Calixpyrroles, calixpyridinopyrroles and calixpyridines
The present invention provides calixpyrrole, calixpyridinopyrrole, and calixpyridine macrocycles, having 4, 5, 6, 7, or 8 heterocyclic rings, as well as syntheses, derivatives, conjugates, multimers, and solid supports thereof. Such macrocycles have proved to be effective and selective ion- and neut...
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| creator | WILLIAM E. ALLEN VLADIMIR KRAL JOHN W. GENGE VINCENT LYNCH ANDREAS GEBAUER JONATHAN L. SESSLER CHRISTOPHER T. BROWN ANDREI ANDRIEVSKY PETRA I SANSOM PHILIP A. GALE |
| description | The present invention provides calixpyrrole, calixpyridinopyrrole, and calixpyridine macrocycles, having 4, 5, 6, 7, or 8 heterocyclic rings, as well as syntheses, derivatives, conjugates, multimers, and solid supports thereof. Such macrocycles have proved to be effective and selective ion- and neutral molecule-binding agents forming supramolecular ensembles, and ion- and neutral molecule-separation agents. The macrocycles are fully meso-non-hydrogen-substituted porphyrinogens, a few molecules of which were previously known but not recognized as possessing anion- or molecule-binding properties. The binding mode is noncovalent, primarily that of hydrogen-bonding, thereby providing a new mode for liquid chromatography, that of Hydrogen Bonding Liquid Chromatography. Further useful applications of the macrocycles provided herein include environmental remediation by removal of undesired ions or neutral molecules, and removal of phosphate for kidney dialysis. |
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The macrocycles are fully meso-non-hydrogen-substituted porphyrinogens, a few molecules of which were previously known but not recognized as possessing anion- or molecule-binding properties. The binding mode is noncovalent, primarily that of hydrogen-bonding, thereby providing a new mode for liquid chromatography, that of Hydrogen Bonding Liquid Chromatography. 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ALLEN</creatorcontrib><creatorcontrib>VLADIMIR KRAL</creatorcontrib><creatorcontrib>JOHN W. GENGE</creatorcontrib><creatorcontrib>VINCENT LYNCH</creatorcontrib><creatorcontrib>ANDREAS GEBAUER</creatorcontrib><creatorcontrib>JONATHAN L. SESSLER</creatorcontrib><creatorcontrib>CHRISTOPHER T. BROWN</creatorcontrib><creatorcontrib>ANDREI ANDRIEVSKY</creatorcontrib><creatorcontrib>PETRA I SANSOM</creatorcontrib><creatorcontrib>PHILIP A. GALE</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>WILLIAM E. ALLEN</au><au>VLADIMIR KRAL</au><au>JOHN W. GENGE</au><au>VINCENT LYNCH</au><au>ANDREAS GEBAUER</au><au>JONATHAN L. SESSLER</au><au>CHRISTOPHER T. BROWN</au><au>ANDREI ANDRIEVSKY</au><au>PETRA I SANSOM</au><au>PHILIP A. GALE</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Calixpyrroles, calixpyridinopyrroles and calixpyridines</title><date>1997-10-29</date><risdate>1997</risdate><abstract>The present invention provides calixpyrrole, calixpyridinopyrrole, and calixpyridine macrocycles, having 4, 5, 6, 7, or 8 heterocyclic rings, as well as syntheses, derivatives, conjugates, multimers, and solid supports thereof. Such macrocycles have proved to be effective and selective ion- and neutral molecule-binding agents forming supramolecular ensembles, and ion- and neutral molecule-separation agents. The macrocycles are fully meso-non-hydrogen-substituted porphyrinogens, a few molecules of which were previously known but not recognized as possessing anion- or molecule-binding properties. The binding mode is noncovalent, primarily that of hydrogen-bonding, thereby providing a new mode for liquid chromatography, that of Hydrogen Bonding Liquid Chromatography. Further useful applications of the macrocycles provided herein include environmental remediation by removal of undesired ions or neutral molecules, and removal of phosphate for kidney dialysis.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record> |
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| subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY CHEMISTRY DECONTAMINATION ARRANGEMENTS THEREFOR DERIVATIVES THEREOF HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES MEASURING MEDICAL OR VETERINARY SCIENCE METALLURGY NUCLEAR ENGINEERING NUCLEAR PHYSICS NUCLEIC ACIDS NUCLEOSIDES NUCLEOTIDES ORGANIC CHEMISTRY PEPTIDES PERFORMING OPERATIONS PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL PHYSICS PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES PROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULARRADIATION OR PARTICLE BOMBARDMENT SEPARATION SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS SUGARS TESTING THEIR RELEVANT APPARATUS TRANSPORTING TREATING RADIOACTIVELY CONTAMINATED MATERIAL |
| title | Calixpyrroles, calixpyridinopyrroles and calixpyridines |
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