Biomedical subjects

Ronald Y Dong

Publications and source records attributed to Ronald Y Dong.

15 recordsLinked to original sources

PubMed2006

Intercalated smectic a phases in banana-shaped liquid crystals with carbonate end groups.

Novel, symmetrical, bent-core mesogens, namely substituted 1,3-phenylenebis{4'-[(ethoxycarbonyl)oxy]-1,1'-biphenyl}-4-carboxylates, are prepared with carbonate groups at both ends of the molecules. The mesophase properties are investigated for different electron-donating and -withdrawing substituents connected to the central ring at different positions. These compounds exhibit nematic and/or smectic A intercalated (SmA(int)) mesophases. Electro-optical studies show a very significant electric-field-induced biaxiality that is fast (<1 ms) and large (0.03) associated with a high birefringence (0.33 at 500 nm, 10 V mum(-1) field) for the unsubstituted analogue. For one substance this effect is observable from above 100 degrees C down to room temperature. Such electric-field-induced biaxiality may find practical applications in fast electro-optic modulation devices.

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PubMed2006

Deuterium NMR of the TGBA* phase in chiral liquid crystals.

A deuterium NMR (DNMR) study of the TGBA* (twist grain boundary smectic A*) phase in an NMR magnetic field of 9.4 T for the chiral compound 4-[4'-(1-methyl heptyloxy)] biphenyl 4-(10-undecenyloxy) benzoate (11EB1M7) is reported. The deuterium two-dimensional (2D) exchange spectra were observed for the first time in this phase. The present study allows us to learn how the helicoidal structures arrange in an external magnetic field. To derive quantitative kinetic parameters of this novel phase, both 1D and 2D experimental spectra were simulated by means of a jump diffusion model. By comparing the experimental and simulated spectra, an accurate determination of the dynamic parameters in the TGBA* phase was obtained. Furthermore, the twist angle between two neighboring smectic A blocks is found as 26 +/- 10 degrees, which is consistent with the X-ray results for similar chiral liquid crystals. The diffusion constant (D(parallel)) is estimated to be 3.2 x 10(-12) m(2)/s at 379.5 K.

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PubMed2006

Comparative study of planar motion in monomeric and dimeric discotics.

Deuterium NMR spectra are reported in powder samples of discotic monomer and dimer as a function of temperature in their column Col(ho) phases. To simulate the observed powder patterns, a threefold jump model is used in the monomer, while in the related dimer the libration motion of the monomeric core is described using the infinitesimal jump method under a restricting potential due to the spacer. By comparing the diffusive rates for the two samples, it is concluded that the planar motion in the dimer is at least 30 times smaller than that of the monomer. This could lead to an enhancement of charge and energy transport in discotic dimer systems.

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PubMed2006

NMR angle-dependent spectral study of core dynamics in a discotic columnar phase.

A detailed (2)H NMR study of a discotic monomer is reported in its columnar phase at 61.4 MHz. A simulation of angular-dependent spectral patterns and/or signal intensities of the aromatic deuterons is shown to provide information on the small step (or jump) diffusion rates in the low temperature region of the D(ho) phase, where the motion is in the intermediate motion regime. In the high end of this phase, the motion falls into the fast motion regime and spectral patterns become insensitive to the diffusion rate. In such a case, angular-dependent NMR signal intensities were used to give the required dynamic information. The diffusive motion about the columnar axis is found to be thermally activated with an activation energy of 69 kJ/mol. Deuteron spin-lattice relaxation rates were measured at 61.4 MHz and interpreted by a conventional rotational diffusion model in order to complement and compare with the above study when possible.

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PubMed2006

13C and 2H NMR study of structure and dynamics in banana B2 phase of a bent-core mesogen.

In this paper, the difficulty in orienting the B(2) phase of the banana mesogen 1,3-Phenylene-bis 4-[4-(10-undecenyloxy)-benzoyloxy] benzoate (Pbis11BB) in a relatively high magnetic field is reported based on some observations using both (13)C and (2)H NMR. (2)H NMR spectra recorded for the two labeled isotopomers of Pbis11BB in the isotropic and B(2) phases are shown here. Preliminary results on the deuteron spin-spin relaxation (T(2)) data are reported at 61 MHz in order to underline the peculiar slow dynamics of banana-shaped liquid crystals (BLC), and these results are discussed in the framework of recent studies on similar BLC. The molecular structure and dynamics in the B(2) and crystalline phases are also studied by (13)C solid-state NMR techniques. The results also point to the slow dynamics in the B(2) phase of Pbis11BB. In particular, two-dimensional MAS exchange experiment has been performed to shed light on the molecular conformation structure of the five-ring banana core in the crystalline phase of Pbis11BB, and to compare with that of quantum mechanical calculations reported in the literature.

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PubMed2006

Interlayer self-diffusion and structure of chiral smectic phases studied by 2H NMR exchange experiment.

A deuterium two-dimensional exchange NMR technique is used to study the chiral smectic C (SmC*) and chiral subphases (SmC*(Fi1), SmC*(Fi2)) of a smectogen (s)-1-methylheptyl 4'-(4-n-decyloxy-benzoyloxy)biphenyl-4-carboxylate (10B1M7). The aim is to demonstrate how this technique can be combined with sample rotation in the magnetic field to obtain the fast translational self-diffusion constant along the helical pitch in the SmC* phase and to shed light on the structure of helicoidal superlattice in the three-layer SmC*(Fi1) and four-layer SmC*(Fi2) phases. The cross-peak intensities in the 2D exchange spectrum are sensitive to the disposition of molecules in the three- and four-layer base unit. The results support the "asymmetric Clock model" as an appropriate description of the ferrielectric phases in this compound.

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PubMed2006

Structure and dynamics of chiral ferrielectric phases by deuteron NMR.

The results of studying angular dependent spectral parameters in a magnetic field are reported in the chiral smectic C phases of a smectogen 1-methylheptyl -(4-n-decyloxybenzoyloxy)-biphenyl-4-carboxylate. Our data provide direct evidence of a phase transition between two ferrielectric phases in this compound, viz. three-layer (SmC*(FiI)) and four-layer (SmC*(FiII)) superlattices. Simulation of spectral patterns of the methyl (C10) deuterons obtained after an aligned sample is rotated by 90 degrees in the magnetic field rules out the "clock model" for the three-layer and four-layer structures in these ferriphases. Instead, our data obtained under a magnetic field (9.4 T) seem to favor an "asymmetric clock model" for the interlayer packing. Interlayer jump rate is also obtained from the simulation of angular dependent spectra in these ferrielectric phases, and compared with those in the antiferroelectric SmC*(A) phase.

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PubMed2005

NMR study of orientational ordering in the chiral- phase of partially deuterated smectic liquid crystals.

Carbon-13 NMR spectroscopy is used to probe the orientational ordering in the tilted chiral smectic phase of two partially deuterated liquid crystals. Quantitative analyses of the chemical shifts of the aromatic carbons in the smectic- and - phases enable us to obtain the location of the long molecular axis of the core and the off-diagonal order parameter of the molecular core in the smectic- phase. The advantage of knowing the ordering information of these molecules in their mesophases from deuteron studies is demonstrated in this work, as they can be used to guide the assignments. The temperature behaviors of the chemical shifts from the aromatic sites in the helical structure of the smectic- phase is caused by both an increase of the tilt angle and a change in the orientation of the principal frame that describes the molecular ordering.

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PubMed2005

Headgroup motion in a lyotropic lamellar phase by deuterium and nitrogen-14 relaxation studies.

Deuterium (2H) and nitrogen-14 (14N) NMR spectroscopy were used to investigate the molecular dynamics of a lyotropic liquid crystal. Deuterium spectral densities of motion for the C1 deuterated site on the chain of the molecule decylammonium chloride (DACl) at the Larmor frequency 61.4 MHz and those for the (14)N at the headgroup (NH(3)(+)) at 28.9 MHz are analyzed quantitatively in the lamellar phase of the DACl-d(11)/water binary system to shed light on the headgroup dynamics. The motional model used is the small step rotational diffusion for reorientations plus internal rotations of the methylene group in the strong collision limit. The tumbling motion of the long axis of the DACl molecule in the aggregates seems to be as rigorous as the molecular spinning motion, likely due to the proposed motional model. The similarity of deuterium spectral densities from the C1 and C2/C3 sites may indicate a relatively rigid unit of C1-C2-C3 in the backbone.

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PubMed2005

Interlayer jump diffusion in the smectic-C*A phase by angular-dependent NMR study.

A detailed 2H nuclear magnetic resonance (NMR) study at 61.4 MHz of two chiral smectic C phases of a smectogen 10B1M7, one ferroelectric (SmC*) and the other antiferroelectric (SmC), is reported. Simulation of angular-dependent spectral patterns and/or signal intensities of the methyl deuterons are shown to provide information on the synclinic or anticlinic ordering, as well as the jump diffusion rates at different temperatures in the SmC phase. The molecular self-diffusion constant is determined to be in the range of 0.2-1.2 x 10(-14) m2/s over the temperature range of the SmC phase. Molecular self-diffusion in the SmC* phase should be faster, but remains undetectable by the present approach. Furthermore, the phase biaxiality in these phases is found to be vanishingly small. The critical magnetic field for unwinding the helical structure of 10B1M7 is found to be relatively high.

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PubMed2005

Chain dynamics in a chiral C phase by deuteron spin relaxation study.

Molecular reorientations and internal conformational transitions of an aligned chiral liquid crystal (LC) 10B1M7 are studied by means of deuterium spin-lattice relaxation in its smectic A (SmA) and smectic C* (SmC*) phase. The motional model which is applicable to uniaxial phases of many LCs is found to be adequate even when the phase is a tilted SmC* phase. The deuterium NMR spectrum in this phase cannot discern rotations of the molecular director about the pitch axis. The basic assumption is that the phase biaxiality is practically unobservable. However, the relaxation rates can be accounted for by the tilt angle between the molecular director and the layer normal in the SmC* phase. The tumbling motion appears to show a higher activation energy upon entering from the uniaxial SmA into the SmC* phase.

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PubMed2005

Orientational ordering of a bent-core mesogen by two-dimensional 13C NMR spectroscopy.

Various two-dimensional (2D) NMR techniques are reported on a bent-core mesogen 4,6-dichloro-1,3-phenylenebis[4'-(9-decenyloxy)-1,1'-biphenyl] carboxylate in its nematic and solid phases in order to unambiguously assign its carbon-13 NMR spectrum. The (13)C chemical shifts from the molecular core were studied as a function of temperature to extract its molecular geometry and orientational order tensor. To this end, the chemical shift anisotropy tensors of some carbon sites were measured in the solid state of this mesogen using a recent method called the separation of undistorted powder patterns by effortless recoupling (SUPER). The average bending angle subtended by the two arms of the bent-core structure is determined to be 148.7 degrees. The C-H dipolar couplings obtained from the separated local field (SLF) experiment for the aromatic rings are used to find the local order parameter tensors.

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PubMed2004

Structure and order of a homologous series of bent-core molecules: a 13C NMR study.

A carbon-13 NMR study in a series of bent-core (banana-shaped) molecules is reported. In 1, 3- phenylene bis[4'-alkenyloxy biphenyl]-4-carboxylate derivatives the position of the chlorine substituent(s) connected to the central phenyl ring and/or the terminal chain length of the compounds were varied. By analyzing the observed chemical shift anisotropies, the order parameters S and bending angles in their nematic phase are compared. The biphenyl moiety on each arm of the molecular core is found to form a nonzero twist angle.

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PubMed2002

Flow alignment in a shearing nematic liquid crystal near a charged surface.

The flow alignment angle theta(eff)(y) and effective rotational viscosity coefficient gamma(eff)1 are investigated for polar liquid crystals (LCs), such as 4-n-octyloxy-4'-cyanobiphenyl (8OCB), in the vicinity of a charged bounding surface. gamma(eff)1 and theta(eff)(y) are calculated, for the stationary regime, in the framework of the conventional Ericksen-Leslie theory. Calculations of gamma(eff)1, for the homeotropic alignment of 8OCB molecules, at a charged indium tin oxide-coated glass plate show an increase in gamma(eff)1 up to 7.8%.

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PubMed2002

Deuterium NMR relaxation in the smectic-A phase of a chiral smectogen.

Correlated internal rotations are studied for a deuterated decyloxy chain in the chiral liquid crystal, 1-methylheptyl 4(')-(4-n-decyloxy-benzoyloxy)biphenyl-4-carboxyate (10B1M7) using deuteron spin-lattice relaxation and quadrupolar splitting measurements. The present study is limited to the uniaxial smectic-A phase of 10B1M7, in which the observed deuterium nuclear magnetic resonance spectra show well-resolved peaks. The deuteron Zeeman (T(1Z)) and quadrupolar (T(1Q)) spin-lattice relaxation times are simultaneously determined for the methylene deuterons using the Wimperis broadband pulse sequence at two different Larmor frequencies. The quadrupolar splittings at each temperature are modeled by the additive potential method to obtain the orienting potential of mean torque. A decoupled model using 683 conformations for the decyloxy chain is used to explain the observed relaxation rates. In this model, the overall reorientation is described by a small step rotational diffusion model, while both gauche migration and gauche pair production as well as the so called one- and two-bond motions are allowed to occur in the chain. Transition rates for the chain dynamics and the overall rotational diffusion constants are obtained using a global target analysis of the relaxation data of 10B1M7.

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