A homochiral metal–organic porous material for enantioselective separation and catalysis
Explore this paper's citation graph
Summary
The synthesis of a homochiral metal–organic porous material that allows the enantioselective inclusion of metal complexes in its pores and catalyses a transesterification reaction in an enantiOSElective manner is reported.
- Type
- article
- Published
- 2000-04-27
- Cited by
- 3,286
- References
- 28
- OpenAlex
- https://openalex.org/W1628423641
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:1159701
Keywords
Enantioselective synthesis, Catalysis, Enantiopure drug, Metal-organic framework, Materials science
References
- Design and synthesis of an exceptionally stable and highly porous metal-organic framework
- Immobilization of a Soluble Metal Complex in an Organic Network. Remarkable Catalytic Performance of a Porous Dialkoxyzirconium Polyphenoxide as a Functional Organic Zeolite Analogue
- Preparation, Clathration Ability, and Catalysis of a Two-Dimensional Square Network Material Composed of Cadmium(II) and 4,4'-Bipyridine
- Functional Organic Analogues of Zeolites Based on Metal–Organic Coordination Frameworks
- From Condensed Lanthanide Coordination Solids to Microporous Frameworks Having Accessible Metal Sites
- Crystal Engineering of Stacked Aromatic Columns. Three-Dimensional Control of the Alignment of Orthogonal Aromatic Triads and Guest Quinones via Self-Assembly of Hydrogen-Bonded Networks
- Molecular Tectonics. Porous Hydrogen-Bonded Networks with Unprecedented Structural Integrity
- Catalysis by Organic Solids. Stereoselective Diels−Alder Reactions Promoted by Microporous Molecular Crystals Having an Extensive Hydrogen-Bonded Network
- Selective binding and removal of guests in a microporous metal–organic framework
- Crystal structure of a copper complex of 2-carboxypentonic acid; a decomposition product of dehydroascorbic acid
- Functional Micropore Chemistry of Crystalline Metal Complex-Assembled Compounds
- Shape-Induced, Hexagonal, Open Frameworks: Rubidium Ion Complexed Cucurbituril.
- Spontaneous assembly of a hinged coordination network
- Assembly of porphyrin building blocks into network structures with large channels
- SMTP-1: The First Functionalized Metalloporphyrin Molecular Sieves with Large Channels.
- Nanoporous Molecular Sandwiches: Pillared Two-Dimensional Hydrogen-Bonded Networks with Adjustable Porosity
- Topochemical Conversion of a Hydrogen-Bonded Three-Dimensional Network into a Covalently Bonded Framework.
- Variable Pore Size, Variable Chemical Functionality, and an Example of Reactivity within Porous Phenylacetylene Silver Salts
- Exchange Properties of the Three-Dimensional Coordination Compound 1,3,5-Tris(4-ethynylbenzonitrile)benzene·AgO3SCF3
- Three‐Dimensional Framework with Channeling Cavities for Small Molecules: [M2(4, 4′‐bpy)3(NO3)4]·xH2On (M Co, Ni, Zn)
Cited by
- Homochiral 3D lanthanide coordination networks with an unprecedented 4(9)6(6) topology.
- A homochiral metal-organic material with permanent porosity, enantioselective sorption properties, and catalytic activity.
- One-dimensional copper(II) coordination polymers bridged both by mu-trans-oxamidates and phenyldicarboxylates: Synthesis, crystal structure and DNA binding studies.
- Functionalized coordination space in metal-organic frameworks.
- Copper(II) complexes of mono-anionic glutamate: anionic influence in the variations of molecular and supramolecular structures.
- Oriented nanoscale films of metal-organic frameworks by room-temperature gel-layer synthesis.
- Induction in urothermal synthesis of chiral porous materials from achiral precursors.
- Homochiral frameworks formed by reactions of lanthanide ions with a chiral antimony tartrate secondary building unit.
- Molecular tectonics: homochiral coordination networks based on combinations of a chiral neutral tecton with Hg(II), Cu(II) or Ni(II) neutral complexes as metallatectons.
- Metal oxide-coated three-dimensional graphene prepared by the use of metal-organic frameworks as precursors.
- Photoinduced postsynthetic polymerization of a metal-organic framework toward a flexible stand-alone membrane.
- Anodized Aluminum Oxide Templated Synthesis of Metal-Organic Frameworks Used as Membrane Reactors.
- Time-Resolved In Situ Liquid-Phase Atomic Force Microscopy and Infrared Nanospectroscopy during the Formation of Metal–Organic Framework Thin Films
- A Three-dimensional MOF Assembled by Metal-organic Tapes Comprising of Copper(II) Tetranuclear Clusters and 5-Sulfoisophthalates
- Chemical inhibition through conformational stabilization of Rho GTPase effectors.
- Porphyrin Network Materials: Chemical Exploration in the Supramolecular Solid-State
- A novel approach to carbon dioxide capture and storage
- Designing metal-organic frameworks for catalytic applications.
- Poly[[diaquacobalt(II)]-di-μ-4-cyanobenzoato-κ4O:O']
- Large-scale generation and screening of hypothetical metal-organic frameworks for applications in gas storage and separations.
Related papers
- Efficacious and Rapid Metal- and Solvent-Free Synthesis of Enantiopure Oxazolines.
- A Valuable Synthetic Route to the Enantiopure Functionalized N-Substituted Aziridines
- Synthesis of Enantiopure γ-Lactones via a RuPHOX-Ru Catalyzed Asymmetric Hydrogenation of γ-Keto Acids
- Synthesis of Enantiopure 5-Substituted 2,3-Methanopyrrolidines by Cyclization of Enantiopure α-Branched α-N-Homoallylamino Nitriles
- Chirality preservation in pyrrolinone iron tetracarbonyl complexes – a route to enantiopure 5-substituted pyrrolinones
- Synthesis of an enantiopure syn-benzocyclotrimer through regio-selective cyclotrimerization of a halonorbornene derivative under palladium nanocluster conditions
- Stereoselective Addition of Racemic Allenylzinc onto Enantiopure N-tert-Butanesulfinimines
- Enantiopure Guanidine Bases For Enantioselective Enone Epoxidations: 1, Acyclic Guanidines
- Synthesis of Enantiopure o-Hydroxybenzylamines by Stereoselective Reduction of 2-Imidoylphenols: Application in the Catalytic Enantioselective Addition of Diethylzinc to Aldehydes
- Enantioselective syntheses of trans-3,4-difluoropyrrolidines and investigation of their applications in catalytic asymmetric synthesis.