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Amphiphiles, chiral molecular self-assembly

The monolayer in a multi-component system has been attracting attention from the viewpoints of fundamental understanding on molecular self-assembly [1], as well as its applications for surface modifiers [2], biosensing [3-5], photoswitching [6] and electrical devices [7]. In this system, whether amphiphilic molecules are miscible or immiscible in the monolayer is important for its properties. Therefore, a systematic tmder-standing on the phase separation mechanism in a mixed monolayer appears to be an essential step in the design and constmction of functionalized structures in the system. The phase separation in a monolayer state depends on many factors involving electrostatic interaction, molecular chirality and so on besides thermodynamic parameters such as the subphase temperature and surface pressure. Hence, for... [Pg.103]

Besides molecular shapes and amphiphilicity, chirality also has a large influence on LC self assembly, leading to series of LC phases with helical superstructures, reduced symmetry, and chirality induced frustration [43-46]. [Pg.9]

Figure 10 Self-assembled nanotubes can be obtained through a rolling mechanism (chiral molecular packing) or packing directly from the monomer. The structures of amphiphilic molecules used in nanotube formation (a) diacetylenic phospholipids, (b) diacetylenic N-aldonamides, (c, d, and e) glucose glycolipids, (f) sphingolipids, (g) glucophospholipid amphiphiles, (h) amphiphile with a serine head. R and R groups represent a variety of alkyl, alkenyl, or alkynyl groups. (Reproduced with permission from Ref. 52. The Chemical... Figure 10 Self-assembled nanotubes can be obtained through a rolling mechanism (chiral molecular packing) or packing directly from the monomer. The structures of amphiphilic molecules used in nanotube formation (a) diacetylenic phospholipids, (b) diacetylenic N-aldonamides, (c, d, and e) glucose glycolipids, (f) sphingolipids, (g) glucophospholipid amphiphiles, (h) amphiphile with a serine head. R and R groups represent a variety of alkyl, alkenyl, or alkynyl groups. (Reproduced with permission from Ref. 52. The Chemical...
The systems described above formed linearly extended, fibrous self-assemblies, although the morphological structures depended on amphiphiles. The molecular arrangement in fibers were maintained by the formation of concentric multilamellar bilayer, besides hydrophobic interaction and hydrogen bonding, except C Asp fibers with chiral character. The assemblies underwent temperature-dependent fibril-vesicle transition. The fibril-vesicle transition resulted from the rearrangement of bilayers. Generally, multilamellar layers were diminished in ves-... [Pg.66]


See other pages where Amphiphiles, chiral molecular self-assembly is mentioned: [Pg.169]    [Pg.285]    [Pg.302]    [Pg.133]    [Pg.142]    [Pg.49]    [Pg.319]    [Pg.4]    [Pg.523]    [Pg.538]    [Pg.173]    [Pg.21]    [Pg.2147]    [Pg.1535]    [Pg.558]    [Pg.64]    [Pg.86]    [Pg.180]    [Pg.36]   


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Amphiphiles self-assembly

Amphiphilic molecular assemblies

Chiral self-assembly

Chirality molecular

Molecular Self-Assembling

Molecular assemblies amphiphiles

Molecular self-assembly

Self-assembled amphiphiles

Self-assembled molecular

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