Lyotropic liquid crystal

A liquid crystalline mesophase is called lyotropic (a portmanteau of lyo- "dissolve" and -tropic "change" ) if formed by dissolving an amphiphilic mesogen in a suitable solvent, under appropriate conditions of concentration, temperature and pressure.[1] [2] A mixture of soap and water is an everyday example of a lyotropic liquid crystal.

A highly viscous cubic phase gel made of polysorbate 80, water, and liquid paraffin.

Historically, the term was used to describe the common behavior of materials composed of amphiphilic molecules upon the addition of a solvent. Such molecules comprise a water-loving hydrophilic head-group (which may be ionic or non-ionic) attached to a water-hating, hydrophobic group.

The micro-phase segregation of two incompatible components on a nanometer scale results in different type of solvent-induced extended anisotropic[3] arrangement, depending on the volume balances between the hydrophilic part and hydrophobic part. In turn, they generate the long-range order of the phases, with the solvent molecules filling the space around the compounds to provide fluidity to the system.[4]

In contrast to thermotropic liquid crystals, lyotropic liquid crystals have therefore an additional degree of freedom, that is the concentration that enables them to induce a variety of different phases. As the concentration of amphiphilic molecules is increased, several different type of lyotropic liquid crystal structures occur in solution. Each of these different types has a different extent of molecular ordering within the solvent matrix, from spherical micelles to larger cylinders, aligned cylinders and even bilayered and multiwalled aggregates.[5]

Types of lyotropic systems

Examples of amphiphilic compounds are the salts of fatty acids, phospholipids. Many simple amphiphiles are used as detergents. A mixture of soap and water is an everyday example of a lyotropic liquid crystal.

Biological structures such as fibrous proteins showings relatively long and well-defined hydrophobic and hydrophilic ‘‘blocks’’ of aminoacids can also show lyotropic liquid crystalline behaviour.[6]

Amphiphile self-assembly

A typical amphiphilic flexible surfactant can form aggregates through a self-assembly process that results of specific interactions between the molecules of the amphiphilic mesogen and those of the non-mesogenic solvent.

In aqueous media, the driving force of the aggregation is the "hydrophobic effect". The aggregates formed by amphiphilic molecules are characterised by structures in which the hydrophilic head-groups expose their surface to aqueous solution, shielding the hydrophobic chains from contact with water.

For most lyotropic systems aggregation occurs only when the concentration of the amphiphile exceeds a critical concentration (known variously as the critical micelle concentration (CMC) or the critical aggregation concentration (CAC)).

At very low amphiphile concentration, the molecules will be dispersed randomly without any ordering. At slightly higher (but still low) concentration, above the CMC, self-assembled amphiphile aggregates exist as independent entities in equilibrium with monomeric amphiphiles in solution, but with no long ranged orientational or positional (translational) order. As a result, phases are isotropic (i.e. not liquid crystalline). These dispersions are generally referred to as 'micellar solutions', often denoted by the symbol L1, while the constituent spherical aggregates are known as 'micelles'.

At higher concentration, the assemblies will become ordered. True lyotropic liquid crystalline phases are formed as the concentration of amphiphile in water is increased beyond the point where the micellar aggregates are forced to be disposed regularly in space. For amphiphiles that consist of a single hydrocarbon chain the concentration at which the first liquid crystalline phases are formed is typically in the range 25–30 wt%.

Liquid crystalline phases and composition/temperature

The simplest liquid crystalline phase that is formed by spherical micelles is the 'micellar cubic', denoted by the symbol I1. This is a highly viscous, optically isotropic phase in which the micelles are arranged on a cubic lattice. At higher amphiphile concentrations the micelles fuse to form cylindrical aggregates of indefinite length, and these cylinders are arranged on a long-ranged hexagonal lattice. This lyotropic liquid crystalline phase is known as the 'hexagonal phase', or more specifically the 'normal topology' hexagonal phase and is generally denoted by the symbol HI.

At higher concentrations of amphiphile the 'lamellar phase' is formed. This phase is denoted by the symbol Lα and can be considered the lyotropic equivalent of a smectic A mesophase.[1] This phase consists of amphiphilic molecules arranged in bilayer sheets separated by layers of water. Each bilayer is a prototype of the arrangement of lipids in cell membranes.

For most amphiphiles that consist of a single hydrocarbon chain, one or more phases having complex architectures are formed at concentrations that are intermediate between those required to form a hexagonal phase and those that lead to the formation of a lamellar phase. Often this intermediate phase is a bicontinuous cubic phase.

Schematic showing the aggregation of amphiphiles into micelles and then into lyotropic liquid crystalline phases as a function of amphiphile concentration and of temperature.

In principle, increasing the amphiphile concentration beyond the point where lamellar phases are formed would lead to the formation of the inverse topology lyotropic phases, namely the inverse cubic phases, the inverse hexagonal columnar phase (columns of water encapsulated by amphiphiles, (HII) and the inverse micellar cubic phase (a bulk liquid crystal sample with spherical water cavities). In practice inverse topology phases are more readily formed by amphiphiles that have at least two hydrocarbon chains attached to a headgroup. The most abundant phospholipids that are found in cell membranes of mammalian cells are examples of amphiphiles that readily form inverse topology lyotropic phases.

Even within the same phases, self-assembled structures are tunable by the concentration: For example, in lamellar phases, the layer distances increase with the solvent volume. Since lyotropic liquid crystals rely on a subtle balance of intermolecular interactions, it is more difficult to analyze their structures and properties than those of thermotropic liquid crystals.

The objects created by the amphiphiles are usually spherical (as in the case of micelles), but may also be disc-like (bicelles), rod-like, or biaxial (all three micelle axes are distinct). These anisotropic self-assembled nano-structures can then order themselves in much the same way as thermotropic liquid crystals do, forming large-scale versions of all the thermotropic phases (such as a nematic phase of rod-shaped micelles).

Host molecules

It is possible that specific molecules are dissolved in lyotropic mesophases, where they can be located mainly inside, outside, or at the surface of the aggregates.

Some of such molecules act as dopants, inducing specific properties to the whole phase, other ones can be considered simple guests with limited effect on the surrounding environment but possibly strong consequences on their physico-chemical properties, and some of them are used as probe to detect molecular-level properties of the whole mesophase in specific analytical techniques.[7]

Rod-like macromolecules

The term lyotropic has also been applied to the liquid crystalline phases that are formed by certain polymeric materials, particularly those consisting of rigid rod-like macromolecules, when they are mixed with appropriate solvents.[8] Examples are suspensions of rod-like viruses such as the Tobacco Mosaic Virus as well as man-made colloidal suspensions of non-spherical colloidal particles. Cellulose and cellulose derivatives form lyotropic liquid crystal phases as do nanocrystalline ( nanocellulose ) suspensions. [9] Other examples include DNA and Kevlar, which dissolve in sulfuric acid to give a lyotropic phase. It is noted that in these cases the solvent acts to lower the melting point of the materials thereby enabling the liquid crystalline phases to be accessible. These liquid crystalline phases are closer in architecture to thermotropic liquid crystalline phases than to the conventional lyotropic phases. In contrast to the behaviour of amphiphilic molecules, the lyotropic behaviour of the rod-like molecules does not involve self-assembly.

References
  1. Baron, M. (2003). "Definitions of Basic Terms Relating to Low-Molar-Mass and Polymer LIQUID CRYSTALS (IUPAC Recommendations 2001)". Pure Appl. Chem. 73 (5): 845–895. doi:10.1351/pac200173050845.
  2. Self-Assembled Supramolecular Architectures: Lyotropic Liquid Crystals N. Garti, P. Somasundaran, R. Mezzenga, Eds, Wiley 2012 https://onlinelibrary.wiley.com/doi/book/10.1002/9781118336632
  3. Lagerwall, Jan P.F.; Giesselmann, Frank (2006). "Current Topics in Smectic Liquid Crystal Research". ChemPhysChem. 7 (1): 20–45. doi:10.1002/cphc.200500472. PMID 16404767.
  4. Qizhen Liang; Pengtao Liu; Cheng Liu; Xigao Jian; Dingyi Hong; Yang Li. (2005). "Synthesis and Properties of Lyotropic Liquid Crystalline Copolyamides Containing Phthalazinone Moieties and Ether Linkages". Polymer. 46 (16): 6258–6265. doi:10.1016/j.polymer.2005.05.059.
  5. Lewis 2006, pp. 194
  6. Lewis 2006, pp. 191
  7. Domenici, Valentina; Marchetti, Alessandro; Cifelli, Mario; Veracini, Carlo Alberto (2009). "Dynamics of Partially Oriented L-Phenylalanine-d8 in the CsPFO/H2O Lyotropic System via 2H NMR Relaxation Studies". Langmuir. 25 (23): 13581–13590. doi:10.1021/la901917m.
  8. Blumstein, Alexandre, ed. (1985). Polymeric Liquid Crystals. Springer US. doi:10.1007/978-1-4899-2299-1. ISBN 978-1-4899-2301-1.
  9. Klemm, Dieter; Kramer, Frederike; Moritz, Sebastian; Lindstrom, Tom; Ankerfors, Mikael; Gray, Derek; Dorris, Annie (2011). "Nanocellulose:A New Family of Nature-Based Materials". Angewandte Chemie International Edition. 50 (24): 5438–5466. doi:10.1002/anie.201001273. PMID 21598362.

Bibliography
  • Laughlin R.G. (1996). The Aqueous Phase Behaviour of Surfactants. London: Academic Press. ISBN 0-12-437760-2.
  • Fennell Evans D. and Wennerström H. (1999). The Colloidal Domain. New York: Wiley VCH. ISBN 0-471-24247-0.
  • Jin, Hyoung-Joon; Park, Jaehyung; Valluzi, Regina; Kim, Ung-Jin; Cebe, Peggy; Kaplan, David L. (2006). "Bioprocessing of Silk Proteins Controlling Assembly". In Lewis, Randolph V.; Renugopalakrishnan, V. (eds.). Bionanotechnology. Protein to Nanodevices. Springer. ISBN 978-1-4020-4219-5.
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