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

2019 ◽  
Vol 21 (24) ◽  
pp. 13078-13089 ◽  
Author(s):  
Zeinab Parsouzi ◽  
Greta Babakhanova ◽  
Mojtaba Rajabi ◽  
Rony Saha ◽  
Prabesh Gyawali ◽  
...  

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 (NTB) phase transition.

1980 ◽  
Vol 35 (11) ◽  
pp. 1384-1388 ◽  
Author(s):  
Gerd Heppke ◽  
Reinhard Hopf ◽  
Bernd Kohne ◽  
Klaus Praefcke

The synthesis and the phase transition temperatures of homologous liquid crystalline 4(4-alkyloxybenzoyloxy)-4'-cyanoazobenzenes with alkyl chain length n = 1-12 and n = 16 are reported. All compounds exhibit smectic A phases; the SA phase region being interrupted by a "re-entrant" nematic phase for alkyl chain lengath n ≥ 9.


2017 ◽  
Vol 41 (14) ◽  
pp. 6514-6522 ◽  
Author(s):  
Yuki Arakawa ◽  
Yukito Sasaki ◽  
Kazunobu Igawa ◽  
Hideto Tsuji

A novel class of hydrogen bonding liquid crystalline benzoic acids with alkylthio groups was established and their phase transition behavior was investigated in detail.


2019 ◽  
Author(s):  
Richard Mandle ◽  
John W. Goodby

We compare the order parameters, orientational distribution functions (ODF) and heliconical tilt angles of the TB phase exhibited by a liquid-crystalline dimer (CB7CB) to a tetramer (O47) and hexamer (O67) by SAXS/WAXS. Following the N-TB phase transition we find that all order parameters decrease, and while 〈P2 〉 remains positive 〈P4 〉 becomes negative. For all three materials the order parameter 〈P6 〉 is near zero in both phases. The ODF is sugarloaf-like in the nematic phase and volcano-like in the TB phase, allowing us to estimate the heliconical tilt angle of each material and its thermal evolution. The heliconical tilt angle appears to be largely independent of the material studied despite the differing number of mesogenic units.


2012 ◽  
Vol 1403 ◽  
Author(s):  
Christain Melchert ◽  
M. Behl ◽  
A. Lendlein

ABSTRACTThe control of phase transition behavior in liquid crystalline polymers could enable potential application in the field of actuators and sensors by enabling a higher actuator performance of liquid crystalline elastomers (LCE). In this context the phase transition behavior of siloxane based liquid crystalline copolymers synthesized from 1,1,3,3-tetramethyldisiloxane, 2-methyl-1,4-bis[4-(4-pentenyloxy)benzoyl]hydroquinone (M-MeHq), and 2-tert-butyl-1,4-bis[4-(4-pentenyloxy)benzoyl]hydroquinone (M-tBHq) was explored. The selected monomers provided different thermal stabilities of the nematic phase, while the non-flexible siloxane spacer suppressed a smectic phase. The mesogenic properties were studied by means of differential scanning calorimetry (DSC), polarizing optical microscopy (POM), and wide angle X-ray scattering (WAXS). With increasing fraction of M-MeHq the nematic phase of the copolymer was stabilized and a tailoring of relatively low TNI was achieved.


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