Index Name

Zuniga, C.

Alternative Writings

Zuñiga, C.;   Zúñiga, C.

Co-authors

Aguilera, C.;   Alderete, J.;   Bartulin, J.;   Belmar, J.;   Decap, J.;   Fuentes, G.;   Gallardo, H.;   Haase, W.;   Hernandez, S.;   Hernández, S.;   Hidalgo, P.;   Jimenez, V.;   Marcos, M.;   Martinez, R.;   Muller, H.;   Munoz, C.;   Müller, H.;   Müller, H.J.;   Omenat, A.;   Parra, M.;   Perez, C.;   Ramirez, A.;   Retamal, J.;   Ros, B.;   Schumacher, E.;   Serrano, J.L.;   Sierra, T.;   Soto, E.;   Taylor, T.R.;   Vera, V.;   Vergara, J.;   Villouta, S.;   Villouta, Sh.;   Zarraga, M.;   Zunza, H.;   Zárraga, M.

Publication Titles

1982: Mesogenic heterocyclic structures
1986: Thermotropic properties of unsymmetrically substituted N,N'-diarylpiperazine derivatives
1987: Synthesis and mesogenic properties of N'-(4-acylphenyl)-N-alkylpiperazines
1987: Synthesis and mesomorphic properties of N-n-alkyl-N'-[4-(2-cyanoethenylphenyl)]piperazines
1988: Mesomorphic properties of N-alkyl-N'-[4-(2-carbethoxyethenylphenyl)]piperazines
1990: Synthesis and mesogenic properties of N-n-alkyl-N'-(4-n-pentyloxyphenyl)piperazines
1990: Synthesis and mesomorphic properties of 2,5-di-(4-N-alkyloxyphenyl)thiazolo[5,4-d]thiazoles
1991: Synthesis and mesomorphic properties of 2-N-hexyl-6-(4-N-alkoxybenzoyloxy)quinoline
1992: 3,5-Disubstituted 1,2,4-oxadiazoles: synthesis and properties
1992: Heterocyclic liquid crystals. 6-n-Pentyloxy-2-[4-n-alkyloxystyryl] quinolines
1993: Synthesis of amides derived from 1,3,4-thiadiazole as a mesogenic unit
1995: Schiff bases: synthesis and mesomorphic properties
1995: Synthesis and mesomorphic behavior of 2,5-disubstituted 1,3,4-oxadiazoles
1995: Synthesis and mesomorphic properties of 5-(p-n-alkoxy)phenyl-2-(p-n-octyloxy)benzylideneamino-1,3,4-thiadiazoles
1996: Synthesis and mesogenic properties of 6-n-decyloxy-2-(alkoxybenzylidenamino)benzothiazoles
1996: Synthesis and mesomorphic properties of 6-n-decyloxy-2-[4'-(N-alkoxyphenylimino)methyl]quinolines (IV)
1997: 1,3,4-Oxadiazole imines: synthesis and mesomorphic properties
1997: Synthesis and mesomorphic properties of azo compounds derived from phenyl- and thienyl-1,3,4-thiadiazole
1999: New liquid crystals containing the benzothiazole unit: amides and azo compounds
1999: Synthesis and mesomorphic properties of 2,6-disubstituted derivatives of quinoline: amides and esters
1999: Synthesis of new mesogenic compounds having the isoflavone core group
2000: New Schiff's bases containing 1,3,4-thiadiazole and 1,3,4-oxadiazole units: a study of the effect of the heterocyclic ring and the position of the lateral alkoxy group on liquid crystalline properties
2001: Azo compounds and Schiff 's bases derived from 5-(4-pyridyl)-2-amino-1,3,4-thiadiazole: synthesis, mesomorphic properties and structural study by semi-empirical calculations
2002: Symmetric esters derived from 1,3,4-oxadiazole: synthesis, mesomorphic properties and structural study by semi-empirical calculations
2002: Synthesis, mesomorphic properties and structural study by semi-empirical calculations of amides containing the 1,3,4-thiadiazole unit
2003: Esters derived from 7-decanoyloxychromone-3-carboxylic acid: synthesis and mesomorphic properties
2003: Hydrogen-bonded complexes between mesogenic heterocyclic Schiff's bases and mesogenic 4-n-nonyloxybenzoic acid: mesomorphic behaviour, FTIR study and PM3 semi-empirical calculations
2004: Synthesis and mesomorphic properties of esters derived from Schiff's bases containing 1,3,4-thiadiazole
2005: New chiral Schiff's bases with a 1,3,4-thiadiazole ring in the mesogenic core: synthesis, mesomorphic and ferroelectric properties
2008: Synthesis and mesomorphic properties of 3-(4-n-alkyloxyarylaminomethylene)chroman-2,4-diones

Sources

Bol. Soc. Chil. Quim., 27, 144
Bol. Soc. Chil. Quim., 37, 195
Bol. Soc. Chil. Quim., 37, 241
Bol. Soc. Chil. Quim., 38, 325
Bol. Soc. Chil. Quim., 40, 175
Bol. Soc. Chil. Quim., 41, 209
Bol. Soc. Chil. Quim., 42, 507
J. Chem. Soc., Perkin Trans. II, 1987, 1881
J. Prakt. Chem./Chem.-Ztg., 337, 239
J. Prakt. Chem./Chem.-Ztg., 337, 325
Liq. Cryst., 20, 253
Liq. Cryst., 26, 389
Liq. Cryst., 26, 75
Liq. Cryst., 26, 9
Liq. Cryst., 27, 995
Liq. Cryst., 28, 1659
Liq. Cryst., 29, 1375
Liq. Cryst., 29, 647
Liq. Cryst., 30, 1319
Liq. Cryst., 30, 297
Liq. Cryst., 31, 1531
Liq. Cryst., 32, 457
Liq. Cryst., 35, 157
Mol. Cryst. Liq. Cryst., 132, 235
Mol. Cryst. Liq. Cryst., 150B, 237
Mol. Cryst. Liq. Cryst., 159, 127
Mol. Cryst. Liq. Cryst., 180B, 297
Mol. Cryst. Liq. Cryst., 185, 131
Mol. Cryst. Liq. Cryst., 206, 131
Z. Naturforsch. B, 52b, 1533


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

Blättern: Seitenanfang