F-Term-List

(Not Translated)
4H027 Liquid crystal substances
C09K19/00 -19/60@Z
C09K19/00-19/58 BA BA00
KINDS OF LIQUID CRYSTALS
BA01 BA02 BA03 BA04 BA05 BA06 BA07 BA08
. Nematic liquid crystals . . Cholesteric or chiral nematic liquid crystals . Smectic liquid crystals . . Smectic A liquid crystals . . Smectic C liquid crystals . . Chiral smectic C and ferroelectric liquid crystals . . Antiferroelectric liquid crystals . Discotic liquid crystals
BA11 BA12 BA13 BA14 BA15 BA16
. Polymer liquid crystals . . Main chain type . . Side chain type . . Composite type . Lyotropic liquid crystals . Other liquid crystals
BB BB00
DISPLAY SYSTEMS OF LIQUID CRYSTALS
BB01 BB02 BB03 BB04 BB05 BB06 BB07 BB08 BB09 BB10
. Dynamic scattering . Guest host . TN . STN . Cholesteric-nematic phase transition . Double refraction control . Thermal writing . Optical writing . Surface stabilised ferroelectric liquid crystals . Antiferroelectric liquid crystals
BB11 BB12 BB13
. Polymer dispersion liquid crystals or dispersed type liquid crystals . Microencapsulated liquid crystals . Other display systems
BC BC00
DRIVE METHODS OF LIQUID CRYSTALS
BC01 BC02 BC03 BC04 BC05 BC06 BC07 BC08 BC09 BC10
. Static drive . Time division drive or dynamic drive . . Simple matrix drive . Active matrix drive . . TFT or thin film transistor system . . MIM system . Beam address system . . Thermal writing system . . Optical writing system . Other drive methods
BD BD00
PROPERTIES OF LIQUID CRYSTALS OR LIQUID CRYSTAL COMPOSITIONS
BD01 BD02 BD03 BD04 BD05 BD06 BD07 BD08 BD09 BD10
. Chemical stability or physical stability . Operative temperature range . Viscosity . Voltage . . Threshold voltage . . Steepness . Refractive index anisotropy . Response speed . Dielectric constant anisotropy . . Positive dielectric constant anisotropy
BD11 BD12 BD13 BD14 BD15 BD16 BD17 BD18 BD19 BD20
. . Negative dielectric constant anisotropy . Orientation property . . Pretilt angle . Chirality . . Reverse domain . . Helical pitch . Ferroelectricity . Tilt angle . Spontaneous polarisation . Contrast
BD21 BD22 BD23 BD24
. Visual characteristics . Hysteresis . Temperature dependency . Other properties
BE BE00
METHODS OF SPECIFYING CLAIMS
BE01 BE02 BE03 BE04 BE05 BE06 BE07
. Specification by chemical properties . Specification by physical properties . Specification by electric properties . Specification by incomplete structure . Specification by compositions or combination of a plurality of compounds . Specification by special applications . Specification by other methods
CA CA00
RING STRUCTURES CONTAINING BENZENE RING ONLY
CA01 CA02 CA03 CA04 CA05 CA06 CA07 CA08 CA09 CA10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CB CB00
RING STRUCTURES CONTAINING TWO BENZENE RINGS ONLY
CB01 CB02 CB03 CB04 CB05 CB06 CB07 CB08 CB09 CB10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CC CC00
RING STRUCTURES CONTAINING TWO BENZENE RINGS ONLY; PH-COO-PH
CC01 CC02 CC03 CC04 CC05 CC06 CC07 CC08 CC09 CC10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CD CD00
RING STRUCTURES CONTAINING TWO BENZENE RINGS ONLY; PH-PH
CD01 CD02 CD03 CD04 CD05 CD06 CD07 CD08 CD09 CD10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CE CE00
RING STRUCTURES CONTAINING THREE BENZENE RINGS ONLY
CE01 CE02 CE03 CE04 CE05 CE06 CE07 CE08 CE09 CE10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CF CF00
RING STRUCTURES CONTAINING THREE BENZENE RINGS ONLY; PH-COO-PH-PH, PH-OOC-PH-PH
CF01 CF02 CF03 CF04 CF05 CF06 CF07 CF08 CF09 CF10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CG CG00
RING STRUCTURES CONTAINING THREE BENZENE RINGS ONLY; PH-PH-PH
CG01 CG02 CG03 CG04 CG05 CG06 CG07 CG08 CG09 CG10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CH CH00
RING STRUCTURES CONTAINING FOUR BENZENE RINGS ONLY
CH01 CH02 CH03 CH04 CH05 CH06 CH07 CH08 CH09 CH10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CJ CJ00
RING STRUCTURES CONTAINING PH AND CYCLOHEXANE ONLY
CJ01 CJ02 CJ03 CJ04 CJ05 CJ06 CJ07 CJ08 CJ09 CJ10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CK CK00
RING STRUCTURES CONTAINING ONE PHENYL AND ONE CYCLOHEXANE ONLY
CK01 CK02 CK03 CK04 CK05 CK06 CK07 CK08 CK09 CK10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CL CL00
RING STRUCTURES CONTAINING ONE PHENYL AND ONE CYCLOHEXANE ONLY; CY-COO-PH, PH-COO-CY
CL01 CL02 CL03 CL04 CL05 CL06 CL07 CL08 CL09 CL10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CM CM00
RING STRUCTURES CONTAINING ONE PHENYL AND ONE CYCLOHEXANE ONLY; CY-PH
CM01 CM02 CM03 CM04 CM05 CM06 CM07 CM08 CM09 CM10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CN CN00
RING STRUCTURES CONTAINING TWO PHENYLS AND ONE CYCLOHEXANE ONLY
CN01 CN02 CN03 CN04 CN05 CN06 CN07 CN08 CN09 CN10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CP CP00
RING STRUCTURES CONTAINING TWO PHENYLS AND ONE CYCLOHEXANE ONLY; IMAGE 54)
CP01 CP02 CP03 CP04 CP05 CP06 CP07 CP08 CP09 CP10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CQ CQ00
RING STRUCTURES CONTAINING TWO PHENYLS AND ONE CYCLOHEXANE ONLY; PH-PH-CY, PH-CY-PH
CQ01 CQ02 CQ03 CQ04 CQ05 CQ06 CQ07 CQ08 CQ09 CQ10
. All substituents being unsubstituted R or OR . at least one of substituents being one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CR CR00
RING STRUCTURES CONTAINING ONE PHENYL AND TWO CYCLOHEXANE ONLY
CR01 CR02 CR03 CR04 CR05 CR06 CR07 CR08 CR09 CR10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CS CS00
RING STRUCTURES CONTAINING ONE PHENYL AND TWO CYCLOHEXANES ONLY; IMAGE 55)
CS01 CS02 CS03 CS04 CS05 CS06 CS07 CS08 CS09 CS10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CT CT00
RING STRUCTURES CONTAINING ONE PHENYL AND TWO CYCLOHEXANES ONLY; CY-CY-PH, CY-PH-CY
CT01 CT02 CT03 CT04 CT05 CT06 CT07 CT08 CT09 CT10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CU CU00
RING STRUCTURES CONTAINING TOTAL OF FOUR OF BENZENE RINGS AND CYCLOHEXANES
CU01 CU02 CU03 CU04 CU05 CU06 CU07 CU08 CU09 CU10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CV CV00
RING STRUCTURES CONTAINING CYCLOHEXANE ONLY
CV01 CV02 CV03 CV04 CV05 CV06 CV07 CV08 CV09 CV10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CW CW00
RING STRUCTURES CONTAINING TWO CYCLOHEXANES ONLY
CW01 CW02 CW03 CW04 CW05 CW06 CW07 CW08 CW09 CW10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
CX CX00
RING STRUCTURES CONTAINING THREE CYCLOHEXANES ONLY
CX01 CX02 CX03 CX04 CX05 CX06 CX07 CX08 CX09 CX10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DA DA00
RING STRUCTURES CONTAINING HETERO RING (1N)
DA01 DA02 DA03 DA04 DA05 DA06 DA07 DA08 DA09 DA10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DB DB00
RING STRUCTURES COMPOSED OF TWO RINGS INCLUDING HETERO RING (1N).
DB01 DB02 DB03 DB04 DB05 DB06 DB07 DB08 DB09 DB10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DC DC00
RING STRUCTURES COMPOSED OF THREE RINGS INCLUDING HETERO RING (1N)
DC01 DC02 DC03 DC04 DC05 DC06 DC07 DC08 DC09 DC10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DD DD00
RING STRUCTURES CONTAINING HETERO RING (2N)
DD01 DD02 DD03 DD04 DD05 DD06 DD07 DD08 DD09 DD10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DE DE00
RING STRUCTURES BEING COMPOSED OF TWO RINGS INCLUDING HETERO RING (2N)
DE01 DE02 DE03 DE04 DE05 DE06 DE07 DE08 DE09 DE10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DF DF00
RING STRUCTURES BEING COMPOSED OF THREE RINGS INCLUDING HETERO RING (2N)
DF01 DF02 DF03 DF04 DF05 DF06 DF07 DF08 DF09 DF10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DG DG00
RING STRUCTURES CONTAINING HETERO RING (3 OR 4N)
DG01 DG02 DG03 DG04 DG05 DG06 DG07 DG08 DG09 DG10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DH DH00
RING STRUCTURES CONTAINING HETERO RING (O)
DH01 DH02 DH03 DH04 DH05 DH06 DH07 DH08 DH09 DH10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DJ DJ00
RING STRUCTURES CONTAINING OTHER HETERO RINGS
DJ01 DJ02 DJ03 DJ04 DJ05 DJ06 DJ07 DJ08 DJ09 DJ10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DK DK00
RING STRUCTURES CONTAINING NAPHTHALENE RINGS OR TETRALIN RINGS.
DK01 DK02 DK03 DK04 DK05 DK06 DK07 DK08 DK09 DK10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DL DL00
RING STRUCTURES CONTAINING CONDENSED RINGS HAVING RING HETERO ATOMS
DL01 DL02 DL03 DL04 DL05 DL06 DL07 DL08 DL09 DL10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DM DM00
RING STRUCTURES CONTAINING OTHER CONDENSED RINGS
DM01 DM02 DM03 DM04 DM05 DM06 DM07 DM08 DM09 DM10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O inked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DN DN00
RING STRUCTURES CONTAINING OPTICALLY-ACTIVE RINGS
DN01 DN02 DN03 DN04 DN05 DN06 DN07 DN08 DN09 DN10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DP DP00
RING STRUCTURES CONTAINING OTHER RINGS
DP01 DP02 DP03 DP04 DP05 DP06 DP07 DP08 DP09 DP10
. All substituents being unsubstituted R or OR . at least one of substituents being others . . at least one of substituents being substituted R or OR . . at least one of substituents being CN NO2 or X . . . CN NO2 and X not being side chain groups . Optically-active substituents . . C linked to asymmetric carbon . . O linked to asymmetric carbon . . Atoms other than C O and H linked to asymmetric carbon . . Double chiral
DQ DQ00
NOT HAVING RING STRUCTURES
DQ01 DQ02
. showing liquid crystal properties . not showing liquid crystal properties
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