References of "Tschierske, Carsten"
     in
Bookmark and Share    
Full Text
Peer Reviewed
See detailEffects of chain branching and chirality on liquid crystalline phases of bent-core molecules: blue phases, de Vries transitions and switching of diastereomeric states
Ocak, Hale; Bilgin-Eran, Belkiz; Prehm, Marko et al

in Soft Matter (2011), 7(18), 8266-8280

Bent-core molecules based on a resorcinol bisbenzoate core with a series of distinct substituents in different positions at the central resorcinol core have been synthesized and characterized. The focus ... [more ▼]

Bent-core molecules based on a resorcinol bisbenzoate core with a series of distinct substituents in different positions at the central resorcinol core have been synthesized and characterized. The focus is on the effect of branched terminal groups in the racemic and chiral forms on the mesomorphic properties. These were investigated by differential scanning calorimetry, optical polarizing microscopy, X-ray diffraction, electro-optic and dielectric methods. Only bent-core mesogens derived from 4- cyanoresorcinol exhibit liquid crystalline phases and the mesophases of these compounds are strongly influenced by the branching and enantiomeric composition of the terminal chains. Depending on the structure of the rod-like wings and the enantiomeric composition, cybotactic nematic phases (NcybC), BPIII-like isotropic mesophases (BPIIIcybC*) and various polar and apolar smectic phases (SmA, SmC, SmC*, SmCsPA, SmCsPA*) are formed. For one compound, a de Vries type smectic phase is observed and it appears that with decreasing temperature, order develops in two steps. First, at the SmA to SmC transition, the tilt direction becomes long range ordered and in a second step a long range ordering in bend direction takes place. Hence, for the optically active compound a transition from chirality induced polar switching to bend induced (shape induced) antiferroelectricity takes place. In this SmCsPA* phase a homogeneous layer chirality is induced under an applied electric field which interacts with the fixed molecular chirality leading to the energetically favoured diastereomeric state and giving rise to a field direction dependent uniform tilt director orientation. Field reversal induces a flipping of the layer chirality, which first leads to the less favorable diastereomeric state, and then this slowly relaxes to the more stable one by a spontaneous reversal of the tilt direction. [less ▲]

Detailed reference viewed: 119 (1 UL)
Full Text
Peer Reviewed
See detailTailor-designed polyphilic promotors for stabilizing dispersions of carbon nanotubes in liquid crystals
Kühnast, Martin; Tschierske, Carsten; Lagerwall, Jan UL

in Chemical Communications (2010), (46), 6989-6991

We present a potent multifunctional molecular design concept for promoting the dispersion of carbon nanotubes (CNTs) in thermotropic liquid crystals (LCs), making CNT-in-LC dispersions of unprecedented ... [more ▼]

We present a potent multifunctional molecular design concept for promoting the dispersion of carbon nanotubes (CNTs) in thermotropic liquid crystals (LCs), making CNT-in-LC dispersions of unprecedented stability possible and broadening the scope of potential applications. [less ▲]

Detailed reference viewed: 102 (1 UL)
Full Text
Peer Reviewed
See detailTowards efficient dispersion of carbon nanotubes in thermotropic liquid crystals
Schymura, Stefan; Kühnast, Martin; Lutz, Vanessa et al

in Advanced Functional Materials (2010), 20(19), 3350-3357

Motivated by numerous recent reports indicating attractive properties of composite materials of carbon nanotubes (CNTs) and liquid crystals (LCs) and a lack of research aimed at optimizing such composites ... [more ▼]

Motivated by numerous recent reports indicating attractive properties of composite materials of carbon nanotubes (CNTs) and liquid crystals (LCs) and a lack of research aimed at optimizing such composites, the process of dispersing CNTs in thermotropic LCs is systematically studied. LC hosts can perform comparably or even better than the best known organic solvents for CNTs such as N-methyl pyrrolidone (NMP), provided that the dispersion process and choice of LC material are optimized. The chemical structure of the molecules in the LC is very important; variations in core as well as in terminal alkyl chain influence the result. Several observations moreover indicate that the anisotropic nematic phase, aligning the nanotubes in the matrix, per se stabilizes the dispersion compared to a host that is isotropic and thus yields random tube orientation. The chemical and physical phenomena governing the preparation of the dispersion and its stability are identified, taking into account enthalpic, entropic, as well as kinetic factors. This allows a guideline on how to best design and prepare CNT–LC composites to be sketched, following which tailored development of new LCs may take the advanced functional material that CNT–LC composites comprise to the stage of commercial application. [less ▲]

Detailed reference viewed: 95 (0 UL)