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Bent-core liquid crystals, a class of mesogenic compounds with non-linear molecular structures, are well known for their unconventional mesophases, characterized by complex molecular (and supramolecular) ordering and often featuring biaxial and polar properties. In the nematic phase, their unique behavior is manifested in the formation of nano-sized biaxial clusters of layered molecules (cybotactic groups). While this prompted their consideration in the quest for nematic biaxiality, experimental evidence indicates that the cybotactic order is only short-ranged and that the nematic phase is macroscopically uniaxial. By combining atomic force microscopy, neutron reflectivity and wide-angle grazing-incidence X-ray scattering, here, we demonstrate that multilayer films of a bent-core nematic, deposited on silicon by a combined Langmuir–Blodgett and Langmuir–Schaefer approach, exhibit macroscopic in-plane ordering, with the long molecular axis tilted with respect to the sample surface and the short molecular axis (i.e., the apex bisector) aligned along the film compression direction. We thus propose the use of Langmuir films as an effective way to study and control the complex anchoring properties of bent-core liquid crystals. [ABSTRACT FROM AUTHOR]

Students in the second-semester organic chemistry laboratory perform a Wittig reaction between butylidenetriphenylphosphorane (an ylide) and benzaldehyde and determine the relative percentages of the cis and trans isomers of the 1-phenyl-1-pentene product. Because of the highly reactive nature of this unstabilized ylide, students are introduced to working under anhydrous and inert atmosphere conditions. Students prepare the ylide by treatment of butyltriphenylphosphonium bromide with THF solutions of the lithium, sodium, or potassium salt of hexamethydisilazide (HMDS), either alone or in the presence of added LiBr, NaBr, or KBr. After reaction with the benzaldehyde, [superscript 1]H NMR spectroscopy and gas chromatography are used to determine the relative percentages of the cis and trans isomers of the product. By combining their results, students observe that in the absence of lithium the percentage of cis isomer is approximately 90%, whereas in the presence of lithium the percentage of cis isomer is much lower (29-59% depending on the conditions). A discussion led by the instructor develops the mechanistic rationale for understanding these unexpected results. (Contains 1 table, 2 figures and 1 scheme.)

Bent-core mesogens (BCMs) are a class of thermotropic liquid crystals featuring several unconventional properties. However, the interpretation and technological exploitation of their unique behavior have been hampered by the difficulty of controlling their anchoring at surfaces. To tackle this issue, we report the nanoscale structural characterization of BCM films prepared using the Langmuir–Blodgett technique. Even though BCMs are quite different from typical amphiphilic molecules, we demonstrate that stable molecular films form over water, which can then be transferred onto silicon substrates. The combination of Brewster angle microscopy, atomic force microscopy, and X-ray reflectivity measurements shows that the molecules, once transferred onto a solid substrate, form a bilayer structure with a bottom layer of flat molecules and an upper layer of upright molecules. These results suggest that Langmuir–Blodgett films of BCMs can provide a useful means to control the alignment of this class of liquid crystals. [ABSTRACT FROM AUTHOR]

In previous research, we have found that the incorporation of three lateral substituents on bent-core oxadiazole-based liquid crystals has allowed for the presence of a nematic phase that supercooled to room temperature. X-ray diffraction (XRD) studies of these derivatives have confirmed that the nematic phase consists of cybotactic clusters. Moreover, the wide-angle XRD pattern showed a splitting indicative of local biaxial ordering within this phase. In this paper, we report the phase behaviour of two series of compounds that contain up to four lateral methyl groups. In one series, the arrangement of the lateral groups is symmetrical, and in the other case, the groups are not symmetrically distributed. All of the non-symmetric derivatives supercool to room temperature in the nematic phase, while symmetric derivatives tend to crystallise well above room temperature. XRD analysis of all of these compounds indicates the presence of cybotactic order. However, a splitting of the wide-angle XRD pattern is observed only in derivatives with lateral groups on the outer benzene rings, regardless of their supercooling behaviour, indicating the crucial influence of these substituents on the molecular packing. [ABSTRACT FROM AUTHOR]

This paper describes the synthesis and phase behavior of new oxazole containing liquid crystals. These compounds are related to oxadiazole derivatives which show a cybotactic nematic phase. The compounds described here possess a lateral bromo or chloro substituent and, in some cases, lateral methyl groups as well. Derivatives without lateral methyl groups exhibit enantiotropic behavior, while derivatives with lateral methyl groups show only monotropic behavior. However, several of the latter compounds supercool to room temperature in the nematic phase. In addition, the nematic phase of these derivatives retain fluidity to much lower temperatures than was observed for the oxadiazole analogs. [ABSTRACT FROM AUTHOR]

We have previously demonstrated that the incorporation of lateral methyl groups on oxadiazole-based liquid crystals leads to relatively low-temperature cybotactic nematic phases which, in some cases, supercool to room temperature. We report here the synthesis and phase behaviour of related compounds that possess lateral halogen groups and in some cases, lateral methyl groups as well. Derivatives with three lateral substituents (one halogen and two methyl groups) in a specific pattern supercool in the nematic phase to room temperature. As was the case with the previously reported trimethylated derivatives, the low-temperature nematic phase is glassy in nature. Two of the new trisubstituted derivatives (with bromo and chloro groups) remain in the nematic phase upon subsequent heating until transitioning to the isotropic phase indicating that the low-temperature nematic phase may be more stable than that shown by the trimethylated analogue. Preliminary X-ray diffraction analysis confirms the presence of a tilted cybotactic nematic phase. In addition, the splitting observed in the wide-angle scattering feature is indicative of enhanced local biaxial packing. [ABSTRACT FROM PUBLISHER]

A series of new liquid crystalline compounds based on the 2,5-bis-(p-hydroxyphenyl)-1,3,4-oxadiazole (ODBP) core was synthesized in an effort to access the biaxial nematic phase at low temperatures. Derivatives with secondary terminal alkoxy groups and derivatives with either two or four lateral methyl groups were prepared. Secondary alkoxy terminal groups either suppressed mesophase formation altogether or increased the nematic onset temperature relative to primary groups. The dimethylated derivatives showed significant reductions in the nematic onset temperatures compared to the previously reported unmethylated compounds. The tetramethylated analogs generally possessed low clearing temperatures, but exhibited only monotropic mesomorphism. [ABSTRACT FROM AUTHOR]

A series of diphenylacetylene derivatives were synthesized to serve as ligands for metal alkyne complexes. The target compounds, alkyl 4′-(4-phenylethynylbenzoyloxy)-biphenyl-4-carboxylates, were prepared using a three-step synthetic procedure. Both the diphenylacetylene derivatives as well as their immediate precursors, alkyl 4′-(4-iodobenzoyloxy)-biphenyl-4-carboxylates, exhibit liquid crystalline behavior. The diphenylacetylene derivatives possess large liquid crystalline phase ranges and high clearing temperatures. Synthetic details and the phase behavior of these compounds are discussed. [ABSTRACT FROM AUTHOR]

The possibility of biaxial orientational order in nematic liquid crystals is a subject of intense current interest. We explore the tendencies toward local and global biaxial ordering in the recently synthesized trimethylated oxadiazole-based bent-core mesogens with a pronounced asymmetric (bow-type) shape of molecules. The combination of x-ray diffraction and optical studies suggests that the biaxial order is expressed differently at the short- and long-range scales. Locally, at the scale of a few molecules, x-ray-diffraction data demonstrate biaxial packing. However, above the mesoscopic scale, the global orientational order in all three compounds is uniaxial, as evidenced by uniform homeotropic alignment of the nematic phase which is optically tested over the entire temperature range and by the observations of topological defects induced by individual and aggregated colloidal spheres in the nematic bulk. [ABSTRACT FROM AUTHOR]

The possibility of biaxial orientational order in nematic liquid crystals is a subject of intense current interest. We explore the tendencies toward local and global biaxial ordering in the recently synthesized trimethylated oxadiazole-based bent-core mesogens with a pronounced asymmetric (bow-type) shape of molecules. The combination of x-ray diffraction and optical studies suggests that the biaxial order is expressed differently at the short- and long-range scales. Locally, at the scale of a few molecules, x-ray-diffraction data demonstrate biaxial packing. However, above the mesoscopic scale, the global orientational order in all three compounds is uniaxial, as evidenced by uniform homeotropic alignment of the nematic phase which is optically tested over the entire temperature range and by the observations of topological defects induced by individual and aggregated colloidal spheres in the nematic bulk.