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    • 3. 发明申请
    • NEW CLASS OF HIGH HYPERPOLARIZABILITY ORGANIC CHROMOPHORES AND PROCESS FOR SYNTHESIZING THE SAME
    • 新型超高灵敏度有机色素及其合成方法
    • WO0009613A2
    • 2000-02-24
    • PCT/US9916274
    • 1999-07-26
    • PACIFIC WAVE IND INC
    • DALTON LARRY RFETTERMAN HAROLD RWANG FANGSTEIER WILLIAMHARPER AARON WREN ALBERT SMICHAEL JOSEPH
    • C08K5/00C09B23/01C09B23/14C09B
    • C08K5/0041C09B23/0066C09B23/0075C09B23/0091C09B23/145
    • A new class of high hyperpolarizability organic chromophores and a process for synthesizing the same. The chromophores incorporate at least one organic substituent and are formed in consideration of molecular shapes and a spatial anisotropy of intermolecular interactions. The chromophores are processed into hardened material lattices to lock-in poling induced electric-optic activity. Preferred organic substituents are alkyl, aryl, and isophorone groups. A composite including the organic chromophore, in a preferred embodiment, includes a polymer such as a poly(methylmethacrylate), polyimide, polyamic acid, polystyrene, polycarbonate or polyurethane. The optimized chromophores result in hardened electro-optic polymers suitable for electro-optic modulators and other devices such as optical switches. These modulators can be configured to work at high frequencies and in arrays for applications in communications and network connections. In addition, they can be implemented in series and parallel combinations in phased array radar, signal processing and sensor technology applications.
    • 一类新的超超极化有机发色团及其合成方法。 考虑到分子形状和分子间相互作用的空间各向异性,发色团引入至少一个有机取代基并形成。 发色团被加工成硬化材料晶格以锁定极化诱导的电光活动。 优选的有机取代基是烷基,芳基和异佛尔酮基团。 在优选的实施方式中,包含有机发色团的复合物包括聚合物如聚(甲基丙烯酸甲酯),聚酰亚胺,聚酰胺酸,聚苯乙烯,聚碳酸酯或聚氨酯。 优化的发色团产生适用于电光调制器和其他设备(如光开关)的硬化电光聚合物。 这些调制器可以配置为工作在高频和阵列中,用于通信和网络连接的应用。 另外,它们可以在相控阵雷达,信号处理和传感器技术应用中以串联和并联组合方式实施。
    • 5. 发明专利
    • Ultraminiature fiber optic pressure transducer and method of fabrication
    • AU3462901A
    • 2001-08-14
    • AU3462901
    • 2001-01-29
    • PACIFIC WAVE IND INC
    • FETTERMAN HAROLD RBUKSHPUN LEONIDMICHAEL JOSEPH
    • A61B5/00A61B5/0215A61B5/03G01L9/00A61B5/02G01L7/08
    • A method of batch fabrication of ultraminiature fiber optic pressure transducers including the steps of: providing a first substrate with a first sacrificial layer formed thereover; forming a plurality of light reflective diaphragm structures on the first sacrificial layer; forming a plurality of fiber stopper structures on the light reflective diaphragm structures; forming a plurality of fiber alignment cavity structures on the fiber stopper structures, the light reflective diaphragm structures, fiber stopper structures and fiber alignment cavity structures providing a plurality of fiber alignment assemblies; providing a second substrate with a second sacrificial layer formed thereover; forming a plurality of ferrule structures over the second sacrificial layer; inputting a plurality of fibers into the ferrule structures and sealing each of the ferrule structures to the fiber inserted therein, the ferrule structures and the fibers providing a plurality of fiber-ferrule assemblies; etching the second sacrificial layer releasing the fiber-ferrule assemblies; inputting the fiber-ferrule assemblies into the fiber alignment assemblies and sealing each of the fiber alignment assemblies to the fiber-ferrule assembly inserted therein, the fiber alignment assemblies and the fiber-ferrule assemblies providing a plurality of fiber optic pressure transducers; and etching the first sacrificial layer releasing the fiber optic pressure transducers.
    • 6. 发明专利
    • Polymers containing polyene-bridged second-order nonlinear optical chromophores and devices incorporating the same
    • AU9277901A
    • 2002-04-15
    • AU9277901
    • 2001-09-18
    • PACIFIC WAVE IND INC
    • ZHANG CHENGFETTERMAN HAROLD RSTEIER WILLIAMMICHAEL JOSEPH
    • C08K5/00C09B23/01C09B23/14G02F1/065G02F1/21G02F1/225G02F1/361G02F1/35F21V9/00
    • Polymers containing polyene-bridged second-order nonlinear optical chromophores and devices incorporating the same are disclosed. The chromophores are functionalized and incorporated into a series of polymers ranging from linear polyesters, linear poly[ester-imide]s, chain-crosslinked polyesters/poly[ester-imide]s, to crosslinked star-shaped/dendritic macromolecules. An exemplary preferred polymer is a linear chain polymer formed from a dihydroxy-functionalized polyene-bridged chromophore, a diacid or diacid dichloride, and a diol. In a preferred embodiment, the diol structure also includes at least one imide group. Another exemplary preferred polymer is a crosslinked polymer comprised of a linear chain polymer formed from a dihydroxy-functionalized polyene-bridged chromophore, a diacid or diacid dichloride and a diol. The crosslinking is realized by thermally induced cyclolization of trifluorovinylethers which are attached to the diol co-monomer and/or chromophore in the linear chain polymer chain. In a preferred embodiment, the diol structure also includes at least one imide group. Another exemplary preferred polymer is a crosslinked polymer made from crosslinkable star-shaped high molecular weight (larger than 2,000) structure containing polyene-bridged chromophores. In a preferred embodiment, the crosslinking groups are multiple trifluorovinylether groups located at the periphery of the star-shaped structure. Another exemplary preferred polymer is a crosslinked polymer made from crosslinkable dendritic structure having a chromophore core and one or more dendrons. In a preferred embodiment, the crosslinking groups are multiple trifluorovinylether groups located at the periphery of the dendritic structure.
    • 7. 发明专利
    • Sterically stabilized second-order nonlinear optical chromophores
    • AU5331301A
    • 2001-10-23
    • AU5331301
    • 2001-04-09
    • PACIFIC WAVE IND INC
    • ZHANG CHENGFETTERMAN HAROLD RSTEIER WILLIAMMICHAEL JOSEPH
    • C08K5/00C09B23/01C09B23/14G02F1/065G02F1/21G02F1/361G02F1/35F21V9/00
    • Sterically stabilized second-order nonlinear optical chromophores and devices incorporating the same are embodied in a variety of chromophore materials. An exemplary preferred chromophore includes an electron donor group, an electron acceptor group and a ring-locked bridge structure therebetween, with the bridge structure being directly connected to the electron donor via a single bond. Another exemplary preferred chromophore includes an electron donor group, an electron acceptor group and a ring-locked bridge structure between the electron donor group and the electron acceptor group, with two free double bonds, one located between the donor and the bridge and the other located between the (fused) ring bridge and the acceptor. Another exemplary preferred chromophore includes an electron donor group, an electron acceptor group, and a bridge structure therebetween, with the chromophores having no carbon-carbon double bond between the donor and the (fused) ring bridge. In this class, there is only one unlocked carbon-carbon double bond between the (fused) ring bridge and the acceptor. Another exemplary preferred chromophore includes an electron donor group, an electron acceptor group, and a ring-locked bridge structure therebetween, with a built-in electron-withdrawing cyano group on the last ring of the (fused) bridge. Another exemplary preferred chromophore includes any electron donor group, an electron acceptor group including a linear conjugated triene bearing four cyano groups, and any bridge structure therebetween.