Works about RESORCINARENES
Results: 139
Encapsulation in Charged Droplets Generates Distorted Host‐Guest Complexes**.
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- Chemistry - A European Journal, 2023, v. 29, n. 71, p. 1, doi. 10.1002/chem.202302112
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Doxorubicin delivery by polymer nanocarrier based on N-methylglucamine resorcinarene.
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- Supramolecular Chemistry, 2020, v. 32, n. 2, p. 150, doi. 10.1080/10610278.2020.1714620
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Efficient syntheses of π-electron deficient macrocycles.
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- Supramolecular Chemistry, 2020, v. 32, n. 2, p. 119, doi. 10.1080/10610278.2019.1711091
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Selective recognition of small hydrogen bond acceptors by a calix[6]arene-based molecular container.
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- Supramolecular Chemistry, 2020, v. 32, n. 1, p. 23, doi. 10.1080/10610278.2019.1679374
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Mechanism for efficient separation of eugenol and eugenol acetate with β-cyclodextrin as a selective solvent.
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- Supramolecular Chemistry, 2019, v. 31, n. 12, p. 767, doi. 10.1080/10610278.2019.1702663
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A reactive and environmentally friendly protocol for expeditious synthesis of various resorcinarenes using zinc hydrogen sulfate.
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- Supramolecular Chemistry, 2019, v. 31, n. 6, p. 377, doi. 10.1080/10610278.2019.1598557
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Host-guest complexes of C-propyl-2-bromoresorcinarene with aromatic <italic>N</italic>-oxides<sup>*</sup>.
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- Supramolecular Chemistry, 2018, v. 30, n. 5/6, p. 445, doi. 10.1080/10610278.2017.1414217
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Supramolecular nanoscale systems based on amphiphilic tetramethylensulfonatocalix[4]resorcinarenes and cationic polyelectrolyte with controlled guest molecule binding.
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- Supramolecular Chemistry, 2017, v. 29, n. 4, p. 278, doi. 10.1080/10610278.2016.1219034
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Covalently assembled resorcin[4]arenes and molecular tweezers: a chiral recognition rationale by NMR.
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- Supramolecular Chemistry, 2016, v. 28, n. 7/8, p. 647, doi. 10.1080/10610278.2015.1111373
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Calixarenes and resorcinarenes as scaffolds for supramolecular metallo-enzyme mimicry.
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- Supramolecular Chemistry, 2014, v. 26, n. 7/8, p. 454, doi. 10.1080/10610278.2013.877137
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Synthesis of a Zn-salen resorcinarene-based cavitand and its fluorescence response to nitro compounds.
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- Supramolecular Chemistry, 2014, v. 26, n. 3/4, p. 245, doi. 10.1080/10610278.2013.852673
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Influence of amidoammonium calix[4]resorcinarenes on methyl orange protolytic equilibrium: supramolecular indicator systems.
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- Supramolecular Chemistry, 2013, v. 25, n. 12, p. 831, doi. 10.1080/10610278.2013.809085
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Preparation of partially functionalised resorcinarene derivatives.
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- Supramolecular Chemistry, 2013, v. 25, n. 12, p. 777, doi. 10.1080/10610278.2013.803108
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Complexation of enantiomerically pure tetraalkylammonium cations by ethyl resorcinarene.
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- Supramolecular Chemistry, 2013, v. 25, n. 9-11, p. 609, doi. 10.1080/10610278.2013.808344
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Anion binding to a tetracopper resorcinarene-based complex.
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- Supramolecular Chemistry, 2013, v. 25, n. 3, p. 158, doi. 10.1080/10610278.2012.738297
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Reduced symmetry triflate-resorcin[4]arenes.
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- Supramolecular Chemistry, 2012, v. 24, n. 8, p. 618, doi. 10.1080/10610278.2012.703324
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The role of the solvation shell decomposition of alkali metal ions in their selective complexation by resorcinarene and its cavitand.
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- Supramolecular Chemistry, 2012, v. 24, n. 6, p. 374, doi. 10.1080/10610278.2012.678358
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Synthesis of PAMAM dendrimers with a resorcinarene core and their metal complexation.
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- Supramolecular Chemistry, 2012, v. 24, n. 1, p. 56, doi. 10.1080/10610278.2011.622385
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Encagement of Gold Nanoclusters in Crosslinked Resorcinarene Shells.
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- Supramolecular Chemistry, 2002, v. 14, n. 2/3, p. 291, doi. 10.1080/10610270290026202
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Peptide-Resorcinarene Conjugates Obtained via Click Chemistry: Synthesis and Antimicrobial Activity.
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- Antibiotics (2079-6382), 2023, v. 12, n. 4, p. 773, doi. 10.3390/antibiotics12040773
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Octacis(2-hydroxyethylated) Calix[4]resorcinarenes Phosphorochloridates as Precursors in Production of Water-Soluble Calix[4]resorcinarene and Phosphoramidates.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 10, p. 2038, doi. 10.1134/S1070363221100170
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Pre-organized oligomodified resorcinarene ligands. Preparation, structure, and complex formation.
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- Russian Journal of General Chemistry, 2014, v. 84, n. 4, p. 745, doi. 10.1134/S1070363214040240
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Synthesis of new heterofunctionalized resorcinarene derivatives.
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- Russian Journal of General Chemistry, 2012, v. 82, n. 2, p. 276, doi. 10.1134/S107036321202017X
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Use of Titanium Complexes Bearing Diphenolate or Calix[n]arene Ligands in α-Olefin Polymerization and the ROP of Cyclic Esters.
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- Catalysts (2073-4344), 2020, v. 10, n. 2, p. 210, doi. 10.3390/catal10020210
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One-Pot Synthesis of Novel Dibenzoxanthenes, Diarylbutanes, and Calix[4]resorcinarenes via Consecutive Pyrrolidine Ring-Closure/Ring-Opening Reactions.
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- Journal of Chemistry, 2019, p. 1, doi. 10.1155/2019/3424319
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Comparative Study of the Antioxidant Activity of the Conformers of C -tetra(4-methoxyphenyl)calix[4]resorcinarene.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 18, p. 10010, doi. 10.3390/ijms251810010
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Interactions of Sodium Salicylate with β-Cyclodextrin and an Anionic Resorcin[4]arene: Mutual Diffusion Coefficients and Computational Study.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 4, p. 3921, doi. 10.3390/ijms24043921
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The Role of Calix[n]arenes and Pillar[n]arenes in the Design of Silver Nanoparticles: Self-Assembly and Application.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 4, p. 1425, doi. 10.3390/ijms21041425
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Solid Lipid Nanoparticle-Based Calix[n]arenes and Calix-Resorcinarenes as Building Blocks: Synthesis, Formulation and Characterization.
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- International Journal of Molecular Sciences, 2013, v. 14, n. 11, p. 21899, doi. 10.3390/ijms141121899
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Ab initio design of drug carriers for zoledronate guest molecule using phosphonated and sulfonated calix[4]arene and calix[4]resorcinarene host molecules.
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- Journal of Materials Science, 2018, v. 53, n. 7, p. 5125, doi. 10.1007/s10853-017-1930-8
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Recent Advances in Halogen Bonded Assemblies with Resorcin[4]arenes.
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- Chemical Record, 2021, v. 21, n. 2, p. 386, doi. 10.1002/tcr.202000140
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Supramolecular Polymerization Engineered with Molecular Recognition.
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- Chemical Record, 2015, v. 15, n. 5, p. 837, doi. 10.1002/tcr.201500012
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New salt structures based on aminomethylated calix[4]-resorcinarenes and (1-hydroxyethane-1,1-diyl)bisphosphonic acid.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 2, p. 312, doi. 10.1134/S1070428017020324
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Oxygen isotope speedometry in granulite facies garnet recording fluid/melt–rock interaction (Sør Rondane Mountains, East Antarctica).
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- Journal of Metamorphic Geology, 2019, v. 37, n. 7, p. 1037, doi. 10.1111/jmg.12490
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Efficient ethylene purification by a robust ethane-trapping porous organic cage.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24042-7
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- Article
Styrene Hydroformylation with Cavity‐Shaped Ligands.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 47, p. 4951, doi. 10.1002/ejic.201900974
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Reactions of resorcinarene with N,N-dimethylcarbamoyl and N,N-dimethylthiocarbamoyl chlorides: factors affecting the process performance.
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- ARKIVOC: Online Journal of Organic Chemistry, 2016, p. 325, doi. 10.3998/ark.5550190.p009.492
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Retention behavior of resorcinarene-based cavitands on C<sub>8</sub> and C<sub>18</sub> stationary phases.
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- Journal of Separation Science, 2015, v. 38, n. 17, p. 2975, doi. 10.1002/jssc.201500153
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Thermodynamics of complex formation between hydroxypropyl-β-cyclodextrin and quercetin in water–ethanol solvents at T = 298.15 K.
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- Journal of Thermal Analysis & Calorimetry, 2019, v. 138, n. 1, p. 417, doi. 10.1007/s10973-019-08136-5
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Calix[4]resorcinarene macrocycles: Synthesis, thermal behavior and crystalline characterization.
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- Journal of Thermal Analysis & Calorimetry, 2019, v. 137, n. 2, p. 529, doi. 10.1007/s10973-018-7978-0
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Tetramethoxy resorcin[4]arene-tetraester derivatives.
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- Journal of Thermal Analysis & Calorimetry, 2015, v. 120, n. 1, p. 653, doi. 10.1007/s10973-014-4314-1
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Synthesis, Characterization, and Nanomedical Applications of Conjugates between Resorcinarene-Dendrimers and Ibuprofen.
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- Nanomaterials (2079-4991), 2017, v. 7, n. 7, p. 163, doi. 10.3390/nano7070163
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Geochemistry and Mineralogy of Basalts from the South Mid-Atlantic Ridge (18.0°–20.6°S): Evidence of a Heterogeneous Mantle Source.
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- Minerals (2075-163X), 2019, v. 9, n. 11, p. 659, doi. 10.3390/min9110659
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Yttrium(III) Nitrate: A Powerful Catalyst for Green and Rapid Synthesis of Some Supramolecules.
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- Journal of the Chinese Chemical Society, 2015, v. 62, n. 1, p. 13, doi. 10.1002/jccs.201400141
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Highly Selective Fluorimetric Turn‐Off Detection of Copper(II) by Two Different Mechanisms in Calix[4]arene‐Based Chemosensors and Chemodosimeters.
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- ChemPlusChem, 2019, v. 84, n. 10, p. 1610, doi. 10.1002/cplu.201900448
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A Glucose‐Responsive Polymer Nanocarrier Based on Sulfonated Resorcinarene for Controlled Insulin Delivery.
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- ChemPlusChem, 2019, v. 84, n. 10, p. 1560, doi. 10.1002/cplu.201900428
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A straightforward route for covalently anchored pyridinium salt onto upper rim of c-methylcalix[4]resorcinarene with selective antibacterial activity against Gram-positive bacteria.
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- Research on Chemical Intermediates, 2016, v. 42, n. 3, p. 1583, doi. 10.1007/s11164-015-2104-4
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Synthesis, Characterization and DFT-D Studies of 2-Aminoethoxycalix[4]resorcinarenes: A Novel Heterogeneous Organocatalyst.
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- Catalysis Letters, 2022, v. 152, n. 10, p. 3017, doi. 10.1007/s10562-021-03895-z
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One-Pot Synthesis of Tweezer-Like Calix[4]resorcinarene Decorated with Pendant Heterocyclic Moieties: An Efficient and Recyclable Heterogeneous PTC for the Preparation of Azidohydrins in Water.
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- Catalysis Letters, 2014, v. 144, n. 9, p. 1636, doi. 10.1007/s10562-014-1300-y
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Substrate-Selective Olefin Hydrogenation with a Cavitand-Based Bis(N-anisyl iminophosphorane).
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 1, p. 70, doi. 10.1002/ejoc.201601125
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