Abstract: The invention provides composite nanofiltration membranes (FIG. 5) with lyotropic liquid crystal (LLC) polymer porous membranes (30) attached to a porous support (20). The LLC membranes are prepared from LLC monomers which form the inverted hexagonal or bicontinuous cubic phase. The arrangement, size, and chemical properties of the pores can be tailored on the molecular level. The composite membrane of the invention is useful for separation processes involving aqueous and nonaqueous solutions as well as gases. Methods for making and using the composite nanofiltration membranes of the inventions are also provided.

Abstract: The invention provides composite nanofiltration membranes with a lyotropic liquid crystal (LLC) polymer composition embedded in or forming a layer on a porous support. The LLC membranes are prepared from LLC monomers which form a bicontinuous cubic (QI) phase. The arrangement, size, and chemical properties of the pores can be tailored on the molecular level. The composite membranes of the invention are useful for separation processes involving aqueous and nonaqueous solutions as well as gases. Methods for making and using the composite nanofiltration membranes of the invention are also provided.

Abstract: The invention provides heteroaryl salts and methods for producing the same. In particular, the invention provides heteroaryl salts of the formula: and methods for producing the same, where M, a, X1, X2, X3, and X4 are those defined herein.

Abstract: The invention provides cross-linked lyotropic liquid crystal (LLC) copolymers having ordered nanometer-sized pores lined with functional groups. The copolymers are formed by copolymerizing LLC monomers with strong LLC character and functionalized monomers with no or weak LLC character to form an LLC phase. Both the LLC monomers and the functionalized monomers contain hydrogen-bonding groups and hydrogen-bonding is believed to assist in the formation of the LLC phase of the blended mixture. Different classes of functional groups useful for the invention include, but are not limited to, acidic groups, basic groups, catalytic groups, oxidizing agents, reducing agents, polymerization initiators, binding agents, optically active groups, and electrically active groups. The invention also provides methods for making the cross-linked LLC copolymers of the invention.

Abstract: A method and device for storing and dispensing a fluid includes providing a vessel configured for selective dispensing of the fluid therefrom. Provided within a vessel is a nanocomposite material comprising an imidazolium surfactant and an integral solvent that is essential to the formation of the nanocomposite material. The fluid is contacted with the nanocomposite material for take-up of the fluid by the polymerized nanocomposite material. The fluid is released from the nanocomposite material and dispensed from the vessel.

Abstract: A method for synthesizing composites with architectural control on the nanometer scale is described. A polymerizable lyotropic liquid-crystalline monomer is used to form an inverse hexagonal phase in the presence of a second polymer precursor solution. The monomer system acts as an organic template, providing the underlying matrix and order of the composite system. Polymerization of the template in the presence of an optional cross-linking agent with retention of the liquid-crystalline order is carried out followed by a second polymerization of the second polymer precursor within the channels of the polymer template to provide an ordered nanocomposite material.

Abstract: The monomer cis-5,6-bis(trimethylsiloxy)-1,3-cyclohexadiene can be polymerized with certain catalysts, such as bis(allyltrifluoroacetato nickel (II)) and bis(allylpentafluorophenoxy nickel II). The resulting polymer is a precursor to poly(para-phenylene). Other substituted cyclohexadienes may also be polymerized by these catalysts to form useful polymers.

Abstract: The monomer cis-5,6-bis(trimethylsiloxy)-1,3-cyclohexadiene can be polymerized with certain nickel II catalysts, such as bis[(allyl)trifluoroacetatonickel(II)], bis[(allyl)pentafluorophenoxynickel(II)], and bis[(allyl)iodonickel(II)]. The resulting polymer is a precursor to poly(para-phenylene). Other substituted cyclohexadienes may also be polymerized by these catalysts to form useful polymers.

Abstract: The monomer cis-5,6-bis(trimethylsiloxy)-1,3-cyclohexadiene can be polymerized with certain catalysts, such as bis(allyltrifluoroacetato nickel (II) and bis(allylpentafluorophenoxy nickel II). The resulting polymer is a precursor to poly(para-phenylene). Other substituted cyclohexadienes may also be polymerized by these catalysts to form useful polymers.

Abstract: The monomer cis-5,6-bis(trimethylsiloxy)-1,3-cyclohexadiene can be polymerized with certain nickel II catalysts, such as bis[(ally)trifluoroacetatonickel(II)], bis[(allyl)pentafluorophenoxynickel(II)], and bis[(allyl)iodonickel(II)]. The resulting polymer is a precursor to poly(para-phenylene). Other substituted cyclohexadienes may also be polymerized by these catalysts to form useful polymers.