Chemical apparatus and process disinfecting – deodorizing – preser – Analyzer – structured indicator – or manipulative laboratory... – Means for analyzing liquid or solid sample
Reexamination Certificate
1998-07-31
2001-09-04
Celsa, Bennett (Department: 1627)
Chemical apparatus and process disinfecting, deodorizing, preser
Analyzer, structured indicator, or manipulative laboratory...
Means for analyzing liquid or solid sample
C422S051000, C422S051000, C422S068100, C422S082010, C435S004000, C435S007100, C435S007400, C435S007500, C436S004000, C436S501000, C436S524000, C436S528000, C436S805000
Reexamination Certificate
active
06284197
ABSTRACT:
FIELD OF THE INVENTION
This invention relates to devices containing liquid crystals which are optionally patterned. Also provided are methods of using these devices as sensors. More particularly, the present invention relates to liquid crystal devices for detecting the interaction an analyte to a recognition moiety that is contained within the device.
BACKGROUND OF THE INVENTION
Liquid crystals possess physical properties which are normally associated with both solids and liquids. Similar to fluids, the molecules in liquid crystals are free to diffuse about, however, a small degree of long range orientational and sometimes positional order is maintained causing the substance to be anisotropic as is typical of solids.
A vast array of organic and metal-containing substances exhibit liquid, crystallinity. A common feature of these molecules is either an elongated or flattened, somewhat inflexible molecular framework which is usually depicted as either cigar- or disk-shaped. The orientational and positional order in a liquid crystal phase is only partial, with the intermolecular forces striking a very delicate balance between attractive and repulsive forces. As a result, liquid crystals display an extraordinary sensitivity to external perturbations (e.g., temperature, pressure, electric and magnetic fields, shearing stress or foreign vapors).
The phenomenon of orientation, or anchoring, of liquid crystals by surfaces has been known nearly as long as have liquid crystals themselves. Anchoring of a liquid crystal by a surface fixes the mean orientation taken by the molecules with respect to the surface. This fixed direction is called the anchoring direction of the liquid crystal. A liquid population of mesogenic molecules can undergo a transition, between two or more anchoring directions, as a result of an external perturbation. Several anchoring transitions have been observed. These transitions involve a change in the orientation of the liquid crystal in the plane of the substrate which can be continuous or discontinuous. The transitions can be induced by a number of different perturbations, including the adsorption of foreign molecules. Such adsorption modifies the interface between the substrate and the liquid crystal, thereby inducing a “switching” between anchoring directions. See, Jerome, B; Shen, Y. R.,
Phys. Rev. E,
48:4556-4574 (1993) and Bechhoefer et al.,
Phase Transitions
33:227-36 (1991).
Past interest in the orientations assumed by liquid crystals near surfaces has been largely driven by their use in electrooptical devices such as flat-panel displays (FPDs). A goal of many studies has, therefore, been the development of methods for the fabrication of surfaces that uniformly orient liquid crystals over large areas. Future uses of liquid crystals in electrooptic devices, in contrast, will rely increasingly on liquid crystals with patterned orientations over small areas (Gibbons et al.
Appl. Phys. Lett.
65:2542 (1994); Bos et al.,
J. Soc. Inf. Disp.
3-4: 195 (1995); Morris et al.,
Emmel, Proc. Soc. Photo-Opt. Instrum. Eng.
2650, 112 (1996); Mural et al., ibid, 1665:230 (1992); Patel et al.,
Opt. Lett.
16:532 (1991); Zhang et al.,
J. Am. Chem. Soc.
114:1506 (1992); W. P. Parker,
Proc. Soc. Photo-Opt. Instrum. Eng.
2689:195 (1996)). For example, light can be diffracted or redirected by using patterned mesogenic layer structures that are tuned by application of a uniform electric field (W. P. Parker,
Proc. Soc. Photo-Opt. Instrum. Eng.
2689:195 (1996)), and FPDs with wide viewing angles and broad gray scales can be fabricated by using pixels that are divided into subpixels, where each sub-pixel is defined by a different orientation of the liquid crystal (Schadt et al.,
Nature
381:212 (1996)). Methods capable of patterning mesogenic layers on curved surfaces are also required for the development of new types of tunable electrooptic mesogenic layer devices, including devices that combine the diffraction of light from the patterned mesogenic layer structure with the refraction of light at the curved surface (Resler et al.,
Opt. Lett.
21:689 (1996); S. M. Ebstein, ibid, p.1454; M. B. Stem,
Microelectron. Eng.
32:369 (1996): Goto et al.,
Jpn. J. Appl. Phys.
31:1586 (1992); Magiera et al.,
Soc. PhotoOpt. Instrum. Eng.,
2774:204(1996)).
Current procedures for the fabrication of patterned mesogenic layer structures use either spatially nonuniform electric fields from patterned electrodes or patterned “anchoring” surfaces. Fringing of electric fields from patterned electrodes prevents high-resolution patterning of mesogenic layers by this method (Gibbons et al.
Appl. Phys. Lett.
65:2542 (1994); Williams et al.,
Proc. Soc. PhotoOpt. Instrum. Eng.
1168:352 (1989)).
Patterned anchoring surfaces have been prepared by using mechanical rubbing of spin-coated polymer films, photolithographic masking, and a second rubbing step performed in a direction orthogonal to the first (Patel et al.,
Opt. Lett.
16:532 (1991); W. P. Parker,
Proc. Soc. Photo-Opt. Instrum. Eng.
2689:195 (1996); Chen et al.,
Appl. Phys. Lett.
67:2588 (1995)). This method of patterning mesogenic layers on surfaces is complex and suffers from the disadvantages of rubbing-based methods, such as the generation of dust and static charge. Recently developed photo-alignment techniques for orienting mesogenic layers provide promising alternatives (Gibbons et al.
Appl. Phys. Lett.
65:2542 (1994); Schadt et al.,
Nature
381:212 (1996); Chen et al.,
Appl. Phys. Lett.
68:885 (1996); Gibbons et al.,
Nature
351:49 (1991); Gibbons et al., ibid 377:43 (1995); Shannon et al. 368:532 (1994); Ikeda et al.,
Science
268:1873 (1995); Schadt et al.,
Jpn. J. Appl. Phys.
34:3240.(1995)). However, because light-based methods generally require surfaces to be spin-coated by uniformly thin films of photopolymer, and because the orientations of mesogenic layers on photo-aligned surfaces are determined by the angle of incidence of the light used for alignment, these methods are not easily applied to the patterning of mesogenic layers on nonplanar surfaces.
The methods of the present invention permit fabrication of complex mesogenic layer structures in two simple processing steps. Surfaces can be patterned with regions of mesogenic layers that differ in shape and have sizes ranging from micrometers to centimeters. The mesogenic layers can also be patterned on nonplanar surfaces (mesogenic layers have been anchored within pores of alumina and vycor glass coated with surface-active reagents, Crawford. et al.
Phys. Rev. E
53:3647 (1996), and references therein). The present invention differs from this past work in two principal ways. (i) Scale: Mesogenic layers have been anchored on curved surfaces with radii of curvature that are large compared with the thickness, of the mesogenic layer. The local state of the mesogenic layer is similar to that of mesogenic layers anchored on a planar surface and thus properties of the mesogenic layer are not dominated by elastic energies caused by curvature. Methodologies used for anchoring mesogenic layers on planar surfaces (for example, twisted nematic cells) can be translated to our curved surfaces; and (ii) Patterns: The methods of the invention allow the formation of patterned curved surfaces.
Self-assembled monolayers formed by the chemisorption of alkanethiols on gold are likely to now be the most intensively characterized synthetic organic monolayers prepared to date. See, Ulman, A., 1991,
An Introduction to Ultrathin Organic Films: From Langmuir-Blodgett to Self Assembly
(San Diego, Calif.: Academic Press); Dubois, L. H. et al., 1992,
Annu. Rev. Phys. Chem.,
43, 437. These monolayers form spontaneously during immersion of evaporated films of gold in solutions of alkanethiols as a result of chemisorption of sulfur on the (111) textured surface of the films. The molecules self-organize into a commensurate
—
3×
—
3R30° lattice on the surface of the Au(111). See, “Porter, M. D. 1987,
J. Am. Chem. Soc.,
109, 3559; Camillone III, N. et al., 1993,
Chem.
Abbott Nicholas L.
Dubrovsky Timothy B.
Gupta Vinay K.
Shah Rahul
Skaife Justin J.
Celsa Bennett
The Regents of the University of California
Townsend and Townsend / and Crew LLP
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