2009
DOI: 10.1080/15421400903065739
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Synthesis and Phase Transition Behavior of Novel Liquid Crystal Tetramers

Abstract: We synthesized novel liquid crystal tetramers possessing cyanobiphenyl and phenylpyrimidine moieties, and investigated their phase transition behavior. The liquid crystal tetramers exhibited nematic (N) and smectic A (SmA) phases. X-ray diffraction measurements suggest that the SmA phase has an intercalated structure. We discuss the transition behavior of the newly designed tetramers in terms of their molecular shape.

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Cited by 4 publications
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“…These molecules exhibit a remarkable odd-even effect in their transition properties, which depends on the length and parity of the flexible spacer. The structure property relationships in LC trimers and tetramers have been studied by a number of researchers [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20], and we have also studied odd-even effects in LC trimers (1) [21] and tetramers (2) [22]. The molecules (1) and (2) contain two kinds of flexible spacers, namely O(CH 2 ) m O and COO(CH 2 ) n O groups.…”
Section: Introductionmentioning
confidence: 99%
“…These molecules exhibit a remarkable odd-even effect in their transition properties, which depends on the length and parity of the flexible spacer. The structure property relationships in LC trimers and tetramers have been studied by a number of researchers [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20], and we have also studied odd-even effects in LC trimers (1) [21] and tetramers (2) [22]. The molecules (1) and (2) contain two kinds of flexible spacers, namely O(CH 2 ) m O and COO(CH 2 ) n O groups.…”
Section: Introductionmentioning
confidence: 99%