Functional monomers for molecular recognition and catalysis

Details Functional monomers for molecular recognition and catalysis Functional monomers for molecular recognition and catalysis

2005-03-22

2005-03-22

Pezzuto, Helen L. (Department: 1713)

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

Synthetic resins

Polymers from only ethylenic monomers or processes of...

C526S199000, C526S200000, C526S243000, C526S248000, C526S250000, C526S288000, C526S292900

Reexamination Certificate

active

06870021

ABSTRACT:
The present invention refers to new classes of polymerisable monomers, to molecularly imprinted polymers obtainable by polymerisation of at least one of the monomers and a cross linking monomer in the presence of a template molecule. The obtained polymers may be used for separation of enantiomers, diastereomers of the template molecule, and also for separation of the template molecule or template molecule analogues from structurally related compounds.

REFERENCES:
patent: 2868796 (1959-01-01), Cislak
patent: 3281487 (1966-10-01), Rowe, Jr. et al.
patent: 5310648 (1994-05-01), Arnold et al.
patent: 5401825 (1995-03-01), Kurz
patent: 5444129 (1995-08-01), Kurz
patent: 5786428 (1998-07-01), Arnold et al.
patent: 5858296 (1999-01-01), Domb
patent: 6063637 (2000-05-01), Arnold et al.
patent: 6217901 (2001-04-01), Perrott et al.
patent: 6310110 (2001-10-01), Markowitz et al.
patent: 9720639 (1997-06-01), None
patent: 9807671 (1998-02-01), None
patent: WO 0155095 (2001-08-01), None
Research News, Polymerizable Amidines—Adhesion Mediators and Binding Sites for Molecular Imprinting, Günter Wulff, et al., Advanced Materials 1998, 10, No. 12, pp. 957 to 959.
Polymer-and template-related factors influencing the efficiency in molecularly imprinted solid-phase extractions, Börje Sellergren, Department of Inorganic Chemistry and Analytical Chemistry, Johannes Gutenberg University Mainz, J.J. Becherweg 24, 55099 Mainz, Germany, trends in analytical chemistry, vol. 18, No. 3, 1999, pp. 164 to 174.
International, File CAPLUS, CAPLUS accession No. 1995:613658, Document No. 123:10053, Ritter, Helmut et al.: “Polymerizable mesoions. 2. Radical polymerization and 1,4-dipolar polycycloaddition of a 4-vinylphenyl-modified mesoionic 4,6-dioxo-1,3-diazine”; Macromol. Rapid Commun. (1995), 16(6), 407-15.
Tetrahedron, vol. 29, 1973, R. Fuks, “N-Alkylation of Nitriles—I.A. General Synthesis of Substituted Amidines” pp. 2147 to 2151.
International, File CAPLUS, CAPLUS accession No. 1976:493728, Document No. 85:93728, Tomoi, Masao et al.: “N-Alkylpentamethylphosphoramides: novel catalysts in two-phase reactions”; & Chem. Lett. (1976), (5), 473 to 476.
International, File CAPLUS, CAPLUS accession No. 1987:138532, Document No. 106:138532, Benmaarouf-Khallaayoun, Z et al.: “Hydroboration of unsaturated amines. XI. Regio-and stereoselectivity of boron hydrides with respect to N-phosphorylated propargylic amines”; & J. Organomet. Chem. (1986), 306(3), 283 to 293.
Tetrahedron Letters, vol. 11, 1976, Bernard Corbel et al., “N-Propargylphosphoramides—Nouveaux Reactifs de Synthese” pp. 835 to 838.
International, File CAPLUS, CAPLUS accession No. 1976:106103, Document No. 84:106103, Kondo, Koichi et al.: “Synthesis of functional polymers containing carbodiimide groups”; & Technol. Rep. Osaka Univ. (1975), 25(1254-1275), 487-9.
International, File CAPLUS, CAPLUS accession No. 1980:76011, Document No. 92:76011, Sinyavskii, V.G. et al.: “Synthesis of 2- and 4-isocyanatostyrenes and their derivatives”; & Deposited Doc. (1978), VINITI 3283-78, 12 pp.
Bulletin of the Chemical Society of Japan, vol. 52, No. 2, 1979, Hiroyoshi Kamogawa et al., “Syntheses of Polymerizable Carbodiimides Bearing a Terminal Vinyl Group” pp. 533 to 535.
International, File CAPLUS, CAPLUS accession No. 1971:111672, Document No. 74-111672, Shur, A.M. et al.: “Synthesis and study of some monomers, containing additional chemically active groups”; & Sb. Nauch. Statei, Kishinev. Gos. Univ., Estestv. Mat. Nauki (1969), 118-29.
J. Am. Chem. Soc., vol. 110, 1988, Margaret C. Etter et al., “1,3-Bis(m-nitrophenyl)urea: An Exceptionally Good Complexing Agent for Proton Acceptors” pp. 5896 to 5897.
Trends in biochemical sciences, vol. 19, Jan. 1994, Klaus Mosbach, “Molecular imprinting” pp. 9 to 14.
J. Am. Chem. Soc., vol. 110, No. 17, 1988, Börje Sellergren et al., “Highly Enantioselective and Substrate-Selective Polymers Obtained by Molecular Imprinting Utilizing Noncovalent Interactions. NMR and ChromotographicStudies on the Nature of Recognition” pp. 5853 to 5860.

Affiliated with

Also associated with

Rating

Functional monomers for molecular recognition and catalysis does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Functional monomers for molecular recognition and catalysis, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Functional monomers for molecular recognition and catalysis will most certainly appreciate the feedback.

Rate now

Comments { 0 }

Profile ID: LFUS-PAI-O-3400334