Informationen zur Darstellung dieser Seite in älteren Browsern
LCI Publisher Universitaet Hamburg

Index Name

Wingen, Rainer

Alternative Writings

Wingen, R.

Co-authors

Amakawa, Haruki;   Beresnev, L.A.;   Blatter, Karsten;   Bremer, Matthias;   Dübal, H.-R.;   Dübal, Hans-Rolf;   Escher, C.;   Escher, Claus;   Escher, Klaus;   Fujiwara, Hidenori;   Fuss, Robert W.;   Gay, Jürgen;   Günther, D.;   Günther, Dieter;   Haase, W.;   Harada, Takamara;   Harada, Takamasa;   Harnischfeger, Peter;   Heckmeier, Michael;   Hemmerling, W.;   Hemmerling, Wolfgang;   Heppke, Gerd;   Hornung, B.;   Hornung, Barbara;   Illian, G.;   Illian, Gerd;   Illian, Gerhard;   Inoguchi, Yoshio;   Ji, Li;   Junghans, Claas;   Kalbeitzel, Anke;   Kaltbeitzel, A.;   Kaltbeitzel, Anke;   Klasen, Melanie;   Klasen-Memmer, Melanie;   Li, J.;   Li, Ji;   Lötzsch, Detlef;   Magerstaedt, Micheal;   Mancro, Javier;   Manero, J.;   Manero, Javier;   Michalski, Britta;   Morr, Michael;   Murakami, Mikio;   Müller, I.;   Müller, Ingrid;   Nagao, Kazuya;   Nonaka, T.;   Nonaka, Toshiaki;   Ogawa, A.;   Ogawa, Ayako;   Ohlendorf, D.;   Ohlendorf, Dieter;   Pauluth, Detlef;   Pfeiffer, M.;   Pfirmann, Ralf;   Rieger, H.;   Rösch, N.;   Rösch, Norbert;   Scherowsky, Günter;   Schlosser, H.;   Schlosser, Hubert;   Schmidt, W.;   Schmidt, Wolfgang;   Sefkow, Michael;   Sharma, N.K.;   Takeichi, Ayako;   Takeuchi, Ayako;   Wegener, P.;   Weller, Clarissa;   de Meijere, Armin

Publication Titles

1987: Binary liquid crystal systems with two eutectics
1988: Chiral aryl-2,3-epoxyalkyl ether and their corresponding thio compounds, and their use as dopants in liquid-crystal phases
1988: Chiral aryloxypropionic acid esters and their use as dopants in liquid-crystal phases
1988: New liquid-crystal 5-phenylpyrimidine derivatives with smectic C or chiral smectic C phases and their preparation
1988: New phenyl-pyrimidine derivatives with S{\sub C}-phases
1988: New practical broad range FLC-mixtures for display application
1988: Optically active 1-acylproline esters and their use as dopants in liquid-crystal compositions
1988: Three classes of new chiral dopants: synthesis and physical qualification as dopants for practical ferroelectric liquid crystal mixtures
1988: Use of optically active 1,3-dioxolan-4 carboxylic acid esters as dopants in liquid-crystal mixtures new optically active esters, and liquid-crystal mixtures and electrooptical devices containing them
1989: Liquid-crystal 1-substituted piperidine-4-carboxylic acid esters, their preparation, and their use in liquid-crystal mixtures and electrooptical devices
1989: Liquid-crystal cyclopropylalkyl or -alkenyl heterocycles, their preparation, and their use in liquid-crystal mixtures and electrooptical devices
1989: Liquid-crystal phenylpyrimidine cyclohexanecarboxylic acid esters, their preparation, and liquid-crystal mixtures and electrooptical devices containing them
1989: Liquid-crystal phenylpyrimidine derivatives, their preparation, and their use in liquid-crystal mixtures and electrooptical devices
1990: Optically active 1,3-dioxolane derivatives containing mesogenic group in the 4-position, their preparation, and liquid-crystal mixtures and display devices containing them
1990: Optically active esters of 5-ethyl- and 5-vinyl-1,3-dioxolan-4-carboxylic acid, their preparation, their use as dopants in liquid-crystal mixtures, and liquid-crystal mixtures and display devices containing them
1990: Optically active mesogenic-group-containing dioxolane derivatives for liquid-crystal display devices
1990: Optically active oxiran-2-carboxylic acid esters and optically active 1,3-dioxolan-4-carboxylic acid esters, their use as dopants in liquid-crystal mixtures, and liquid-crystal mixtures containing them
1990: Optically active tetrahydrofuran-2-carboxylic acid esters, and their use in liquid crystal compositions as dopants
1990: Preparation of cyclopropylalkyl-substituted arenes as liquid crystals
1990: Preparation of organosilylalkyl or organosilylalkenyl compounds and liquid crystal mixtures containing them therein
1991: A new class of compounds for ferroelectric liquid crystal mixtures
1992: Chiral azetidinone derivatives and their use as dopants in liquid crystalline mixtures
1992: Chiral dopant for ferroelectric liquid crystals with very high value of inducing spontaneous polarization
1992: Chiral oxazolidinone derivatives, their preparation, and ferroelectric liquid-crystal mixtures and switching and display devices containing them
1992: Chiral oxazolidinone derivatives, their preparation, their use as dopants in liquid-crystal mixtures, and electrooptical switching and display devices using the mixtures
1992: Cyclohexylphenylpyrimidines, their preparation, and ferroelectric liquid - crystal mixtures and display devices containing them
1992: Cyclohexylphenylpyrimidines, their use in liquid crystal media, the media, and ferroelectric switches and displays using the media
1992: Ferroelectric liquid crystals in high information content displays
1992: Ferroelectric liquid-crystal mixtures containing aromatic mercapto compounds, and electrooptical switching and display devices using them
1992: Fluoropyridine derivatives and ferroelectric liquid - crystal mixtures and switching and display devices using them
1992: Preparation and use of 4-fluoro-pyrimidine derivatives as components for ferroelectric liquid crystal mixtures, the mixtures, and liquid crystal switches and displays using them
1992: Preparation of ferroelectric liquid-crystalline siloxanes for use in electrooptical components
1992: Pyridylpyrimidines, their preparation, and their use in liquid - crystal mixtures and display devices
1992: Surface stabilized ferroelectric liquid crystals (SSFLC) - a promising technology for high resolution displays
1992: trans-2,2'-(1,4-cyclohexanediyl)bis(pyrimidine) derivatives, a method for their preparation and their use in nematic or ferroelectric liquid crystals
1993: 3-cyclohexylpropionic acid derivatives and their use in ferroelectric liquid crystal mixtures
1993: Chiral oxiranylmethylethers and their use as dopants in liquid crystal mixtures
1993: Chiral stabilized complex ligands and macrocycles and their uses in liquid crystal displays
1993: Compounds with only a single side chain for use in liquid crystal mixtures
1993: Preparation of 3-alkyl-2-fluoro-6-phenylpyrazines and analogs as liquid crystal components
1994: 4-hydroxy-2,3,5-trifluorobenzoic acid and a process for its preparation
1994: Novel compounds for use in liquid-crystal compositions
1994: Preparation of (benzyloxy)halobiaryls as liquid crystal components
1994: Preparation of arylboronic acid as precursors for liquid crystal mixture
1994: Preparation of poly(heteroaryl) compounds as liquid crystal components
1994: Preparation of poly[(hetero)aryl] compounds as liquid crystal components
1994: Trifluorophenylene derivatives and their use in liquid-crystal mixtures and electrooptical devices
1995: Cyclopropylalkyl or -alkenyl or heterocyclic compounds, process for their preparation and their use in liquid-crystalline mixtures
1995: Preparation of [1,3,4]-thiadiazole liquid crystal precursors
1995: Preparation of liquid crystal phenanthrene derivatives
1995: Preparation of phenanthridine derivatives as liquid crystal components
1996: Preparation of 1,8-difluoroisoquinoline-derivative liquid crystal compounds
1996: Preparation of arylisoquinolines as liquid crystal components
1996: Preparation of aryloxotetrahydroisoquinolines as liquid crystal components
1996: Preparation of aryltetrahydroisoquinolines as liquid crystal components
1996: Preparation of substituted pyridazinones as liquid crystal components
1996: Tetracyclic compound and its use in liquid crystal mixture for liquid crystal display
1996: Tricyclic compound and its use in liquid crystal mixture for liquid crystal display
1997: Difluorophenylpyrimidylpyridine derivatives and liquid -crystal mixtures and ferroelec. switching and/or display devices using them
1997: Ferroelectric liquid crystal mixture for display device
1997: Preparation of fluorophenanthrenes as liquid crystal components
1997: Preparation of liquid crystal compounds as liquid crystal display devices and optical switches
1997: Preparation of tricyclic compounds such as phenanthrene derivatives and ferroelectric liquid crystal composition containing them
1999: Chip card with bistable ferroelectric liquid crystal display
1999: Fluorinated phenanthrene derivative and its use in liquid crystalline mixture
1999: Material characteristics of an active matrix LCD based upon chiral smectics
1999: Monostable ferroelectric active matrix display
1999: Monostable ferroelectric active matrix display and its preparation and use
1999: Monostable ferroelectric active-matrix display
1999: Polyfluorinated cyclohexane derivatives and liquid-crystal mixtures and switching and/or display devices using them
2000: FLC materials for active and passive matrix displays
2000: Ferroelectric active matrix liquid crystal display with expanded working temperature range
2000: Fluorinated azole and liquid crystal mixture containing the same
2001: Active matrix liquid crystal display with improved high contrast
2001: Cyclohexane derivative and its use in liquid crystalline mixture
2001: Cyclopentane derivative and its use in ferroelectric liquid crystalline mixture
2001: Cyclopentene derivative and its use in liquid crystalline mixture
2001: Fluorinated thiophene derivative and its use in ferroelectric liquid crystalline mixture
2001: Furan derivative and its use in ferroelectric liquid crystalline mixture
2001: Isoxazole derivative and its use in ferroelectric liquid crystalline mixture
2001: Isoxazole derivatives and their use in liquid crystalline mixtures
2001: Preparation of 2,7-disubstituted phenanthrenes and their use in liquid crystal mixtures
2001: Preparation of hydrogenated phenanthrenes and their use in liquid crystal mixtures
2001: Thiazole derivative and its use in ferroelectric liquid crystalline mixture
2002: 5-Arylindane derivatives and ferroelectric liquid crystal mixture containing same
2002: Chiral smectic and monostable ferroelectric liquid crystal mixtures for active matrix panel display
2002: Fluorinated (dihydro)phenanthrene derivatives and their use in liquid crystalline media
2002: Fluorinated fluorenes and their use in liquid crystal mixtures for liquid crystal displays
2002: Liquid crystal mixture suitable for active matrix liquid crystal display using ECB (electrically controlled birefringence) effects
2002: Polyfluorinated fluorenes and their use in liquid crystal mixtures for inverse mode liquid crystal display
2003: Active matrix liquid crystal device and smectic liquid crystal mixture
2003: Fluoridated anthracene compound and its use in liquid crystal mixture for display
2003: Fluoridated cyclopenta[a]naphthalene compound and its use in liquid crystal mixture for display
2003: Fluoridated cyclopenta[b]naphthalene compound and its use in liquid crystal mixture for display
2003: Fluorinated naphthalene derivatives, liquid crystal compositions and liquid crystal displays containing them
2003: Fluorinated polycycles and their use in liquid - crystal mixtures
2004: Fluoridated oxaanthracene and its use in liquid crystal mixture suitable for ECB-, IPS-, or VA- liquid crystal display
2005: Chiral smectic liquid crystal mixture
2005: Fluorinated condensed aromatic compound and its use in liquid crystal mixture for liquid crystal display
2005: Fluorinated xanthene and its use in liquid crystal mixture for liquid crystal display
2005: Preparation of fluoridated heterocycles and their use in liquid crystal mixtures
2005: Preparation of fluoridated polycyclene and their use in liquid crystal mixtures
2005: Procedure for the production liquid crystalline ethers by silane reduction of the corresponding carboxylate ester
2005: Process for the preparation of liquid crystalline ethers by the reduction of the corresponding ester compounds

Sources

AT 346031 T (2006/12/15)
Adv. Mater., 4, 189
DE 10.001.644 (2000/07/20)
DE 10101020 A1 (2002/07/18)
DE 10101021 A1 (2002/07/18)
DE 10344661 B3 (2005/06/09)
DE 19.500.768 (1995/09/28)
DE 19.502.178 (1995/08/03)
DE 19.517.025 (1996/11/14)
DE 19.517.038 (1996/11/14)
DE 19.517.051 (1996/11/14)
DE 19.517.056 (1996/11/14)
DE 19.517.060 (1996/11/14)
DE 19.524.230 (1997/01/09)
DE 19.732.160 (1999/01/28)
DE 19.748.818 (1999/05/20)
DE 19.748.819 (1999/05/06)
DE 19.825.484 (1999/12/09)
DE 19.825.487 (1999/12/09)
DE 19.825.488 (1999/12/09)
DE 19.857.352 (2000/06/15)
DE 19941655 A1 (2001/03/08)
DE 3.633.968 (1988/04/07)
DE 3.638.119 (1988/05/11)
DE 3.644.522 (1988/07/14)
DE 3.709.618 (1988/10/06)
DE 3.713.273 (1988/11/03)
DE 3.731.638 (1989/04/27)
DE 3.731.639 (1989/03/30)
DE 3.744.024 (1989/07/06)
DE 3.827.599 (1990/02/15)
DE 3.827.600 (1990/02/15)
DE 3.832.502 (1990/03/29)
DE 3.832.503 (1990/03/29)
DE 3.907.601 (1990/09/13)
DE 3.915.804 (1990/11/15)
DE 4.023.028 (1992/01/23)
DE 4.023.216 (1992/01/23)
DE 4.025.236 (1992/02/13)
DE 4.100.176 (1992/07/09)
DE 4.116.751 (1992/11/26)
DE 4.133.719 (1993/04/15)
DE 4.143.139 (1993/07/01)
DE 4.236.103 (1994/04/28)
DE 4.236.104 (1994/04/28)
DE 4.236.105 (1994/04/28)
DE 4.236.106 (1994/04/28)
DE 4.402.986 (1995/08/03)
DE 4.432.970 (1996/03/21)
DE 4.434.974 (1996/04/04)
DE 4.434.975 (1996/04/04)
DE 4.446.880 (1996/07/04)
EP 318.423 (1989/05/31)
EP 351.746 (1990/01/24)
EP 471.201 (1992/02/19)
EP 475.444 (1992/03/18)
EP 477.901 (1992/04/01)
EP 520.292 (1992/12/30)
EP 532.916 (1993/03/24)
EP 541.081 (1993/05/12)
EP 552.658 (1993/07/28)
EP 602.549 (1994/06/22)
EP 602.596 (1994/06/22)
Ferroelectrics, 114, 241
Ferroelectrics, 246, 143
Ferroelectrics, 84, 89
Ferroelectrics, 85, 393
JP 09.031.028 (1997/02/04)
JP 09.031.459 (1997/02/04)
JP 2001081466 A (2001/03/27)
JP 2001226301 A (2001/08/21)
JP 2003176244 A (2003/06/24)
JP 2003226876 A (2003/08/15)
JP 2004292451 A (2004/10/21)
JP 2005097259 A (2005/04/14)
JP 2005314417 A (2005/11/10)
Jpn. J. Appl. Phys., Part 2, 27, L2241
Liq. Cryst., 26, 1599
Mol. Cryst. Liq. Cryst., 151, 225
Mol. Materials, 2, 73
Proc. SPIE-Int. Soc. Opt. Eng., 1665, 90
US 2006011886 A1 (2006/01/19)
US 5.407.599 (1995/04/18)
US 6.485.797 (2002/11/26)
US 6515163 B2 (2003/02/04)
US 6616989 B1 (2003/09/09)
US 6670514 B2 (2003/12/30)
US 6737125 B2 (2004/05/18)
US 6759103 B2 (2004/07/06)
US 6793984 B2 (2004/09/21)
US 6929834 B2 (2005/08/16)
US 6955838 B2 (2005/10/18)
US 7014890 B2 (2006/03/21)
US 7052742 B1 (2006/05/30)
US 7297378 B2 (2007/11/20)
WO 2005103200 A1 (2005/11/03)
WO 9.211.241 (1992/07/09)
WO 9.212.974 (1992/08/06)
WO 9.426.720 (1994/11/24)
WO 9.704.039 (1997/02/06)
WO 9.724.351 (1997/07/10)
WO 9.960.441 (1999/11/25)
WO 9.964.538 (1999/12/16)


Seiteninfo: Impressum | Last Change 1. Mai 2010 by Volkmar Vill und Ron Zenczykowski

Blättern: Seitenanfang