Polymerizable higher diamondoid derivatives

Details Polymerizable higher diamondoid derivatives Polymerizable higher diamondoid derivatives

2005-02-22

2005-02-22

Hightower, P. Hampton (Department: 1711)

Synthetic resins or natural rubbers -- part of the class 520 ser

Synthetic resins

From phenol, phenol ether, or inorganic phenolate

C528S272000, C528S288000, C528S310000, C528S322000, C528S344000, C528S350000, C528S353000, C525S437000, C525S440030, C526S262000

Reexamination Certificate

active

06858700

ABSTRACT:
Higher diamondoid derivatives capable of taking part in polymerization reactions are disclosed as well as intermediates to these derivatives, polymers formed from these derivatives and methods for preparing the polymers.

REFERENCES:
patent: 3457318 (1969-07-01), Capaldi
patent: 3832332 (1974-08-01), Thompson
patent: 4142036 (1979-02-01), Feinstein
patent: 4952747 (1990-08-01), Alexander
patent: 4952748 (1990-08-01), Alexander
patent: 4952749 (1990-08-01), Alexander
patent: 4982049 (1991-01-01), Alexander
patent: 5015758 (1991-05-01), Pilgrim et al.
patent: 5017734 (1991-05-01), Baum
patent: 5019660 (1991-05-01), Chapman et al.
patent: 5019665 (1991-05-01), Partridge
patent: 5053434 (1991-10-01), Chapman
patent: 5238705 (1993-08-01), Hayashi et al.
patent: 5245104 (1993-09-01), Cullick
patent: 5256391 (1993-10-01), Chen et al.
patent: 5268513 (1993-12-01), Shen
patent: 5298666 (1994-03-01), Shen
patent: 5306851 (1994-04-01), Wu
patent: 5308661 (1994-05-01), Feng et al.
patent: 5347063 (1994-09-01), Shen
patent: 5367051 (1994-11-01), Narang et al.
patent: 5369213 (1994-11-01), Shen
patent: 5380947 (1995-01-01), Chen
patent: 5382684 (1995-01-01), Moini
patent: 5397488 (1995-03-01), Chen
patent: 5410092 (1995-04-01), Shen
patent: 5414189 (1995-05-01), Chen
patent: 5416188 (1995-05-01), Chiang et al.
patent: 5430193 (1995-07-01), Shen
patent: 5449531 (1995-09-01), Zhu et al.
patent: 5455072 (1995-10-01), Bension et al.
patent: 5461184 (1995-10-01), Swanson
patent: 5462680 (1995-10-01), Brois et al.
patent: 5462776 (1995-10-01), Gruen
patent: 5498812 (1996-03-01), Bradway
patent: 5576355 (1996-11-01), Chen
patent: 5635581 (1997-06-01), Chiang et al.
patent: 5695847 (1997-12-01), Browne
patent: 5739376 (1998-04-01), Bingel
patent: 5861135 (1999-01-01), Tanabe et al.
patent: 5874175 (1999-02-01), Li
patent: 5880154 (1999-03-01), Boukrinskaia
patent: 6080470 (2000-06-01), Dorfman
patent: 6162412 (2000-12-01), Fujimori
patent: 6235851 (2001-05-01), Ishii
patent: 6300410 (2001-10-01), Shachat et al.
patent: 0399851 (1996-11-01), None
patent: WO 9213909 (1992-08-01), None
patent: WO 9506019 (1995-03-01), None
patent: WO 9511472 (1995-04-01), None
Aczel, et al., “Stability of Adamantane and its Derivatives to Coal-liquefaction Conditions, and its implications toward the organic structure of Coal”,Fuel, vol. 58, pp. 228-230, (Mar. 1979).
Badziag, P., et al., “Nanometre-sized Diamonds are More Stable than Graphite”,Nature, vol. 343, pp. 244-245, and 517.
Bagrii, Ye, et al., “Catalytic Breakdown of Paraffinic Hydrocarbons in the Presence of Adamantanes”,Petrol. Chem USSR, vol. 30, No. 2, pp. 131-134, (1990).
Balaban, et al., Systemic Classification and Nomenclature of Diamond Hydrocarbons-I,Tetrahedron, 34, pp. 3599-3606, (1978).
Baughman, GL, “Dibromination of Adamantane”, Publication Unknown, vol. 29, pp. 238-240 (Jan. 1964).
Bingham, RC, et al., “Recent Developments in the Chemistry of Adamantane and Related Polycyclic Hydrocarbons”,Chemistry of Adamantanes, Ch. 18, pp. 1-101 (1970).
Bott, Von K., “Synthese von Adamantan-und Norbornan chloressigsauren mit Trichlorathylen”,Angew. Chem., vol. 79, pp. 943-945 (1967).
Broich, F., “Carbonsauresynthesen mit 1,1-Dichlorathylen”,Angew. chem., vol. 78, pp. 932-936 (1966).
Cammas, S., et al., “Poly(β-malic acid): Obtaining High Molecular Weights by Improvement of the Synthesis Route”,Polymer, vol. 37, No. 18, pp. 4215-4220 (1996).
Chung, et al., Recent Development in High-Energy Density Liquid Fuels,Energy and Fuels, 13, pp. 641-649, (1999).
Courtney, T., et al., “The Chemistry of Diamantane: Part 1—Synthesis and Some Functionalisation Reations”, J.C.S.Perkin I, pp. 2691-2696 (1972).
Dahl, J., et al., Diamondoid Hydrocarbons as Indicators of Natural Oil Cracking,Nature, 399, pp. 54-57, (1999).
Drexler, Eric K.,Nanosystems: Molecular Machinery Manufacturing and Computation, John Wiley & Sons, pp. 238-249, (1992).
Fort, Jr., et al., Adamantane: Consequences of the Diamondoid Structure,Chem. Rev., 64, pp. 277-300, (1964).
Haaf, W., “Untersuchungen uber die Ritter-Reacktion”, pp. 3359-3369 (1963).
Hala, V.S., et al., “Analyse Unds erwendung on Pyrolyseol”,Jahrgang, pp. 85-87, (Feb. 1971) In German- English Abstract on p. 85.
Koch, H., “Direkte Syntese der Adamantan-carbonsaure-(1)”,Eingengangen Am., 29, p. Z 944 (1960).
Landa, S., “Adamantane and Its Homologues”,Current Science, V. 52, pp. 485-489 (1963).
Liaw, Der-Jang, et al., “Synthesis and Characterization of new Polyamides and Polyimides Prepared from 2,2-bix[4-(4-aminophenoxy)phenyl]adamantane”,Macromol. Chem. Phys., 200, No. 6, pp. 1326-1332 (1999).
Lin, et al., Natrual Occurrence of Tetramantane (C22H36), Pentamantane (C26H32), and Hexamantane (C30H36) in a Deep Petroleum Reservoir,Fuel, 74:10, pp. 1512-1521, (1995).
Machacek, V., et al., “Let Od Objeveni Adamantanu”,Chemicke Listy/svazek, pp. 753-761, (1982) Russian—English Abstract on p. 761.
McKervey, Synthetic Approaches to Large Diamondoid Hydrocarbonds,Tetrahedron, 36, pp. 971-992 (1980).
Moine, L., et al., “Polymers of Malic Acid Conjugated with the 1-adamantyl Moiety as Lipophilic Pendant Group”,Polymer, vol. 38, No. 12, pp. 3121-3127 (1997).
Moiseev, IK, et al., “Reactions of Adamantanes in Electrophilic Media”,Russian Chem. Reviews, vol. 68, No. 12, pp. 1001-1120 (1999).
Neavel, R., “Liquefaction of Coalinhydrogen-donor and Non-donor Vehicles”,Fuel, vol. 55, pp. 237-242 (1976).
Oya, A, et al., “Carbonization of Adamantanes to a Graphitizable Carbon”,Fuel, vol. 60, pp. 667-669, (Aug. 1981).
Petrov, A., “Hydrocarbons of Adamantane Series as Indicies of Petroleum Catagenesis Process”,Advances in Organic Geo Chemistry, 6thInternational Meeting on Organic Geochemistry, pp. 517-522 (1973).
Prusova, D., Liquid Chromatography of Adamantanes and Carbon Adsorbents,J. Chrom, 234, pp. 1-11, (1982).
Rollman, L., et al., “Adamantanes From Petroleum, with Zeolites”, American Chemical Study, 210thACS National Meeting, Abstract and paper, Aug. 20, 1995).
Sandia National Laboratories (2000), World's First Diamond Micromachines Created at Sandia, Press Release, (Feb. 22, 2000), www.Sandia.gov.
Shen, M., et al., Finite TdSymmetry Models for Diamond: From Adamantane to Superadamantane (C35H36),J. Am., Chem. Soc., vol. 114, No. 2, pp 497-505, (1992).
Smith, G., et al., “Some Reactions of Adamantane and Adamantane Derivatives”,publication unknown, vol. 26, pp. 2207-2212 (1961).
Stetter, H., et al., “Monofunktionelle Adamantan-Derivate”,Angew. Chem., 71, pp. 429-430 (1959).
Supryadkina, NY, et al., “Catalytic Dealkylation of Alkyladamantanes”,Petrol. Chem., USSR, vol. 28, No. 2, pp. 103-110, (1988).
Tominaga, K., et al., “Next-generation Fine Chemicals Raw Material-Adamantane”,Chem Econ&Eng. Review, vol. 17, No. 10, pp. 23-29, (Oct. 1985).
Vodicka, L., et al., “High Performance Liquid Chromatography of Halogeno Derivatives of Adamantane and Diamantane”,J. Chrom, 270, pp. 199-205, (1983).
von Schleyer, P., et al., “Nonacyclo[11.7.1.12,18.03,16.04,13.05,10.06,14.07,11.015,20]-Docosane, a Bastard Tetramantane”,J. of the Am. Chem. Soc., 90:8, lettter to the editor, Aug. 28, 1968.
von R. Schleyer, P., et al., “The Preparation and Reactivity of 2-Substituted Derivatives”,Frick Chemical Laboratory, vol. 83, pp. 182-187 (1967).
Wingert, W., “G.c.-m.s. Analysis of Diamondoid Hydrocarbons in Smackover Petroleums”,Fuel, vol. 71, pp. 37-42, (Feb. 1992).

Affiliated with

Also associated with

Rating

Polymerizable higher diamondoid derivatives does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Polymerizable higher diamondoid derivatives, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Polymerizable higher diamondoid derivatives will most certainly appreciate the feedback.

Rate now

Comments { 0 }

Profile ID: LFUS-PAI-O-3493840