Works matching DE "PORPHYRIN synthesis"
Results: 193
Regioregular Polythiophene-Porphyrin Supramolecular Copolymers for Optoelectronic Applications.
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- Macromolecular Chemistry & Physics, 2016, v. 217, n. 3, p. 445, doi. 10.1002/macp.201500280
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Framework Porphyrins: One‐Pot Synthesis of Framework Porphyrin Materials and Their Applications in Bifunctional Oxygen Electrocatalysis (Adv. Funct. Mater. 29/2019).
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- Advanced Functional Materials, 2019, v. 29, n. 29, p. N.PAG, doi. 10.1002/adfm.201970198
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One‐Pot Synthesis of Framework Porphyrin Materials and Their Applications in Bifunctional Oxygen Electrocatalysis.
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- Advanced Functional Materials, 2019, v. 29, n. 29, p. N.PAG, doi. 10.1002/adfm.201901301
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Nanoparticles of Chlorin Dimer with Enhanced Absorbance for Photoacoustic Imaging and Phototherapy.
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- Advanced Functional Materials, 2018, v. 28, n. 26, p. 1, doi. 10.1002/adfm.201706507
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Porous Porphyrin‐Based Organosilica Nanoparticles for NIR Two‐Photon Photodynamic Therapy and Gene Delivery in Zebrafish.
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- Advanced Functional Materials, 2018, v. 28, n. 21, p. 1, doi. 10.1002/adfm.201800235
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Alterations in the porphyrin biosynthesis and antioxidant responses to chilling and heat stresses in Oryza sativa.
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- Biologia Plantarum, 2015, v. 59, n. 2, p. 341, doi. 10.1007/s10535-015-0505-2
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Synthesis, Electrochemical and Photochemical Studies on π‐Extended Mono‐β‐Functionalized Porphyrin Dyads.
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- ChemPhotoChem, 2019, v. 3, n. 3, p. 151, doi. 10.1002/cptc.201800165
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Self-assembly of uncharged amphiphilic porphyrins and incorporation of C 60 fullerenes in water.
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- Supramolecular Chemistry, 2016, v. 28, n. 7/8, p. 634, doi. 10.1080/10610278.2015.1092535
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A convenient synthesis of a porphyrin cross-linked polymer, its application as a size selective heterogeneous catalyst and a comparison with a porphyrin-cored hyperbranched polymer.
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- Supramolecular Chemistry, 2016, v. 28, n. 7/8, p. 617, doi. 10.1080/10610278.2015.1083102
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Synthesis, Spectral, and Coordination Properties of Halogen-Substituted Tetraarylporphyrins.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 3, p. 459, doi. 10.1134/S1070363219030150
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Synthesis and Estimation of Radical Scavenging Activity of Tetra(meso-aryl)porphyrins Containing 2,6-Dimethoxyphenol Unit.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 8, p. 1635, doi. 10.1134/S1070363218080145
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Fullerene-containing porphyrins: Synthesis and potential practical applications.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 9, p. 2145, doi. 10.1134/S1070363216090322
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Synthesis of water-soluble copolymers containing porphyrin fragments in the side chain.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 6, p. 1505, doi. 10.1134/S1070363216060475
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Synthesis of novel thiophosphorylated meso-substituted porphyrin.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 11, p. 2670, doi. 10.1134/S1070363215110298
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Calculation of equilibrium formation constants of complexes with a polydentate oligomer.
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- Russian Journal of General Chemistry, 2014, v. 84, n. 3, p. 424, doi. 10.1134/S1070363214030037
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Synthesis, physicochemical and coordination properties of 5,15-diphenyltetramethyltetraethylporphyn nitro derivatives.
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- Russian Journal of General Chemistry, 2012, v. 82, n. 3, p. 488, doi. 10.1134/S1070363212030218
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1,3,5,7-Tetrasubstituted adamantanes as frameworks in the design of assemblies of porphyrin macrocycles.
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- Doklady Chemistry, 2017, v. 474, n. 2, p. 129, doi. 10.1134/S0012500817060039
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Synthesis of carborane conjugates based on the maleimide derivative of 5,10,15,20-tetraphenylporphyrin.
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- Doklady Chemistry, 2014, v. 458, n. 1, p. 165, doi. 10.1134/S0012500814090018
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Insight into the Interaction of Cationic Porphyrin-Anthraquinone Hybrids with Hsp90: In Silico Analysis.
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- Journal of Mathematical & Fundamental Sciences, 2018, v. 50, n. 3, p. 303, doi. 10.5614/j.math.fund.sci.2018.50.3.6
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Reductive Functionalization of Graphenides With Nickel(II) Porphyrin Diazonium Compounds.
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- Physica Status Solidi - Rapid Research Letters, 2017, v. 11, n. 11, p. n/a, doi. 10.1002/pssr.201700306
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Special Issue of "Porphyrins and Phthalocyanines".
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- Chinese Journal of Chemistry, 2016, v. 34, n. 10, p. 947, doi. 10.1002/cjoc.201690025
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5-Aminolevulinic Acid Improves Nutrient Uptake and Endogenous Hormone Accumulation, Enhancing Low-Temperature Stress Tolerance in Cucumbers.
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- International Journal of Molecular Sciences, 2018, v. 19, n. 11, p. 3379, doi. 10.3390/ijms19113379
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Effects of Light-Emitting Diode Irradiation on Growth Characteristics and Regulation of Porphyrin Biosynthesis in Rice Seedlings.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 3, p. 641, doi. 10.3390/ijms18030641
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Differential Antioxidant Responses and Perturbed Porphyrin Biosynthesis after Exposure to Oxyfluorfen and Methyl Viologen in Oryza sativa.
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- International Journal of Molecular Sciences, 2015, v. 16, n. 7, p. 16529, doi. 10.3390/ijms160716529
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Synthesis and Spectral Evaluation of Some Unsymmetrical Mesoporphyrinic Complexes.
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- International Journal of Molecular Sciences, 2012, v. 13, n. 7, p. 8112, doi. 10.3390/ijms13078112
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Cyclodextrin-Templated Porphyrin Nanorings.
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- Angewandte Chemie, 2014, v. 126, n. 30, p. 7904, doi. 10.1002/ange.201402917
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Towards True Carbaporphyrinoids: Synthesis of 21-Carba-23-thiaporphyrin.
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- Angewandte Chemie, 2014, v. 126, n. 19, p. 4985, doi. 10.1002/ange.201310999
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Synthesis and Switching the Aromatic Character of Oxatriphyrins(2.1.1).
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- Angewandte Chemie, 2014, v. 126, n. 11, p. 3036, doi. 10.1002/ange.201310129
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On the Molecular Structure and Bonding in a Lithium Bismuth Porphyrin Complex: LiBi(TPP)<sub>2</sub>.
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- Angewandte Chemie, 2014, v. 126, n. 6, p. 1620, doi. 10.1002/ange.201308672
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Silver-Mediated Formation of a Cofacial Porphyrin Dimer with the Ability to Intercalate Aromatic Molecules.
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- Angewandte Chemie, 2013, v. 125, n. 46, p. 12318, doi. 10.1002/ange.201306510
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Highly sensitive free-base-porphyrin-based thin-film optical waveguide sensor for detection of low concentration NO<sub>2</sub> gas at ambient temperature.
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- Journal of Materials Science, 2018, v. 53, n. 15, p. 10822, doi. 10.1007/s10853-018-2374-5
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Variations in functional substitution of the macroheterocycle and structure of stable rhenium(V) porphyrins.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 9, p. 1361, doi. 10.1134/S1070428014090218
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Systematic Investigation of Porphyrin-Thiophene Conjugates for Ternary Bulk Heterojunction Solar Cells.
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- Advanced Energy Materials, 2016, v. 6, n. 20, p. n/a, doi. 10.1002/aenm.201600957
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Controlling the Photophysics of Aromatic Guests Using a Cyclic Porphyrin Dimer: Synthesis, Structure, and Encapsulation‐Mediated "ON‐OFF" Switch.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 31, p. 3629, doi. 10.1002/ejic.201900639
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Synthesis of substituted meso-tetraphenylporphyrins in mixed solvent systems.
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- ARKIVOC: Online Journal of Organic Chemistry, 2013, p. 389
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Synthesis and characterization of p-extended porphyrins as potential precursors for the formation of columnar mesophases: Design principles for columnar mesophases need revision?
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- ARKIVOC: Online Journal of Organic Chemistry, 2011, p. 29
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Thermal studies of metalloporphyrins with metals in different oxidation states.
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- Journal of Thermal Analysis & Calorimetry, 2013, v. 112, n. 1, p. 11, doi. 10.1007/s10973-012-2860-y
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Identification of PEPT2 as an important candidate molecule in 5-ALA-mediated fluorescence-guided surgery in WHO grade II/III gliomas.
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- Journal of Neuro-Oncology, 2019, v. 143, n. 2, p. 197, doi. 10.1007/s11060-019-03158-3
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Radiolabelled porphyrins in nuclear medicine.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2014, v. 57, n. 4, p. 304, doi. 10.1002/jlcr.3166
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Molecular insights into the human ABCB6 transporter.
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- Cell Discovery, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41421-021-00284-z
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Charge Carrier Dynamics and pH Effect on Optical Properties of Anionic and Cationic Porphyrin-Graphene Oxide Composites.
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- Journal of Electronic Materials, 2018, v. 47, n. 5, p. 2897, doi. 10.1007/s11664-018-6139-3
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Concentrations of Irgarol in selected marinas of Oahu, Hawaii and effects on settlement of coral larval.
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- Ecotoxicology, 2012, v. 21, n. 1, p. 1, doi. 10.1007/s10646-011-0752-8
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Effects of δ-aminolevulinic acid, and lactulose supplements in weaning piglets.
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- Journal of Animal Science, 2016, v. 94, p. 132, doi. 10.2527/msasas2016-282
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Intraoperative photodynamic diagnosis of lymph node metastasis in esophageal cancer patients using 5-aminolevulinic acid.
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- Oncology Letters, 2015, v. 10, n. 5, p. 3035, doi. 10.3892/ol.2015.3685
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Plasma protoporphyrin IX following administration of 5-aminolevulinic acid as a potential tumor marker.
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- Molecular & Clinical Oncology, 2015, v. 3, n. 4, p. 57, doi. 10.3892/mco.2015.549
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Budget impact of incorporating one instillation of hexaminolevulinate hydrochloride blue-light cytoscopy in transurethral bladder tumour resection for patients with non-muscle-invasive bladder cancer in Sweden.
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- BJU International, 2016, v. 117, n. 6B, p. E102, doi. 10.1111/bju.13261
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Base-Promoted Selective Activation of Benzylic Carbon-Hydrogen Bonds of Toluenes with Rhodium(III) Porphyrin Chloride: Synthetic Scopes and Mechanism.
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- Journal of the Chinese Chemical Society, 2013, v. 60, n. 7, p. 779, doi. 10.1002/jccs.201200635
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Efficient Synthesis of Arylenedioxy-Bridged Porphyrin Dimers through Catalyst-Free Nucleophilic Aromatic Substitution.
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- ChemPlusChem, 2020, v. 85, n. 1, p. 217, doi. 10.1002/cplu.201900670
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Panchromatic π-Extended Porphyrins from Conjugation with Quinones.
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- ChemPlusChem, 2016, v. 81, n. 5, p. 477, doi. 10.1002/cplu.201600115
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Metallomesogens with Luminescent Behaviour: Palladium Complexes Derived from Alkylamide Tetraarylporphyrins.
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- ChemPlusChem, 2016, v. 81, n. 3, p. 253, doi. 10.1002/cplu.201600015
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