Novel asymmetrical single- and double-chiral
liquid crystal diads with wide blue phase ranges
†
Chong-Lun Wei,aTe-Cheng Chen,aPutikam Raghunath,bMing-Chang Linb and Hong-Cheu Lin*a
In this study, two series of novel asymmetrical single- and double-chiral liquid crystal diads using a central linker to link two different mesogenic cores were successfully synthesized. The effects of the position of chiral centers and the number of aromatic rings on the mesomorphic and electro-optical properties were investigated. We found that diads III-N (where N ¼ A, B, C and D) have better mesophasic properties than II-N (where N ¼ A, B, C, D and E). Compared with III-C with a chiral center at the terminal alkoxyl chain, diad III-D exhibited the widest temperature range of BPI (ca. 31C) as the chiral center was introduced to the central linker. Besides III-D, BPs were also observed in diads II-B and III-B with a chiral center at the central spacer. According to our experimental results and molecular modeling, the mesomorphic properties and temperature ranges of BPs will be affected by the values of biaxiality and dipole moment, along with the bent shape of molecular geometry. Therefore, we demonstrated the first example of asymmetrical single- and double-chiral liquid crystal diads involved chiral centers located at the central linker to exhibit BPs, including the mesophases of BPI and BPIII, which might offer new BP single-components to the future applications of eutectic liquid crystal mixtures with wide BP ranges.
Introduction
It is well known that liquid crystal molecules may reveal many different mesophases, including nematic,1 smectic,2 chole-steric,3 and blue phases, and these are attributed to their chemical structures, such as molecular congurations with specic shapes and dipole moments. Among these mesophases, blue phase liquid crystals (BPLCs) are observed between isotropic phase and chiral nematic (N*) phase during cooling process, which have less applications due to their narrow mesophasic ranges (usually about 1 K).4It has been reported that BPLCs aggregate into internal helical alignments called “double twist cylinders (DTC)”,5,6 where are three types of BPLCs: blue phase I (BPI), blue phase II (BPII) and blue phase III (BPIII). The packing structures of these three BPLCs are described as follows: BP I is a body-center cubic structure, BP II is a simple cubic structure,7,8and BP III is the same symmetry as the isotropic phase with arbitrary orientation.9,10 BPLCs have different performances in the eld of optoelectronics: among all BPs, BP III has the fastest response speed,11and BP II shows smaller hysteresis and faster response time than BP I.12Though
very narrow ranges of BPLCs were observed, polymer stabilized BPLCs was rst discovered by Kikuchi et al. to extend the temperature range of BPs phase over 60 C.13 Since BPLC arrangements were stabilized by the polymer network design to enlarge the BPLC ranges, general interests have been attracted to develop BPLCs recently. Some advantages in the elds of optoelectronics and photonics are listed as follows:14,15 fast response time (about sub-millisecond), no alignment layer required,16and free of typical birefringence.17
Nowadays, several research groups have reported numerous methods to induce the blue phase and enlarge the temperature range of blue phase, which were accomplished either by struc-tural modications or mixture optimizations. For example, Yang et al. utilized hydrogen bonds to stabilized BPLCs, where two complimentary hydrogen-bonded moieties were self-assembled by hydrogen bonds to form a BP complex with a wide temperature range about 23 C.18In addition, they also tried to dope hydrogen-bonded bent-shaped and T-shaped molecules to stabilize BPs.19 Pivnenko et al. synthesized bimesogens structures to induce BPLCs with a BP temperature range ca. 44C.20Besides, U-shaped molecules have also been doped with a chiral additive to extend the BP range success-fully.21There are some reports demonstrated that several biaxial nametic LCs doped with certain amounts of chiral materials can enhance the temperature range of BPs.22–24 Although BPLCs have so many benets, very limited single-component BPLC molecules with wide BPLC ranges have been developed so far. aDepartment of Materials Science and Engineering, National Chiao Tung University,
Hsinchu, Taiwan, Republic of China. E-mail: [email protected]
bCenter for Interdisciplinary Molecular Science, Department of Applied Chemistry,
National Chiao Tung University, Hsinchu, Taiwan, Republic of China
† Electronic supplementary information (ESI) available. See DOI: 10.1039/c4ra13943g
Cite this: RSC Adv., 2015, 5, 4615
Received 6th November 2014 Accepted 5th December 2014 DOI: 10.1039/c4ra13943g www.rsc.org/advances
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linked aexible spacer between a rod and a cholesterol meso-genic unit which exhibited a wide range of BPs.35Our previous research also reported a bent-core oxadiazole-based liquid crystal to possess a blue phase with a wide range of ca. 30C.36 In this study, we synthesized two series of novel asymmet-rical single- and double-chiral liquid crystal diads with an odd-number spacer to link two different mesogenic rods and introduced chiral centers into the central linker and/orexible terminus of the diads. We demonstrated the effects of the number of aromatic rings and the positions of the chiral centers on the mesophasic behaviors of LCs. Interestingly, we found one of the double-chiral liquid crystal diad exhibited BPI with a wide temperature range about 31 C. Moreover, the phase transition sequences, electric-optical properties, Kerr constants and theoretical calculations of molecular modeling were investigated in this report.
Experimental
Spectroscopic analysis1H NMR spectra were recorded on a Bruker Unity 300 MHz
spectrometer using DMSO-d6, CDCl3 and THF-d8 as solvents. Elemental analyses (EA) were performed on a Heraeus CHN-OS RAPID elemental analyzer. Synchrotron powder X-ray diffrac-tion (XRD) measurements were performed at beam-line BL17A equipped with magnetic of the National Synchrotron Radiation Research Center (NSRRC), Taiwan, where the wavelength of X-ray was 1.33336 ˚A. The powder samples were packed in a capillary tube and heated by a heat gun, for which the temperature controller is programmable by a PC with a PID feedback system. The scattering angle theta was calibrated by a mixture of silver behenate and silicon.
Molecular simulation method
The gas phase optimization of all asymmetrical structures of liquid crystal diads II-N (N¼ A, B, C, D and E) and III-N (where N ¼ A, B, C and D) was carried out with the generalized gradient approximation (GGA) density functional B97D along with dispersion correction37using the standard 6-31G(d,p) basis set. The predicted minima were further conrmed by frequency calculations at the same level. Only the lowest energy confor-mations are reported here. The electrostatic potential derived charges (ESP) were calculated according to Merz–Singh–Koll-man (MK) scheme38at the B97D/6-31G(d,p) level of theory. ESP results were used to compute maps of electrostatic potential. The results of all the calculations reported in this work were
phase transitions were determined by differential scanning calorimetry (DSC, model: Perkin Elmer Pyris 7) under N2at a heating and cooling rate of 1C min1. The performance of optical properties was determined in the range of blue phase temperature and the optical transmittance was studied with a function of applied electric ACeld at 2 kHz. The transmittance with 100% and 0% were calibrated by that the cell under parallel polarizers. The distance between electrodes was 10mm and the cell gap was maintained at 7.5mm by spacers. Preparation of materials
(i) (S)-6-((40-Cyano-[1,10-biphenyl]-yl)oxy)-methylhexyl 4-((4-((4-((R)-octan-2-yloxy)benzoyl)oxy)benzoyl)oxy)benzoate, (III-D). The synthesis of compound III-D was shown in Scheme 1. To a stirred solution of M1 (3.0 g, 9.7 mmol), M2 (2.42 g, 4.9 mmol) and 4-(N,N-dimethylamino)pyridine (DMAP) (0.13 g, 1.06 mmol)
in dry dichloromethane (100 mL),
N,N-dicyclohex-ylcarbodiimide (DCC) (2.35 g, 11.6 mmol) was added and the reaction mixture stirred at room temperature overnight under nitrogen. The resulting precipitate of dicyclohexylurea (DCU) wasltered off and washed with an excess of dichloromethane (20 mL). The solvent was evaporated and the crude product was
puried by silica gel chromatography (n-hexane/
dichloromethane ¼ 1 : 1 v/v) and then recrystallized from methanol/dichloromethane (5 : 1 v/v) to afford compound III-D as a white solid in 78% yield. 1H NMR (300 MHz, CDCl3): d (ppm) 8.27 (d, J ¼ 8.7 Hz, 2H), 8.17 (d, J ¼ 8.7 Hz, 2H), 8.14 (d, J¼ 9.0 Hz, 2H), 7.71–7.63 (m, 4H), 7.54 (d, J ¼ 8.7 Hz, 2H), 7.40 (d, J ¼ 8.7 Hz, 2H), 7.31 (d, J ¼ 9.0 Hz, 2H), 7.02–6.98 (m, 4H), 4.53–4.51 (m, 1H), 4.37 (t, J ¼ 6.3 Hz, 2H), 4.09 (m, 2H), 1.92–1.84 (m, 5H), 1.52–1.33 (m, 15H), 1.35 (d, J ¼ 6.6 Hz, 3H), 0.91 (t, J¼ 6.6 Hz, 3H). Anal. calcd for C49H51NO8: C, 75.27, H, 6.57, N, 1,79; found: C, 75.31, H, 6.62, N, 1.83%.
Results and discussion
Chemical synthesisAs illustrated in Fig. 1, series II-N (where N¼ A, B, C, D and E) and III-N (where N¼ A, B, C and D) were synthesized according to Schemes S1–S4 (see the ESI†), where one of the mesogenic rods in series III are longer than series II, along with B, C and D represent single- and double-chiral diads, respectively. These compounds with high purities were fully characterized by1 H-and13C-NMR, as well as mass ESI spectra (see the ESi†.) Mesophasic and thermal properties
As shown in Table 1, the phase transition temperatures, enthalpies and mesophasic ranges of the asymmetrical liquid
crystal diads were determined by differential scanning calo-rimetry (DSC) and polarizer optical microscope (POM). The transition temperature of BPs–chiral nematic (N*) was deter-mined by POM (at a cooling rate of 0.5C min1) due to their undetectable enthalpy changes by DSC. To realize the effect of
various asymmetrical congurations, including different
numbers (or positions) of chiral centers and aromatic rings, on mesophasic and thermal properties of these asymmetrical single- and double-chiral liquid crystal diads, the comparison of all compounds are described as follows:
(i) Compounds II-N (where N ¼ A, B, C, D and E).
Compound II-A (no chiral center) exhibits a phase transition sequence of iso–nematic (N)–smectic A (SmA)–crystal. We tried to introduce a single chiral center to the central linker and exible terminus of diads II-B and II-C, respectively. In contrast to II-C, diad II-B revealed BPIII (ranging 3.4C) due to the chiral center located at the central spacer, which induced twisting
power but didn't diminish the interactions of mesogenic cores. However, as the chiral center was shied to the terminal alkoxyl chain, the mesophases were totally vanished in II-C due to a stronger chiral twisting of the chiral center closer to the rigid core. Moreover, we also introduced double chiral centers to both central linker andexible terminus of diad II-D, which do not have any mesophases due to even a stronger chiral twisting than II-C to further eliminate mesogenic interactions of meso-phases. The strongest chiral twisting of both diads II-C and II-D to reduce the mesogenic interactions of rigid cores were also evidenced by their lowest crystallization (as well as isotropiza-tion) temperatures among all diads. Among these described chiral diads (II-B, II-C and II-D), only diad II-B with a single chiral center at the central spacer displayed mesophases, including BPIII. Hence, another single chiral diad II-E was introduced to investigate the effects of chiral center position at the central spacer, which showed a phase transition sequence of iso–N*–crystal. Diad II-E with a chiral center at the central spacer possessed a mesophase of N*, but BPIII was absence in II-E due to the different location of chiral center in contrast to II-B. Accordingly, a single chiral center located at the appro-priate position of the central linker was required for diad II-B to obtain BPIII.
(ii) Compounds III-N (where N¼ A, B, C and D). The phase transition sequence of compound III-A is similar to II-A, i.e., iso–N–SmA–crystal, but III-A has higher transition temperatures and wider mesophasic ranges (i.e., N and SmA) than II-A due to the longer rigid core of III-A with a strongerp–p interaction. Similar to II-B and II-C, a single chiral center was introduced to the central spacer andexible terminus of diads III-B and III-C, respectively. In comparison with III-C, single-chiral diad III-B exhibited BPI (ranging 1.5C) due to the chiral center located at the central spacer. Nevertheless, as the chiral center was shied to the terminal alkoxyl chain, III-C had similar mesophases of III-B, i.e., N* and SmA, but BPI was totally disappeared in III-C due to a stronger chiral twisting of the chiral center closer to the rigid core. Because of the same reason, compared with III-B, Scheme 1 Synthesis of III-D.
Fig. 1 Chemical structures of compounds II-N (where N¼ A, B, C, D and E) and III-N (where N¼ A, B, C and D).
most transition temperatures and both mesophasic ranges of N* and SmA were reduced in III-C. Accordingly, SmA was totally removed and BPI (ranging 31C) was induced in double-chiral diad III-D owing to the introduction of double chiral centers to both central spacer andexible terminus. Similarly, the stron-gest chiral twisting of diad III-D to decrease the mesogenic interactions of rigid cores was also evidenced by its lowest phase transition temperatures among all diads in series III.
(iii) Comparison of series II and III. All phase transition temperatures of the corresponding phases in compounds III-N were higher than those of compounds II-N (where N¼ A, B, C, D and E) because of the longer rigid core of series III-N (where N¼ A, B, C and D) with strongerp–p interactions. Among all diads, only diads II-C and II-D did not have any mesophases owing to their strongest chiral twisting with less mesogenic interactions of shorter rigid cores. In contrast to II-C and II-D, compounds III-C and III-D with a longer rigid core possessed strongerp–p interactions to compensate the chiral twisting thus to preserve the molecular assembly of mesophases. Interestingly, among all asymmetrical diads, BPs only exited in single-chiral diads II-B, III-B and double-chiral diad III-D, which all possessed chiral centers at central spacer. Compared with BPIII of II-B, the other diads III-B and III-D possessed BPI owing to their longer rigid core. Above all, double-chiral diad III-D was discovered to possess the widest BP temperature range among all diads, which is therst molecular design of liquid crystal diad with double-chiral centers (at both central spacer and exible terminus) in the literature.
Optical and XRD investigations
Regarding the blue phases of diads II-B, III-B and III-D, we investigated the phase transitions by POM on cooling process (cooling rate 0.5C min1). Fig. 2(a)–(d) show the phase tran-sitions of iso–BPIII–N*–SmA in II-B, respectively. In addition,
the POM texture of III-B at 181.0C upon cooling (0.5C min1) is also illustrated in Fig. S1.† Meanwhile, the phase transitions of iso–BPI–N* in III-D are shown in Fig. 3(a)–(c), respectively. All phase transitions were investigated by XRD measurements and their related data are shown in Fig. S2† and Table S2† of the ESI. Generally, sharp reection peaks of XRD patterns (representing layer d-spacings) were observed in the small angle area of the smectic phase (including SmA), but only broad peaks were revealed in the wide angle area of the N and N* phases. As shown in Table S2† (see the ESI), II-A and II-B processed d-spacing values of 41.8 ˚A and 43.4 ˚A, respectively. In addition, III-A, III-B and III-C also exhibited d-spacing values of 49.7 ˚A, 50.1 ˚A and 45.7 ˚A, respectively. Their d-spacing values (d) were a little larger than their corresponding molecular lengths (L) by the theoretical simulation (shown below), which suggested the d-spacing values of the SmA phase in these diads are interdigitated layer arrangements (i.e., L < d < 2L). Therefore, the SmA phase was veried not only by the focal-conic fan texture of POM photo-images but also by the d-spacing values of sharp reection peaks. The II-B behavior of BPIII could be veried by the rotation of the polarizer (see Fig. 4). As the polarizer was rotated clockwise
II-E Iso 41.8 [0.10] N* 30.9 [0.83] Cr 10.9
III-A Iso 195.0 [1.12] N 119.1 [2.99] SmA 63.0 [1.51] Cr
75.9 56.1
III-B Iso 182.2 [0.94] BPI 180.7cN* 106.2 [2.44] SmA 72.5 [1.22] Cr
1.5 74.5 33.7
III-C Iso 109.5 [11.76] N* 87.6 [5.43] SmA 79.7 [2.03] Cr
21.9 7.9
III-D Iso 108.0 [0.36] BPI 76.6cN* 51.9 [1.63] Cr 31.4 24.7
aPeak temperatures in the DSC proles obtained during the rst heating and cooling cycles at a rate of 1C min1.bIso¼ isotropic phase; BPIII ¼
blue phase III; BPI¼ blue phase I; N ¼ nematic phase; N* ¼ chiral nematic phase; SmA ¼ smectic A phase; Cr ¼ crystal.cThe transition to this phase was observed under the polarizing optical microscope and it was too weak to be recognized by the DSC. (Phase transition temperatures and enthalpies of heating process are shown in Table S1.)
Fig. 2 POM textures of II-B upon cooling (0.5C min1). (a) Isotropic state at 100C. (b) Blue phase III at 92.1C. (c) Chiral nematic phase at 80.2C. (d) Smectic A phase at 60.1C. (Scale bar: 40mm. White arrows are the directions of polarizers and analyzers.)
by a small angle of 10from the crossed position, the color was changed from blue to light blue (Fig. 4(a)). Upon rotating the polarizer counterclockwise by the same angle (10) from the crossed position, the color was changed from blue to red (Fig. 4(c)). The POM observations also indicated that the phase of BPIII has selective reection colors according to their pitch lengths, which were examined by changing the cross angles in the polarizer and analyzer of POM.
Electro-optical studies
In order to investigate the electro-optical switching behavior in the blue phase of diads II-B and III-D, a rectangular wave function of the ACeld at a frequency of 2 kHz was applied to measure the optical transmittance. Fig. 5 shows the voltage– transmittance curve at T TI-BP¼ 2C, where the black lines with solid squares and circle squares represent the trans-mittance of compound II-B upon increasing and decreasing voltages, respectively. The red lines with solid dots and circle dots stand for the transmittance of III-D upon increasing and decreasing voltages, respectively. Both II-B and III-D showed enhanced transmittance by increasing the electric eld. As transmittance reached 10% and 90% in the V–T curve, we found that III-D had higher respective electricalelds (11.5 and 17.2 V mm1) than II-B (10.2 and 15.6 Vmm1). In addition, in-plane-switching (IPS) cells were utilized to realize the V–T hysteresis by increasing the voltage to saturation. Because hysteresis will inuence the grayscale of liquid crystal device, the hysteresis should be minimized for real applications.40The denition of
hysteresis is DV/Von (DV is the voltage difference between the forward and backward directions at half of the peak transmittance and Von is the driving voltage).41 The electro-optical switching exhibited that II-B did not have any hysteresis (0%), but III-D was observed to have a large hysteresis (27%). Compared with II-B, the higher applied voltages (10% and 90% transmittance in the V–T curve) and hysteresis of III-D were due to a larger number of aromatic rings in III-D with strongerp–p interactions.
The values of response time for diads II-B and III-D were obtained from the electro-optical response curves of Fig. S3(a) and (b),† respectively (see the ESI). As summarized in Fig. 6, their values of response time were measured with a rectangular wave function of the ACeld (at a frequency of 2 kHz) for the rise and decay processes at T TI-BP¼ 2C. The denitions of the rise time (son) and decay time (soff) are the response time values for 90% transmittance change by increasing and Fig. 3 POM textures of III-D upon cooling (0.5C min1). (a) Isotropic
state at 112.3C. (b) Blue phase I (platelet textures with different colors and stripes) at 86.2C. (c) Chiral nematic phase at 65.1C. (Scale bar: 40mm. White arrows are the directions of polarizers and analyzers.)
Fig. 4 Optical images of II-B observed by POM at 92.7C (a) polarizer was rotated clockwise by a small angle of 10. (b) Polarizer and analyzer were orthogonal. (c) Polarizer was rotated counterclockwise by a small angle of 10. (White arrows are the directions of polarizers and analyzers.)
Fig. 5 Optical transmittance of diads II-B and III-D in BPs (at T TI-BP¼ 2C).
Fig. 6 Diads II-B and III-D in the BP at T TI-BP¼ 2C. (a)
Electric-field dependence of the response times for the rise processes. (b) Electric-field dependence of the response times for the decay processes. (c) Electric-field dependence of the total response times.
the values of rise time (son) and decay time (soff) have opposite trends for diads II-B and III-D. As a result, the values of total response time (stotal¼ son+ soff) in Fig. 6(c) are enhanced by increasing voltage, which has the same trend as the decay time (soff) due to the larger values ofsoffwith more contributions to stotalcompared with those ofson. According to Table S3,† the average values of total response time (stotal¼ son+soff) for II-B and III-D are 2.74 and 3.56 ms, respectively, where II-B has the fastest total response time.
According to the denition of the Kerr effect,45,46the formula: Dninduced ¼ lKE2, whereDn is the electric eld-induced bire-fringence, l is the wavelength of light, K is the Kerr constant and E is the electric-eld. The Kerr constants of II-B and III-D in their corresponding BPs were 2.2 1011 and 2.7 1011 mV2, respectively, where BPI of III-D demonstrated the largest Kerr constant. The BPs with largeeld-induced birefringences would cause the orientation changes of the ordered molecules easily. In contrast to nitrobenzene with a well-known and large Kerr constant 2.2 1012mV2,47II-B and III-D possessed Kerr constants 10 times larger than nitrobenzene might have useful applications in the future.
Theoretical simulation
As alluded to above, we carried out geometry optimization at the B97D/6-31G(d,p) level for all asymmetrical liquid crystal diads II-N (N¼ A, B, C and D) and III-N (where N ¼ A, B, C and D) to analyze the structural variations. The main geometric parame-ters for the ground states of lowest energy conformations of II-B, III-B and III-D bearing chiral centers at the central linker and/or terminal alkoxyl chain are summarized in Table 2 with molecule length, breadth, bent angle and dipole moment, which can inuence the temperature range and stabilization of blue pha-ses (BPs). In addition, the related data of the other compounds without BPs are shown in Tables S3–S5 (see ESI†).
Hence, a similar molecular structure with a more bent shape (i.e., a smaller bent angle in Fig. 7) should have a larger biaxiality (i.e., a larger difference between W1and W2). These parameters are dened as following: L (length along the long axis), biaxiality equals W1/W2 (W1: width along the short axis normal to the benzene plane and W2: width along the short axis parallel to the benzene plane) and bent angles are measured as the angles between the centers of therst, central and nal benzene rings of the bent-core structures (see Fig. 7 and Table 2).
Table 2 Calculated lengths, breadths, bent angles and dipole moments of molecular structures in optimized asymmetrical liquid crystal diads at the B97D level with the 6-31G(d,p) basis set
Compounds Length L (˚A) Breadth W1(˚A) Breadth W2(˚A)
Biaxial parameter
(W1/W2) Bent anglea(deg)
Dipole moment (Debye, D)
II-B 39.5 8.8 6.0 1.47 139.4 10.9
III-B 45.0 10.8 6.4 1.69 141.1 13.1
III-D 43.2 12.1 6.5 1.86 132.1 13.2
aBent angle () measured as the angle between therst, central and nal benzene rings' centers of the bent-core structures. The dipole moments of the lowest energy structures are given (see ESI Tables S4–S6).
Fig. 7 Molecular models of the lowest energy conformations for single molecules of diads (a) III-D (b) III-B and (c) II-B.
Comparing the BP temperature range of compound II-B and III-B, diad II-B (3.4C) has a little wider BP range than III-B
(1.5C), but diad III-B has one more aromatic ring than II-B.
To explain this result, the difference of biaxiality, dipole moment and bent angle are further investigated between II-B and III-B. Although the values of biaxiality and dipole moment for diad III-B (biaxiality parameter1.69 and dipole moment 13.1 D) are larger than those of II-B (biaxiality parameter 1.47 and dipole moment10.9 D), diad II-B (139.4) has a
more bent shape than III-B (141.1). In this study, we found that the bent shape of molecular geometry is useful to stabilize the BPs so that the BP temperature range of diad II-B (3.4C) is
wider than III-B (1.5C). On the other hand, diad III-D has one
more chiral center at the terminal alkoxyl chain than III-B but the BP temperature range of III-D (31.4C) is much wider than
that of III-B (1.5C). In order to explain this phenomenon, the
differences of biaxiality, dipole moment and bent angle were studied between III-D and III-B. As shown in Table 2, diad III-D (biaxiality parameter1.86 and dipole moment 13.2 D) has larger values of biaxiality and dipole moment than III-B (biax-iality parameter1.69 and dipole moment 13.1 D). Besides, the molecular geometry of III-D (132.1) is more bent than that of III-B (141.1) so that diad III-D (31.4C) with a more bent shape (i.e., a larger biaxiality) is observed to have a wide temperature range of BP. In the investigation of biaxiality, bent angle and dipole moment effects on widening and stabilizing the BP temperature range, the large values of biaxiality and dipole moment, along with the bent shape of molecular geometry are found to be useful to extend and stabilize the temperature range of BP.
The electrostatic potential maps of all diads III-D, III-B and II-B calculated at the B97D/6-31G(d,p) level are shown in Fig. 8. The results reveal that the red color refers to the electron-rich
and the blue color refers to more positive charge and thus the green color signies the zero electrostatic potential. The highest negative potential (red) is always located at the C(O)]O and C]N functionalities. In addition, the remaining electrostatic potential maps of the other diads are also shown in the ESI Fig. S5.†
Conclusions
Two series of novel asymmetrical chiral liquid crystal diads II-N (where N¼ A, B, C, D and E) and III-N (where N ¼ A, B, C and D) were synthesized to possess two different mesogenic units which were linked together by an odd-number spacer. The effects of the position of chiral centers and the number of aromatic rings on the mesophasic properties (especially for BPs) were investigated. Among these diads, II-B exhibited blue phase III (BPIII) and diads III-B and III-D revealed blue phase I (BPI), where III-D showed the widest temperature of BPI (31C). The
effects of the number of aromatic rings and the position of chiral centers on the behavior of mesophases, electric-optical properties and Kerr constants were systemically investigated. Based on the molecular modeling, we found that the large values of biaxiality and dipole moment, along with the bent shape of molecular geometry are useful to extend and stabilize the temperature range of BPs. Consequently, therst report of asymmetrical single- and double-chiral liquid crystal diads containing a chiral center at the central linker is illustrated to exhibit BPs, including the mesophases of BPI and BPIII. The single-component discoveries of novel liquid crystal diads with wide BP ranges will pave a new way to optimize BP ranges in the eutectic mixtures for future applications.
Acknowledgements
This project wasnancially supported by the National Science Council of Taiwan (ROC) through funding (no. NSC 101-2113-M-009-013-MY2 and NSC 102-2221-E-009-174). We are grateful to the National Center for High-performance Computing for computer time and facilities. The powder XRD measurements were supplied by beam-line BL17A (charged by Dr Jey-Jau Lee) of the National Synchrotron Radiation Research Center (NSRRC) in Taiwan.
Notes and references
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