CN1036071C - Liquid crystal compound containing perfluoro-benzene-ring and preparation method thereof - Google Patents
Liquid crystal compound containing perfluoro-benzene-ring and preparation method thereof Download PDFInfo
- Publication number
- CN1036071C CN1036071C CN92108444A CN92108444A CN1036071C CN 1036071 C CN1036071 C CN 1036071C CN 92108444 A CN92108444 A CN 92108444A CN 92108444 A CN92108444 A CN 92108444A CN 1036071 C CN1036071 C CN 1036071C
- Authority
- CN
- China
- Prior art keywords
- compound
- reaction
- cdcl
- hour
- fnmr
- 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 - Fee Related
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The present invention relates to a liquid crystal compound and a preparation method thereof, wherein the liquid crystal compound contains one or more than one perfluoro-benzene ring, one or more than one conjugate bridge bond and two to five aromatic rings. The present invention is a tail-end alkyne compound prepared by a nucleophilic substitution or Grignard reaction and a hydrolyzing reaction of trimethyl silicon-based pentafluorobenzene acetylene or pentafluorobenzene ethene, or is prepared by self-oxidation coupling, or a HecK reaction, or an esterifying reaction after oxidation into acid or hydrolyzing and esterifying reactions of acyl group products of the HecK reaction. The method is convenient and simple, and the liquid crystal compound has the advantages of low phase change temperature and wide ranges.
Description
The present invention relates to liquid crystalline cpd and preparation method thereof, specifically, is a kind of organic lcd compound and preparation method who contains perfluoro-benzene-ring.
Since finding liquid crystal in 1888, the character that has many uniquenesses owing to liquid crystal is with a wide range of applications.For example in chemical industry, liquid crystal can be used as orderly solvent, promotes the organic chemistry orientation response, and stereoisomerism is selected, the optical rotatory substance enrichment with separate; Can improve chromatogram selectivity and separation efficiency as chromatographic stationary liquid; The liquid crystal state functional membrane has the extremely good separation efficiency of selective penetrating quality.In electronic industry, liquid crystal is owing to have the incomparable superior character of many other materials, as: power consumption is extremely low, driving voltage is low, response speed is fast, shows under bright light environments etc., thereby obtain application more and more widely aspect electronic display technology and microtronics.Just because of above-mentioned successful application and development, impel people synthetic and studied up to ten thousand kinds of different liquid crystalline cpds.
According to condition and composition that liquid crystal forms, liquid crystal can be divided into two big classes: thermotropic liquid crystal and lytropic liquid crystals.Can divide into nematic (being called for short N) from the microtexture and the phase of thermotropic liquid crystal phase, smectic type (being called for short S) and cholesteric (being called for short C).Molecule in the smectic liquid crystal is layered arrangement, and perpendicular when molecular long axis and layer plane, and intermolecular relative position is not regular arrangement, and when promptly molecule can and rotate in the free translation of layer plane, this mesomorphic phase was smectic type A phase (S
A); Smectic C phase (being called for short Sc) molecular arrangement and movement characteristic are with S
AMutually similar, different is molecular long axis and is not orthogonal to layered planes, but is inclined to an angle that is not equal to 90 ° with layer plane.When the molecule of Sc in mutually was chirality, this mesomorphic phase just was called chirality smectic C phase (Sc*).Sc* has reduced the symmetry of state of aggregation mutually, has ferroelectricity [J.Phys (Paris) .Lett.36,69 (1975)], makes first optoelectronic switch [Springer Verlag, Berlin, 222 (1980)] fast in 1980.Replace one or two hydrogen in the liquid crystal nuclear can effectively reduce the transformation temperature of liquid crystal with fluorine atom, obtained the very good ferroelectric liquid crystal material of many performances [JP 01,272 552 (89,272 552); JP 01,294 653 (89,294 653); US 4,737 313; JP 63,175 095 (88,75 095)] and other liquid crystal material [JP 10,301 638 (89,301 638); EP 321 984 (1989); WO 89 05, and 792; Mol.Cryst.Liq.Cryst., 1,67 (1981)], even the work that has replaces the hydrogen atom on the flexible side-chains that is connected liquid crystal nuclear two ends with fluorine atom, also obtained ideal results [JP 02,11570 (90,11570); JP01,283 258 (89,283 258)].Because the huge applications potentiality of liquid crystal material, people are still at liquid crystal material of constantly exploring excellent property and preparation method thereof.
The object of the invention provides a class and contains liquid crystalline cpd of perfluoro-benzene-ring and preparation method thereof, and this compounds contains one or more perfluoro-benzene-ring at least.
Specifically, to provide the molecule formula be Y-A-E-B-G in the present invention
k-C
l-H
m-D
n-Z's contains the strong liquid crystalline cpd of one or more perfluoro-benzene-ring and one or more bridges, and wherein, A, B, C or D are to substituted-phenyl
Or tetrafluoro phenyl
K, l, m or n=0 or 1, Y=R or OR, R=C
1-14Straight chain, side chain or chirality alkyl, Z-OR, R, COOR ', NO
2, CN or X, R '=C
1-10Straight chain, side chain or chirality alkyl, X is a halogen: E, G or H=singly-bound or bridged bond, bridged bond be-C ≡ C-,-C ≡ C-C ≡ C-,-COO-.
Liquid crystalline cpd of the present invention contains a bridged bond owing to be rod shaped liquid crystal between ring and the ring at least, has promptly increased length-to-diameter ratio, make bar-shaped feature obvious, because the strong conjugation between ring and ring or bridge and the ring has strengthened the rigidity of examining, be beneficial to the formation of mesomorphic phase again.In the flexible end group of compound, when unsaturated ester or alkoxyl group are arranged, participate in the conjugation of rigid nuclear equally, thereby also strengthened the rigidity of molecule, it is synthetic to be beneficial to raising liquid crystal clearing point and liquid crystal.Because the fluorine on the perfluoro-benzene-ring is replaced by other group easily, as-CH
3, halogen ,-NO
2,-OCH
3,-CN etc. therefore can easily obtain the low liquid crystalline cpd of symmetry on the molecular structure, and the general fusing point of this compound are lower, and the mesomorphic phase temperature is also low, and obtaining low temperature liquid crystal also just becomes possibility.Fluorine atom is the very strong atom of a kind of electronegativity, and its volume is near hydrogen atom, and the introducing of four fluorine atoms had both strengthened the polarity of molecule, satisfied the linearly requirement of molecule again, and therefore, the possibility that liquid crystal occurs is very big.The electronegativity of fluorine can make the Cloud Distribution of the molecule after the replacement, and electronic structures such as polarizability help changing liquid crystal property again.Fluorochemicals is littler than corresponding hydrocarbon molecules interphase interaction power, and fusing point or boiling point are low, and the viscosity of the liquid crystal that makes is diminished, and makes the response speed of the material that makes fast.Fluorinated liquid crystal fat-soluble good can mix well with other organic compound, improved the using value that this class contains the perfluoro-benzene-ring liquid crystal.
The present invention also provides a kind of above-mentioned method that contains the liquid crystalline cpd of one or more perfluoro-benzene-rings for preparing.
Wen Jianxun etc. have reported synthetic [Synthesis, 727 (1990): J.Fluorine Chem., 49,293 (1990)] of trimethyl silicon based penta fluoro benzene acetylene and penta fluoro benzene acetylene.Method of the present invention is that raw material synthetic molecules formula is Y-A-E-B-G with these two compounds exactly
k-C
l-H
m-D
n-Z's contains the strong liquid crystalline cpd of one or more perfluoro-benzene-ring and one or more bridges, and wherein, A, B, C or D are to substituted-phenyl
Or tetrafluoro phenyl
K, l, m or n=0 or 1, Y=R or OR, R=C
1-14Straight chain, side chain or chirality alkyl, Z-OR, R, COOR ', NO
2, CN or X, R '-C
1-10Straight chain, side chain or chirality alkyl, X is a halogen: E, G or H=singly-bound or bridged bond, bridged bond be C ≡ C-,-C ≡ C-C ≡ C-,-COO-.
Trimethyl silicon based penta fluoro benzene acetylene and alcohol generate molecular formula in the presence of alkali
To alkoxyl group tetra fluoro benzene acetylene (1).Also can be divided into for two steps, trimethyl silicon based with alcohol reaction generation earlier to alkoxyl group tetra fluoro benzene ethyl-acetylene, be hydrolyzed into compound (1) again.Compound (1) also can be made by penta fluoro benzene acetylene and alcohol reaction.
Trimethyl silicon based penta fluoro benzene acetylene can also increase aromatic ring with the Grignard reagent reaction of the aromatic compound of para-orientation.For example with
RMgBr,
The Grignard reagent reaction can make molecular formula respectively and be
With
Deng compound, can get through hydrolysis
With
Deng.
Can obtain the liquid crystalline cpd of the different rodlike molecule of many structures from the tetra fluoro benzene acetylene of above-mentioned para-orientation.The symmetrical coupling in compound (1) and (3) self can obtain containing two compounds of perfluoro-benzene-ring, as
(4) and
(5) etc.With 1,4-two generations aromatic hydrocarbons reaction, paradiiodobenzene for example, paradibromobenzene or to iodine tribromophenyl etc., can produce aromatic hydrocarbons is centrosymmetric diine class liquid crystalline cpd, as
(26) etc.Fluorine-containing or the not fluorine-containing aralkyl or the alkane reaction of the tetra fluoro benzene acetylene of para-orientation and iodine or bromo, as with X " B-G
k-C
l-H
m-D
n"=Br or I when Z is carboxyl, can obtain product of the present invention through esterification for-Z, wherein X.
Preparation method of the present invention can further describe as follows:
Can obtain (1) compounds in room temperature-50 a ℃ reaction after 0.5-50 hour by trimethyl silicon based penta fluoro benzene acetylene and oxy-compound carrying out nucleophilic substitution reaction in the presence of alkali or the subsalt.As:
If oxy-compound is C
1-14Pure the time, be compound (1).The mol ratio of trimethyl silicon based penta fluoro benzene acetylene, oxy-compound and alkali or subsalt is 1: (1-10): (1-5).Consumption, temperature of reaction and the reaction times of improving oxy-compound and alkali or subsalt are to reacting essentially no influence.Described oxy-compound can be C
1-14Alcohol, the phenol of phenol, perfluor phenol, para-orientation or perfluor phenol, substituting group can be Y or Z.Alkali or subsalt can be the oxyhydroxide and the strong base-weak acid salts of monovalence or divalent metal, as carbonate, supercarbonate, phosphoric acid, hydrophosphate or dihydrogen phosphate, sulphite or hydrosulphite, acetate, this reaction can be carried out in polar solvent, as alcohol, ether, ethyl acetate, Nitromethane 99Min., oil of mirbane, dimethyl formamide isopolarity solvent.The solvent usage quantity can be 0-50 a times of trimethyl silicon based penta fluoro benzene acetylene weight, recommends to use 1-20 doubly.Hydrolysis takes place in reaction simultaneously, trimethyl silicon based leaving away.
Grignard reaction, the tetra fluoro benzene acetylene of trimethyl silicon based penta fluoro benzene acetylene or para-orientation and Grignard reagent reacting by heating in ether solvent can increase the length of compound.Acetylene compound, Grignard reagent and ether solvent mol ratio are 1: (0.5-3): (1-100), optimum proportion is 1: (1-1.5): (4-20).Described Grignard reagent can be
RMgX ',
Deng, X '=Cl, Br, I; Ether solvent is ether, butyl ether, tetrahydrofuran (THF), 1,4-dioxane etc.As with trimethyl silicane penta fluoro benzene acetylene with
Reaction generates
With
Reaction generates
≡ CSiMe
3, all can become intermediate.Reaction times 0.5-50 hour, preferably 10-20 hour; Be preferably under the reflux temperature and carry out.Product is hydrolyzed through oxyhydroxide, carbonate, acetate or the phosphoric acid salt of the 1-2 of 0.001-0.02 mol ratio valency metal again, reaction times 0.5-40 hour, goes trimethyl silicon based.
Autoxidation coupled reaction, but the acetylene compound coupled reaction behind nucleophilic substitution or grignard reaction.Can obtain two acetylene compounds that symmetry contains perfluoro-benzene-ring as compound (1) and (3) through the coupling of autoxidation symmetry, as:
Aerating oxygen during reaction, and add CuX.Reaction can at room temperature be finished, reaction times 1-5 hour.Above-mentioned acetylene compound, as
With the mol ratio of CuX be 1: (0.01-0.20), best 1: (0.03-0.20).React completely and quicken for making, can add organic solvent earlier, make the CuX dissolving, organic solvent can be N,N,N, acetone, tetrahydrofuran (THF) (TFH) etc., and X is a halogen.
Acetylene compound behind nucleophilic substitution or grignard reaction can carry out the Heck reaction.To replacing perfluorophenyl or can passing through Heck prepared in reaction 1 to substituted-phenyl acetylene and halogenide, the two replaced acetylene class liquid crystalline cpds of 2-, reaction adopts two (trihydrocarbyl phosphine) dihalide palladium, two (trihydrocarbyl phosphine) palladium or two (trihydrocarbyl phosphine) Palladous nitrates and CuX to make catalyzer, as:
X "=Br or I, X_=Cl, Br, I, OCOCH wherein
3, NO
3Deng: R ' is C
1-14Alkyl or phenyl.R-X ', HC ≡ C-R ", the mol ratio of palladium compound and CuX is 1: (1-10): (0.01-0.2): (0.02-0.40).During reaction, the having of nitrogenous organic ligand is beneficial to reaction and carries out, nitrogenous organic ligand is the organic ligand that contains a nitrogen-atoms, be tertiary amine, secondary amine, primary amine, pyridine, bipyridine compounds, as Trimethylamine 99, triethylamine, trioctylamine, diethylamine, n-Butyl Amine 99, pyridine, tetramethyl level quadrol, tetraethylethylenediamine etc. with C1-10 alkyl.Temperature of reaction is room temperature-reflux temperature, reaction times 0.5-50 hour.This reaction can be carried out in organic solvent.
Oxidizing reaction by the end alkyne compound that nucleophilic substitution or grignard reaction and hydrolysis reaction make, can be carried out oxidizing reaction and generate carboxylic compound, can use KMnO under acidity or alkaline condition
4Oxidation.Described acidic conditions promptly is to add formic acid or acetic acid and organic solvent in above-mentioned 1mol product, makes solution present acidic conditions PH＜7 o'clock, with the KMnO of 5-8mol
4Backflow 10-50 hour, this reaction can add the C that has of 0.02-0.5mol
9-30The quaternary amine of alkyl carries out esterification, as tetrabutyl chlorination or amine bromide, and trimethylammonium tetradecyl ammonia chloride, trimethylammonium n-octyl chlorination amine, trimethyl benzyl ammonia chloride, tributyl phenyl iodate amine etc.Described alkaline condition is the monovalence metal hydroxides that adds 1-50mol, in the presence of organic solvent and water, with the KMnO of 0.5-4mol
4Reacted 10-50 hour.
Esterification, when product molecule one end that makes with above-mentioned reaction had carboxyl, can esterification take place with alcohol became ester group.Esterification among the present invention can be at SOCl
2Finish carboxylic acid, pure and mild SOCl under existing
2Mol ratio be 1: (1-2): (1-15), temperature of reaction is room temperature-backflow, reaction times 1-10 hour.This reaction also can be at N, and N-dicyclohexyl carbon imide (DCCI) and following to pyrryl pyridine (PPY) or 4-dimethylamino pyridine (DMAP) existence reacts in polar solvent.Described solvent can be ethanol, ethylene dichloride, trichloromethane, ether, glycol dimethyl ether isopolarity solvent.When adopting this method, the mol ratio of described acid, alcohol, DCCI, PPY or DMAP can be 1: (1-20): (1-3): (0.01-0.20).Solvent recommend consumption be acid mole ratio 5-100 doubly.
By the combination of above-mentioned hydrolysis reaction, grignard reaction, autoxidation symmetry coupled reaction, Heck reaction, esterification, can synthesize numerous liquid crystalline cpds that contains a perfluoro-benzene-ring and one or more bridged bonds at least.
Adopt method of the present invention, starting raw material is easy to get, and reaction is simple, and the productive rate height is fit to industrial production.The compound that contains a perfluoro-benzene-ring that the present invention obtains, because of the volume of fluorine atom and hydrogen atom approaching, replace hydrogen with fluorine and can not cause the coplanarity of destroying two rings such as the steric interaction between two aromatic nucleus in the biphenyl liquid crystal nuclear, be prone to mesomorphic phase.Fluorine on the perfluoro-benzene-ring is easily by other little group, as-CH
3,-OCH
3, replacements such as-CN easily obtain the low liquid crystalline cpd of symmetry.Liquid crystalline cpd of the present invention is lower than complete hydrocarbon liquid crystalline cpd fusing point or boiling point, and Intermolecular Forces is little, and viscosity is also less, and it is just faster to make liquid crystal material responses speed, and the liquid crystal phase transition temperature range is wide, and transformation temperature is also lower.Fluorochemicals is fat-soluble good thus, and this class liquid crystalline cpd is with a wide range of applications.
Help further to understand the present invention by following embodiment, but do not place restrictions on content of the present invention.Symbolic representation is as follows among the embodiment: Cryst. or C-crystal; Iso. or the I-isotropic liquid; The Ch.-cholesteryl phase; The S-smectic phase; S
A-smectic A phase; Sc-smectic C phase; The ferroelectric smectic C of Sc*-phase; The N-nematic phase.Embodiment 1.
Synthetic:
In reaction flask, add the trimethyl silicon based pentafluorophenyl group acetylene of 0.1mol, 0.1-5.0mol C
1-14Alcohol, oxyhydroxide, carbonate or the supercarbonate of the 1-2 valency metal of 0.1-0.3mol are as NaOH, Na
2CO
3Deng, the 0-50ml polar solvent is as THF, chloroform, ether etc.React under the room temperature,
19FNMR trace analysis to reaction finishes.Add entry and water-insoluble organic solvent in the reaction solution, tell organic phase, the water organic solvent extraction.Organic phase is through anhydrous Na
2SO
4Drying, desolventize liquid.Product is through column chromatography purification, and sherwood oil is a leacheate.Product analysis behind result and the purifying is as follows: the numbering RUH alkali solvent reaction time (hour) productive rate (%) 1-1 CH
3OH NaOH acetone 10 89.31-2 C
2H
5OH K
2CO
3DMF 72 84.81-3 n-C
3H
7OH K
2CO
3Ether 72 91.01-4 n-C
4H
9OH K
2CO
380 87.01-5 n-C
5H
11OH CaHPO
4DMF 120 89.31-6 n-C
6H
13OH K
2CO
3DMF 100 86.81-7 n-C
7H
15OH K
2CO
3DMF 100 88.11-8 n-C
8H
17OH K
2CO
3DMF 50 83.11-9 n-C
9H
19OH K
2CO
3DMF 120 76.11-10 n-C
12H
25OH K
2CO
3DMF 120 81.8 compounds (1-1), white, needle-shaped crystals
1HNMR (CCl
4/ TMS); (3.48 s, 1H ,-C ≡ CH); 4.15 (s, 3H ,-OCH
3)
19FNMR (CCl
4/ TFA): 60.33 (d, 2F, J=18.8Hz); 81.00 (d, 2F, J=18.8Hz) compound (1-2), light yellow transparent liquid
1HNMR (CCl
4/ TMS): 1.40 (t, 3H, J=6.0Hz ,-CH
3); (3.40 s, 1H ,-C ≡ CH);
4.20 (q, 2H ,-OCH
2-)
19FNMR (CCl
4/ TFA): 60.83 (d, 2F, J=18.8Hz); 80.67 (d, 2F, J=18.8Hz) compound (1-3), light orange transparent liquid
1HNMR (CCl
4/ TMS): 0.96 (t, 3H, J=6.0Hz ,-CH
3); 1.73 (m, 2H ,-CH
2-);
(3.36 s, 1H ,-C ≡ CH); 4.13 (t, 2H, J=6.0Hz ,-OCH
2-)
19FNMR (CCl
4/ TFA): 60.67 (d, 2F, J=18.8Hz); 80.37 (d, 2F, J=18.8Hz) compound (1-4), light yellow liquid
1HNMR (CCl
4/ TMS): 0.83-1.76 (m, 7H ,-C
3H
7); (3.26 s, 1H ,-C ≡ CH);
4.11 (t, 2H ,-OCH
2-, J=6.0Hz)
19FNMR (CCl
4/ TFA): 60.57 (d, 2F, J=18.8Hz); 80.50 (d, 2F, J=18.8Hz) compound (1-5), pale orange liquid
1HNMR (CCl
4/ TMS): 0.80-1.80 (m, 9H ,-(CH
2)
3CH
3); (3.30 s, 1H ,-C ≡ CH);
4.10 (t, 2H, J=6.0Hz ,-OCH
2-)
19FNMR (CCl
4/ TFA): 60.97 (d, 2F); 80.68 (d, 2F) compound (1-6), light yellow liquid
1HNMR (CCl
4/ TMS): 0.70-1.90 (m, 11H ,-(CH
2)
4CH
3); (3.30 s, 1H ,-C ≡ CH);
4.12 (t, 2H, J=6.0Hz ,-OCH
2-)
19FNMR (CCl
4/ TFA): 60.50 (d, 2F); 80.33 (d, 2F) compound (1-7), light yellow liquid
1HNMR (CCl
4/ TMS): 0.70-1.80 (m, 13H ,-(CH
2)
5CH
3); (3.30 s, 1H ,-C ≡ CH);
4.10 (t, 2H, J=6.0Hz ,-OCH
2-)
19FNMR (CCl
4/ TFA): 60.82 (d, 2F); 80.55 (d, 2F) compound (1-8), light yellow liquid
1HNMR (CCl
4/ TMS): 0.80-1.80 (m, 15H ,-(CH
2)
6CH
3); (3.32 s, 1H ,-C ≡ CH);
4.14 (t, 2H, J=6.0Hz ,-OCH
2-)
19FNMR (CCl
4/ TFA): 60.5 (d, 2F); 80.5 (d, 2F) ultimate analysis: calculated value % C 63.58, H 5.77, and F 24.36
Measured value % C 63.62, H 5.86, F 24.32 compounds (1-9), light brown liquid
1HNMR (CCl
4/ TMS): 0.75-1.80 (m, 17H ,-(CH
2)
7CH
3); (3.31 s, 1H ,-C ≡ CH);
4.12 (t, 2H, J=6.0Hz ,-OCH
2-)
19FNMR (CCl
4/ TFA): 60.65 (d, 2F); 80.33 (d, 2F) compound (1-10), faint yellow semisolid
1HNMR (CCl
4/ TMS): 0.80-1.80 (m, 23H ,-(CH
2)
10CH
3); (3.30 s, 1H ,-C ≡ CH);
4.10 (t, 2H, J=6.0Hz ,-OCH
2-)
19FNMR (CCl
4/ TFA): 60.50 (d, 2F); 80.40 (d, 2F) embodiment 2.
Synthesizing (1-11),
With the trimethyl silicon based pentafluorophenyl group acetylene of 6.08g, 5.0ml s-(-)-2-methyl-1-butene alcohol, 9.0gK
2CO
2Place reaction flask with 10ml DMF, ℃ reaction is 30-50 hour in room temperature～50, and 60-65 ℃ was reacted 5 hours,
19The FNMR analytical reaction are complete.Add 80ml water and 100ml ether, tell the ether layer after the vibration, water layer extracted with diethyl ether three times merge organic phase, are washed till neutrality with saturated NaCl solution, add anhydrous Na
2SO
4Drying, remove desolvate light yellow transparent liquid 5.40g, productive rate 90.3%.
1HNMR(CCl
4/TMS)：0.82-1.90(m，9H)；3.3(s，1H，-C≡CH)；
3.94 (d, 2H, J=6.0Hz, OCH
2)
19FNMR (CCl
4/ TFA): 60.47 (m, 2F); 80.47 (m, 2F) embodiment 3.
Synthesizing (2):
With the trimethyl silicon based pentafluorophenyl group acetylene of 0.01mol, the 1-20ml polar solvent, as THF, ether places in the three-necked bottle, stirs to drip 0.01-0.03mol down
Grignard reagent finished in 1 hour, continued at stirring at room 2-5 hour reflux 1-30 hour.Subsequently, with the acidifying of 0.5-10% inorganic acid aqueous solution, layering adds the 50-500ml ether extraction, and extracting solution is drained or column chromatography, and sherwood oil is a leacheate, steams to desolventize the acquisition crystal.Numbering R fusing point (℃) productive rate (%) 2-1 n-C
4H
9-59.2 82.62-2 n-C
6H
1366.2 60.92-3 n-C
8H
17-51.2 69.82-4 n-C
10H
21-52.2 60.02-5 n-C
12H
25-53.4 62.5 products are yellow or yellow tabular crystal, and the product analysis result is as follows: compound (2-1):
1HNMR (CDCl
3/ TMS): 0.30 (s, 9H, 3 CH
3); 0.98 (t, 3H, J=4.8Hz, CH
3); 1.26-1.98 (m, 4H); 4.00 (t, 2H, J=4.2Hz, CH
2O); (7.16 AA ' BB ' be, phenyl ring)
19FNMR (CDCl
3/ TFA): 58.6 (m, 2F); 66.0 (m, 2F) IR (KBr, cm
-1): 2900 (m, C-H); 2140 (w, C ≡ C); 1610 (m, hydrogen phenyl ring);
1490 (vs, fluorobenzene rings); 1250 (s, C-O-C) compound (2-2):
1HNMR (CDCl
3/ TMS): 0.22 (s, 9H, 3 CH
3); 0.84 (t, 3H, J=4.8Hz, CH
3); 1.12-1.92 (m, 8H); 3.92 (t, 2H, J=4.8Hz, CH
2O); (7.10 AA ' BB ' be, phenyl ring)
19FNMR (CDCl
3/ TFA): 59.0 (m, 2F); 68.2 (m, 2F) IR (KBr, cm
-1): 2910 (m, C-H); 2150 (w, C ≡ C); 1615 (m, hydrogen phenyl ring);
1480 (vs, fluorobenzene rings); 1250 (s, C-O-C) compound (2-3):
1HNMR (CDCl
3/ TMS): 0.22 (s, 9H, 3 CH
3): 0.84 (t, 3H, J=4.2Hz, CH
3); 1.08-1.92 (m, 12H); 3.92 (t, 2H, J=4.8Hz, CH
2O); (7.09 AA ' BB ' be, phenyl ring)
19FNMR (CDCl
3/ TFA): 59.0 (m, 2F); 60.2 (m, 2F) IR (KBr, cm
-1): 2900 (m, C-H); 2160 (w, C ≡ C); 1615 (m, hydrogen phenyl ring);
1490 (vs, fluorobenzene rings); 1250 (s, C-O-C) compound (2-4):
1HNMR (CDCl
3/ TMS): 0.30 (s, 9H, 3 CH
3): 0.88 (t, 3H, J=4.2Hz, CH
3); 1.08-2.00 (m, 16H); 4.00 (t, 2H, J=4.8Hz, (H
2O); (7.16 AA ' BB ' be, phenyl ring)
19FNMR (CDCl
3/ TFA): 59.2 (m, 2F); 66.2 (m, 2F) IR (KBr, cm
-1): 2900 (m, C-H); 2140 (w, C ≡ C); 1610 (m, hydrogen phenyl ring);
1495 (vs, fluorobenzene rings); 1260 (s, C-O-C) compound (2-5):
1HNMR (CDCl
3/ TMS): 0.34 (s, 9H, 3 CH
3); 0.90 (t, 3H, J=4.2Hz, CH
3); 1.08-2.04 (m, 20H); 4.02 (t, 2H, J=4.8Hz, CH
2O); (7.16 AA ' BB ' be, phenyl ring)
19FNMR (CDCl
3/ TFA): 58.8 (m, 2F); 65.8 (m, 2F) IR (KBr, cm
-1): 2910 (m, C-H); 2150 (w.C ≡ C); 1810 (m, hydrogen phenyl ring);
1480 (vs, fluorobenzene rings); 1250 (s, C-O-C) embodiment 4.
0.05mol compound (2) is dissolved in the 10-100ml polar solvent (as methyl alcohol or ethanol), adds 0.5-1.0N alkaline solution 0.2-20ml, separate out a large amount of white needle-like crystals.Continue stirring reaction under the room temperature after 0.5-40 hour, add entry and make precipitation fully.Filter, get the white powder solid.Product can be through organic solvent-water recrystallization, as acetone (or toluene)-water etc., the water white transparency needle-like crystal.Numbering R fusing point (℃) productive rate (%) 3-1 n-C
4H
9-50.1 90.13-2 n-C
6H
13-47.2 95.43-3 n-C
8H
17-45.2 94.93-4 n-C
10H
21-48.5 94.23-5 n-C
12H
23-42.3 95.4 analytical resultss are as follows: compound (3-1):
1HNMR (CDCl
3/ TMS): 0.90 (t, 3H, J=4.2Hz, CH
3); 1.10-1.88 (m, 4H); (3.64 s, 1H, C ≡ C-H); 4.02 (t, 2H, J=4.8Hz, OCH
2); 7.14 (AA ' BB ', phenyl ring)
19FNMR (CDCl
3/ TFA): 60.2 (M, 2F); 66.2 (M, 2F) IR (KBr, cm
-1): 3300 (m, C ≡ C-H); 2910 (m, C-H); 1615 (s, hydrogen phenyl ring);
1490 (vs, fluorobenzene rings): 1280 (s, C-O-C) compounds (3-2): 1HNMR (CDCl
3): 0.88 (t, 3H, J=4.2Hz, CH
3); 1.10-1.94 (m, 8H); (3.60 s, 1H, C ≡ C-H); 4.00 (t, 2H, J=4.8Hz, OCH
2); 7.16 (AA ' BB ', phenyl ring)
19FNMR (CDCl
3/ TFA): 60.6 (m, 2F); 66.6 (m, 2F) IR (KBr, cm
-1): 3310 (m, C ≡ C-H); 2900 (m, C-H); 1610 (s, hydrogen phenyl ring);
1480 (vs, fluorobenzene rings); 1260 (s, C-O-C) compound (3-3):
1HNMR (CDCl
3): 0.88 (t, 3H, J=4.2Hz, CH
3); 1.08-1.94 (m, 12H); (3.62 s, 1H, C ≡ C-H); 4.00 (t, 2H, J=4.8Hz, OCH
2); 7.16 (AA ' BB ', phenyl ring)
19FNMR (CDCl
3/ TFA): 60.6 (m, 2F); 66.6 (m, 2F) IR (KBr, cm
-1): 3300 (m, C ≡ C-H); 2900 (m, C-H); 1610 (m, hydrogen phenyl ring);
1480 (vs, fluorobenzene rings); 1260 (s, C-O-C) compound (3-4):
1HNMR (CDCl
3): 0.90 (t, 3H, J=4.2Hz, CH
3); 1.08-2.02 (m, 16H); (3.64 s, 1H, C ≡ C-H); 4.00 (t, 2H, J=4.8Hz, OCH
2); 7.12 (AA ' BB ', phenyl ring)
19FNMR (CDCl
3/ TFA): 60.6 (m, 2F); 66.6 (m, 2F) IR (KBr, cm
-1): 3205 (m, C ≡ C-H); 2850 (m, C-H); 4610 (m, hydrogen phenyl ring);
1490 (vs, fluorobenzene rings); 1280 (s, C-O-C) compound (3-5):
1HNMR (CDCl
3): 0.88 (t, 3H, J=4.2Hz, CH
3); 1.12-1.96 (m, 20H); (3.62 s, 1H, C ≡ C-H); 4.00 (t, 2H, J=4.8Hz, OCH
2); 7.18 (AA ' BB ', phenyl ring)
19FNMR (CDCl
3/ TFA); 60.8 (m, 2F); 66.0 (m, 2F) IR (KBr, cm
-1): 3300 (m, C ≡ C-H); 2850 (m, C-H); 1610 (m, hydrogen phenyl ring);
1490 (vs, fluorobenzene rings); 1290 (s, C-O-C) embodiment 5.
Synthesizing (4):
In three-necked bottle, add 5mg CuCl or CuBr, 5ml acetone, 0.5ml N, N, N, N-Tetramethyl Ethylene Diamine (TMEDA), 200mg
Aerating oxygen.After 1-4 hour, detect, show that reaction is complete, add 1-50ml water, separate out a large amount of white precipitates, filter with TLC.Product gets white needle-like crystals with the acetone-water recrystallization, and productive rate is greater than 83%, 57.1 ℃ of fusing points.Ultimate analysis: calculated value C 63.79% H 5.66% F 25.25%
Measured value C 64.01% H 5.97% F 24.96%
1HNMR (CDCl
3/ TMS): 0.90 (t, 6H, J=4.2Hz, 2CH
3); 1.04-1.98 (m, 24H);
4.18 (t, J=4.8Hz, 2OCH
2)
19FNMR (CDCl
3/ TFA): 62.3 (m, 2F); 81.5 (m, 2F) IR (CDCl
3, cm-1): 2900 (s, C-H), 1485 (vs, fluorobenzene rings), 1280 (s, C-O-C) MS (m/e): 602 (M
+, 78.63%), 378 (M
+-224,100.00%) embodiment 6.
Synthesizing (5):
Synthetic method is the same.For example, use
250mg after the filtration, gets white plates crystal 125mg with acetone recrystallization, and productive rate is greater than 66.8%, 141.4 ℃ of fusing points.Ultimate analysis: calculated value C 70.03% H 5.57% F 20.16%
Measured value C 69.62% H 5.49% F 20.11%
1HNMR,
19FNMR does not do owing to can not find appropriate solvent.IR (KBr, cm
-1): 2860 (s, C-H); 1600 (m, hydrogen phenyl ring); 1496 (vs, fluorobenzene rings);
1290(s，C-O-C)MS(m/e)：754(M
+，90.70％)；530(M
+-224，100.00％)
Adopt orthogonal polarizing microscope that the optical texture that compound occurs in heating and cooling process is observed, find that it has liquid crystal liquid crystal property.Adopt the way of heating and cooling, in temperature-fall period, observe the pintongs schlieren texture of nematic liquid crystal (being called for short N) feature.Its thermal behavior list in following formula (warming and cooling rate be 10 ℃/min), wherein Cryst. represents the crystal phase, Iso. represents the isotropic liquid phase.Can find out that from formula nematic phase only appears in this compounds, and the temperature range of mesomorphic phase is very big, up to more than 100 degrees centigrade, this is comparatively rare.
Embodiment 7.
Synthesizing (7): 1.
Synthesizing (6):
In three-necked bottle, put into Pd (PPh
3)
2Cl
235mg, CuI 10mg is at N
2Protection adds to octyloxy tetra fluoro benzene acetylene 0.01mol five fluorine iodobenzenes or five bromofluorobenzene 0.01-0.05mol, Et down
3N 20ml, in room temperature～50 ℃ stirring reaction 5-48 hour.The elimination amine salt desolventizes, and gets white solid, productive rate 80%.The product analysis result is:
19FNMR (CDCl
3/ TFA): 57.62 (d, 2F, J=16.47Hz); 59.17 (q, 2F);
88.87(q，2F)；73.20(t，1F，J＝20.57Hz)：
84.08(t，2F，J＝20.14Hz，16.46Hz)
1HNMR(CDCl
3/TMS)：7.43(d，2H，J＝9.0Hz)；7.02(d，2H，J＝9.0Hz)；
4.04 (t, 2H, J=6.3Hz), 0.71-2.1 (m, 15H) 2.
Synthesizing (7):
In three-necked bottle, put into above-mentioned product (6) 200mg, n-Octanol 0.4-2g, anhydrous K
2CO
30.3-1g, polar solvent (as THF) 1-10ml, room temperature is stirred and is blocked reaction 1-8 hour,
19FNHMR detects, and reacts complete.Filter, desolventize or add the water stopped reaction, extracted with diethyl ether, drying, column chromatography purification, white crystal, 70 ℃ of mp, productive rate 80～85%.
19FNMR (CDCl
3/ TFA) t 60.05 (d, 2F, J=16.9Hz): 78.00 (d, 2F, J=16.9Hz)
1HNMR (CDCl
3, TMS): 4.21 (t, 4H, J=6.3Hz); 0.66-2.06 (m, 30H) IR (KBr, cm
-1): 2920,2850,1655,1520,1500,1455,1390,1195,1055,1000,790,720,600 embodiment 8.
0.8-5mol
0.001-0.02mol Pd (PPh
3)
2Cl
2, 0.001-0.02 mol CuI, 10-100ml Et
3N.Stir down room temperature～50 ℃ reaction 5-100 hour.Remove by filter amine salt, desolventize and raw material, get yellow solid, productive rate 75-85%.Ultimate analysis: calculated value C 66.06% H5.50% F 17.43%
Measured value C 66.24% H 5.08% F 16.35%
1HNMR (CDCl
3/ TMS); (8.0 m, 2H, phenyl ring); (7.5 m, 2H, phenyl ring); 4.2 (m, 2H ,-OCH
2); 3.9 (s, 3H, CH
3O-); 1.0-1.8 (m, 15H ,-C
2H
16)
19FNMR (CDCl
3/ TFA): 41.3 (s, 2F); 23.3 (s, 2F) IR (KBr, cm
-1): 2930 (m ,-CH
3); 2850 (m ,-CH
2-); 1720 (s, C=O);
1610 (m, phenyl ring); 1280 (s, C-O-C): 1500 (s ,-F-) MS (m/e): 436 (M
+, 13.11%); 324 (M
+-112,100.00%; 293 (M
+-112-31,22.36%) embodiment 9.
Synthesizing (9);
Claim 7.0-10.0mmol solid NaOH in an egg type bottle, add 50ml distilled water, stirring and dissolving caustic soda drops into 7.0mmol compound (8), adds 20-100ml ethanol again.When being heated to 75 ℃, the solid ester dissolving continues to be heated to backflow.React after 2-8 hour TLC (sherwood oil: ethyl acetate=9: 1) analyze, find that raw material reacts completely, at this moment solution pH value=8-12.Stopped reaction, white creaming appears in enriching HCl acidifying immediately, adds ether and stirs, and precipitation disappears, at this moment, organic phase pH value=2-3.Use the extracted with diethyl ether organic phase, water layer is washed (20ml * 2) 2 times with ether, merges organic phase, washes with water to neutrality, drains solvent, gets light brown solid 2.81g, productive rate 95.19%.Ultimate analysis: calculated value C 65.40% H 5.21% F 18.01%
Measured value C 65.36% H 5.25% F 18.05%
1HNMR (CDCl
3/ TMS): 8.0 (m, 2H, phenyl ring); (7.5 m, 2H, phenyl ring);
4.2(t，2H，-OCH
2)；1.0-1.8(m；15H，-C
7H
15)
19FNMR(CDCl
3/TFA)：40.3(m，2F)；20.6(m，2F)IR(KBr，cm
-1)：3000-2500(m，-OH)；2950-2900(m，-C-H)；1680(s，C＝O)；
1605 (m, phenyl ring); 1490 (s, fluorobenzene rings); 1450 (w, phenyl ring); MS (m/e): 422 (M
+, 9.79%); 310 (M
+-112,100.00%); 293 (M
+-112-17,7.47%) embodiment 10.
Synthesizing (10):
Compound (10-1～10-6, synthesizing m=1-6) is example with (10-1): in reaction flask, add compound (9) 200.0mg (0.047mmol),
79.2mg (0.52mmol), DCCI107.4mg (0.52mmol) and anhydrous CH
2Cl
210ml.After the mixing, add PPY a small amount of (about 0.05mmol) at once.After at room temperature stirring 8 days, add the 20ml ether, filter, filtrate is washed to neutrality with 5% HAc solution washing (8ml * 5), takes out and desolvates, and gets light yellow solid.Column chromatography, leacheate are sherwood oil: ethyl acetate (9: 1), collect desired product, and boil off solvent, get white solid 170mg, productive rate 66.41%.(10-1～10-6) is synthetic to feed intake and the anhydrous PPY output of output numbering compound 9 pure DCCI output
(mg) (mg) (mg) CH
2Cl
2(mg) (%) a small amount of 180.0 60.7 compounds (10-1) of a small amount of 170.0 64.510-2 of 10-1 200.0 79.2 107.4 10ml 200.0 86.5 107.4 10ml a small amount of 175.0 64.810-3 200.0 93.8 107.4 10ml a small amount of 170.0 62.110-4 200.0 101.1 107.4 10ml a small amount of 140.0 49.410-5 200.0 108.4 107.4 10ml a small amount of 180.0 62.110-6 200.0 115.7 107.4 10ml:1HNMR (CDCl
3/ TMS): 8.04-8.2 (m, 4H); 7.84 (m, 2H); 7.35 (m, 2H); 4.28 (m, 2H, OCH
2); 3.92 (s, 3H, OCH
3); 1.2-2.0 (m, 12H ,-(CH
2)
6-); 0.9 (m, 3H ,-CH
3)
19FNMR (CDCl
3/ TFA): 40.0 (m, 2F); 20.5 (m, 2F) MS (m/e): 556 (M
+, 7.31%); 405 (M
+-151,100.00); 293 (M
+-263,20.46) ultimate analysis: calculated value C 66.91% H 5.04% F 13.67%
Measured value C 66.29% H 4.64% F, 14.25% compound (10-2):
1HNMR (CDCl
3/ TMS): 8.04-8.20 (m, 4H); 7.64 (m, 2H); 7.35 (m, 2H); 4.20-4.48 (m, 4H, OCH
2); 0.7-2.0 (m, 18H)
19FNMR (CDCl
3/ TFA): 40.0 (m, 2F); 20.5 (m, 2F) MS (m/e): 570 (M
+, 5.09), 405 (M
+-165,100.00), 293 (M
+-277,35.68) ultimate analysis: calculated value C 67.37% H 5.26% F 13.33%
Measured value C 66.86% H 5.10% F, 13.16% compound (10-3):
1HNMR (CDCl
3/ TMS): 8.04-8.20 (m, 4H); 7.64 (m, 2H); 7.32 (m, 2H); 4.20-4.36 (m, 4H, 2 OCH
2); 0.8-2.0 (m, 20H)
19FNMR (CDCl
3/ TFA): 40.0 (m, 2F); 20.5 (m, 2F) MS (m/e); 584 (M
+, 7.73), 405 (M
+-179,100.00), 293 (M
+-291,17.10) ultimate analysis: calculated value C 67.81% H 5.48% F 13.01%
Measured value C 67.37% H 5.32% F, 12.82% compound (10-4):
1HNMR (CDCl
3/ TMS): 8.04-8.20 (m, 4H); 7.64 (m, 2H); 7.35 (m, 2H) 4.20-4.40 (m, 4H, 2 OCH
2); 0.8-2.0 (m, 22H)
19FNMR (CDCl
3/ TFA): 40.0 (m, 2F); 20.5 (m, 2F) MS (m/e): 598 (M
+, 7.68), 405 (M
+-193,100.00), 293 (M
+-305,20.13) ultimate analysis: calculated value C 68.23% H 5.69% F 12.71% measured value C 68.22% H 5.30% F, 13.18% compound (10-5):
1HNMR (CDCl
3/ TMS): 8.04-8.20 (m, 4H); 7.64 (m, 2H); 7.35 (m, 2H); 4.20-4.40 (m, 4H, 2 OCH
2); 0.7-2.0 (m, 24H)
19FNMR (CDCl
3/ TFA): 40.0 (m, 2F): 20.5 (m, 2F) compound (10-6):
1HNMR (CDCl
3/ TMS): 8.04-8.20 (m, 4H); 7.64 (m, 2H); 7.35 (m, 2H); 4.20-4.48 (m, 4H, 2 OCH
2); 0.7-2.0 (m, 26H)
19FNMR (CDCl
3/ TFA): 40.0 (m, 2F); 20.5 (m, 2F) ultimate analysis: calculated value C 69.10% H 6.07% F 12.14% measured value C 69.32% H 5.83% F 11.93% embodiment 11.
(these six samples of 10-1～10-6) are for a series of, because their end group chain length difference has caused that the difference of liquid crystal phase under differing temps changes for compound.With Mettler FP52 temperature control warm table, warming and cooling rate is 3 ℃/min, is 0.2 ℃/min when undergoing phase transition, and polarizing microscope amplifies 100 times, and 90 ℃ of crossed polarized lights are observed down, result and the contrast of DSC spectrogram, and the thermal behavior unanimity of sample is an example with (10-8):
(all kinds of phase transition temperatures and the temperature province of 10-1～10-6): numbering m.p., (℃) S phase scope, (℃) S → N, (℃) N phase scope, (℃) c.p., (℃) 10-1 104.6 64.3 168.9 44.0 212.910-2 65.2 88.4 153.6 29.5 183.110-3 68.0 79.8 147.8 22.0 169.810-4 80.7 64.8 145.5 8.7 154.210-5 65.4 79.1 144.5 8.6 153.110-6 71.3 70.6 141.6 4.6 146.2
| Experimental technique | m.p.(℃) S A→N(℃) c.p.(℃) | |
| Temperature-rise period | Polarizing microscope | 71.3 141.6 146.2 |
| DSC | 75.3 142.4 146.4 | |
| Temperature-fall period | Polarizing microscope | 60.1 142.1 146.1 |
| DSC | 55.6 139.9 144.2 |
Result of study shows: (1) this quasi-molecule is along with the increase of end group carbon atom, and the difference of adjacent two clearing points becomes little, finds have S to be inclined to mutually simultaneously and widens and N tends to disappearance volume rule mutually gradually; (2) liquid crystal of this class formation has quite wide transformation temperature zone.Embodiment 12.
Synthetic:
With 200-600mg
100 500mg compounds (1), 10-50mg PdPPh
3)
2Cl
2Reach 10-30mg CuI and place in the three-necked bottle, at N
2Protection adds the anhydrous Et of 5-30ml down
3N, heated and stirred reaction 0.5-3 hour, reaction finishes.Be chilled to room temperature, add the 10-20ml anhydrous diethyl ether, the elimination precipitation, desolventize crystal.Product can be through column chromatography purification, and with alkane or sherwood oil: polar solvent (as acetone, ethyl acetate)=9: 0.5～2 is a leacheate, white plates or needle crystal, productive rate 85-98%.Analytical results is as follows: numbering R fusing point (℃) productive rate (%) 11-1 n-CH
3-100.8 85.211-2 n-C
2H
5-95.4 97.811-3 n-C
3H
7-93.6 87.211-4 n-C
4H
9-90.4 84.611-5 n-C
5H
11-89.5 85.211-6 n-C
6H
13-88.8 89.311-7 n-C
7H
15-77.8 86.311-8 n-C
8H
17-75.4 92.311-9 n-C
9H
19-74.0 90.411-10 n-C
12H
25-72.9 90.8 compounds (11-1):
1HNMR (CCl
4/ TMS): 0.92-1.92 (m, 9H); 4.02-4.32 (m, 5H, OCH
2, OCH
3);
7.30(d)/8.12(d)(AA′BB′，4H，J＝8.0Hz，O-C
6H
4)；
(d)/8.22 7.72 (d) (AA ' BB ', 4H, J=8.0Hz, C ≡ C-C
6H
4-)
19FNMR (CCl
4/ TFA): 60.07 (m, 2F); 80.50 (m, 2F) MS (m/e): 514 (M
+, 2.34%); 307 (M
+-207,100.00%) ultimate analysis: calculated value C 65.37% H 4.31% F 14.77% measured value C 65.45% H 4.01% F, 14.68% compound (11-2):
1HNMR (CCl
4/ TMS): 0.87-1.84 (m, 12H); 4.04-4.34 (m, H, 2 OCH
2);
7.24(d)/8.10(d)(AA′BB′，4H，J＝8.0Hz，O-C
6H
4-)；
(d)/8.19 7.64 (d) (AA ' BB ', 4H, J=8.0Hz, C ≡ C-C
6H
4-)
19FNMR (CCl
4/ TFA); 60.10 (m, 2F); 80.13 (m, 2F) MS (m/e): 528 (M
+, 4.05%); 321M
+-207,100.00%); 293 (M
+-207-28,13.39%) ultimate analysis: calculated value C 65.91% H 4.58% F 14.38%
Measured value C 65.45% H 4.33% F, 14.17% compound (11-3):
1HNMR (CCl
4/ TMS): 0.80-1.97 (m, 14H); 3.97-4.27 (m, 4H, 2 OCH
2);
7.14(d)/7.97(d)(AA′BB′，4H，J＝8.0Hz，O-C
6H
4-)；
(d)/8.09 7.57 (d) (AA ' BB ', 4H, J=8.0Hz, C ≡ C-C
6H
4-)
19FNMR (CCl
4/ TFA): 60.15 (m, 2F); 80.13 (m, 2F) MS (m/e): 542 (M
+, 3.64%); 337 (M
+-205,100.00%); 293 (M
+-205-44,29.90%) ultimate analysis: calculated value C 66.42% H 4.83% F 14.01%
Measured value C 66.60% H 4.74% F, 13.68% compound (11-4):
1HNMR (CCl
4/ TMS): 0.87-2.00 (m, 16H); 4.00-4.30 (m, 4H, 2 OCH
2);
7.17(d)/8.03(d)(AA′BB′，4H，J＝8.0Hz，O-C
6H
4-)；
(d)/8.12 7.60 (d) (AA ' BB ', 4H, J=8.0Hz, C ≡ C-C
6H
4-)
19FNMR (CCl
4/ TFA): 59.90 (m, 2F); 79.67 (m, 2F) MS (m/e): 556 (M
+, 3.94%); 349 (M
+-207,100.00%); 293 (M
+-207-56,23.08%) ultimate analysis: calculated value C 66.90% H 5.07% F 13.65%
Measured value C 67.18% H 4.96% F, 13.37% compound (11-5):
1HNMR (CCl
4/ TMS): 0.90-1.90 (m, 18H); 4.00-4.30 (m, 4H, 2 OCH
2);
7.18(d)/8.00(d)(AA′BB′，4H，J＝8.0Hz，O-C
6H
4-)；
(d)/8.10 7.80 (d) (AA ' BB ', 4H, J=8.0Hz, C ≡ C-C
6H
4-)
19FNMR (CCl
4/ TFA); 60.00 (m, 2F); 79.83 (m, 2F) MS (m/e): 570 (M
+, 5.11%); 363 (M
+-207,100.00%); 293 (M
+-207 70,31.12%) ultimate analysis: calculated value C 67.36% H 5.30% F 13.32%
Measured value C 67.11% H 5.05% F, 13.18% compound (11-6):
1HNMR (CCl
4/ TMS): 0.90-1.88 (m, 20H); 4.05-4.33 (m, 4H, 2 OCH
2);
7.23(d)/8.06(d)(AA′BB′，4H，J＝8.0Hz，O-C
6H
4-)；
(d)/8.15 7.65 (d) (AA ' BB ', 4H, J=8.0Hz, C ≡ C-C
6H
4-)
19FNMR (CCl
4/ TFA): 60.00 (m, 2F); 79.80 (m, 2F) MS (m/e); 584 (M
+, 5.78%); 378 (M
+-206,100.00%); 293 (M
+-205-85,31.69%) ultimate analysis: calculated value C 67.80% H 5.52% F 13.00%
Measured value C 67.61% H 5.56% F, 12.71% compound (11-7):
1HNMR (CCl
4/ TMS): 0.83-1.90 (m, 22H): 4.00-4.30 (m, 4H, 2 OCH
2)
7.14(d)/7.97(d)(AA′BB′，4H，J＝8.0Hz，O-C
6H
4-)；
(d)/8.07 7.57 (d) (AA ' BB ', 4H, J=8.0Hz, C ≡ C-C
6H
4)
19FNMR (CCl
4/ TFA): 60.15 (m, 2F); 80.13 (m, 2F) MS (m/e); 598 (M
+, B, 75%); 392 (M
+-206,100.00%); 293 (M
+-206-99,27.54%) ultimate analysis: calculated value C 68.22% H 5.73% F 12.69%
Measured value C 68.17% H 5.60% F, 12.41% compound (11-8):
1HNMR (CCl
4/ TMS): 0.83-1.90 (m, 24H); 3.93-4.23 (m, 4H, 2 OCH
2);
7.11(d)/7.93(d)(AA′BB′，4H，J＝8.0Hz，O-C
6H
4-)；
(d)/8.01 7.51 (d) (AA ' BB ', 4H, J=8.0Hz, C ≡ C-C
6H
4-)
19FNMR (CCl
4/ TFA): 60.03 (m, 2F); 79.83 (m, 2F) MS (m/e): 612 (M
+, 2.29%); 405 (M
+-207,100.00%); 293 (M
+-207-112,18.26%) ultimate analysis: calculated value C 68.62% H 5.92% F 12.40% measured value C 68.31% H 5.78% F, 12.34% compound (11-9):
1HNMR (CCl
4/ TMS): 0.90-1.90 (m, 26H): 4.00-4.30 (m, 4H, 2 OCH
2);
7.20(d)/8.03(d)(AA′BB′，4H，J＝8.0Hz，O-C
6H
4-)；
(d)/8.13 7.61 (d) (AA ' BB ', 4H, J=8.0Hz, C ≡ C-C
6H
4-)
19FNMR (CCl
4/ TFA): 60.00 (m, 2F); 79.83 (m, 2F) MS (m/e); 626 (M
+, 2.16%); 419 (M
+-207,100.00%); 293 (M
+-207-126,21.38%) ultimate analysis: calculated value C 69.00% H 6.11% F 12.13%
Measured value C 68.98% H 6.20% F, 11.84% compound (11-10):
1HNMR (CCl
4/ TMS): 0.80-1.90 (m, 32H); 3.93-4.20 (m, 4H, 2OCH
2);
7.10(d)/7.93(d)(AA′BB′，4H，J＝8.0Hz，O-C
6H
4-)；
(d)/8.00 7.50 (d) (AA ' BB ', 4H, J=8.0Hz, C=C-C
6H
4-)
19FNMR (CCl
4/ TFA): 60.30 (m, 2F); 79.97 (m, 2F) MS (m/e): 668 (M
+, 1.56%); 461 (M
+-207,100.00%); 293 (M
+-207-168,18.67%) ultimate analysis: calculated value C 70.04% H 6.63% F 11.38%
Measured value C 69.96% H 6.62% F 11.09% embodiment 13.
With orthogonal polarizing microscope (11-1)～(11-10) each compound is observed, and done dsc analysis, transformation temperature is as follows in the heating and cooling process: (temperature: ℃) compound m.p. S
APhase scope S
APhase transformation in → Ch Ch phase scope c.p.11-1 100.8 // 61.6 162.411-2 95.4 14.9 110.3 64.4 174.711-3 93.6 24.4 118.0 46.4 164.411-4 90.4 45.6 136.0 33.2 169.211-5 89.5 35.2 124.7 28.4 153.111-6 88.8 44.0 132.8 21.9 154.711-7 77.8 51.8 129.6 17.9 147.511-8 75.4 54.0 129.4 15.4 144.811-9 74.0 54.3 128.3 11.0 139.311-10 72.9 54.5 127.4 4.7 132.1 temperature-fall periods is as follows: (temperature: ℃) Compound I so → Ch Ch phase scope Ch → SAS
APhase scope S
A→ Sc
*Sc
*Phase scope Sc
*→ Cryst11-1 162.0 61.5 // 100.5
*27.8 72.711-2 174.2 64.6 109.6 13.5 96.1 37.3 58.811-3 164.1 48.9 117.2 22.8 94.4 32.2 62.211-4 168.8 33.1 135.7 44.1 91.6 17.9 73.711-5 152.9 27.7 125.2 35.5 89.7 19.1 70.611-6 154.5 22.1 132.4 42.9 89.5 19.2 70.311-7 147.2 18.2 129.0 51.0 78.0 16.4 61.611-8 144.4 15.3 129.1 51.9 77.2 18.4 58.811-9 139.2 11.2 128.0 48.4 79.6 26.3 53.311-10 132.0 5.0 127.0 45.8 81.2 26.8 these phase transition temperatures of 54.4* are: Ch → Sc*
Result of study shows: (1) resulting fluorinated liquid crystal molecule, along with the increase of end group carbon chain lengths, fusing point reduces, S
APhase range widens and cholesteryl phase trend towards disappearing gradually, simultaneously, clearing point shows tangible odd even rule when end group carbochain not oversize (m＜8), and promptly m has higher clearing point for the even compound, and when the end group carbochain was grown (m 〉=8), the odd even rule was more not obvious; In addition, along with the growth of end chain, the clearing point of each compound is reduction trend, and the difference of adjacent two clearing points is tending towards reducing.(2) Sc appears in this serial fluorinated liquid crystal molecule in temperature-fall period
*Phase, and Sc
*The phase scope is comparatively desirable, adds that the temperature range of whole liquid crystal area is very wide, thereby is a kind of more rising ferroelectric liquid crystal material.Embodiment 14.
Synthesizing (12):
With 0.01-0.5mol Pd (PPh
3)
2Cl
2, 0.05-0.2mol CuI, 1mol compound (1), 1-5mol
And 10-500mlEt
3N places in the reaction flask, back flow reaction 1-5 hour, reacts complete.Add 50-1000ml polar solvent (as ether), remove by filter amine salt, desolventize solid product.Through column chromatography purification, leacheate is non-polar solvent (as a sherwood oil, 14 hydrocarbon etc.): polar solvent (as ethyl acetate, acetone)=9: 0.5-2, obtain white solid.With raw material (18) is example, productive rate 81.31%, 81.6 ℃ of product (12-8) fusing points.
1HNMR(CDCl
3/TMS)：0.80-1.90(m，15H，-C
7H
15)；4.14(t，2H，-OCH2-)；
7.21(d)/7.94(d)(AA′BB′，4H，J＝8.0Hz，-C
6H
4-NO
2)；
7.51(d)/8.01(d)(AA′BB′，4H，J＝8.0Hz，-C≡C C
6H
4)
19FNMR(CDCl
3/TFA)：60.06(m，2F)；79.83(m，2F)
With orthogonal polarizing microscope compound (12-8) is observed, and made dsc analysis, its transformation temperature is as follows:
Embodiment 15.
Synthesizing (13):
With 0.1mol compound (1), 0.1-0.5mol
0.01-0.08molPd (PPh
3)
2Br
2, 0.05-0.2mol CuI and 10-100ml Et
3N at room temperature reacted 1-5 hour, filtered, and removed raw material and obtained product.Also can add the 100ml ether, filter, desolventize or through column chromatography purification.With raw material (1-8) is example, produces and considers 85.1%, 84.8 ℃ of product (138) fusing points.
1HNMR(CDCl
3/TMS)：0.80-1.90(m，15H，-C
7H
15)；4.14(t，2H，-OCH
2-)；
7.41(d)/7.84(d)(AA′BB′，4H，J＝8.0Hz，-C
6H
4Cl)；
7.51(d)/8.01(d)(AA′BB′，4H，J＝8.0Hz，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：60.05(m，2F)；79.90(m，2F)
With orthogonal polarizing microscope compound (13-8) is observed, and made dsc analysis, its transformation temperature
Embodiment 16.
Synthesizing (14):
With 0.1mol compound (1), 0.1-0.5mol
0.001-0.05molPd (PPh
3)
2Cl
2, 0.005mol CuI and 10-100ml bipyridine, back flow reaction 0.5～3 hour.Nucleus magnetic resonance is followed the tracks of, and reacts complete.Add 10-500ml ether or chloroform, filter, get crude product.Through column chromatography purification, leacheate is a dodecane: acetone (or ethyl acetate)=9: 1 gets white crystals.When being raw material with compound (1-8), productive rate 72.7%, 88.0 ℃ of product (14-8) fusing points.
1HNMR(CDCl
3/TMS)：0.36-1.98(m，15H，-C
7H
15)；4.14(t，2H，J＝3.6Hz，
-OCH
2-)；7.44(AA′BB′， 4H，J＝7.2Hz，-C
6H
4-CN)；
7.96(AA′BB′，4H，J＝7.2Hz，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：65.41(m，2F)：84.81(m，2F)
With orthogonal polarizing microscope compound (14-8) is observed, and made dsc analysis, its transformation temperature
Embodiment 17.
Synthesizing (15):
With 0.1mol compound (3), 0.1-0.5mol
0.003mol Pd (PPh
3)
2Cl
2, the copper halide of 0.005mo (as CuI, CuBr, CuCl etc.) and 10-100ml triethylamine, at room temperature-50 ℃ stirring reaction 10-48 hour, the TLC analytical reaction were complete.Purifying gets product after filtration.When being raw material, reacted 20 hours productive rate 80.2%, 103.0 ℃ of product fusing points with compound (3-5).
1HNMR(CDCl
3/TMS)：0.95-2.05(m，23H)：4.12(1，2H，-OCH
2-)；
7.12(AA′BB′，4H，O-C
6H
4-)；7.60(AA′BB′，4H，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：58.9(m，2F)；65.9(m，2F)
With orthogonal polarizing microscope compound is observed, its transformation temperature is as follows:
Embodiment 18.
Synthesizing (16): 1.
(16-1)
In three-necked bottle, add PdLP (C
4H
9)
3)
2Cl
25-20mg, CuI 3-10mg, Bu
3N 10-30ml, compound (3-2) 50-200mg, to n-octyloxy tetrafluoro iodobenzene 100-150mg, heating reflux reaction 4 hours, TLC analyzes, and reacts complete.Remove by filter amine salt.Product column chromatography purification, leacheate are sherwood oil: polar solvent (as ethyl acetate or acetone)=100: 0.5-2.Get white solid, productive rate 70-85%.
1HNMR(CCl
4/TMS)：0.64-2.09(m，13H)；3.96(t，2H，J＝6.0Hz)；
4.26(t，2H，J＝6.0Hz)；7.15(AA′BB′，4H)
19FNMR(CCl
4/TFA)：59.17(m，4F)；66.89(m，2F)；79.69(m，2F)MS(m/e)：612(M
+-29.09％)，430(M
+-182，100.00％)IR(KBr，cm
-1)：2950，2910，2850，1605，1515，1495，1475，1440，1390，
1290，1250，1180，1070，980，840。2.
(16-2)
Removing the change raw material is compound (3-4), and product is with outside acetone-methanol mixed solvent recrystallization, and all the other are the same.Get white solid, productive rate 65.72%.
1HNMR(CCl
4/TMS)：0.64-2.09(m，21H)；3.96(t，2H，J＝6.0Hz)；
4.28(t，2H，J＝6.0Hz)；7.15(AA′BB′，4H)
19FNMR(CDCl
3/TFA)：59.84(m，4F)；67.00(m，2F)；80.00(m，2F)MS(m/e)：668(M
+，100.00％)，430(M
+-238，76.83％)IR(KBr，cm
-1)：2925，2860，1620，1520，1500，1480，1445，1305，1265，
1185，1075，1030，990，830，810，635，535
Find that this compounds is a nematic liquid crystal, transformation temperature is as follows: 16-1
16-2
Embodiment 19.
Synthesizing (17):
With 1mol compound (3), 0.5-1.5mol (s)
0.03molPd (PPh
3)
2Cl
2, 0.08mol CuI and 10-100ml triethylamine place in the reaction flask, stir back flow reaction 1-5 hour down.Reaction solution is chilled to room temperature, filters, and desolventizes.Through column chromatography (sherwood oil: purifying acetone=9: 1), productive rate 75.90%.During with compound (3-3) raw material is example, productive rate 80.0%, 89.5 ℃ of product fusing points.
1HNMR(CDl
3/TMS)：0.85(t，3H，J＝4.2Hz，CH
3)；1.08-1.92(m，12H)；
4.00(t，2H，J＝4.8Hz，CH
2O-)；7.10(AA′BB′，4H，-C
6H
4-)
19FNMR(CDCl
3/TFA)，59.20(m，4F)；66.70(m，2F)；79.70(m，2F)
With orthogonal polarizing microscope compound is observed, its transformation temperature is as follows:
Embodiment 20.
Synthesizing (18):
In reaction flask, add compound (3) 200-400mg, to iodine or p-Nitrobromobenzene 155mg, CuI 5-20mg, PdLP (C
6H
17)
3J
2Cl
220-30mg and 10-30ml triethylamine.At room temperature-50 ℃ stirring reaction 2-48 hour, best 3-10 hour.Remove by filter amine salt, desolventize, roll over alkane (or sherwood oil) recrystallization or with the post layer, sherwood oil is a leacheate, desolventizes, and product is yellow needle-like crystal.Numbering R productive rate %18-1 n-C
4H
9-7518-2 n-C
6H
13-7118-3 n-C
8H
17-7618-4 n-C
10H
21-80.4 product analysis results are as follows: compound (18-1):
1HNMR (CDCl
3/ TMS): 0.97-2.00 (m, 7H); 4.04 (t, 2H, J=6.3Hz); (d)/7.44 7.02 (d) (AA ' BB ', 4H, J=9.0Hz): 7.76 (d)/8.27 (d) (AA ' BB ', 4H, J=8.1Hz)
19FNMR (CDCl
3/ TFA): 59.64 (m, 2F); 66.75 (m, 2F) MS (m/e): 443 (M
+, 50.99%); 387 (M
+-56,100.00%) IR (KBr, cm
-1): 2950,2850,1610,1520,1505,1485,1420,1345,1300,
1260,1185,1185,990,885,855,840,750,690,630,620 compounds (18-2):
1HNMR (CDCl
3/ TMS): 0.78-2.02 (m, 11H): 4.04 (t, 2H, J-6.3Hz); (d)/7.44 7.02 (d) (AA ' BB ', 4H, J=9.0Hz); (d)/8.27 7.76 (d) (AA ' BB ', 4H, J-8.1Hz)
19FNMR (CDCl
3/ TFA): 60.00 (m, 2F); 66.10 (m, 2F) MS (m/e): 471 (M
+, 49.91%); 387 (M
+-84,100.00%) IR (KBr, cm
-1): 2950,2870,1615,1600,1525,1505,1485,1120,1345,1295,1260,1180,1170,1110,1030,980,860,840,750,690,630 compounds (18-3):
1HNMR (CDCl
3/ TMS): 0.69-2.09 (m, 15H); 4.04 (t, 2H, J=6.3Hz); (d)/7.44 7.02 (d) (AA ' BB ', 4H, J=9.0Hz); (d)/8.28 7.78 (d) (AA ' BB ', 4H, J=8.1Hz)
19FNMR (CDCl
3/ TFA): 59.70 (m, 2F); 66.65 (m, 2F) MS (m/e): 499 (M
+, 100.00%); 387 (M
+-112,71.23%) IR (KBr, cm
-1): 2960,2920,2850,1615,1600,1520,1505,1485,1420,
1340，1300，1260，1190，1170，1110，1030，990，870，8
60,845,800,750,690,630 compounds (18-4);
1HNMR (CDCl
3/ TMS): 0.78-2.06 (m, 19H); 4.04 (t, 2H, J=6.3Hz); (d)/7.43 7.02 (d) (AA ' BB ', 4H, J=9.0Hz); (d)/8.28 7.76 (d) (AA ' BB ', 4H, J=8.1Hz)
19FNMR (CDCl
3/ TFA): 59.64 (m, 2F); 66.75 (m, 2F) MS (m/e): 527 (M
+, 100.00%); 388 (M
+-139,73.40%) IR (KBr, cm
-1): 2920,2850,1610,1600,1525,1505,1485,1480,1345,
1300,1260,1180,1165,1025,980,870,855,840,750 embodiment, 21. compounds (18) are as follows according to the transformation temperature that optical texture obtains: compound phase-variable temperature (polarizing microscope) ℃ 18-1
18-2
18-3
18-4
From the transformation temperature of compound (18) as can be seen, the non-constant width of the liquid crystal phase temperature range of this compounds is up to degree more than 100.As material, its operating temperature range is an important indicator, and this compounds of the wide explanation of liquid crystal phase temperature range is good as stability of material.Embodiment 22.
Synthesizing (19):
1-10mg Pd (PPh is being housed
3)
2I
2, 1-5mg CuI, 0.5mmol compound (3) and 0.5-1.0mmol to iodine or parabromobenzoic acid ester, add triethylamine 5-10ml, reflux has a large amount of brown precipitations to produce immediately, carried out FNMR and analyze after 0.5-4 hour, reacts complete.Add organic solvent 10-100ml, as ether, acetone, benzene or the like.Remove by filter triethylamine salt, steam desolventize product.With acetone-methyl alcohol or ethyl alcohol recrystallization, or use column chromatography, and sherwood oil and ethyl acetate (100: 0.5-10) drip washing, drain.Numbering R R ' fusing point (℃) productive rate (%) 19-1 n-C
8H
17-CH
3-124.8 8319-2 n-C
8H
17-C
2H
5-123.2 8319-3 n-C
8H
17-n-C
3H
7-117.6 8419-4 n-C
8H
17-n-C
4H
9-118.4 8519-5 n-C
8H
17-n-C
5H
11-109.3 6619-6 n-C
8H
17-n-C
6H
13-104.2 7019-7 n-C
8H
17-n-C
8H
17-117.8 8519-8 nC
6H
13--CH
2CH (CH
3) C
2H
5108.4 8419-9 nC
8H
17-
114.8 8519-10 n-C
10H
21-
106.7 8219-11 n-C
11H
25-
110.4 85 products are white crystal, analytical results is as follows: compound (19-1):
1HNMR (CDCl
3/ TMS): 0.78-1.94 (m, 15H); 3.94 (s, 3H ,-OCH
3);
4.00(t，2H，J＝5.4Hz，OCH
2)；7.16(AA′BB′，4H，O-C
6H
4-)；
7.84 (AA ' BB ', 4H ,-C ≡ C-C
6H
4-)
19FNMR (CDCl
3/ TFA): 60.1 (m, 2F); 67.3 (m, 2F) MS (m/c): 512 (M
+, 6.54%); 400 (M
+-112,100.00%); 369 (M
+-143,23.69%) IR (KBr, cm
-1): 2900 (s, C-H); 1725 (s, C=O); 1810 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1280 (s, 2 C-O-C) ultimate analysis: calculated value C 70.30% H 5.51% F 14.83%
Measured value C 89.92% H 5.28% F, 14.82% compound (19-2):
1HNMR (CDCl
3/ TMS): 0.78-1.94 (m, 18H); 3.92 (t, 2H, J=6.3Hz ,-OCH
2);
4.32(q，2H，J＝6.3Hz，OCH
2)；7.16(AA′BB′，4H，O-C
6H
4-)；
7.76 (AA ' BB ', 4H ,-C ≡ C-C
6H
4-)
19FNMR (CDCl
3/ TFA): 60.1 (m, 2F); 67.3 (m, 2F) MS (m/e): 526 (M
+, 100.00%); 414 (M
+-112,70.51); 369 (M
+-157,19.32%) IR (KBr, cm
-1): 2960 (s, C-H); 1718 (s, C=O); 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1278 (s, 2 C-O-C) compound (19-3):
1HNMR (CDCl
2/ TMS): 0.72-1.92 (m, 20H); 3.93 (t, 2H, J=6.3Hz ,-OCH
2);
4.23(t，2H，J＝6.3Hz，OCH
2)；7.14(AA′BB′，4H，O-C
6H
4-)；
7.73(AA′RR′，4H，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：60.1(m，2F)；87.3(m，2F)MS(m/e)：540(M
+，89.99％)；428(M
+-112，43.96％)；386(M
+154，36.30％)；
369 (M
+-171,15.22%); 57 (M
+-483,100.00%) IR (KBr, cm
-1): 2900 (s, C-H); 1718 (s, C=O); 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1278 (s, 2 C-O-C) ultimate analysis: calculated value C 71.09% H 5.97% F 14.06%
Measured value C 89.35% H 5.74% F, 13.85% compound (19-4):
1HNMR (CDCl
3/ TMS): 0.78-1.94 (m, 22H); 3.92 (t, 2H, J=6.3Hz ,-OCH
2);
4.32(t，2H，J＝6.3Hz，OCH
2)；7.16(AA′BB′，4H，O-C
6H
4-)；
7.76(AA′BB′，4H，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：60.1(m，2F)；67.3(m，2F)MS(m/e)：554(M
+，71.53％)；442(M
+-112，17.43％)；386(M
+-168，49.40％)；
369 (M
+-185,8.57%); 57 (M
+-494,100.00%) IR (KBr, cm
-1): 2910 (s, C-H); 1718 (s, C=O); 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1278 (s, 2 C-O-C) compound (19-5):
1HNMR (CDCl
3/ TMS): 0.78-1.94 (m, 24H); 3.92 (t, 2H, J=6.3Hz ,-OCH
2);
4.32(t，2H，J＝6.3Hz，OCH
2)；7.16(AA′BB′，4H，O-C
6H
4-)；
7.76(AA′BB′，4H，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：60.1(m，2F)；67.3(m，2F)MS(m/e)：568(M
+，82.80％)；456(M
+-112，12.14％)；386(M
+-182，58.75％)；
369 (M
+-199,7.69%); 57 (M
+-511,100.00%) IR (KBr, cm
-1): 2910 (s, C-H); 1718 (s, C=O); 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1278 (s, 2 C-O-C) compound (19-6);
1HNMR (CDCl
3/ TMS); 0.68-1.92 (m, 26H); 3.92 (t, 2H, J=6.3Hz ,-OCH
2);
4.24(t，2H，J＝6.3Hz，OCH
2)；7.12(AA′BB′，4H，O-C
6H
4-)；
7.76(AA′BB′，4H，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：60.1(m，2F)；67.3(m，2F)MS(m/e)，582(M
+，100.00％)；470(M
+-112，9.43％)；386(M
+-196，85.43％)；
369 (M
+-213,7.00%); 57 (M
+-525,66.64%) IR (KBr, cm
-1): 2910 (s, C-H); 1718 (s, C=O): 1610 (o, phenyl ring);
1480 (vs, fluorobenzene rings): 1110,1278 (s, 2 C-O-C) compound (19-7):
1HNMR (CDCl
3/ TMS): 0.64-1.92 (m, 30H); 3.92 (t, 2H, J=6.3Hz ,-OCH
2);
4.24(t，2H，J＝6.3Hz，OCH
2)；7.12(AA′BB′，4H，O-C
6H
4-)；
7.76(AA′BB′，4H，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：60.1(m，2F)；67.3(m，2F)MS(m/e)：610(M
+，100.00％)；498(M
+-112，8.43％)；386(M
+-224，66.30％)；
369 (M
+-241,7.70%) IR (KBr, cm
-1): 2900 (s, C-H); 1718 (s, C=O); 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1115,1278 (s, 2 C-O-C) ultimate analysis: calculated value C 72.76% H 6.93% F 12.44%
Measured value C 72.50% H 7.12% F, 12.28% compound (19-8):
1HNMR (CDCl
3/ TMS): 0.80-1.94 (m, 2OH); 4.00 (t, 2H, J=6.3Hz, OCH
2);
4.18(d，2H，OCH
2)；7.18(AA′BB′，4H，O-C
6H
4-)；
7.84 (AA ' BB ', 4H ,-C ≡ C-C
6H
4-)
19FNMR (CDCl
3/ TFA): 60.1 (m, 2F); 67.3 (m, 2F) MS (m/e): 540 (M
+, 100.00%); 386 (M
+-154,75.21%); 369 (M
+-171,16.81%) IR (KBr, cm
-1): 2910 (s, C-H); 1718 (s, C=O); 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1278 (s, 2 C-O-C) compound (19-9):
1HNMR (CDCl
3/ TMS): 0.80-1.94 (m, 24H); 4.00 (t, 2H, J=6.3Hz ,-OCH
2);
4.18(d，2H，OCH
2)；7.18(AA′BB′，4H，O-C
6H
4-)；
7.84(AA′BB′，4H，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：60.1(m，2F)；67.3(m，2F)MS(m/e)：568(M
+，60.00％)；456(M
+-112，3.92％)；386(M
+-182，75.21％)；
369 (M
+-199,16.81%); 57 (M
+-511,100.00%) IR (KBr, cm
-1): 2910 (s, C-H); 1718 (s, C=O); 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1278 (s, 2 C-O-C) compound (19-10):
1HNMR (CDCl
3/ TMS): 0.80-1.94 (m, 28H); 4.00 (t, 2H, J=6.3Hz ,-OCH
2);
4.18(d，2H，OCH
2)；7.18(AA′BB′，4H，O-C
6H
4-)；
7.84(AA′BB′，4H，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：60.1(m，2F)；67.3(m，2F)MS(m/e)；596(M
+，100.00％)；386(M
+-210，67.27％)；369(M
+-227，11.17％)；
57 (M
+-539,63.34%) IR (KBr, cm
-1): 2910 (s, C-H); 1718 (s, C=O); 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings): 1110,1278 (s, 2 C-O-C) compound (19-11):
1HNMR (CDCl
3/ TMS): 0.80-1.94 (m, 32H); 4.00 (t, 2H, J=6.3Hz ,-OCH
2);
4.18(d，2H，OCH
2)；7.18(AA′BB′，4H，O-C
9H
4-)；
7.84(AA′BB′，4H，-C≡C-C
6H
4-)
19FNMR(CDCl
3/TFA)：60.1(m，2F)；67.3(m，2F)MS(m/e)：624(M
+，100.00％)；386(M
+-238，45.77％)；369(M
+-255，6.50％)；
57 (M
+-267,55.69%) IR (KBr, cm
-1): 2910 (s, C-H); 1718 (s, C=O); 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1278 (s, 2 C-O-C) embodiment 23. has determined that by orthogonal polarizing microscope and DSC method the transformation temperature of compound (19-1)～(19-7) is: numbering transformation temperature (polarizing microscope) a transformation temperature (DSC) a
T
C-NT
N-IT
C-NT
N-I90.5 ℃ of 120.8 ℃ of 86.8 ℃ of 115.7 ℃ of a of 94.8 ℃ of 131.8 ℃ of 86.8 ℃ of 121.8 ℃ of 19-7 of 99.0 ℃ of 135.1 ℃ of 90.5 ℃ of 127.5 ℃ of 19-6 of 98.1 ℃ of 134.4 ℃ of 95.7 ℃ of 129.3 ℃ of 19-5 of 97.9 ℃ of 154.1 ℃ of 95.8 ℃ of 148.6 ℃ of 19-4 of 109.3 ℃ of 164.3 ℃ of 103.6 ℃ of 158.9 ℃ of 19-3 of 102.8 ℃ of 193.0 ℃ of 93.8 ℃ of 187.9 ℃ of 19-2 of 19-1, the phase transition temperature of temperature-fall period
With polarizing microscope and DSC compound (19-8)～(19-11) has been carried out inter-state research, their mesomorphic phase and transformation temperature see Table: numbering phase temperature (polarizing microscope) 19-8
19-9
19-10
19-11
Embodiment 24.
Synthesizing (20):
Operate same compound (19),, get white crystal with compound (3) with to iodine or the reaction of parabromobenzoic acid benzene alkyl ester.Numbering R R ' fusing point (℃) productive rate (%) 20-1 n-C
8H
17-n-C
4H
9-108.9 8520-2 n-C
6H
13-
106.5 7720-3 n-C
8H
17-
105.6 8020-4 n-C
10H
21-
93.5 7920-5 n-C
12H
25-
109.0 77 products are white crystal, analytical results is as follows: compound (20-1):
1HNMR (CDCl
3/ TMS): 0.64-1.92 (m, 22H); 3.92 (t, 2H, J=6.3Hz, OCH
2);
4.26 (t, 2H, J=6.3Hz, OCH
2); (6.82-8.20 m, 12H, phenyl ring)
19FNMR (CDCl
3/ TFA): 59.7 (m, 2F); 66.6 (m, 2F) MS (m/e): 674 (M
+, 19.40%); 481 (M
+-193,100.00%); 55 (M
+-619,59.91%) IR (KBr, cm
-1): 2960 (s, C-H); 1720,1740 (s, 2 C=O); 1608 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1210,1260 (s, 3 C-O-C) compound (20-2):
1HNMR (CDCl
3/ TMS): 0.72-1.92 (m, 20H); 3.94 (t, 2H, J=6.3Hz, OCH
2);
4.12 (d, 2H, OCH
2); (6.82-8.20 m, 12H, phenyl ring)
19FNMR (CDCl
3/ TFA): 59.7 (m, 2F); 66.6 (m, 2F) MS (m/e): 660 (M
+, 10.72%); 453 (M
+-207,100.00%); 55 (M
+-605,29.44%) IR (KBr, cm
-1), 2910 (s, C-H); 1720,1740 (s, 2 C=O): 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1210,1260 (s, 3 C-O-C) compound (20-3):
1HNMR (CDCl
3/ TMS): 0.72-1.92 (m, 24H); 3.94 (t, 2H, J=6.3Hz, OCH
2);
4.12 (d, 2H, OCH
2); (6.82-8.20 m, 12H, phenyl ring)
19FNMR (CDCl
3/ TFA): 59.7 (m, 2F); 66.6 (m, 2F) MS (m/e): 688 (M
+, 19.56%); 481 (M
+-207,100.00%); 55 (M
+633,40.68%) IR (KBr, cm
-1): 2910 (s, C-H); 1720,1740 (s, 2 C=O): 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1210,1260 (s, 3 C-O-C) compound (20-4):
1HNMR (CDCl
3/ TMS): 0.72-1.92 (m, 28H); 3.94 (t, 2H, J=6.3Hz, OCH
2);
4.12 (d, 2H, OCH
2); (6.82-8.20 m, 12H, phenyl ring)
19FNMR (CDCl
3/ TFA): 59.7 (m, 2F); 66.6 (m, 2F) MS (m/e): 716 (M
+, 10.97%); 509 (M
+-207,84.62%); 55 (M
+-661,100.00%) IR (KBr, cm
-1): 2910 (s, C-H); 1720,1740 (s, 2 C=O); 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1210,1260 (s, 3 C-O-C) compound (20-5):
1HNMR (CDCl
3/ TMS): 0.72-1.92 (m, 32H); 3.94 (t, 2H, J=6.3Hz, OCH
2);
4.12 (d, 2H, OCH
2); (6.82-8.20 m, 12H, phenyl ring)
19FNMR (CDCl
3/ TFA): 59.7 (m, 2F); 66.6 (m, 2F) MS (m/e): 744 (M
+, 3.11%); 537 (M
+-207,18.92%); 55 (M
+-689,100.00%) IR (KBr, cm
-1): 2910 (s, C-H); 1720,1740 (s, 2 C=O): 1610 (s, phenyl ring);
1480 (vs, fluorobenzene rings); 1110,1210,1260 (s, 3 C-O-C) embodiment 25. is by the texture that DSC spectrum and polarized light microscope observing obtain, and (transformation behavior of 20-1～20-5) is as table: number phase temperature (polarizing microscope) 20-1 to determine compound
20-2
20-3
20-4
20-5
Embodiment 26.
Synthesizing (21): 1.
Synthetic:
With 0.5-5g compound (1-11), 0.2-10g is to bromo-iodobenzene, 50-500mg Pd (PPh
3)
2Cl
2Reach 30-200mgCuI and place in the three-necked bottle, at N
2Protection adds 10-100mlEt down
3N.At room temperature-50 ℃ stirring reaction 10-24 hour, the reaction of TLC analysis revealed was complete.Add the 20ml ether, filter, desolventize product.Through column chromatography purification, sherwood oil is a leacheate, gets white half decorating film 2.55g, productive rate 79.9%.
1HNMR (CCl
4/ TMS): 0.82-1.90 (m, 9H); 4.20 (d, 2H, J=6.0Hz); 7.50 (s, 4H)
19FNMR (CCl
4/ TFA); 60.37 (m, 2F); 80.37 (m, 2F) 2.
Synthesizing (21):
With above-mentioned product 0.1mol, compound (1) 0.1-0.5mol, Pd (PPb
3)
2Cl
20.001mol CuBr 0.001-0.01mol places in the three-necked bottle, at N
2Protection adds 5-20mlEt down
3N.Back flow reaction 6 hours.Be chilled to room temperature, filter, desolventize.Or in reaction system, add the 5-50ml polar solvent, and as ether, vinyl acetic monomer etc., the elimination throw out, through column chromatography purification, sherwood oil is a leacheate, gets product.When R is n-C
5H
11-, n-C
6H
13-, n-C
7H
15-, n-C
8H
17-, n-C
9H
19-and n-C
12H
25In-time, productive rate is 78-85%.When R is n-C
8H
17In-time, the product fusing point is 108.3 ℃, productive rate 80.1%.Nuclear magnetic resonance spectroscopy is as follows:
1HNMR (CCl
4/ TMS): 0.80-2.0 (m, 24H); 4.0-4.3 (m, 4H); 7.50 (s, 4H)
19FNMR (CCl
4/ TFA): 60.20 (m, 2F); 80.20 (m 2F) observes this compound with orthogonal polarizing microscope, determines that its transformation temperature is as follows:
Embodiment 27.
(1) in reaction flask, adds compound
0.01ml, add a small amount of formic acid or acetum, make to be under the acidic conditions, add organic solvent, as ethylene dichloride, ether, dioxane, KMnO
40.05-0.40mol backflow 10-50 hour.Can add during reaction and have C
12-30The quaternary amine 0.0002-0.005mol of alkyl as trimethylammonium tetradecyl ammonium chloride, tetrabutyl chlorination or brometo de amonio, methyl three n-octyl chlorination ammoniums, trimethyl benzyl ammonia chloride, tributyl phenyl ammonium iodide etc., carries out to add fast response.Reaction is used the mineral acid acidifying after finishing, with reductive agent such as NaHSO
3Take off into colourlessly, organic solvent extraction desolventizes, and obtains
(22), productive rate 89.8%.
(2) use
0.1mol, add 0.05-0.40mol KMnO
4, 0.1-5mol 1 valency metal hydroxides as NaOH, at organic solvent, as reaction in dioxane, THF or methylene dichloride and water 10-50 hour, obtains white solid, productive rate 30-75%.Also can be in the reaction with phase-transfer catalyst, quaternary ammonium salt compound 0.002-0.05mol as described above, productive rate 40-80%.Work as R=n-C
7H
15-time, productive rate 71.4%.MS(m/e)：384(M
+，72.80％)；340(M
+-44，16.39％)；286(M
+-98，100.00％)
1HNMR(CD
3COCD
3/TMS)：0.30-1.60(m，13H)；3.50(t，2H，OCH
2)；
6.70(AA′BB′，4H)
19FNMR(CD
3COCD
3/TFA)：65.52(m，2F)；67.67(m，2F)
(3)
Synthesizing (24):
Use compound
0.1mol, use 0.1mol SOCl with p-hydroxybenzoic acid chirality isopentyl ester 0.1-0.2mol reaction
2Perhaps 0.1mol DCCI/0.001mol PPY in methylene dichloride or ether back flow reaction 1-10 hour, obtains compound (24), productive rate 61.2-90%, 100.2 ℃ of product fusing points.
1HNMR(CDCl
3/TMS)：0.76-2.04(m，24H)；4.00(t，2H，J＝4.8Hz)；
4.14 (d, 2H, COOCH
2); 7.16 (AA ' BB ', 4H); 7.73 (AA ' BB ', 4H)
19FNMR (CDCl
3/ TFA): 58.3 (m, 2F): 63.8 (m, 2F) MS (m/e): 538 (M
+, 9.48%); 381 (M
+-207,100.00%) IR (KBr, cm
-1): 2000 (s, C-H); 1750,1715 (s, 2C=O); 1605 (m, hydrogen phenyl ring);
1470 (vs, fluorobenzene rings); 1275,1225,1100 (s, C-O-C) ultimate analyses: calculated value C 67.35% H 6.12% F 12.92%
Measured value C 67.94% H 6.13% F 12.67%
Adopt orthogonal polarizing microscope that the optical texture that compound (24) occurs in heating and cooling process is observed, find that this compounds presents cholesteryl phase and ferroelectric liquid crystals (Sc*) two mesomorphic phases mutually, its texture is changed to:
Embodiment 28.
Synthesizing (25):
With 0.1mol compound (3),
Or
0.1-O.3mol, Pd[P (C
4H
9)
3]
2Cl
20.002-0.01mol, CuCl 0.003-0.01mol and 0.1molEtNH
2At room temperature stirring reaction 10-50 minute, be added dropwise to sulfuric acid or hydrochloric acid, produce yellow mercury oxide.Use ether extraction, the saturated common salt water washing is to neutrality, anhydrous Na
2SO
4Drying desolventizes.Perhaps, get light yellow crystal through column chromatography purification.Productive rate 78-85%.When being raw material with compound (3-1), productive rate 80.1%, 155.2 ℃ of product (25-1) fusing points.
1HNMR(CDCl
3/TMS)：0.90(t，3H，J＝4.2Hz，CH
3)；1.10-1.88(m，4H)；
4.02 (t, 2H, J=4.8Hz); 7.14 (AA ' BB ', 4H); 7.98 (AA ' BB ', 4H)
19FNMR (CDCl
3/ TFA): 60.2 (m, 2F); 66.2 (m 2F) has carried out inter-state research with polarizing microscope and DSC to this compounds, and is as follows as the mesomorphic phase and the transformation temperature of compound (25-1),
Embodiment 29.
Synthesizing (26):
In the 100ml three-necked bottle, put into Pd (PPh
3)
2Cl
250mg, CuI 15mg, I-C
6H
4-I 0.55g, and at N
2Protection adds compound (1) 1g, pyridine 40ml down.At room temperature-50 ℃ stirring reaction 5-24 hour.Behind the elimination pyridinium salt, column chromatography, leacheate are sherwood oil: ethyl acetate (100: 2) gets yellow solid 1.05g, productive rate 95.4%.Further purify, can get yellow needle-like crystal with acetone-methanol mixed solvent recrystallization.Numbering R productive rate (%) 24-1 n-C
3H
7-8824-2 n-C
4H
9-9024-3 n-C
5H
11-8824-4 n-C
6H
13-9524-5 n-C
7H
15-7824-6 n-C
8H
17-95.424-7 n-C
9H
19-9224-8 n-C
12H
25-84 analytical resultss are as follows: compound (26-1), and yellow needle-like crystal:
19FNMR (CDCl
3/ TFA): 61.0 (d, 2F, J=18.8Hz); 80.3 (d, 2F, J=18.6Hz)
1HNMR (CDCl
3/ TMS): 7.57 (s, 4H); 4.31 (t, 4H, J=6.3Hz);
1.24-1.93(m，4H)；1.01(t，6H，J＝6.3Hz)MS(m/e)：538(M
+，50.41％)；454(M
+-84，100％)IR(KBr，cm
-1)：2950，1640，1520，1490，1440，1390，1260，1090，1115，
985,840,800,690,545 compounds (26-2), yellow needle-like crystal:
19FNMR (CDCl
3/ TFA): 61.0 (d, 2F, J=18.6Hz); 80.3 (d, 2F, J=18.8Hz)
1HNMR (CDCl
3/ TFA): 7.57 (s, 4H); 4.31 (t, 4H, J=6.3Hz);
1.29-1.98(m，8H)；1.01(t，6H，J＝6.3Hz)MS(m/e)：566(M
+，54.30％)；454(M
+-112，100％)；57(M
+-509，32.13％)IR(KBr，cm
-1)：2960，1640，1520，1500，1490，1475，1440，1390，1260，
1120,985,840,800,690 compounds (26-3), white needle-like crystals:
19FNMR (CDCl
3/ TF
A): 61.2 (d, 2F, J=18.6Hz); 80.6 (d, 2F, J=18.6Hz)
1HNMR (CDCl
3/ TMS): 7.57 (s, 4H); 4.31 (t, 4H, J=6.3Hz); 0.77-1.98 (m, 18H) MS (m/e): 594 (M
+, 66.43%); 454 (M
+-140,100%) IR (KBr, cm
-1): 2970,2870,1520,1505,1490,1440,1410,1390,1140,
1130,1020,1010,985,840,800,695,545 compounds (26-4), faint yellow needle-like crystal:
19FNMR (CDCl
3/ TFA): 61.0 (d, 2F, J=18.6Hz); 80.3 (d, 2F, J=18.6Hz)
1HNMR (CDCl
3/ TMS): 7.57 (s, 4H); 4.29 (t, 4H, J=6.3Hz); 0.75-1.99 (m, 22H) MS (m/e): 622 (M
+, 61.96%); 454 (M
+-168,100%) IR (KBr, cm
-1): 2900,2850,1640,1520,1490,1440,1390,1130,
1020,985,840,690,545 ultimate analyses: theoretical value C, 65.59% H, 4.82% F 24.44%
Measured value C 66.58% H 4.88% F, 24.55% compound (26-5), yellow needle-like crystal:
19FNMR (CDCl
3/ TF
A): 61.2 (d, 2F, J=18.6Hz); 80.6 (d, 2F, J=18.6Hz)
1HNMR (CDCl
3/ TMS): 7.57 (s, 4H); 4.30 (t, 4H, J=6.3Hz); 0.76-2.00 (m, 26H) MS (m/e): 650 (M
+, 55.20%); 454 (M
+-196,100%) IR (KBr, cm
-1): 2960,2930,2860,1645,1520,1490,1440,1405,1390,
1260,1145,1130,1020,1010,985,840,690,545 compounds (28-6), yellow needle-like crystal: 19FNMR (CDCl
3/ TFA): 61.0 (d, 2F, J=18.8Hz); 80.3 (d, 2F, J=18.6Hz)
1HNMR (CDCl
3/ TMS): 7.57 (s, 4H); 4.30 (t, 4H, J=6.3Hz); 0.74-2.00 (m, 30H) MS (m/e): 678 (M
+, 87.33%): 454 (M
+-224,100%) IR (KBr, cm
-1): 2910,2840,1640,1520,1490,1440,1390,1140,1125,
1020,1005,985,840,895,550 ultimate analyses: calculated value C 67.26%, H 5.60%, and F 22.42%
Measured value C 66.43%, H 5.72%, F 22.40% compound (26-7), yellow needle-like crystal:
19FNMR (CDCl
3/ TFA): 61.2 (d, 2F, J=18.6Hz); 80.6 (d, 2F, J=18.6Hz)
1HNMR (CDCl
3/ TMS); 7.57 (s, 4H); 4.30 (t, 4H, J=6.3Hz); 0.73-2.02 (m, 34H) MS (m/e): 706 (M
+, 41.69%); 454 (M
+-252,100%); 57 (M
+-649,71.77%) IR (KBr, cm
-1): 2950,2900,2850,1640,1520,1490,1485,1440,1390,
1260,1140,1125,1020,985,840,800,695,545 compounds (26-8), white needle-like crystals:
19FNMR (CDCl
3/ TFA): 61.1 (d, 2F, J=18.6Hz); 80.7 (d, 2F, J=18.6Hz)
1HNMR (CDCl
3/ TMS): 7.58 (s, 4H): 4.29 (t, 4H, J=6.3Hz); 0.75-1.97 (m, 46H) MS (m/e): 790 (M
+, 35.30%); 454 (M
+-336,83.41%);
71(M
+-719，45.79％)；57(M
+-733，100％)IR(KBr，cm
-1)：2900，2840，1640，1520，1500，1490，1470，1440，1405，
1385,1135,1000,985,840,690,545 ultimate analysis: theoretical value C, 69.87% H, 6.84% F 19.24%
Measured value C 69.80% H 6.87% F 19.55% embodiment 30.
The transformation temperature and the temperature range that get compound (26) with polarized light microscopic method and DSC method side are as shown in the table: (℃) code T
C → NT
N → IT
I → NT
N → CΔ T
N heats upΔ T
The N coolingThe phase transition temperature that 24-1 192.6 194.1 193.4 191.6 1.5 1.824-2 159.1 189.5 189.1 157.4 30.4 30.724-3 125.4 167.8 167.0 124.4 42.4 42.624-4 115.4 160.3 159.9 113.5 44.9 46.424-5 118.4 150.1 149.9 111.4 31.7 32.524-6 120.0 146.1 146.0 118.7 26.1 27.324-7 114.3 137.1 136.9 112.4 22.8 24.524-8 108.4 122.5 122.4 106.2 14.1 16.2 compounds (26) obtain according to DSC spectrum and temperature range (℃) code TC → NT
N → IT
I → NT
N → CΔ T
N heats upΔ T
The N cooling24-1 181.05 189.26 183.93 175.13 8.21 8.8024-2 155.04 184.45 182.07 148.37 29.41 33.7024-3 121.29 162.42 159.92 116.54 41.13 43.3824-4 116.01 153.30 151.00 105.56 37.29 45.4424-5 112.97 141.98 139.83 108.51 29.01 31.3224-6 121.55 145.09 140.08 110.95 23.54 29.1324-7 109.70 132.06 129.88 104.93 22.36 24.9524-8 104.30 117.63 115.46 99.23 13.33 16.23 results show the growth with liquid crystal molecule two ends flexible chain, and fusing point and clearing point descend. Embodiment 31.Synthesizing (27):
Operation, the same compound of proportioning (10).With R=n
4-C
8H
17-be example, productive rate 81%, product are white crystal, 104.0 ℃ of fusing points.
1HNMR(CDCl
3/TMS)：0.64-1.92(m，18H)；4.25(t，2H，J＝6.3Hz，OCH
2)；
4.40 (d, 2H, OCH
2); 7.68 (AA ' BB ', 4H); 7.88 (AA ' BB ', 4H)
19FNMR (CDCl
3/ TFA): 60.5 (m, 2F); 80.3 (m, 2F) .IR (KBr, cm
-1): 2950 (s, C-H); 1715,1740 (two C=O): 1605 (s, phenyl ring);
1490 (vs, fluorobenzene rings); 1110,1200,1260 (s, three C-O-C) MS (m/e): 570 (M
+, 6.30%); 363 (M
+-207,100.00%); 293 (M
+-277,64.22%)
With polarizing microscope and DSC this compounds has been carried out inter-state research, for example the mesomorphic phase of above-claimed cpd and transformation temperature are as follows:
Claims (10)
- One kind to prepare molecular formula be Y-A-E-B-G k-C l-H m-D nThe method of the perfluor liquid crystalline cpd that contains one or more perfluoro-benzene-ring and one or more bridged bond of-Z, its A, B, C or D are OrK, l, m or n=0 or 1; Y=OR or R, R=C 1-14Straight chain, side chain or chirality alkyl; Z=R, COOR ', NO 2, CN or X, R '=C 1-10Straight chain, side chain or chirality alkyl, X=F, Cl, Br or I; E, G or H are singly-bound or bridged bond, bridged bond is-C ≡ C-,-COO-or-C ≡ C-C ≡ C-, it is characterized in that making respectively by following method:
(1) trimethyl silicon based penta fluoro benzene acetylene and oxy-compound are in the presence of alkali or subsalt, room temperature-50 ℃ reaction 0.5-50 hour; The mol ratio of trimethyl silicon based penta fluoro benzene acetylene, oxy-compound and alkali or subsalt is 1: (1-10): (1-5); Described oxy-compound is
Or ROH; Alkali or subsalt are oxyhydroxide, carbonate, supercarbonate, phosphoric acid, hydrophosphate, sulphite or hydrosulphite, the acetate of monovalence or divalent metal; Reaction can be carried out in polar solvent, and solvent load is 0-50 a times of trimethyl silicon based penta fluoro benzene acetylene weight,
(2) trimethyl silicon based penta fluoro benzene acetylene and Grignard reagent are in ether solvent reacting by heating 0.5-50 hour, wherein, Grignard reagent be RMgX ', MgX ',X '=Cl, Br, I; Ether solvent is ether, butyl ether, tetrahydrofuran (THF) or 1, the 4-dioxane; The tetra fluoro benzene acetylene of trimethyl silicon based penta fluoro benzene acetylene or para-orientation, Grignard reagent and ether solvent mol ratio are 1: (0.5-3): (1-100), product is dissolved in the polar solvent, oxyhydroxide, carbonate, acetate or the phosphoric acid salt (0.001-0.02 mol ratio) that add 1-2 valency metal are hydrolyzed, reaction times 0.5-40 hour
(3) carry out the oxidizing reaction of terminal alkynes by the product of (1) or (2), be in acidic conditions and the organic solvent 1 mole of KMnO of the product of described (1) or (2) adding formic acid or acetic acid with the 5-8 mole 4Backflow 10-50 hour, can add the C that has of 0.02-0.5 mole 9-30The quaternary amine catalysis of alkyl; Perhaps the oxyhydroxide of 1 valency metal of 1-50 mole, organic solvent and water exist down, with the KMnO of 0.5-4 mole 4Reacted 10-50 hour,(4) by the aromatic alkyne compounds in the presence of oxygen and CuX, room temperature autoxidation symmetry coupled reaction 1-5 hour, the aromatic alkyne compounds is OrX is a halogen, and aromatic alkyne compounds and CuX mol ratio are 1: (0.01-0.20), can add the organic solvent that dissolves CuX in the reaction,
(5) the tetra fluoro benzene acetylene and the bromine or iodine thing of trimethyl silicon based penta fluoro benzene acetylene or the para-orientation that makes by (1) or (2), in the presence of two (trihydrocarbyl phosphine) halogenation palladium, two (trihydrocarbyl phosphine) palladium or two (trihydrocarbyl phosphine) Palladous nitrates and CuX and organic solvent, room temperature-reflux temperature reacted 0.5-50 hour, wherein iodine or bromide are X '-G-X "; X "-G-Z, X " G-C-H m-D n-Z, X " G-COOH or X "-G-C-H m-D n-COOH, "=Br or I, alkyl is C to X in the palladium compound 1-10Alkyl or phenyl, the mol ratio of above-mentioned acetylene compound, bromine or iodine thing, palladium compound and CuX is 1: (1-10): (0.01-0.2): (0.02-0.40),(6) make the compound of an end band carboxyl by (3) or (5), can with ROH at SOCl 2Carry out esterification under existing, mol ratio is followed successively by 1: (1-2): (1-15), temperature of reaction is room temperature-reflux temperature, and the reaction times is 1-10 hour,(7) make the compound of an end band carboxyl by (3) or (5), can with ROH at N, N-dicyclohexyl carbimide and following to pyrryl pyridine or the existence of 4-dimethylamine pyridine, in polar solvent, carry out esterification, reaction times is 1-10 hour, carboxylic compound, ROH, N, are 1 to the mol ratio of pyrryl pyridine or 4-dimethylamine pyridine at N-dicyclohexyl carbimide: (1-20): (1-3): (0.01-0.20). - 2. preparation method as claimed in claim 1, it is characterized in that the reaction in the presence of two (trihydrocarbyl phosphine) halogenide and CuX at (4) described acetylene compound and bromine or iodine thing, also add the organic ligand that contains a nitrogen-atoms, tertiary amine, bipyridine, ethylenediamines compound, acetylene compound is 1 with containing ammonia organic ligand mol ratio: (1-10).
- 3. one kind as claim 1 or described preparation method, it is characterized in that described tertiary amine is Trimethylamine 99, triethylamine, Tributylamine, and the ethylenediamines compound is a tetraethylethylenediamine.
- 4. one kind as claim 1,2 or 3 described preparation methods, the described liquid crystalline cpd of its feature be or
- 5. one kind as claim 1,2 or 3 described preparation methods, and Ji Tezheng is that described liquid crystalline cpd is
- 6. one kind as claim 1,2 or 3 described preparation methods, it is characterized in that described liquid crystalline cpd is
- 7. one kind as claim 1,2 or 3 described preparation methods, it is characterized in that described liquid crystalline cpd is
- 8. one kind as claim 1,2 or 3 described preparation methods, it is characterized in that described liquid crystalline cpd is
- 9. one kind as claim 1,2 or 3 described preparation methods, it is characterized in that described liquid crystalline cpd is
- 10. one kind as claim 1,2 or 3 described preparation methods, it is characterized in that described liquid crystalline cpd is
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN92108444A CN1036071C (en) | 1992-06-04 | 1992-06-04 | Liquid crystal compound containing perfluoro-benzene-ring and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN92108444A CN1036071C (en) | 1992-06-04 | 1992-06-04 | Liquid crystal compound containing perfluoro-benzene-ring and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1066458A CN1066458A (en) | 1992-11-25 |
| CN1036071C true CN1036071C (en) | 1997-10-08 |
Family
ID=4943551
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN92108444A Expired - Fee Related CN1036071C (en) | 1992-06-04 | 1992-06-04 | Liquid crystal compound containing perfluoro-benzene-ring and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1036071C (en) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1059459C (en) * | 1997-12-15 | 2000-12-13 | 中国科学院上海有机化学研究所 | Liquid crystal compound contg. cyclohexyl and perfluoro benzene ring and preparing process thereof |
| JP2005255578A (en) * | 2004-03-10 | 2005-09-22 | Fuji Photo Film Co Ltd | Compound, liquid crystal composition and optical material |
| JPWO2012005310A1 (en) * | 2010-07-08 | 2013-09-05 | 旭硝子株式会社 | Fluorine-containing aromatic compounds, organic semiconductor materials, and organic thin film devices |
| CN102031120B (en) * | 2010-11-17 | 2013-07-10 | 上海天问化学有限公司 | Fluorine-containing liquid crystal of 4-(2,3,5,6-tetrafluo-R substituent phenethyl) benzoic acid-4'-fluo-4-biphenyl ester |
| CN102020553B (en) * | 2010-11-17 | 2013-10-30 | 上海天问化学有限公司 | P-alkyl group substituted-4-fluorophenylacetic acid, synthesis method and application thereof |
| CN102153454B (en) * | 2011-01-28 | 2013-08-07 | 上海天问化学有限公司 | Ultrahigh-fluorine-substituted liquid crystal compound with CF2O bridge bond, synthetic method and application |
| CN103059875A (en) * | 2011-10-24 | 2013-04-24 | 财团法人工业技术研究院 | Liquid crystal compound and liquid crystal display comprising same |
| CN102585838B (en) * | 2012-01-12 | 2014-01-08 | 上海天问化学有限公司 | 4-[(4-R alkoxy 2,3,5,6-tetrafluorophenyl)ethyl]benzoic acid(4-R1 alkoxy) phenyl ester fluoride liquid crystal compound |
| CN102827614A (en) * | 2012-09-24 | 2012-12-19 | 上海天问化学有限公司 | Negative liquid crystal containing 2, 3, 5, 6-tetra-fluorine phenylene, as well as synthesis method and application of negative liquid crystal |
| CN103333697B (en) * | 2013-07-16 | 2015-06-03 | 福建省邵武市永晶化工有限公司 | Nematic negative liquid crystal containing 2,3,5,6-tetrafluorotolane, synthetic method and application |
| CN104194800B (en) * | 2014-08-11 | 2016-03-09 | 福建省邵武市永晶化工有限公司 | Fluoric bis(diphenyl)acetylene nematic negative liquid crystal, synthetic method and application |
| CN104531165B (en) * | 2014-12-12 | 2016-10-05 | 西安彩晶光电科技股份有限公司 | Two fluoro-[(4-alkoxyl-2,3,5,6-tetrafluoro phenyl) ethyl)-side fluorophenyl-side fluoro-4-4-trifluoromethylphenopendant] methane and preparation and application thereof |
| CN114805122B (en) * | 2021-01-22 | 2024-03-01 | 江苏和成新材料有限公司 | Esterification reaction method |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS628839A (en) * | 1985-07-05 | 1987-01-16 | Fujitsu Ltd | Controlling method for inching of vehicle equiped with automatic transmission |
| GB2190373A (en) * | 1986-04-01 | 1987-11-18 | Central Glass Co Ltd | Trifluoromethylbenzoyl bromide and conversion of same to bromobenzotrifluoride |
| DE4111998A1 (en) * | 1990-04-13 | 1991-10-17 | Merck Patent Gmbh | Liq. crystal mixt. with wide nematic phase range etc. - contg. one or more substd. alkyl 1,4-cyclohexylene phenylene fluoride(s) |
-
1992
- 1992-06-04 CN CN92108444A patent/CN1036071C/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS628839A (en) * | 1985-07-05 | 1987-01-16 | Fujitsu Ltd | Controlling method for inching of vehicle equiped with automatic transmission |
| GB2190373A (en) * | 1986-04-01 | 1987-11-18 | Central Glass Co Ltd | Trifluoromethylbenzoyl bromide and conversion of same to bromobenzotrifluoride |
| DE4111998A1 (en) * | 1990-04-13 | 1991-10-17 | Merck Patent Gmbh | Liq. crystal mixt. with wide nematic phase range etc. - contg. one or more substd. alkyl 1,4-cyclohexylene phenylene fluoride(s) |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1066458A (en) | 1992-11-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1036071C (en) | Liquid crystal compound containing perfluoro-benzene-ring and preparation method thereof | |
| CN1143973A (en) | Novel polymerisable liquid-crystalline compounds | |
| CN104449762B (en) | Fluorinated liquid crystal containing difluoro-methoxy bridged bond and combinations thereof thing | |
| JPS63307837A (en) | Optical active compound | |
| DE19982965B3 (en) | Liquid crystalline compound with a negative value of dielectric anisotropy | |
| CN101768447B (en) | Polyfluoric terphenyl liquid crystal compound and synthesis method and use thereof | |
| CN1911888A (en) | 2,3,2,'3' tetrafluoro diphenyl acetylene derivative, its composition, preparation method and use | |
| CN1214036A (en) | Bisalkenyl derivatives, liquid crystalline compounds and liquid crystal compsns. | |
| CN1911880A (en) | Multifluoro substituted diphenyl acetylene derivative, composition containing multifluoro substituted diphenyl acetylene derivatire, its preparation method and use | |
| CN87101284A (en) | Preparation of liquid crystalline cyclohexylbenzene derivatives and novel nematic mixtures containing them | |
| WO2018018708A1 (en) | Tricyclic super-fluorine liquid crystal compound, and synthetic method and application thereof | |
| CN103242854B (en) | Fluorine-containing liquid crystal compound | |
| JP5526686B2 (en) | Difluorobenzene derivatives and liquid crystal compositions containing the same. | |
| CN1158142A (en) | Process for producing liquid cyrstal mixtures | |
| CN105884626B (en) | A kind of synthetic method of 2 aminoidan derivatives and products thereof | |
| CN109181712A (en) | A kind of benzofuran liquid-crystal compounds and combinations thereof with difluoromethyl ether bridged bond | |
| JP4521738B2 (en) | Benzothiazole compound, process for producing the same, liquid crystal composition, and liquid crystal element | |
| CN1356969A (en) | Compound having tetrahydronalphthalene skeleton and liquid crystal compsn. contg. same | |
| JP2005048007A (en) | Liquid crystal composition containing trifluoro naphthalene derivative, display element and liquid crystalline compound | |
| CN101153000A (en) | Difluorbenzol-derivat und herstellungsverfahren dafur | |
| JP5382406B2 (en) | 1- (Trifluoromethoxy) naphthalene derivative | |
| JP5708994B2 (en) | Compound having fluorinated oxabicyclononane structure and liquid crystal composition thereof | |
| JP2007261952A (en) | Chroman derivative and liquid crystal composition containing the compound | |
| JP4219061B2 (en) | Cyclohexenyl derivative | |
| CN1153807A (en) | Liquid crystalline compound replaced by fluorine containing group, liquid crystal composition, and liquid crystal display device |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C06 | Publication | ||
| PB01 | Publication | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C15 | Extension of patent right duration from 15 to 20 years for appl. with date before 31.12.1992 and still valid on 11.12.2001 (patent law change 1993) | ||
| OR01 | Other related matters | ||
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |