電常數ε⊥
、垂直介電與介電絕對值的比值ε⊥
/|Δε|及平均彈性常數Kave
,在與通式I的化合物協同作用後,對液晶組合物的穿透率及對比度形成了顯著的改善。
由上述實施例1-8可知,本發明的液晶組合物均具有高的清亮點、大的光學各向異性、大的介電各向異性、較高的垂直於分子軸的介電常數ε⊥
、較高的垂直介電與介電絕對值的比值ε⊥
/|Δε|及較高的平均彈性常數Kave
,包含該些液晶組合物的液晶顯示器件均具備穿透率佳、對比度高的效果。本發明的液晶組合物可滿足液晶顯示器件對功耗低、顯示效果好的要求,在IPS模式、FFS模式及VA模式型液晶顯示器中具有較高的應用價值。
申請人聲明,本發明通過上述實施例來說明本發明的一種包含二苯並衍生物的液晶組合物及液晶顯示器件,但本發明並不局限於上述工藝步驟,即不意味著本發明必須依賴上述工藝步驟才能實施。所屬技術領域的技術人員應該明瞭,對本發明的任何改進,對本發明所選用原料的等效替換及輔助成分的添加、具體方式的選擇等,均落在本發明的保護範圍和公開範圍之內。
以上實施方式只為說明本發明的技術構思及特點,其目的在於讓熟悉此項技術的人瞭解本發明內容並加以實施,並不能以此限制本發明的保護範圍,凡根據本發明精神實質所做的等效變化或修飾,都應涵蓋在本發明的保護範圍內。
Claims (9)
- 一種包含二苯並衍生物的液晶組合物,該液晶組合物包含至少一種通式I的化合物,以及至少一種通式II的化合物:
其中, R表示-H、鹵素、-CN、含有1-12個碳原子的直鏈或支鏈烷基、、 或,而含有1-12個碳原子的直鏈或支鏈烷基、、或 中的一個或不相鄰的至少兩個-CH2-可分別獨立地被-CH=CH-、-C≡C-、 -O-、-S-、-CO-、-CO-O-或-O-CO-替代,而含有1-12個碳原子的直鏈或支鏈 烷基、、或中的一個或至少兩個-H可分別獨立地被-F或-Cl 取代;Rx表示-H、含有1-12個碳原子的直鏈或支鏈的烷基,而含有1-12個碳原子的直鏈或支鏈的烷基中的一個或不相鄰的至少兩個-CH2-可分別獨立地被-CH=CH-、-C≡C-、-O-、-S-、-CO-、-CO-O-或-O-CO-替代,而含有1-12個碳原子的直鏈或支鏈的烷基中的一個或至少兩個-H可分別獨立地被-F或 -Cl取代,Rx與環中任意碳原子相連接; R1和R2各自獨立地表示含有1-12個碳原子的直鏈或支鏈的烷基、、 或,而含有1-12個碳原子的直鏈或支鏈的烷基中的一個或不相 鄰的至少兩個-CH2-可分別獨立地被-CH=CH-、-C≡C-、-O-、-S-、-CO-、-CO-O-或-O-CO-替代,而含有1-12個碳原子的直鏈或支鏈的烷基中的一個或至少兩個-H可分別獨立地被-F或-Cl取代,R1和R2與通式II中氧原子相連的原子均為碳原子; 環表示、、、或,前述基團中 的一個或至少兩個環中單鍵可被雙鍵替代; 環表示、或;或中 的一個或至少兩個-CH2-可被-O-替代,一個或至多兩個環中單鍵可被雙鍵替 代;中的一個或至少兩個-H可被-F或-Cl取代,一個或至少兩個環 中-CH=可被-N=替代; 環表示,中的一個或至少兩個-H可被-F 或-Cl取代,一個或至少兩個環中-CH=可被-N=替代;Z1表示-(CH2)aO-或-(CH2)aS-,其中a表示0至7的整數;Z2表示-O-、-S-、-CO-O-、-O-CO-、-CF2O-、-OCF2-、-CH2O-、-CH2S-、-OCH2-、-SCH2-、-CH2-、-CH2CH2-、-(CH2)4-、-CH=CH-CH2O-、-C2F4-、-CH2CF2-、-CF2CH2-、-CF=CF-、-CH=CF-、-CF=CH-、-CH=CH-、-C≡C-或單鍵;L1和L2各自獨立地表示-F;X表示-S-或-O-; n表示0、1或2,其中當n表示2時,環相同或不同,Z2相 同或不同; m表示0、1或2,當m表示2時,環相同或不同; 其中,該液晶組合物還包含至少一種環僅為、、 或的通式I的化合物,前述基團中的一個或至少兩個環中單鍵 可被雙鍵替代。 - 如請求項1所述之液晶組合物,其中,n表示0或1。
- 如請求項1所述之液晶組合物,其中,該液晶組合物中含有至少一種X表示-O-的通式I的化合物。
- 如請求項1所述之液晶組合物,其中,通式I的化合物占液晶組合物總重量的0.1-40%。
- 如請求項5所述之液晶組合物,其中,通式II的化合物占液晶組合物總重量的0.1-30%。
- 如請求項1所述之液晶組合物,其中,該液晶組合物中還包含一種或至少兩種通式M的化合物
其中,RM1和RM2各自獨立地表示含有1-12個碳原子的直鏈或支鏈的烷基、 、或,而含有1-12個碳原子的直鏈或支鏈的烷基中的一個 或不相鄰的至少兩個-CH2-可分別獨立地被-CH=CH-、-C≡C-、-O-、-CO-、-CO-O-或-O-CO-替代; 環、環和環各自獨立地表示或 ,中的一個或至少兩個-CH2-可被-O-替代,中 的至多一個-H可被鹵素取代;ZM1和ZM2各自獨立地表示單鍵、-CO-O-、-O-CO-、-CH2O-、-OCH2-、-CH=CH-、-C≡C-、-CH2CH2-、-(CH2)4-、-CF2O-、-OCF2-或-CF2CF2-; nM1表示0、1、2或3,其中當nM1=2或3時,環相同或不同, ZM2相同或不同。 - 如請求項1所述之液晶組合物,其中,該液晶組合物還包含一種或至少兩種通式N的化合物
其中,RN1和RN2各自獨立地表示含有1-12個碳原子的直鏈或支鏈的烷基、 、或,而含有1-12個碳原子的直鏈或支鏈的烷基中的一個 或不相鄰的至少兩個-CH2-可分別獨立地被-O-、-CO-、-CO-O-或-O-CO-替代, 而含有1-12個碳原子的直鏈或支鏈的烷基、、或中的一個 或至少兩個-H可分別獨立地被-F或-Cl取代;RN1、RN2中的至少一個與通式N中環結構相連的原子為碳原子; 環和環各自獨立地表示或, 中的一個或至少兩個-CH2-可被-O-替代,中的一個或至 少兩個-H可被-F或-Cl取代,一個或至少兩個環中-CH=可被-N=替代; ZN1和ZN2各自獨立地表示單鍵、-CO-O-、-O-CO-、-CH2O-、-OCH2-、-CH2CH2-、-(CH2)4-、-CF2O-、-OCF2-或-CF2CF2-;LN1和LN2各自獨立地表示-H或甲基;nN1表示0、1、2或3,nN2表示0或1,且0nN1+nN2 3,其中當nN1=2 或3時,環相同或不同,ZN1相同或不同。 - 一種包含如請求項1至8中任一項所述之液晶組合物的液晶顯示器件。
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| CN115491211B (zh) * | 2022-09-08 | 2023-08-01 | 重庆汉朗精工科技有限公司 | 一种负性液晶组合物及其在液晶显示装置中的应用 |
| CN116496795B (zh) * | 2022-11-17 | 2025-11-14 | Tcl华星光电技术有限公司 | 液晶组合物及液晶显示面板 |
| CN118165740B (zh) * | 2022-12-09 | 2025-04-25 | 江苏和成显示科技有限公司 | 一种液晶组合物及液晶显示器件 |
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