ArticlePDF Available

Abstract and Figures

Physical properties of new thermotropic antiferroelectric liquid crystal have been studied. Experiments were done by use of complementary methods such as differential scanning calorimetry, polarizing optical microscopy and X-ray powder diffractometry. Acquired data from X-ray powder diffractometry was examined under application of quantum chemical approach. It has been found that compound studied exhibits stable enantiotropic antiferroelectric SmC∗A phase in the wide temperature range while ferroelectric phase SmC∗ is very narrow.
Content may be subject to copyright.
a,a b c c a
b
a
b
c
A
A
∗ ∗
A
A
6 13 6 13
µ
µ
◦ ◦
3
106
k
k
A
◦ ◦
A
5
1525
k
k
TONSET
HS k
TONSET
HS
8.116.37
6.315.15
17.642.68
7.816.04
6.114.87
18.144.03
8.316.89
6.515.56
18.344.68
8.517.37
6.715.87
18.044.16
8.417.14
6.615.72
17.843.67
8.517.15
6.615.75
17.944.00
8.518.38
6.716.15
17.442.60
Cr 80.3
SmC
A
134.0
SmC138.3
Is Is 143.3
SmC137.8
SmC
A
72.7
Cr
2θ
15
a b c α βγ
P m 2 (2||Y
∗ ∗
A
A
Article
Full-text available
The structure of the antiferroelectric smectic C*A phase is investigated for two liquid crystals with almost identical molecular structures, except for chiral centers. The X-ray diffraction results determined the crystal unit cell parameters, smectic layer spacing, average distance within layers, and correlation length of the short-range positional order. The coefficients of thermal expansion are determined for the crystal phases. The molecular modeling with the semi-empirical PM7 method and density functional theory calculations with the def2TZVPP basis set and B3LYP-D3(BJ) functional are applied to determine the tilt angle of molecules from the experimental smectic layer spacing. The most probable conformations are then selected based on a comparison with the tilt angle measured by the electro–optic method, known from the previous results. In the most suitable molecular models, the chiral chain makes an approximately 90° angle with the molecular core, and some fragments in the fluorinated part of the achiral terminal chain are in the gauche conformation.
Article
Full-text available
A general symmetry argument is presented, and experiments on newly synthesized p-decyloxybenzylidene p'-amino 2-methyl butyl cinnamate are described, demonstrating that chiral smectic C and H liquid crystals are ferroelectric. Some of the properties of this new class of ferro-electrics are discussed. Un argument généraI de symétrie est présenté et des expériences sur le p-décyloxybenzylidène p'-aminocinnamate de méthyl-2 butyle sont décrites démontrant que les smectiques C et H chiraux sont ferroélectriques. Quelques propriétés de cette nouvelle famille de ferroélectriques sont discutées.
Article
A method for accurate and efficient local density functional calculations (LDF) on molecules is described and presented with results. The method, Dmol for short, uses fast convergent three‐dimensional numerical integrations to calculate the matrix elements occurring in the Ritz variation method. The flexibility of the integration technique opens the way to use the most efficient variational basis sets. A practical choice of numerical basis sets is shown with a built‐in capability to reach the LDF dissociation limit exactly. Dmol includes also an efficient, exact approach for calculating the electrostatic potential. Results on small molecules illustrate present accuracy and error properties of the method. Computational effort for this method grows to leading order with the cube of the molecule size. Except for the solution of an algebraic eigenvalue problem the method can be refined to quadratic growth for large molecules.
Article
Recent extensions of the DMol3 local orbital density functional method for band structure calculations of insulating and metallic solids are described. Furthermore the method for calculating semilocal pseudopotential matrix elements and basis functions are detailed together with other unpublished parts of the methodology pertaining to gradient functionals and local orbital basis sets. The method is applied to calculations of the enthalpy of formation of a set of molecules and solids. We find that the present numerical localized basis sets yield improved results as compared to previous results for the same functionals. Enthalpies for the formation of H, N, O, F, Cl, and C, Si, S atoms from the thermodynamic reference states are calculated at the same level of theory. It is found that the performance in predicting molecular enthalpies of formation is markedly improved for the Perdew–Burke–Ernzerhof [Phys. Rev. Lett. 77, 3865 (1996)] functional. © 2000 American Institute of Physics.
Article
New chiral liquid crystalline materials containing a keto group and two lactate units attached to the mesogenic core have been synthesized and studied. All the new compounds show the paraelectric SmA, ferroelectric SmC* and antiferroelectric SmC*A phases each over rather broad temperature ranges. The properties of the phases were characterized by DSC, electro-optical and dielectric studies. The spontaneous polarization, tilt angle, helical pitch, and switching times were determined for the polar phases.
Article
The experimental and theoretical vibrational spectroscopic study of one of a novel antiferroelectric liquid crystals (AFLC), known under the MHPSBO10 acronym, have been undertaken. The interpretation of both FT-IR and FT-Raman spectra was focused mainly on the solid-state data. To analyze the experimental results along with the molecular properties, density functional theory (DFT) computations were performed using several modern theoretical approaches. The presented calculations were performed within the isolated molecule model, probing the performance of modern exchange-correlations functionals, as well as going beyond, i.e., within hybrid (ONIOM) and periodic boundary conditions (PBC) methodologies. A detailed band assignment was supported by the normal-mode analysis with SQM ab initio force field scaling. The results are supplemented by the noncovalent interactions analysis (NCI). The relatively noticeable spectral differences observed upon Crystal to AFLC phase transition have also been reported. For the most prominent vibrational modes, the geometries of the transition dipole moments along with the main components of vibrational polarizability were analyzed in terms of the molecular frame. One of the goals of the paper was to optimize the procedure of solid-state calculations to obtain the results comparable with the all electron calculations, performed routinely for isolated molecules, and to test their performance. The presented study delivers a complex insight into the vibrational spectrum with a noticeable improvement of the theoretical results obtained for significantly attracting mesogens using modern molecular modeling approaches. The presented modeling conditions are very promising for further description of similar large molecular crystals.
Article
We construct a generalized gradient approximation (GGA) for the density {ital n}{sub xc}({ital r},{ital r}+{ital u}) at position {ital r}+{ital u} of the exchange-correlation hole surrounding an electron at {ital r}, or more precisely for its system and spherical average {l_angle}{ital n}{sub xc}({ital u}){r_angle}=(4{pi}){sup {minus}1}{integral}{ital d}{Omega}{sub {ital u}}{ital N}{sup {minus}1}{integral}{ital d}{sup 3}{ital r} {ital n}({ital r}){ital n}{sub xc}({ital r},{ital r}+{ital u}). Starting from the second-order density gradient expansion, which involves the local spin densities {ital n}{sub {up_arrow}}({ital r}),{ital n}{sub {down_arrow}}({ital r}) and their gradients {nabla}{ital n}{sub {up_arrow}}({ital r}),{nabla}{ital n}{sub {down_arrow}}({ital r}), we cut off the spurious large-{ital u} contributions to restore those exact conditions on the hole that the local spin density (LSD) approximation respects. Our GGA hole recovers the Perdew-Wang 1991 and Perdew-Burke-Ernzerhof GGA{close_quote}s for the exchange-correlation energy, which therefore respect the same powerful hole constraints as LSD. When applied to real systems, our hole model provides a more detailed test of these energy functionals, and also predicts the observable electron-electron structure factor. {copyright} {ital 1996 The American Physical Society.}
Article
Generalized gradient approximations (GGA{close_quote}s) for the exchange-correlation energy improve upon the local spin density (LSD) description of atoms, molecules, and solids. We present a simple derivation of a simple GGA, in which all parameters (other than those in LSD) are fundamental constants. Only general features of the detailed construction underlying the Perdew-Wang 1991 (PW91) GGA are invoked. Improvements over PW91 include an accurate description of the linear response of the uniform electron gas, correct behavior under uniform scaling, and a smoother potential. {copyright} {ital 1996 The American Physical Society.}
  • M A Neumann
M.A. Neumann, J. Appl. Crystallogr. 36, 356 (2003).