A convenient one-pot synthesis, and characterisation of the ω-bromo-1-(4-cyanobiphenyl-4’-yl) alkanes (CBnBr)

A convenient synthetic route based on a sodium-mediated aromatic cross-coupling reaction is described for the multi-gram preparation of the ω-bromo-1-(4-cyanobiphenyl-4’−yl) alkanes (CBnBr, n = 2–10). These materials are not only key intermediates in the synthesis of oligomers and polymers but also exhibit fascinating liquid crystal behaviour in their own right. Nematic behaviour is observed for n⩾5, and the nematic-isotropic transition temperature, TNI, increases in essentially a linear manner on n. The properties of the ω-bromo-1-(4-cyanobiphenyl-4’−yloxy) alkanes (CBOnBr, n = 2–9) are also reported, and nematic behaviour is seen for n⩾3. The values of TNI show a weak odd-even effect on n in which the odd members show the higher values. The sense of this alternation is opposite to that seen for the 4-alkyloxy-4’-cyanobiphenyls, and this is attributed to the steric bulk of the bromine atom. The absence of smectic behaviour for both the CBnBr and CBOnBr series is attributed largely to electrostatic interactions that would arise from the concentration of the bromine atoms at the layer interfaces in an interdigitated smectic phase. A comparison of a range of cyanobiphenyl-based materials containing a chain with a terminal polar or polarisable group suggests that their phase behaviour is governed largely by their average molecular shapes

Molecular curvature and the twist-bend liquid crystal phases: the effect of the spacer

The synthesis and characterisation of ten members of the 4[{[4({5[4((4-cyanophenyl)phenyl]oxy)pentoxy}yl)phenyl]methylidene}amino] phenyl 4-alkyloxybenzoates is presented. These dimers are referred to using the acronym CBO5OIBeOm in which m refers to the number of carbon atoms in the terminal chain and varies from 1 to 10. The CBO5OIBeOm series exhibits nematic (N), twist-bend nematic (NTB), and smectic A (SmA) phases depending on the length of the terminal chain. Although the NTB phase is observed, these dimers do not exhibit the twist-bend smectic C (SmCTB) phases. By comparison, the structurally similar CB6OIBeOm series does exhibit the SmCTB phases, and this strongly suggests that the formation of the SmCTB phase is more sensitive to molecular curvature than that of the NTB phase

A kinetic study of the formation of smectic phases in novel liquid crystal ionogens

[EN] A multi-rate non-isothermal kinetic analysis of the isotropic-melt to liquid crystalline phase transition of novel liquid crystalline ionogenic copolymers, LCIs, the 10-(4-methoxyazobenzene-4'-oxy)decyl methacrylate]-co-2-(acrylamido-2-methyl-1-propanesulfonic acid)s, 10-MeOAzB/AMPS, copolymers, has been performed by means of calorimetric experiments. An analytical methodology which includes the study of the phase transition rate parameter, the determination of the activation energies by using Kissinger and Flynn-Wall-Ozawa models, and the study of the phase transition kinetics by the use of the Avrami theory, has been applied. The formation of the mesophases from the isotropic state occurred close to thermodynamic equilibrium. The results evidence the presence of several individual processes in the formation of liquid crystalline phases from the melt and a strong dependence of phase transition rates and activation energies with acid contents. A decrease in the phase transition rate, related to a decrease in the overall change of the transition entropy, has been observed. The final inhibition of the liquid crystal (LC) behaviour is ascribed to an exponential increase in the activation energy of the phase transition, promoted by strong acid aggregation. An optimum composition of the 10-MeOAzB/AMPS copolymers to achieve the dual characteristics of LCIs (ionogenic and liquid crystalline behaviour) requires acid concentrations capable of promoting structure-forming effects on the LC phases and the evolution of phase separated morphologies.The authors would like to acknowledge the Spanish Ministry of Science and Innovation, through the Research Projects ENE2007-67584-C03, UPOVCE-3E-013, ENE2011-28735-C02-01, IT-2009-0074 and three FPI and FPU predoctoral grants, and the financial support of the Generalitat Valenciana, through the Grisolia and Forteza programs and the ACOMP/2011/189 program. The Vice-rectorate for Research of UPV is also thanked for additional support through the PAID 05-09-4331, PAID-05-11/2806, and PAID 06-11-2037 projects.Martinez-Felipe, A.; Badia, J.; Santonja Blasco, L.; Imrie, C.; Ribes Greus, MD. (2013). A kinetic study of the formation of smectic phases in novel liquid crystal ionogens. European Polymer Journal. 49(6):1553-1563. https://doi.org/10.116/j.eurpolymj.2013.01.021S1553156349

Ionically conducting and photoresponsive liquid crystalline terpolymers: Towards multifunctional polymer electrolytes

[EN] We have prepared a series of new ionically conducting polymer electrolytes consisting of side-chain liquid crystal terpolymers with mesogenic azobenzenes, sulfonic acid groups and methyl methacrylate. The poly[10-(4-methoxyazobenzene -4'-oxy)decyl methacrylate] -co-poly[2-acrylamido-2-methyl-1-propanesulfonic acid]-copoly [methyl methacrylate]s, 10-MeOAzB/AMPS/MMA terpolymers, were synthesised by a one-pot conventional radical polymerisation. All samples were characterised by NMR, GPC/SEC, FT-IR, POM, XRD, DSC, UV-visible spectrophotometry and EIS. The terpolymers have light responsive properties, and exhibit liquid crystallinity over a wide range of compositions. Above a certain threshold of AMPS content, the 10-MeOAzB/AMPS/MMA terpolymers exhibit ionic conductivities in the 10(-8)-10(-4)S.cm(-1) range, with signs of decoupling of ionic mobility from segmental motions of the polymer.ARG and AMF thank the financial support of the Generalitat Valenciana, through the Grisolia and Forteza programs, and the Spanish Ministry of Science and Innovation, through the Research Projects ENE2007-67584-C03 and UPOVCE-3E-013 and the awarding of two FPI and FPU pre-doctoral grants. AMF and NFKA would like to thank the Royal Academy of Engineering for the award of the Newton Research Collaboration Programme grant NRCP1516/4/61. AMF acknowledges the School of Engineering of the University of Aberdeen for financial support.Vanti, L.; Alauddin, SM.; Zaton, D.; Aripin, N.; Giaccinti-Baschetti, M.; Imrie, C.; Ribes-Greus, A.... (2018). Ionically conducting and photoresponsive liquid crystalline terpolymers: Towards multifunctional polymer electrolytes. European Polymer Journal. 109:124-132. https://doi.org/10.1016/j.eurpolymj.2018.08.033S12413210

A kinetic study of the formation of smectic phases in novel liquid crystal ionogens

A multi-rate non-isothermal kinetic analysis of the isotropic-melt to liquid crystalline phase transition of novel liquid crystalline ionogenic copolymers, LCIs, the 10-(4-methoxyazobenzene-4′-oxy)decyl methacrylate]-co-2-(acrylamido-2-methyl-1-propanesulfonic acid)s, 10-MeOAzB/AMPS, copolymers, has been performed by means of calorimetric experiments. An analytical methodology which includes the study of the phase transition rate parameter, the determination of the activation energies by using Kissinger and Flynn-Wall-Ozawa models, and the study of the phase transition kinetics by the use of the Avrami theory, has been applied. The formation of the mesophases from the isotropic state occurred close to thermodynamic equilibrium. The results evidence the presence of several individual processes in the formation of liquid crystalline phases from the melt and a strong dependence of phase transition rates and activation energies with acid contents. A decrease in the phase transition rate, related to a decrease in the overall change of the transition entropy, has been observed. The final inhibition of the liquid crystal (LC) behaviour is ascribed to an exponential increase in the activation energy of the phase transition, promoted by strong acid aggregation. An optimum composition of the 10-MeOAzB/AMPS copolymers to achieve the dual characteristics of LCIs (ionogenic and liquid crystalline behaviour) requires acid concentrations capable of promoting structure-forming effects on the LC phases and the evolution of phase separated morphologies

Molecular flexibility in the design of low molar mass liquid crystals

SIGLEAvailable from British Library Document Supply Centre- DSC:DX85536 / BLDSC - British Library Document Supply CentreGBUnited Kingdo

Liquid crystal dimers and the twist‐bend phases: non‐symmetric dimers consisting of mesogenic units of differing lengths.

The syntheses and characterisation of the 4‑[{[4‑({n‑[4‑(4 cyanophenyl)phenyl]‑n‑yl}oxy)phenyl]-methylidene}amino]phenyl-4-alkoxybenzoates (CBnOIBeOm) are reported with n= 8 and 10 and m= 1-10. The two series display fascinating liquid crystal polymorphism. All twenty reported homologues display enantiotropic nematic (N) phase at high temperature. When the length of the spacer (n) is greater than that of the terminal chain (m), the twist-bend nematic (NTB) phase is observed at temperatures below the N phase. As the length of the terminal chain is increased and extends beyond the length of the spacer up to three smectic phases are observed on cooling the N phase. One of these smectic phases has been assigned as the rare twist-bend smectic C subphase, the SmCTB‑α phase. In all the smectic phases, a monolayer packing arrangement is seen, and this is attributed to the anti-parallel associations of the like mesogenic units

A twist-bend nematic phase driven by hydrogen bonding

The liquid crystalline phase behavior of 4-[6-(4'-cyanobiphenyl-4-yl)hexyloxy]benzoic acid (CB6OBA) and 4-[5-(4'-cyanobiphenyl-4-yloxy)pentyloxy]benzoic acid (CBO5OBA) is described. Both acids show an enantiotropic nematic phase attributed to the formation of supramolecular complexes by hydrogen bonding between the benzoic acid units. In addition, CB6OBA provides the first example of hydrogen bonding driving the formation of the twist-bend nematic phase. The observation of the twist-bend nematic phase for CB6OBA, but not CBO5OBA, is attributed to the more bent molecular shape of the complexes formed by the former, reinforcing the view that shape is a key factor in stabilizing this new phase. Temperature-dependent FTIR spectroscopy reveals differences in hydrogen bonding between the two nematic phases shown by CB6OBA which suggest that the open hydrogen-bonded complexes may play an important role in stabilizing the helical arrangement found in the twist-bend nematic phase

New insights into the liquid crystal behaviour of hydrogen-bonded mixtures provided by temperature-dependent FTIR spectroscopy

The phase behaviour of equimolar mixtures of 6-(4'-cyanobiphenyl-4-yl)hexyloxybenzoic acid (CB6OBA) with either 1-(4-butylazobenzene-4'-oxy)-5-(4-oxypyridine)pentane (BuABO5OPyr) or 1-(4-butylazobenzene-4'-oxy)-6-(4-oxypyridine)hexane (BuABO6OPyr) is reported. CB6OBA shows a monotropic twist-bend nematic phase and an enantiotropic nematic phase whereas the two pyridyl-based components do not exhibit liquid crystallinity. Both equimolar mixtures (CB6OBA/BuABOnOPyr) show enantiotropic nematic phases. The nematic-isotropic transition temperature and associated entropy change are higher for the CB6OBA/BuABO6OPyr mixture than for the CB6OBA/BuABO5OPyr mixture. This may be accounted for in terms of the average shapes of the hydrogen-bonded 1:1 complexes formed between the two differing components in the mixtures. However, Fourier transform infrared spectroscopy reveals that this complex is not formed quantitatively, but instead a complex mixture exists over the complete temperature range studied, involving the 1:1 complex, both cyclic and open acid dimers, free acid and hence, free BuABOnOPyr molecules

Symmetric and non-symmetric chiral liquid crystal dimers

The synthesis and characterisation of three sets of non-symmetric liquid crystal dimers consisting of a cholesterylbased unit and either 4-methoxybiphenyl, 4-cyanobiphenyl or (S)-2-methylbutyl 40oxybiphenyl-4-carboxylate are described. The transitional properties of these non-symmetric dimers are compared to those of the corresponding parent symmetric dimers. The symmetric dimers exhibit only chiral nematic or nematic phase behaviour. By contrast, members of the non-symmetric dimer series containing either 4-cyanobiphenyl or (S)-2-methylbutyl 40- oxybiphenyl-4-carboxylate groups exhibit smectic behaviour. The former series show an interdigitated smectic A phase while for the latter the structure of the smectic A phase depends on the length of the flexible spacer. Specifically, for short spacer lengths a monolayer arrangement is seen while for long spacers an intercalated smectic A phase is formed. For an intermediate spacer length, the small-angle X-ray scattering pattern for the intercalated smectic A phase reveals short-range incommensurate structural fluctuations associated with the monolayer smectic A phase. The driving force for the formation of the intercalated phase may be an electrostatic interaction between the electron rich carbonyl linking group attached to the cholesteryl unit and the electron deficient aromatic unit while the monolayer arrangement may be stabilised by the van der Waals interactions between the cholesteryl unit and the alkyl chains. Blue phases are observed only for a small number of these non-symmetric dimers and these all contain an odd-membered spacer. This is in accord with the rather general observation that blue phases are observed for odd-membered non-symmetric dimers and not their even-membered counterparts