Molecular dynamics of a main-chain liquid crystalline polyester below the crystalline to nematic phase transition

1997 ◽  
Vol 93 (8) ◽  
pp. 1605-1612 ◽  
Author(s):  
Valeria Arrighi ◽  
Julia S. Higgins
2016 ◽  
Vol 38 ◽  
pp. E331-E341 ◽  
Author(s):  
Stefanos Koutsoumpis ◽  
Sotiria Kripotou ◽  
Natalia Nikonorova ◽  
Polycarpos Pissis

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.


2002 ◽  
Vol 35 (3) ◽  
pp. 736-745 ◽  
Author(s):  
Jrjeng Ruan ◽  
Jason J. Ge ◽  
Anqiu Zhang ◽  
Jin Shi ◽  
Shy-Yeu Wang ◽  
...  

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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