Pretransitional behavior of viscoelastic parameters at the nematic to twist-bend nematic phase transition in flexible n-mers

被引:24
|
作者
Parsouzi, Zeinab [1 ]
Babakhanova, Greta [2 ,3 ]
Rajabi, Mojtaba [1 ]
Saha, Rony [1 ]
Gyawali, Prabesh [1 ]
Turiv, Taras [2 ,3 ]
Wang, Hao [2 ,3 ]
Baldwin, Alan R. [1 ]
Welch, Chris [4 ]
Mehl, Georg H. [4 ]
Gleeson, J. T. [1 ]
Jakli, Antal [1 ,2 ,3 ]
Lavrentovich, Oleg D. [1 ,2 ,3 ]
Sprunt, Samuel [1 ]
机构
[1] Kent State Univ, Dept Phys, Kent, OH 44242 USA
[2] Kent State Univ, Adv Mat & Liquid Crystal Inst, Kent, OH 44242 USA
[3] Kent State Univ, Chem Phys Interdisciplinary Program, Kent, OH 44242 USA
[4] Univ Hull, Dept Chem, Kingston Upon Hull HU6 7RX, N Humberside, England
基金
美国国家科学基金会; 英国工程与自然科学研究理事会;
关键词
ELASTIC-CONSTANTS; MESOPHASES; DIMERS;
D O I
10.1039/c9cp00984a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report dynamic light scattering measurements of the orientational (Frank) elastic constants and associated viscosities among a homologous series of a liquid crystalline dimer, trimer, and tetramer exhibiting a uniaxial nematic (N) to twist-bend nematic (N-TB) phase transition. The elastic constants for director splay (K-11), twist (K-22) and bend (K-33) exhibit the relations K-11 > K-22 > K-33 and K-11/K-22 > 2 over the bulk of the N phase. Their behavior near the N-N-TB transition shows dependency on the parity of the number (n) of the rigid mesomorphic units in the flexible n-mers. Namely, the bend constant K-33 in the dimer and tetramer turns upward and starts increasing close to the transition, following a monotonic decrease through most of the N phases. In contrast, K-33 for the trimer flattens off just above the transition and shows no pretransitional enhancement. The twist constant K-22 increases pretransitionally in both even and odd n-mers, but more weakly so in the trimer, while K-11 increases steadily on cooling without evidence of pretransitional behavior in any n-mer. The viscosities associated with pure splay, twist-dominated twist-bend, and pure bend fluctuations in the N phase are comparable in magnitude to those of rod-like monomers. All three viscosities increase with decreasing temperature, but the bend viscosity in particular grows sharply near the N-N-TB transition. The N-N-TB pretransitional behavior is shown to be in qualitative agreement with the predictions of a coarse-grained theory, which models the N-TB phase as a "pseudo-layered" structure with the symmetry (but not the mass density wave) of a smectic-A* phase.
引用
收藏
页码:13078 / 13089
页数:12
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