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  • 1995-1999  (4)
  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 5012-5028 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report on a new, more precise structural characterization of n-octadecane thiol monolayer self-assembled on the UHV-prepared Au(001) surface using a combination of helium atom diffraction, grazing incidence x-ray diffraction, and x-ray reflectivity measurements. Our results show that the equilibrated alkane chains form a two dimensional distorted hexagonal structure with lattice constants a=5.77±0.06 A(ring), b=4.81±0.02 A(ring), and α=53.1±0.46°. The alkane chains are tilted 33.5±1.0° from the surface normal and the tilt direction is ∼6.8±1.0° away from the elongated next-nearest-neighbor direction. The Au–thiol interface is found to have an unusual p(1×4) structure formed by an excess of Au atoms, which are believed to be produced in the dereconstruction process of the clean hexagonal Au(001) surface during the chemisorption of thiols. We propose that this Au interfacial layer modulates the height of the alkane chains resulting in a highly corrugated top surface, which forms a c(2×8) structure as observed by atom diffraction. These structural findings reveal a novel interplay between the head group/substrate interaction and the interchain van der Waals interaction which determines not only the alkane chain packing but also the structure of the interfacial layer of the substrate. Our studies also demonstrate that rich, complementary structural information can be obtained about the topmost surface, the chain packing, the interface arrangement, and the substrate of this and similar systems by the combination of atomic beam and synchrotron x-ray characterization techniques. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 2456-2462 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The morphologies of several styrene–isoprene miktoarm star copolymers have been examined by small angle x-ray scattering and electron microscopy. Three of these polymers were of the three-armed A2B type, and six were four-armed A3B miktoarms. The ordered microphase-separated morphologies displayed by these polymers were seen to be highly dependent on the architecture of the chains, and were quite different from those that occur in the corresponding linear block copolymers. These results can be quite well explained by a theory of Milner which is based on the bending energy of the microphase interface and the ability of the chains to stretch away from the interface between the microphases. We speculate that the small differences between the observations and theoretical predictions are due to the effects of the compression of chains in small gaps between adjacent domains. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 16 (1995), S. 299-307 
    ISSN: 1572-9567
    Keywords: confinement ; SFA ; Surface Forces Aparatus ; X-Ray Surface Forces Apparatus ; XSFA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We describe the newly invented X-Ray Surface Forces Apparatus (X-SFA) which allows the simultaneous measurement of forces and collective structures of confined complex fluids under static and flow conditions. The structure of the smectic liquid crystal 8CB (4-cyano-4′-octylbiphenyl) f confined between two mica surfaces with separation ranging from 4000 to 20,000 A was measured. At small gaps and no shear, the smectic layers take on distinct stable orientations, including the bulk forbidden “h” orientation. which persist under low shear ( $$\dot \gamma $$ ⩽ 30 s−1). However, at higher shear rates $$\dot \gamma $$ ⩽ 360 s−1) the shear acts to dramatically order and align the smectic layers into a single“a” orientation.
    Type of Medium: Electronic Resource
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