Answers are grounded in this paper and cite their sources.
A new series of chiral tolane with aliphatic end chains ranging from heptyloxy to dodecyloxy has been synthesized and characterized. The mesomorphic properties have been analyzed by optical microscopy on pure compounds and mixtures, D.S.C, electro-optical and pitch measurements. This series displays a very rich polymesomorphism including SA, SC*α, SC*, SC*FI, SC*A, SI*A, and SJ* phases with reference to the compound MHPOBC through miscibility test. One of the characteristic of this sene is the two SC*FI phases (SC*FI1 and SC*FI2) between SC* and SC*A phases. The electro-optical measurements were carried out with the classical SSFLC geometry. The threshold field is measured in each tilted mesophase; this one is peculiarly high in SJ*, SI*A and SC*A phase (respectively more than 6; 4 and 1V/μm). In the SC*FI phase one can note a first plateau between 0.3V/μm an 0.7V/μm, and the saturation is reached at 1V/μm. Helical pitch measurement shows a strong variation of the pitch at the SC*A-SC*FI and SC*FI-SC* transitions.
No takes yet. Share an insight, caveat, or question.
Cluzeau et al. (1995) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: