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1.
In this article, optical properties of four fluoro-substituted 4-propyl-4′-[(4-ethylphenyl)ethynyl] biphenyls and liquid crystal mixture A are presented in the terahertz (THz) range. Birefringence, refractive indices and absorption coefficients for ordinary and extraordinary ray of liquid crystals are described in the range of 0.3 to 3.0 THz. It shows that the measured parameters are dependent on the number and placement of fluorine atoms in the molecules. Measurements have been performed using time-pulsed spectroscopy.  相似文献   

2.
The refractive index and absorption coefficient of blue phase liquid crystals are investigated by terahertz time-domain spectroscopy system. Four phases, including isotropic phase, BPII, BPI, and cholesteric phase are investigated. The refractive index of liquid crystal sample is dependent on the temperature, which is related to the different phases. In our experiment, in the frequency range of 0.2–1.2 THz, the refractive index of BPII and BPI is about 1.620 and 1.625, respectively. For BPII and BPI, the measured absorption coefficients increase with the increase of frequency, with absorption peak appearing at 1.11 and 1.05 THz, respectively. These properties of BPLC provide useful information for BPLC-based terahertz components such as phase shifter, wave-plates and so on.  相似文献   

3.
ABSTRACT

In this work, the terahertz (THz) absorption of homologous series of isothiocyanobiphenyls (nBT) and 4-(trans-4?-n-alkylcyclohexyl)isothiocyanato-benzene (nCHBT) are simulated by using the density functional theory (DFT) method. Numerical results show that absorption of the tested nematic liquid crystals (NLCs) varies up to 0.04 in the broad range of 0.3–20.0 THz and takes maximum value in the range of 9–14 THz.

In addition, the values of molecular polarisabilities (αo, αe) increase with the increase in the number of carbon atoms in the alkyl chain, while refractive indices (no, ne) decreases. The calculated birefringence (Δn) values for nCHBT are approximately twice as large as the birefringence value for nBT. It is crucial to examine these series of nematic liquid crystals at THz frequencies due to the role of soft matter in various switchable THz components.  相似文献   

4.
The measurement of absorption spectra using angle-dependent terahertz (THz) time-domain spectroscopy for amino acid single crystals of l-cysteine and l-histidine is reported for the first time. Linearly polarized THz radiation enables us to observe angle-dependent far-infrared absorption spectra of amino acid single crystals and determine the direction of the oscillating dipole of the molecules in the 20-100 cm(-1) range. By comparing the THz spectra of a single crystal and powder, we found that there was a clear hydrogen-bond peak in the crystal spectrum as a result of the larger hydrogen-bond network. The low-temperature THz spectra of amino acid microcrystals showed more intermolecular vibrational modes than those measured at room temperature. An ab initio frequency calculation of a single amino acid molecule was used to predict the intramolecular vibrational modes. The validity of the calculation models was confirmed by comparing the results with experimentally obtained data in the Raman spectral region.  相似文献   

5.
Fluorinated aromatics is generally chosen as mesogenic cores to design novel liquid crystal compounds. Here, a series of benzoxazole derivatives with laterally multifluorinated biphenyl units, 2-(3′,3-difluoro ?4′-alkoxy-1,1′-biphenyl-4-yl)-benzoxazole derivatives (coded as nPF(3)PF(3)Bx), are synthesized and characterized, where methyl and nitro moieties are selected as terminal groups to investigate the effects of different polar substituents on the liquid crystal properties. The compounds nPF(3)PF(3)Bx show enantiotropic mesophases with mesophase ranges of 0–40°C and 0–63°C on heating and cooling for hydrogen-terminated derivatives (nPF(3)PF(3)BH), 43–93°C and 54–123°C for methyl-terminated ones (nPF(3)PF(3)BM), 60–108°C and 74–152°C for nitro terminated ones (nPF(3)PF(3)BN), respectively. They exhibit photoluminescence emission peaks at 390–392 nm and UV–vis absorption bands with maxima at 327–330 nm, respectively. The results reveal that lateral multifluoro substituents lead to a decrease in melting/clearing points, while electron-withdrawing terminal nitro moiety results in increases in both melting point and mesophase range.  相似文献   

6.
Terahertz (THz) absorption is a fingerprint property of materials, due to the underlying low-frequency vibration/phonon modes being strongly dependent on the chemical constitutions and microscopic structures. The low excitation energies (0.414-41.4 meV) are related to two intrinsic properties of THz vibrations: the potential energy surfaces (PESs) are shallow, and the vibrationally excited states are usually populated via thermal fluctuations. The shallow PESs make the vibrations usually anharmonic, leading to redshifted vibrational excited state absorption; combined with considerable vibrational excited states population, characteristic THz signals are usually redshifted and congested with varying degrees at different temperatures. Combining existing experimental THz spectra at low temperatures, first principles vibration analysis, and the Morse potential, we developed a semi-empirical model to evaluate the anharmonicity of the low-frequency modes. The model was benchmarked with purine molecular crystal to generate THz spectra at different temperatures, the results were consistent with experiments. The good agreement suggests this model would facilitate the application of THz spectroscopy in molecular crystal characterization.  相似文献   

7.
Raman spectra of pure and 2 wt.% gold nanoparticles (GNPs) dispersed liquid crystalline compound 4-n-Hexyloxy-4?- cyanobiphenyls (6OCB) has been recorded as a function of temperature from room temperature (solid crystal) to 80°C (isotropic liquid) in the spectral region of 500–2500 cm?1. The variation of Raman spectral parameters (peak positions and line width) with temperature is used to explain the changes in molecular alignment and its effect on inter-/intra-molecular interactions at crystal-Nematic (K-N) transition. To understand the change in molecular structure during phase transition and on account of dispersion of gold nanoparticles in pure liquid crystal more precisely, two spectral regions 1000–1500 cm?1 and 1500–2400 cm?1 have been selected separately. From the detailed study, it is concluded that increased orientational/vibrational freedom of the molecules as well as delocalisation of electron clouds results in the spectral anomalies at K-N transition. The geometrical structure of 6OCB was optimised using density functional theory (DFT) and theoretical Raman spectra have been obtained for comparison with experimental spectra. The tentative assignment of vibrational modes observed in our region of study was calculated based on potential energy distribution (PED) using vibrational energy distribution analysis (VEDA) calculation.  相似文献   

8.
This paper describes the synthesis and characterisation of several liquid crystal (LC) compounds having a tolane core structure and a trifluoromethoxy terminal group. The mesomorphic properties, mid-wave infrared (IR) absorption and birefringence were investigated. These materials exhibit low absorption in mid-wave IR regions (MWIR) and high birefringence (Δn ~ 0.26–0.29). The impact of fluorine substitution was investigated. Compounds with monofluorine exhibit wide mesophase temperature (88.5°C), and the mesomorphic behaviour weakened with increasing fluorine atom. The results show that they are promising LC materials for applications in the MWIR.  相似文献   

9.
A new series of donor–acceptor–donor (D–A–D) type luminescent mesogens carrying 2-methoxy-3-cyanopyridine as a central core linked with variable alkoxy chain lengths (m = 6 and 8) as terminal substituents was synthesized and characterized using spectral methods. The newly synthesized molecules were subjected to single-crystal X-ray diffraction (SCXRD), powder X-ray diffraction (PXRD), differential scanning calorimetric (DSC), polarizing optical microscopy (POM), and fluorescence emission studies in order to ascertain their mesogenic and photophysical properties. The SCXRD data on 4a and 4b reveal that the presence of short intermolecular contacts, viz. C–H···N, C–H···O, C–H···π, and π···π interactions, is responsible for their crystal packing. The measured torsion angle values indicate that molecules possess distorted non-planar structure. The DSC, POM, and PXRD studies confirm that all the molecules show thermotropic liquid crystalline behaviour and exhibit rectangular columnar phase. Further, their UV–visible and fluorescence spectral studies reveal that the target molecules are luminescent displaying a strong absorption band in the range of 335–340 nm and a blue fluorescence emission band in the range of 395–425 nm (both in solution and film state) with good fluorescence quantum yields (10–49 %).  相似文献   

10.
ABSTRACT

Polymer dispersed liquid crystal (PDLC) systems based on a smectic liquid crystal embedded in polyvinylalcohol-boric acid (PVAB) as biocompatible carrying matrix were prepared and characterised. The smectic liquid crystal contains biologically friendly structural blocks and was designed to have a direct isotropic–smectic transition and a mesophase stability range at human body temperature. The resulted PDLCs were characterised from morphological and thermotropic aspects by polarised light microscopy (POM), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and Raman microspectroscopy, and their surface properties were determined by contact angle measurements and surface energy calculations.

It was concluded that the electron-deficient PVAB matrix constrains the ester liquid crystal to grow as spherical droplets with planar anchoring. The droplet diameter was comprised in the range 4–11 µm, with a predominant droplet population around 7 µm and a narrower polydispersity as the amount of the liquid crystal in the polymeric matrix increases. The resulted PDLC films exhibited versatile morphology and surface properties which allow targeting of their application.  相似文献   

11.
The terahertz (THz) spectrum of the pharmaceutical (1R,2S)‐(?)‐ephedrine from 8.0 to 100.0 cm?1 is investigated at liquid‐nitrogen (78.4 K) temperature. The spectrum exhibits several distinct features in this range that are characteristic of the crystal form of the compound. A complete structural analysis and vibrational assignment of the experimental spectrum is performed using solid‐state density functional theory (DFT) and cryogenic single‐crystal X‐ray diffraction. Theoretical modeling of the compound includes an array of density functionals and basis sets with the final assignment of the THz spectrum performed at a PW91/6‐311G(d,p) level of theory, which provides excellent solid‐state simulation agreement with experiment. The solid‐state analysis indicates that the seven experimental spectral features observed at low temperature consist of 13 IR‐active vibrational modes. Of these modes, nine are external crystal vibrations and provide approximately 57 % of the predicted spectral intensity. This study demonstrates that the THz spectra of complex pharmaceuticals may be well reproduced by solid‐state DFT calculations and that inclusion of the crystalline environment is necessary for realistic and accurate simulations.  相似文献   

12.
A series of 2-(3?-fluoro-4?-alkoxy-1,1?-biphenyl-4-yl)-benzoxazole liquid crystals (coded as nPF(3)PBx) were prepared, where a lateral fluorine substituent, as well as methyl, chlorine and nitro terminal groups, was introduced into the molecules to investigate the effects of different polar substituents on the liquid crystal properties. The mesomorphic and photophysical properties were investigated. The results show that compounds nPF(3)PBx have enantiotropic mesophases; meanwhile, they exhibit UV–vis absorption bands with maxima at 323–326 nm and photoluminescence emission peaks at 389–395 nm, respectively. It is noted that nPF(3)PBx with terminal polar groups or electron-withdrawing groups (NO2, Cl) display higher clearing temperatures and wider mesophase range than those of the corresponding homologues with terminal non-polar groups or electron-donating groups (CH3, H). Meanwhile, compared with two lateral fluorine-substituted analogues containing 3,5-difluorophenyl unit, lateral monofluoro-substituted nPF(3)PBx display enhanced mesophase range both in heating and cooling except for terminal methyl-substituted compounds, as well as show obvious red-shifted UV–vis absorption bands and photoluminescence emission, which are attributed to the enhanced dipole–dipole interaction caused by increased dipole moment.  相似文献   

13.
D-、L-和DL-青霉胺的太赫兹时域光谱   总被引:8,自引:0,他引:8  
利用太赫兹时域光谱技术(THz-TDS)对D-、L-和DL-青霉胺的研究发现, 三种样品在0.2 THz到1.8 THz波段的吸收光谱存在显著差异, 实验结果表明, THz吸收光谱能够鉴别青霉胺对映异构体, 这一特点将可以用于青霉胺药物的检测. 本文利用纯D-、L-青霉胺的THz吸收光谱, 对D-、L-青霉胺混合样品的THz吸收光谱进行拟合, 证明可以用THz光谱定量分析混合样品中D-、L-青霉胺的相对含量. 这项研究为手性药物分子检测和分析提供了新的实验方法, 也对深入了解手性药物与生物靶分子之间相互作用提供了启示.  相似文献   

14.
Single crystals of nonlinear optical material l-glutamic acid hydrochlorobromide (LGHCB) were grown by slow evaporation technique from its aqueous solution. Optically good quality crystals of dimension 20 × 10 × 2 mm3 were obtained. The lattice parameters for the grown crystals were determined using single crystal X-ray diffraction study. The LGHCB crystal belongs to non-centrosymmetric P212121 space group. The crystal structure was resolved by direct method and refined by full matrix least-square method using SHELXL-97. Using the powder X-ray diffraction study, the crystallinity of the grown crystal was confirmed and the diffraction peaks are indexed. From Fourier transform infrared spectroscopy study, the various functional groups present in LGHCB crystal were elucidated. The UV–Vis-NIR absorption spectrum was recorded in the range of 200–2,000 nm, and the lower cut off wavelength is ~235 nm. Optical band gap of the grown crystal was found to be 5.22 eV. Thermal properties of LGHCB crystal were studied by thermogravimetric analysis and derivative thermogravimetric analysis. The second harmonic generation efficiency of LGHCB crystal was confirmed by Kurtz’s powder technique.  相似文献   

15.
In this article electromagnetic simulations of tunable terahertz metamaterial infiltrated with nematic liquid crystal are described. A full-wave analysis technique based on the finite-difference time-domain (FDTD) method was done by employing QuickWave 3D electromagnetic solver. Scattering parameter analysis shows a resonant frequency shift of 0.8 THz obtained by reorienting the layered highly birefringent nematic liquid crystal. Effective refractive index for operation frequency varies from negative to positive values.  相似文献   

16.
Hydroxyhexyl esters of alkoxy and halostilbene carboxylic acids were prepared and studied for thermal, liquid crystalline and fluorescent properties. The decomposition temperatures were determined thermogravimetrically and the compounds were found stable at least up to 200°C. Differential scanning calorimetry (DSC) indicated two mesophases in alkoxystilbene caboxylates. The smectic nature of the liquid crystal (LC) compounds was identified from the optical textures and confirmed through X-ray diffraction (XRD) measurements, where SmA, SmB and CrE mesophases were observed. The compounds 3a-g and 3h-k show single absorption maxima in UV-visible spectra at around 338 and 322 nm, respectively. All the alkoxy compounds emit blue light in solution and in solid state in the wavelength range of 422–425 nm.  相似文献   

17.
A photoresponsive azobenzene molecule DCAZO2 with two cholesteryl groups linked to both sides of the azobenzene group is doped in a mixture of nematic liquid crystal E7 and chiral dopant S811 (61.9 wt% E7, 36.1 wt% S811 and 2.0 wt% DCAZO2). Cooled from isotropic phase to 33.0°C, chiral nematic liquid crystal (N*LC) was formed in the sample and then the temperature was kept unchanged at 33.0°C. UV light irradiation induces the transcis photoisomerisation and thus an obvious phase transition. When the azobenzene groups isomerise to a cis-saturated state, the UV light was turned off and the white light was turned on at the same time. The bent-shaped cis isomer then turns back to the planar trans isomer gradually. A blue–green platelet texture representing cubic blue phase (BP) was observed and the size of the platelets was increased along with the cistrans isomerisation. UV–vis absorption spectra indicate that the photoinduced BP exists when the isomerisation degree is between 79% and 18%, and further cistrans isomerisation change BP back into N*LC. The large geometric structure of the cholesteryl groups and the large bent angle θ of the cis isomer are supposed to be responsible for the interesting result.  相似文献   

18.
In the present study, an environment-friendly sample preparation method termed ionic liquid-based dispersive liquid–liquid microextraction combined with flame atomic absorption spectrometry has been developed for the determination of Pb(II) ion in water samples prior to flame atomic absorption spectrometry determination. In this method, ionic liquid was used as an extraction solvent instead of the organic solvent used in the conventional dispersive liquid–liquid microextraction (DLLME) assay, and there is no need for a chelating agent. Several variables that may affect extraction efficiencies, including pH, the volume of ionic liquid, the type and volume of disperser solvent, salt addition, and the time for centrifugation and extraction were studied and optimised. Under the optimised conditions, the calibration curve exhibited linearity over the range of 20.0–1000.0 μg L?1. The enrichment factor and the limit of detection based on 3Sb/m were 35.0 and 5.9 μg L?1, respectively. Seven replicate determination of a solution containing of 100.0 μg L?1 Pb(II) ions gave a relative standard deviation of ±2.1%. Finally, the feasibility of the proposed method for Pb(II) determination was assessed by the analysis of certi?ed reference material and various water samples and the satisfactory results were obtained.  相似文献   

19.
Frequency- and temperature-dependent dielectric and switching parameters of a room temperature tri-component antiferroelectric liquid crystal mixture W-287 have been determined. Dielectric, optical texture and thermodynamic studies show wide room temperature range antiferroelectric SmC*a (?91.1°C to <–25°C) phase in addition to high temperature paraelectric SmA* (?2.6°C) and ferroelectric SmC* (?4.4°C) phases. The dielectric studies carried out in the frequency range of 1–35 MHz under planar anchoring condition of the molecules show five different relaxation modes appearing in the SmA*, SmC* and SmC*a phases. Using Curie–Weiss law fit, ferroelectric SmC* to paraelectric SmA* transition temperature has been found to be 91.8°C. The dielectric response of SmC*a phase exhibits unusually three relaxation modes due to collective as well as individual molecular processes in addition to phason mode in the SmC* phase and amplitudon mode in the SmA* phase. Spontaneous polarisation, switching time and rotational viscosity have also been determined. The maximum value of PS is ?300 nC/cm2, whereas viscosity is moderate. Switching time is of the order of few milli seconds.  相似文献   

20.
含硫氨基酸的太赫兹光谱   总被引:1,自引:0,他引:1  
王雪美  王卫宁 《化学学报》2008,66(20):2248-2252
利用太赫兹时域光谱(THz-TDS)技术研究室温条件下多晶含硫氨基酸L-蛋氨酸(Met)和L-半胱氨酸(Cys)的光谱特性, 得到相应的吸收谱和折射率谱, 表明含硫氨基酸在THz波段具有区别于其它氨基酸的显著特征. 在实验测量的有效光谱范围0.2~2.8 THz内, L-蛋氨酸的THz吸收峰分别位于1.06, 1.88和2.70 THz; L-半胱氨酸的吸收峰分别位于1.40, 1.70, 2.33和2.61 THz, 两种氨基酸的平均折射率均为1.44. 利用GAUSSIAN 03软件包中的Hartree-Fock理论计算了蛋氨酸双分子的低频振动谱, 表明了与蛋氨酸各吸收峰对应的分子微观振动模式, 并对实验光谱进行了解析讨论.  相似文献   

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