Reference health
Efficient One‐Pot Synthesis of Water‐Compatible Molecularly Imprinted Polymer Microspheres by Facile RAFT Precipitation Polymerization
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Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
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The 46 checked references that resolve
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Molekular geprägte Polymere mit einem Gedächtnis für kleine Moleküle, Proteine oder Kristalle
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Imprinted Polymers with Memory for Small Molecules, Proteins, or Crystals
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Configurational biomimesis in drug delivery: molecular imprinting of biologically significant molecules
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Molecular imprinting science and technology: a survey of the literature for the years up to and including 2003
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Non‐covalent molecular imprinting with emphasis on its application in separation and drug development
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Molecular Imprinting: Synthetic Materials As Substitutes for Biological Antibodies and Receptors
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Polymerizable Amidines—Adhesion Mediators and Binding Sites for Molecular Imprinting
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Tailor-Made Receptors by Molecular Imprinting
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Imprinted Polymers Prepared with Stoichiometric Template−Monomer Complexes: Efficient Binding of Ampicillin from Aqueous Solutions
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Synthetic Peptide Receptors: Molecularly Imprinted Polymers for the Recognition of Peptides Using Peptide−Metal Interactions
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An Artificial Riboflavin Receptor Prepared by a Template Analogue Imprinting Strategy
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An Artificial Riboflavin Receptor Prepared by a Template Analogue Imprinting Strategy
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A Stoichiometric Molecularly Imprinted Polymer for the Class‐Selective Recognition of Antibiotics in Aqueous Media
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A Stoichiometric Molecularly Imprinted Polymer for the Class‐Selective Recognition of Antibiotics in Aqueous Media
resolves10.1073/pnas.92.11.4788
Mimics of the binding sites of opioid receptors obtained by molecular imprinting of enkephalin and morphine.
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Influence of template basicity and hydrophobicity on the molecular recognition properties of molecularly imprinted polymers
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Probing the molecular basis for ligand-selective recognition in molecularly imprinted polymers selective for the local anaesthetic bupivacaine
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Preparation of molecularly imprinted polymer microspheres via reversible addition–fragmentation chain transfer precipitation polymerization
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An efficient approach to obtaining water-compatible and stimuli-responsive molecularly imprinted polymers by the facile surface-grafting of functional polymer brushes via RAFT polymerization
resolves10.1039/c1sm05497j
Controlled synthesis of water-compatible molecularly imprinted polymer microspheres with ultrathin hydrophilic polymer shells via surface-initiated reversible addition-fragmentation chain transfer polymerization
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Reversible addition–fragmentation chain transfer (RAFT) radical polymerization and the synthesis of water-soluble (co)polymers under homogeneous conditions in organic and aqueous media
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Advances in the synthesis of amphiphilic block copolymers via RAFT polymerization: Stimuli-responsive drug and gene delivery☆
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Water-Compatible Molecularly Imprinted Polymers Obtained via High-Throughput Synthesis and Experimental Design
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Removal of Estrogenic Pollutants from Contaminated Water Using Molecularly Imprinted Polymers
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Preparation of a novel molecularly imprinted polymer using a water-soluble crosslinking agent
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Uniform-sized molecularly imprinted polymer for (S)-naproxen selectively modified with hydrophilic external layer
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Novel surface modified molecularly imprinted polymer focused on the removal of interference in environmental water samples for chromatographic determination
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Chromatographic comparison of bupivacaine imprinted polymers prepared in crushed monolith, microsphere, silica-based composite and capillary monolith formats
resolves10.1039/b906117g
Water-compatible imprinted polymers for selective depletion of riboflavine from beverages
resolves10.1016/j.eurpolymj.2009.01.021
New restricted access materials combined to molecularly imprinted polymers for selective recognition/release in water media
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Assay System for the Herbicide 2,4-Dichlorophenoxyacetic Acid Using a Molecularly Imprinted Polymer as an Artificial Recognition Element
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Facile RAFT Precipitation Polymerization for the Microwave-Assisted Synthesis of Well-Defined, Double Hydrophilic Block Copolymers and Nanostructured Hydrogels
resolves10.1002/ange.201001461
RAFT Synthesis of Sterically Stabilized Methacrylic Nanolatexes and Vesicles by Aqueous Dispersion Polymerization
resolves10.1002/anie.201001461
RAFT Synthesis of Sterically Stabilized Methacrylic Nanolatexes and Vesicles by Aqueous Dispersion Polymerization
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Biocompatible, Antifouling, and Thermosensitive Core−Shell Nanogels Synthesized by RAFT Aqueous Dispersion Polymerization
resolves10.1016/j.bios.2006.04.014
Preparation of molecularly imprinted polymers using nitroxide-mediated living radical polymerization
resolves10.1002/ange.200352565
Reversible Switching between Superhydrophilicity and Superhydrophobicity
resolves10.1002/anie.200352565
Reversible Switching between Superhydrophilicity and Superhydrophobicity
The 15 references without a DOI — listed, not checked
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no DOI — not checkedMolecularly Imprinted Polymers: Man‐Made Mimics of Antibodies and Their Applications in Analytical Chemistry. Techniques and instrumentation in analytical chemistry
no DOI — not checkedMolecular Imprinting: from Fundamentals to Applications
no DOI — not checkedMolecularly Imprinted Materials. Science and Technology
no DOI — not checkedMolecular Imprinting of Polymers
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no DOI — not checkedNote that the characteristic FTIR absorption peaks of PEG chains were overlapped with those of the poly(4‐VP‐co‐EGDMA) cores in the MIP and CP microspheres grafted with PEG brushes.
no DOI — not checkedA slight decrease in the specific template binding of the MIP microspheres grafted with PNIPAAm brushes (Mn=24 800) in pure water could be attributed to the relatively low Macro‐CTA efficiency during the RAFTPP process owing to its too high molecular weight [14b]which might lead to MIP microspheres with a lower grafting density of polymer brushes as revealed by their relatively higher static water contact angles in comparison with those grafted with shorter PNIPAAm brushes (see Table S2 entries 5–10).
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