Heteroatom-containing diamondoid transistors

Active solid-state devices (e.g. – transistors – solid-state diode – Organic semiconductor material

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C257SE51001

Reexamination Certificate

active

10622046

ABSTRACT:
These heterodiamondoids are diamondoids that include heteroatoms in the diamond lattice structure. The heteroatoms may be either electron donating, such that an n-type heterodiamondoid is created, or electron withdrawing, such that a p-type heterodiamondoid is made. Bulk materials may be fabricated from these heterodiamondoids, and the techniques involved include chemical vapor deposition, polymerization, and crystal aggregation. Junctions may be made from the p-type and n-type heterodiamondoid based materials, and microelectronic devices may be made that utilize these junctions. The devices include diodes, bipolar junction transistors, and field effect transistors.

REFERENCES:
patent: 3457318 (1969-07-01), Capaldi et al.
patent: 3832332 (1974-08-01), Thompson
patent: 4225734 (1980-09-01), McMurry
patent: 5017734 (1991-05-01), Baum et al.
patent: 5019660 (1991-05-01), Chapman et al.
patent: 5051785 (1991-09-01), Beetz, Jr. et al.
patent: 5057894 (1991-10-01), Ikeda et al.
patent: 5072264 (1991-12-01), Jones
patent: 5075757 (1991-12-01), Ishii et al.
patent: 5099296 (1992-03-01), Mort et al.
patent: 5107315 (1992-04-01), Kumagai et al.
patent: 5112775 (1992-05-01), Iida et al.
patent: 5117267 (1992-05-01), Kimoto et al.
patent: 5132749 (1992-07-01), Nishibayashi et al.
patent: 5144380 (1992-09-01), Kimoto et al.
patent: 5171632 (1992-12-01), Heeger et al.
patent: 5177585 (1993-01-01), Welbourn
patent: 5210431 (1993-05-01), Kimoto et al.
patent: 5223721 (1993-06-01), Iida et al.
patent: 5278431 (1994-01-01), Das
patent: H1287 (1994-02-01), Zeisse et al.
patent: 5294814 (1994-03-01), Das
patent: 5306928 (1994-04-01), Kimoto et al.
patent: 5331183 (1994-07-01), Sariciftci et al.
patent: 5352908 (1994-10-01), Kobashi et al.
patent: 5371378 (1994-12-01), Das
patent: 5371382 (1994-12-01), Venkatesan et al.
patent: 5382684 (1995-01-01), Moini et al.
patent: 5382809 (1995-01-01), Nishibayashi et al.
patent: 5389799 (1995-02-01), Uemoto
patent: 5400427 (1995-03-01), Ashjian et al.
patent: 5414189 (1995-05-01), Chen et al.
patent: 5449531 (1995-09-01), Zhu et al.
patent: 5454880 (1995-10-01), Sariciftci et al.
patent: 5455432 (1995-10-01), Hartsell et al.
patent: 5470505 (1995-11-01), Smith et al.
patent: 5476812 (1995-12-01), Kimoto et al.
patent: 5478650 (1995-12-01), Davanloo et al.
patent: 5531184 (1996-07-01), Muranaka et al.
patent: 5541423 (1996-07-01), Hirabayashi
patent: 5600156 (1997-02-01), Nishibayashi et al.
patent: 5632812 (1997-05-01), Hirabayashi
patent: 5653800 (1997-08-01), Kucherov et al.
patent: 5656828 (1997-08-01), Zachai et al.
patent: 5747118 (1998-05-01), Bunshah et al.
patent: 5792256 (1998-08-01), Kucherov et al.
patent: 5903015 (1999-05-01), Shiomi et al.
patent: 6110276 (2000-08-01), Yu et al.
patent: 6162412 (2000-12-01), Fujimori et al.
patent: 6235851 (2001-05-01), Ishii et al.
patent: 6274837 (2001-08-01), Windischmann et al.
patent: 6335245 (2002-01-01), Park et al.
patent: 6340393 (2002-01-01), Yoshida
patent: 6352884 (2002-03-01), Yu et al.
patent: 6376276 (2002-04-01), Oishi et al.
patent: 6861569 (2005-03-01), Dahl et al.
patent: 2002/0016414 (2002-02-01), Lau et al.
patent: 2004/0059145 (2004-03-01), Liu et al.
patent: 2545292 (1979-04-01), None
patent: 0272418 (1988-06-01), None
patent: 0286306 (1988-10-01), None
patent: 1071141 (2001-01-01), None
patent: 1088875 (2001-04-01), None
patent: 2001026541 (2001-01-01), None
patent: 2001026591 (2001-01-01), None
patent: WO 88/02792 (1988-04-01), None
patent: WO 92/13909 (1992-08-01), None
patent: WO 95/06019 (1995-03-01), None
patent: WO 02/00505 (2002-01-01), None
patent: WO02/057201 (2002-07-01), None
patent: WO 02/058139 (2002-07-01), None
patent: 03/050066 (2003-06-01), None
patent: WO03/005066 (2003-06-01), None
patent: WO 2004/009577 (2004-01-01), None
International Search Report from PCT/US03/22630 dated Aug. 20, 2004.
Das, K.K., “Electronic Applications of Diamond Films and Coatings” fromDiamond Films and Coatings, pp. 381-410, Noyes Publications, R.F. Davis, editor, Park Ridge New Jersey (1993).
Partial ISR from PCT/US03/22630 mailed May 28, 2004.
U.S. Appl. No. 10/046,486, filed Jan. 16, 2002.
Askeland, D.R., “Electrical Conductivity”, Chapter 17, pp. 664-667,The Science and Engineering of Materials Second Edition, J. Donald Childress ed. (1989).
Balaban et al., Systematic Classification and Nomenclature of Diamond Hydrocarbons -I,Tetrahedron34:3599-3606 (1978).
Baugman, G.I., “Dibromination of Adamantane”, (1964).
Becker et al, “A Short Synthese of 1-azaadamantan-4-one and the 4r and 4s Isomers of 4-Amino-1-azaadamantane”,Synthesis11:1080-1802 (1992).
Bingham, R.C. et al., Chapter 18 of “Chemistry of Adamantanes”,Springer-Verlag(1971).
Bishop, R., et al., “Detection of Non-Conjugative Interactions in Rigid Cyclic Molecules by Using Carbon-13 N.M.R. Shift Values”,Aust. J. Chem. 40:249-255 (1987).
Black, R.M. et al., “Adamantane Chemistry. Part 3. Abnormal Hypoiodite Reactions of 2-Substituted Adamantan-2-ols; Synthetic Routes to 4-Oxahomo-and 2-Oxa-adamantanes, and 7-Substituted-bicyclo[3.3.1]nona-3-ols”,J. Chem. Soc. Perkins Trans. I 410-418 (1980).
Blaney et al, “Chemistry of Diamantane, Part II. Synthesis of 3,5-disubstituted Derivatives”,Synthetic Communications3(6):435-439 (1973).
Boudjouk et al, “Synthesis and Reactivity of 1-Silaadamantyl Systems”,Journal of Organometallic Chemistry2:336-343 (1983).
Boudjouk et al, “The Reaction of Magnesium with cis-1,3,5-Trsi(bromomethyl)cyclohexane. Evidence For a Soluble Tri-grignard”,Journal of Organometallic Chemistry281:C21-C23 (1985).
Bubnov et al, “A Novel Method of Synthesis of 1-azaadamantane from 1-boraadamantane”,Journal of Organometallic Chemistry412:1-8 (1991).
Cao, G.Z., “Nitrogen and Phosphorus Doping in CVD Diamond”,Diamond, edited by M.H. Nazare and A.J. Neves, INSPEC pp. 345-347 (2001).
Chakrabarti et al., “Chemistry of Adamantane. Part II. Synthesis of 1-Adamantyloxyalkylamines”,Tetrahedron Letters60:6249-6252 (1968).
“Computation Concepts”Chem3D Molecular Modeling and Analysis User's Guide, Chapter 9, pp. 123-144.
Courtney, T., Johnston, D.E. McKervey, M.A. and Rooney, J.J., “The Chemistry of Diamantanes. Part 1. synthesis and Some Functionalisation Reactions”,J. Chem. Soc. Perkin I2691-2696 (1972).
Das, K.K., “Electronic Applications of Diamond Films and Coatings”, from Diamond Films and Coatings: Development, Properties, and Applications, Robert F. Davis, Ed.,Noyes Publications, pp. 381-410 (1993).
DeFranceschi, S., et al., “Electronics and the Single Atom”,Nature417:701-702 (2002).
Eguchi et al, “A Novel Route to the 2-Aza-adamantyl System via Photochemical Ring Contraction of Epoxy 4-Azahomoadamantanes”,Journal of Organometallic Chemistry, Commun., 1147-1148 (1984).
Fernandez, M.J., et al., “NMR Study of 1-Azatricyclo[3.3.13-7]decane Derivatives”,J. Heterocyclic Chem. 26:307-312 (1989).
Fernandez, M.J., et al., “Synthesis, Structural and Conformational Study of 4-α-(or β)-p-Chlorobenzoyloxy-1-azaadamantane Hydrochloride”,J. Heterocyclic Chem. 26:349-353 (1989).
Fleming, I., et al., “A New Oxindole Synthesis”,J. Chem. Soc. Perkin Trans. 1:617-626 (1991).
Fort, Jr., et al., “Stereochemistry of Hydride Reductions of 4,8-Dihalo-2-thiaadamantanes and Related Thiabicyclo[3.3.1]nonanes”,J. Org. Chem.52:2396-2399 (1987).
Fox, M.A., et al., “Transmission of Electronic Effects by Icosahedral Carboranes; Skeletal Carbon-13 Cehmical Shifts and Ultraviolet-Visible Spectra of Substituted aryl-p-carboranes (1,12-dicarba-closo-dodecaboranes)”,J. Chem. Soc., Dalton Trans. 401-411 (1998).
Fritz, G., et al., “Silicon-Carbon Compound with a Carborundum Structure”, Abstract,Angew, Chem, Internat. Edit. 9(6) (1970).
Fritz, G., et al., “Uber die Isolierung Hoherer Carbosilane aus der Pyrolyse des Tetra

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Heteroatom-containing diamondoid transistors does not yet have a rating. At this time, there are no reviews or comments for this patent.

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

Rate now

     

Profile ID: LFUS-PAI-O-3940974

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.