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1                                              Lyotropic aggregation of rhodoxanthin (E/Z)-isomer mixtu
2 (E/Z)-ratios by thermal (E/Z)-isomerization, lyotropic aggregation, and two different formulation tec
3  structures that exhibit thermotropic and/or lyotropic behavior.
4 derivative capable of self-assembling into a lyotropic chiral nematic phase in aqueous solution.
5 s are carried out using Sunset Yellow FCF, a lyotropic chromonic LC with a small twist elastic consta
6 orphology, and deposition patterns of drying lyotropic chromonic liquid crystal droplets.
7                                In this work, lyotropic chromonic liquid crystals (LCLCs) are confined
8 nd templating has been demonstrated by using lyotropic chromonic liquid crystals (LCLCs) as these mat
9 ent measurements of the elastic constants in lyotropic chromonic liquid crystals (LCLCs) have reveale
10 r growth, the intrinsic tumbling behavior of lyotropic chromonic liquid crystals can be suppressed, w
11                              Achiral nematic lyotropic chromonic liquid crystals have been reported t
12                 However, upon confinement of lyotropic chromonic liquid crystals in cylindrical geome
13 rticles in linear defects-disclinations in a lyotropic colloidal cholesteric liquid crystal: a contin
14                                  Thus, these lyotropic DDQCs are long-lived metastable morphologies,
15 celles into previously unrecognized, aqueous lyotropic dodecagonal quasicrystals (DDQCs), which exhib
16 inued susceptibility to LOR (associated with lyotropic formation of the hexagonal II phase) and assoc
17 interfacial water within a "normal" (Type I) lyotropic gyroid phase formed by a gemini dicarboxylate
18 icelles and cylinders up to the formation of lyotropic hexagonal or lamellar phases results from coop
19  aspartate, chloride, etc., produce a marked lyotropic (Hofmeister) effect on the repetitive structur
20    This material is based on a polymerizable lyotropic (i.e., amphiphilic) liquid crystal (1) that fo
21  mesogenic properties, both thermotropic and lyotropic (in DMF) mesophases were observed in one of me
22 ces self-assembly into both thermotropic and lyotropic lamellar liquid crystalline (LC) phases.
23 d bacteria when swimming in solutions of the lyotropic LC disodium cromoglycate (DSCG).
24 lue phases, achiral bent-core LCs, etc.) and lyotropic LCs (DNA LCs, nanocellulose LCs, and graphene
25 patterning, templating, and when extended to lyotropic LCs, a process leading to uniform-sized spheri
26  of azobenzene photosurfactants (AzoPS) into lyotropic liquid crystal (LLC) phases, which are explore
27                                          The lyotropic liquid crystal (LLC) systems consist of amphip
28 r concentration, the helical polymer forms a lyotropic liquid crystal (LLC) that further orients unid
29            The antibiotic squalamine forms a lyotropic liquid crystal at very low concentrations in w
30          The mechanical strengthening of the lyotropic liquid crystal by the two-tailed 1,2-dioleoyl-
31                                 The obtained lyotropic liquid crystal engineering design rules can be
32  of gas (CO(2)) diffusion across a prototype lyotropic liquid crystal membrane.
33       Here we show that topologically-active lyotropic liquid crystal nanoparticles (LCNPs) can trigg
34 media, the vast majority have supported some lyotropic liquid crystal phase formation.
35  We focus upon the generation of 'dilutable' lyotropic liquid crystal phases with two- and three-dime
36 ation of this unique class of nonamphiphilic lyotropic liquid crystal shares enormous similarity to t
37                                          The lyotropic liquid crystal state formed by these polymers
38      Thus, we have experimentally realized a lyotropic liquid crystal system that can be truly engine
39 l of polystyrene nanosphere templates from a lyotropic liquid crystal-templated silica sol-gel matrix
40 hat combines living swimming bacteria with a lyotropic liquid crystal.
41  strength of the cubic-phase monoolein/water lyotropic liquid crystal.
42  fraction, dispersed polymer nanofibers form lyotropic liquid crystalline (LC) mesophases with comple
43 ollable, rapid, and continuous production of lyotropic liquid crystalline (LLC) nanoparticles (both c
44 pack into a previously unknown, low-symmetry lyotropic liquid crystalline Frank-Kasper sigma phase.
45                                  Lipid based lyotropic liquid crystalline mesophases have demonstrate
46 remarkable array of tunable and pH-sensitive lyotropic liquid crystalline mesophases including the in
47                       Ordered nanostructured lyotropic liquid crystalline mesophases may form in sele
48  in modulating the biophysical properties of lyotropic liquid crystalline nano-self-assemblies.
49     Here we have engineered highly sensitive lyotropic liquid crystalline nanoparticles that reversib
50 s electrodeposited from the hexagonal (H(I)) lyotropic liquid crystalline phase are shown to be excel
51                 We report the discovery of a lyotropic liquid crystalline phase based on a 3-D hexago
52 tion, suspensions were prepared in which the lyotropic liquid crystalline phase behavior of the hybri
53 the metal, in the simultaneous presence of a lyotropic liquid crystalline phase of nonionic surfactan
54 chemically deposited from the hexagonal (H1) lyotropic liquid crystalline phase of the nonionic surfa
55            It is based on the formation of a lyotropic liquid crystalline phase on the surface of the
56 round a prolate ellipsoidal type I hexagonal lyotropic liquid crystalline phase.
57 iquid interface, similar to the formation of lyotropic liquid crystalline phases by common surfactant
58   The outstanding diverse functionalities of lyotropic liquid crystalline phases found in nature and
59                                    They form lyotropic liquid crystalline phases in helicogenic solve
60         These copolymers form uncrosslinked, lyotropic liquid crystalline phases of large micelles be
61 he formation of the known classes of lipidic lyotropic liquid crystalline phases, their structure, an
62  the high mesogen concentration required for lyotropic liquid crystalline spinning.
63 dition of the acidic lipid component to this lyotropic liquid crystalline system reduces its range of
64                      The water solubility of lyotropic liquid crystals (LCs) makes them very attracti
65 rmed of thermodynamically stable cubic phase lyotropic liquid crystals (LLCs) could replace the prese
66                                              Lyotropic liquid crystals (LLCs) have well-defined inter
67 nts of the elastic constants in the micellar lyotropic liquid crystals (LLCs) that are formed by surf
68 ree most common bicontinuous cubic phases in lyotropic liquid crystals and block copolymers.
69  mesophase transition at room temperature in lyotropic liquid crystals constructed from arylazopyrazo
70 monium chloride micelles for the assembly of lyotropic liquid crystals generates new structural compl
71 l evaluation, and therapeutic application of lyotropic liquid crystals in the field of parenteral sus
72 ueous interconnected networks of cubic-phase lyotropic liquid crystals, urate permeates only through
73 to engineer a potentially rich assortment of lyotropic liquid crystals.
74 ilding blocks of both micellar and chromonic lyotropic liquid crystals.
75                            The synthesis and lyotropic liquid-crystalline (LLC) phase behavior of a h
76                                 The aqueous, lyotropic liquid-crystalline phase behavior of the alpha
77 PtGeQ and C(n)PyPtSnSe were templated by the lyotropic liquid-crystalline phase of alkylpyridinium su
78                This is the first new inverse lyotropic liquid-crystalline phase to be reported for tw
79  first use of magnetic-alignment behavior of lyotropic liquid-crystalline polymer macro-nanodiscs (>2
80          Achieving control and tunability of lyotropic materials has been a long-standing goal of liq
81 , and contrary to what is perceived for soft lyotropic materials in general, the self-assembly method
82 ugh liquid-liquid phase separation (LLPS) of lyotropic mesophases from isotropic solutions upon a con
83  mainly (2)H 1D/2D-NMR in chiral polypeptide lyotropic mesophases, are presented and analyzed.
84 sses) in the presence of molecular porogens, lyotropic mesophases, supramolecular architectures, emul
85                                              Lyotropic mesophases, where membranes conform to periodi
86 o assemble into high-aspect ratio (>10(3) ), lyotropic nanotubes in the presence of excess acid.
87                                         This lyotropic nematic exhibited the slowest dielectric relax
88 crostructures of reduced graphene oxide in a lyotropic nematic liquid crystal of graphene oxide flake
89 eter of 10 mum, dispersed in water, formed a lyotropic nematic liquid crystal phase.
90 re traditionally classified as thermotropic, lyotropic or polymeric, based on the stimulus that gover
91 hat poly(norbornene) BBPs exhibit long-range lyotropic ordering as a result of their rodlike characte
92 the lack of rigidity necessary to access the lyotropic ordering that underpins the formation of colla
93 OR15amr and COR6.6r on the cryostability and lyotropic phase behavior of liposomes are examined.
94 ll quaternary mixtures showed highly regular lyotropic phase behavior with the same sequence of phase
95                                          The lyotropic phase behaviour of model lipid systems that de
96 ported for two decades and is the only known lyotropic phase whose structure consists of a close pack
97 ction of the fatty acid with ozone, and that lyotropic-phase formation also occurs in more complex mi
98                              We suggest that lyotropic-phase formation likely occurs in the atmospher
99 centrations of water and surfactant in these lyotropic phases also triggers formation of the related
100 el of the uncharged lipid displays the usual lyotropic phases as a function of the relative volume fr
101  self-assembly (PISA) can be used to prepare lyotropic phases comprising diblock copolymer nano-objec
102 ate that the droplets contained crystal-like lyotropic phases including hexagonal and cubic close-pac
103                                              Lyotropic polymer liquid crystals are unique systems for
104 s, which, moreover, exhibit viscoelastic and lyotropic properties.
105 hich forms 2.3 nm diameter water channels by lyotropic self-assembly.
106       The influence of select salts from the lyotropic series (NH(4)Cl, KCl, NaCl, MgCl(2), CaCl(2),
107 e expect an ion's position in the Hofmeister lyotropic series to be determined by a combination of dr
108 e guanidinium cation effect according to the lyotropic series.
109 h layered materials such as thermotropic and lyotropic smectic liquid crystals and block copolymers.
110                        This is unusual for a lyotropic system, where flexibility typically destabiliz
111                     Such phases are found in lyotropic systems (for example, lipid-water, soap-water)
112 e transition temperatures of other lipid and lyotropic systems.

 
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