TY - JOUR
T1 - Highly dichroic benzo-2,1,3-thiadiazole dyes containing five linearly π-conjugated aromatic residues, with fluorescent emission ranging from green to red, in a liquid crystal guest-host system
AU - Zhang, Xuelong
AU - Yamaguchi, Rumiko
AU - Moriyama, Keiichi
AU - Kadowaki, Masami
AU - Kobayashi, Takako
AU - Ishi-i, Tsutomu
AU - Thiemann, Thies
AU - Mataka, Shuntaro
PY - 2006
Y1 - 2006
N2 - A number of fluorescent benzothiadiazole dyes have been synthesised and their optical properties, when dispersed in a liquid crystal host phase, examined. These dyes have five linearly π-conjugated aromatic ring systems (both with and without ethene and 1,3-butadiene spacers). The liquid crystalline host medium, used was the nematic phase of MLC-2039. The emission colours observed ranged from green to red, depending on the unsaturated chains attached at the 4- and 7- positions of the bezo-2,1,3-thiadiazole core. A highly dichroic and efficient fluoresence was observed. The dye 4,7-bis[5-bis(phenylethenyl) thiophen-2-yl]-2,1,3-benzothiadiazole is of particular importance. This is the first example of a dye emitting strong red fluorescence (633 nm). When dispersed in MLC-2039, dichroic ratio values up to 12.3 were obtained.
AB - A number of fluorescent benzothiadiazole dyes have been synthesised and their optical properties, when dispersed in a liquid crystal host phase, examined. These dyes have five linearly π-conjugated aromatic ring systems (both with and without ethene and 1,3-butadiene spacers). The liquid crystalline host medium, used was the nematic phase of MLC-2039. The emission colours observed ranged from green to red, depending on the unsaturated chains attached at the 4- and 7- positions of the bezo-2,1,3-thiadiazole core. A highly dichroic and efficient fluoresence was observed. The dye 4,7-bis[5-bis(phenylethenyl) thiophen-2-yl]-2,1,3-benzothiadiazole is of particular importance. This is the first example of a dye emitting strong red fluorescence (633 nm). When dispersed in MLC-2039, dichroic ratio values up to 12.3 were obtained.
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U2 - 10.1039/b512493j
DO - 10.1039/b512493j
M3 - Article
AN - SCOPUS:32844464074
SN - 0959-9428
VL - 16
SP - 736
EP - 740
JO - Journal of Materials Chemistry
JF - Journal of Materials Chemistry
IS - 8
ER -