Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Compositions to be polymerized by wave energy wherein said...
Reexamination Certificate
2006-04-25
2006-04-25
Rabago, Roberto (Department: 1713)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Compositions to be polymerized by wave energy wherein said...
C522S173000, C522S178000, C522S182000
Reexamination Certificate
active
07034064
ABSTRACT:
A method for attaching a silicon die to a substrate using an adhesive containing an oxetane functionality and an electron acceptor or an electron donor functionality, represented by the formulain which R1is a methyl or ethyl group, R2is a divalent hydrocarbon, X and Y are independently a direct bond, or an ether, ester, or carbamate functionality, Q is a divalent hydrocarbon, and F is an electron donor or electron acceptor functionality.
REFERENCES:
patent: 3867353 (1975-02-01), Hsieh et al.
patent: 4225691 (1980-09-01), Crivello
patent: 5981616 (1999-11-01), Yamamura et al.
patent: 6166100 (2000-12-01), Hiwara et al.
patent: 6207728 (2001-03-01), Sekiguchi et al.
patent: 2002/0089067 (2002-07-01), Crane et al.
patent: 2002/0143112 (2002-10-01), Weinert et al.
patent: 1 095 938 (2001-05-01), None
patent: 2001081149 (2001-03-01), None
patent: 2001-303015 (2001-10-01), None
patent: 2001329112 (2001-11-01), None
patent: 2002150836 (2004-05-01), None
patent: WO 02/06038 02 (2002-01-01), None
patent: WO 02/06038 03 (2002-01-01), None
patent: WO 02/28985 (2002-04-01), None
Ledwith, Anthony: “Possibilities for promoting cationic polymerization by common sources of free radicals”;Polymer 1978, vol. 19; Oct.; pp. 1217-1222.
Sasaki, Hiroshi et al.: “Photoinitiated Cationic Polymerization of Oxetane Formulated with Oxirane”;Journal of Polymer Science Part A; vol. 33; 1995; pp. 1807-1816.
Searles, Scott et al.: “Hydrogen Bonding Ability and Structure of Ethylene Oxides”;This Journal; 73;3704;1951.
Xianming, Hu et al.: “Phase-Transfer Synthesis of Optically Pure Oxetanes Obtained from 1,2,2-Trisubstituted 1,3-Propanediols”;Synthesis May 1995; pp. 533-538.
Fujiwara, Tomoko et al.: “Synthesis and Characterization of Novel Oxetane Macromonomers”;Polymer Preprints 2003; 44(1), 785.
Dhavalikar, R. et al.: “Molecular and Structural Analysis of a Triepoxide-Modified Poly(ethylene terephthalate) from Rheological Data”;Journal of Polymer Science: Part A: Polymer Chemistry; vol. 41, 958-969 (2003); pp. 958-969.
Satoh, Toshifumi et al.: “A Novel Ladder Polymer, Two-Step Polymerization of Oxetanyl Oxirane Leading to a “Fused 15-Crown-4 Polymer” Having a High Li+-Binding Ability”;Macromolecules 2003, 36, 1522-1525.
Chen, Yu et al.: “Synthesis of Multihydroxyl Branched Polyethers by Cationic Copolymerization of 3,3-Bis(hydroxymethyl)oxetane and 3-Ethyl-3-(hydroxymethyloxetane”;Journal of Polymer Science: Part A: Polymer Chemistry, vol. 40, 1991-2002; 2002 Wiley Periodicals, Inc.
Nishimura, Tomonari et al.: “Chemoselective isomerization of amide-substituted oxetanes with Lewis acid to give oxazine derivatives or bicyclic amide acetals”;Chem. Commun., 1998; pp. 43-44.
Miwa, Yoshiyuki et al.: “Polymerization of Bis-Oxetanes Consisting of Oligo-Ethylene Oxide Chain with Lithium Salts as Initiators”; Polym. J., vol. 33, No. 8, 2001; pp. 568-574.
Ichikawa, Eiko et al.: “Synthesis of Oxetanocin A and Related Unusual Nucleosides with Bis(hydroxymethyl)-branched Sugars”;Synthesis 2002, No. 1, 28 12 2001; Georg Thieme Verlag Stuttgart, NY; pp. 1-28.
Minegishi, Shouji et al.: “Synthesis of Polyphosphonates Containing Pendant Chloromethyl Groups by the Polyaddition of Bis(oxetanes)s with Phosphonic Dichlorides”;Journal of Polymer Science:Part A: Polymer Chemistry, vol. 40 3835-3846; 2002 Wiley Periodicals, Inc.
Sasaki, Hiroshi et al.: “Photoinitiated Cationic Polymerization of Oxetane Formulated with Oxirane”;Journal of Polymer Science: Part A: Polymer Chemistry, vol. 33, 1807-1816; 1995 John Wiley & Sons, Inc.
Rosenbaum, Dr. Barry et al.: “Develop Better Coatings”;Omnova Solutions Inc., Akron, OH; pp. 1-5.
Sasaki, Hiroshi: “Application of Oxetane Monomers for UV-Curable Material”; RadTech 2002; Tech. Conf. Proceedings; pp. 64-78.
Carter, Wells et al.: “New Oxetane Derivative Reactive Filuent for Cationic UV Cure”;RadTech 2000; Tech. Proceed.; pp. 641-649.
Crivello, J. V. et al.: “Diaryliodonium Salts as Thermal Initiators of Cationic Polymerization”;Journal of Polymer Science: Polymer Chemistry Ed, vol. 21, 97-109 (1983); John Wiley & Sons, Inc.
Lu, Yong-Hong et al.: “Synthesis of Side-Chain Liquid Crystalline Polyoxetanes Containing 4-(Alkanyloxy)phenyl trans-4-Alkylcyclohexanoate Side Groups”;1995 American Chem. Society; pp. 1673-1680.
Lu, Yong-Hong et al.: “Synthesis of side-chain liquid crystalline polyoxetanes containing 4-dodecanyloxphenyl trans-4-alkylcyclohexanoate side groups”;Polymer Bulletin 32, 551-558 (1994); Springer Verlag.
Hsu, Li-Ling et al.: “Studies on the Synthesis and Properties of Ferroelectric Side Chain Liquid Crystalline Polyoxetanes”;Journal of Polymer Science: Part A: Polymer Chemistry; vol. 35, 2843-2855; (1997); John Wiley & Sons, Inc.
Kawakami, Yusuke et al.: “Synthesis and Thermal Transition of Side-chain Liquid Crystalline Polyoxetanes Having Laterally Attached Mesogenic Group”;Polymer International; 0959-8103/93; Great Britian, 35-40.
Kawakami, Yusuke et al.: “Synthesis of Liquid Crystalline Polymers with a Polyoxetane Main Chain”;Macromolecules; vol. 24, No. 16, 1991; pp. 4531-4537.
Kawakami, Yusuke et al.: “Smectic liquid crystalline polyoxetane with novel mesogenic group”;Polymer Bulletin 25; Springer-Verlag 1991; pp. 439-442.
Crivello, J.V. et al.: “Photoinitiated Cationic Polymerization With Multifunctional Vinyl Ether Monomers”;Journal of Radiation Curing, Jan. 1983; pp. 6-13.
Ishizone, Takashi et al.: “Protection and Polymerization of Functional Monomers. 29. Syntheses of Well-Defined Poly[(4-vinylphenyl)acetic acid], Poly [3-(4-vinylphenyl)propionic acid], and Poly(3-vinylbenzoic acid) by Means of Anionic Living Polymerizations of Protected Monomers Bearing Bicyclic Ortho Ester Moieties”;Macromolecules 1999, 32, 1453-1462.
Sato, Kazuya et al.: “New Reactive Polymer Carrying a Pendant Oxetane Ring”;Macromolecules 1992, 25, 1198-1199; Communications to the Editor.
Moussa, K. et al.: “Light-Induced Polymerization of New Highly Reactive Acrylic Monomers”;Journal of Polymer Science: Part A: Polymer Chemistry, vol. 31, 2197-2203 (1993); John Wiley & Sons, Inc.
Kawakami, Yusuke et al.: “Synthesis of Liquid Crystalline Polyoxetanes Bearing Cyanobiphenyl Mesogen and Siloxane-Containing Substituent in the Repeating Unit”;Polymer Journal, vol. 28, No. 10, pp. 845-850 (1996).
Crivello, J. V. et al.: “Synthesis and Photopolymerization of Silicon-Containing Multifunctional Oxetane Monomers”;J.M.S.-Pure Appl. Chem., A30(2 & 3), pp. 173-187 (1993); Marcel Dekker, Inc.
Chappelow, C. C. et al.: “Photoreactivity of Vinyl Ether/Oxirane-Based Resin Systems”;Journal of Applied Polymer Science, vol. 86, 314-326 (2002); Wiley Periodicals, Inc.
Toagosei Co. Ltd.: “Developing Monomers”, Aug. 2002.
Hou, Jian et al.: “Synthesis of a Star-Shaped Copolymer with a Hyperbranched Poly(3-methyl-3-oxetanemethanol) Core and Tetrahydrofuran Arms by One-Pot Copolymerization”;Macromol. Rapid Commun. 2002, 23, 456-459.
Xu, Jun et al.: “Study On Cationic Ring-Opening Polymerization Mechanism of 3-Ethyl-3-Hydroxymethyl Oxetane”;J. Macromol. Sci.-Pure Appl. Chem., A39(5), 431-445 (2002); Marcel Dekker, Inc.
Suzuki, Hiroshi et al.: “Photo-cationic curable materials using cationic polymerizable monomers such as epoxides and vinyl ether derivatives”;Polymer Preprints 2001, 42(2), 733.
Kanoh, Shigeyoshi et al.: “Monomer-Isomerization Polymerization of 3-Methyl-3-(phthalimidomethyl)oxetane with Two Different Ring-Opening Courses”;Macromolecules 1999, 32, 2438-2448; 1999 American Chemical Society.
Jansen, Johan F.G.A. et al.: “Effect of Dipole Moment on the Maximum Rate of Photoinitiated Acrylat
Gennaro Jane E.
National Starch and Chemical Investment Holding Corporation
Rabago Roberto
LandOfFree
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