Angewandte Chemie International Edition, ISSN 1433-7851, 08/2016, Volume 55, Issue 36, pp. 10717 - 10721
When aprotic Li–O2 batteries discharge, the product phase formed in the cathode often contains two different morphologies, that is, crystalline and amorphous...
amorphous Li2O2 | charge-transport properties | aprotic Li–O2 batteries | oxidation kinetics | aprotic Li–O | amorphous Li | batteries | ELECTRON | CHARGE-TRANSPORT | LI-O-2 BATTERIES | aprotic Li-O-2 batteries | CHEMISTRY, MULTIDISCIPLINARY | O-2 REDUCTION | SOLID-STATE | DEPENDENCE | EVOLUTION | LITHIUM-OXYGEN BATTERIES | AIR BATTERIES | NANOTUBES | Electrochemistry | Superoxide | Chemical properties | Batteries | Chemical synthesis | Electrochemical analysis | Transport properties | Purity | Charge transport | Discharge | Morphology | Metal air batteries | Reaction kinetics | Oxidation | Energy efficiency | Kinetics | Power efficiency | Energy management | Siblings | Crystal structure
amorphous Li2O2 | charge-transport properties | aprotic Li–O2 batteries | oxidation kinetics | aprotic Li–O | amorphous Li | batteries | ELECTRON | CHARGE-TRANSPORT | LI-O-2 BATTERIES | aprotic Li-O-2 batteries | CHEMISTRY, MULTIDISCIPLINARY | O-2 REDUCTION | SOLID-STATE | DEPENDENCE | EVOLUTION | LITHIUM-OXYGEN BATTERIES | AIR BATTERIES | NANOTUBES | Electrochemistry | Superoxide | Chemical properties | Batteries | Chemical synthesis | Electrochemical analysis | Transport properties | Purity | Charge transport | Discharge | Morphology | Metal air batteries | Reaction kinetics | Oxidation | Energy efficiency | Kinetics | Power efficiency | Energy management | Siblings | Crystal structure
Journal Article
Molecules, ISSN 1420-3049, 08/2017, Volume 22, Issue 8, p. 1266
The effects of sulfation of yeast glucans was optimized using response surface methodology. The degree of sulfation was evaluated from 0.11 to 0.75 using...
Sulfated yeast glucans (SYG) | Yeast | Yeast glucans (YG) | Saccharomyces cerevisiae | VITRO | PLEURAN BETA-GLUCAN | CHEMISTRY, ORGANIC | ANTITUMOR ACTIVITIES | yeast | PHOMA-HERBARUM YS4108 | MONOSTROMA-LATISSIMUM | sulfated yeast glucans (SYG) | yeast glucans (YG) | DIET | POLYSACCHARIDES | MICE | PLEUROTUS-OSTREATUS | MARINE | Viscosity | Molecular Weight | Spleen - immunology | Solubility | Glucans - pharmacology | Spleen - cytology | Spleen - drug effects | Antioxidants - chemical synthesis | Antioxidants - pharmacology | beta-Glucans - pharmacology | Spectroscopy, Fourier Transform Infrared | Saccharomyces cerevisiae - chemistry | beta-Glucans - chemical synthesis | Catalase - metabolism | Animals | Lymphocytes | Radiation Injuries, Experimental - drug therapy | Sulfates - chemistry | Glucans - chemistry | Mice | Glucans - chemical synthesis | Superoxide Dismutase - metabolism | Fourier transforms | Liquid chromatography | Response surface methodology | Saccharomyces | High-performance liquid chromatography | Chromatography | Sulfation | Antioxidants | Spectrometry | Glucans | Chemical synthesis | High performance liquid chromatography | Conformation
Sulfated yeast glucans (SYG) | Yeast | Yeast glucans (YG) | Saccharomyces cerevisiae | VITRO | PLEURAN BETA-GLUCAN | CHEMISTRY, ORGANIC | ANTITUMOR ACTIVITIES | yeast | PHOMA-HERBARUM YS4108 | MONOSTROMA-LATISSIMUM | sulfated yeast glucans (SYG) | yeast glucans (YG) | DIET | POLYSACCHARIDES | MICE | PLEUROTUS-OSTREATUS | MARINE | Viscosity | Molecular Weight | Spleen - immunology | Solubility | Glucans - pharmacology | Spleen - cytology | Spleen - drug effects | Antioxidants - chemical synthesis | Antioxidants - pharmacology | beta-Glucans - pharmacology | Spectroscopy, Fourier Transform Infrared | Saccharomyces cerevisiae - chemistry | beta-Glucans - chemical synthesis | Catalase - metabolism | Animals | Lymphocytes | Radiation Injuries, Experimental - drug therapy | Sulfates - chemistry | Glucans - chemistry | Mice | Glucans - chemical synthesis | Superoxide Dismutase - metabolism | Fourier transforms | Liquid chromatography | Response surface methodology | Saccharomyces | High-performance liquid chromatography | Chromatography | Sulfation | Antioxidants | Spectrometry | Glucans | Chemical synthesis | High performance liquid chromatography | Conformation
Journal Article
Angewandte Chemie, ISSN 0044-8249, 08/2016, Volume 128, Issue 36, pp. 10875 - 10879
When aprotic Li–O2 batteries discharge, the product phase formed in the cathode often contains two different morphologies, that is, crystalline and amorphous...
Amorphes Li2O2 | Ladungstransport | Oxidationskinetik | Aprotische Li-O2-Batterien | Electrochemistry | Superoxide | Chemical properties | Batteries | Chemical synthesis
Amorphes Li2O2 | Ladungstransport | Oxidationskinetik | Aprotische Li-O2-Batterien | Electrochemistry | Superoxide | Chemical properties | Batteries | Chemical synthesis
Journal Article
Angewandte Chemie, ISSN 0044-8249, 08/2016, Volume 128, Issue 36, p. 10875
When aprotic Li-O2 batteries discharge, the product phase formed in the cathode often contains two different morphologies, that is, crystalline and amorphous...
Electrochemical analysis | Transport properties | Purity | Superoxide | Charge transport | Batteries | Discharge | Morphology | Metal air batteries | Reaction kinetics | Electrochemistry | Oxidation | Energy efficiency | Kinetics | Power efficiency | Chemical synthesis | Energy management | Siblings | Crystal structure
Electrochemical analysis | Transport properties | Purity | Superoxide | Charge transport | Batteries | Discharge | Morphology | Metal air batteries | Reaction kinetics | Electrochemistry | Oxidation | Energy efficiency | Kinetics | Power efficiency | Chemical synthesis | Energy management | Siblings | Crystal structure
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2014, Volume 53, Issue 48, pp. 13264 - 13268
A combined palladium‐ and photoredox‐catalyzed CH olefination enables the synthesis of indoles. By using visible light, the direct CH activation of aromatic...
Heck reaction | CH functionalization | photocatalysis | superoxide | Superoxide | C-H functionalization | Photocatalysis | ROOM-TEMPERATURE | ELECTRON-WITHDRAWING SUBSTITUENTS | BOND-FORMING REACTIONS | HECK REACTIONS | AROMATIC-SUBSTITUTION | CHEMISTRY, MULTIDISCIPLINARY | OLEFINS | OXIDATIVE CYCLIZATION | EFFICIENT | ALKENYLATION | MOLECULAR-OXYGEN | Indoles - chemical synthesis | Molecular Structure | Catalysis | Palladium - chemistry | Light | Activation | Joining | Synthesis | Indoles | Derivatives
Heck reaction | CH functionalization | photocatalysis | superoxide | Superoxide | C-H functionalization | Photocatalysis | ROOM-TEMPERATURE | ELECTRON-WITHDRAWING SUBSTITUENTS | BOND-FORMING REACTIONS | HECK REACTIONS | AROMATIC-SUBSTITUTION | CHEMISTRY, MULTIDISCIPLINARY | OLEFINS | OXIDATIVE CYCLIZATION | EFFICIENT | ALKENYLATION | MOLECULAR-OXYGEN | Indoles - chemical synthesis | Molecular Structure | Catalysis | Palladium - chemistry | Light | Activation | Joining | Synthesis | Indoles | Derivatives
Journal Article
Chemical Reviews, ISSN 0009-2665, 03/2016, Volume 116, Issue 5, pp. 3029 - 3085
Superoxide ion (O2 •–) is of great significance as a radical species implicated in diverse chemical and biological systems. However, the chemistry knowledge of...
ROOM-TEMPERATURE | ZERO-VALENT IRON | ELECTROGENERATED SUPEROXIDE | ELECTROCHEMICAL REDUCTION | SINGLET OXYGEN | OXYGEN REDUCTION REACTION | HYDROGEN-PEROXIDE | CHEMISTRY, MULTIDISCIPLINARY | SOLUBLE TETRAZOLIUM SALT | CORE-SHELL NANOWIRES | GLASSY-CARBON ELECTRODES | Electrodes | Chemistry Techniques, Synthetic | Refuse Disposal | Superoxides - analysis | Superoxides - chemistry | Hazardous Substances - chemistry | Superoxides - chemical synthesis | Environmental Restoration and Remediation | Ionic Liquids - chemistry
ROOM-TEMPERATURE | ZERO-VALENT IRON | ELECTROGENERATED SUPEROXIDE | ELECTROCHEMICAL REDUCTION | SINGLET OXYGEN | OXYGEN REDUCTION REACTION | HYDROGEN-PEROXIDE | CHEMISTRY, MULTIDISCIPLINARY | SOLUBLE TETRAZOLIUM SALT | CORE-SHELL NANOWIRES | GLASSY-CARBON ELECTRODES | Electrodes | Chemistry Techniques, Synthetic | Refuse Disposal | Superoxides - analysis | Superoxides - chemistry | Hazardous Substances - chemistry | Superoxides - chemical synthesis | Environmental Restoration and Remediation | Ionic Liquids - chemistry
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 07/2012, Volume 53, Issue 28, pp. 3654 - 3657
A protecting group AZMB was introduced to ribonucleosides 3a2-hydroxyl group to facilitate solution phase synthesis of siRNA. The protection and cleavage...
Synthesis (chemistry) | Chlorides | Tetrahedrons | Biocompatibility | Superoxide dismutase | Cleavage | Biological | Gene expression
Synthesis (chemistry) | Chlorides | Tetrahedrons | Biocompatibility | Superoxide dismutase | Cleavage | Biological | Gene expression
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 10/2005, Volume 48, Issue 20, pp. 6400 - 6408
The synthesis of several coumarin Mannich bases is described. The structures of the synthesized compounds were confirmed by spectral and elemental analysis....
SUPEROXIDE | CHEMISTRY, MEDICINAL | REACTIVE OXYGEN | ACID | INHIBITION | SERIES | PROTECTION | DRUGS | 5-LIPOXYGENASE | Arthritis, Experimental - drug therapy | Free Radical Scavengers - chemistry | Rats, Inbred F344 | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Coumarins - chemistry | Male | Structure-Activity Relationship | Immunologic Factors - chemical synthesis | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Mannich Bases - chemical synthesis | Lipoxygenase Inhibitors - chemical synthesis | Lipoxygenase Inhibitors - chemistry | Free Radical Scavengers - chemical synthesis | Mannich Bases - pharmacology | Female | Anti-Inflammatory Agents, Non-Steroidal - chemical synthesis | Immunologic Factors - chemistry | Superoxides - chemistry | Rats | Cyclooxygenase Inhibitors - chemistry | Edema - drug therapy | Mannich Bases - chemistry | Coumarins - pharmacology | Animals | Coumarins - chemical synthesis | Cyclooxygenase Inhibitors - chemical synthesis | Carrageenan | Edema - chemically induced | Immunologic Factors - pharmacology
SUPEROXIDE | CHEMISTRY, MEDICINAL | REACTIVE OXYGEN | ACID | INHIBITION | SERIES | PROTECTION | DRUGS | 5-LIPOXYGENASE | Arthritis, Experimental - drug therapy | Free Radical Scavengers - chemistry | Rats, Inbred F344 | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Coumarins - chemistry | Male | Structure-Activity Relationship | Immunologic Factors - chemical synthesis | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Mannich Bases - chemical synthesis | Lipoxygenase Inhibitors - chemical synthesis | Lipoxygenase Inhibitors - chemistry | Free Radical Scavengers - chemical synthesis | Mannich Bases - pharmacology | Female | Anti-Inflammatory Agents, Non-Steroidal - chemical synthesis | Immunologic Factors - chemistry | Superoxides - chemistry | Rats | Cyclooxygenase Inhibitors - chemistry | Edema - drug therapy | Mannich Bases - chemistry | Coumarins - pharmacology | Animals | Coumarins - chemical synthesis | Cyclooxygenase Inhibitors - chemical synthesis | Carrageenan | Edema - chemically induced | Immunologic Factors - pharmacology
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 1900, Volume 137, Issue 21, pp. 6837 - 6843
Superoxide anion radical (O2 •–) is undoubtedly the most important primary reactive oxygen species (ROS) found in cells, whose formation and fate are...
OXIDATIVE STRESS | DESIGN | MYELOPEROXIDASE | HYDROETHIDINE | ETHIDIUM | BIOLOGY | CHEMISTRY | TISSUES | CHEMISTRY, MULTIDISCIPLINARY | Fluorescent Dyes - chemical synthesis | Cell Line | Fluoresceins - chemistry | Fluorescent Dyes - chemistry | Macrophages - chemistry | Cell Survival | HCT116 Cells | Humans | Alkanesulfonates - chemical synthesis | Fluorescent Dyes - analysis | Superoxides - analysis | Fluoresceins - chemical synthesis | Macrophages - cytology | Zebrafish - embryology | Animals | Alkanesulfonates - chemistry | Mice | Molecular Structure | Hydrogen-Ion Concentration | Flow cytometry | Usage | Probes (Electronic instruments) | Superoxide | Chemical properties | Research | Chemical synthesis
OXIDATIVE STRESS | DESIGN | MYELOPEROXIDASE | HYDROETHIDINE | ETHIDIUM | BIOLOGY | CHEMISTRY | TISSUES | CHEMISTRY, MULTIDISCIPLINARY | Fluorescent Dyes - chemical synthesis | Cell Line | Fluoresceins - chemistry | Fluorescent Dyes - chemistry | Macrophages - chemistry | Cell Survival | HCT116 Cells | Humans | Alkanesulfonates - chemical synthesis | Fluorescent Dyes - analysis | Superoxides - analysis | Fluoresceins - chemical synthesis | Macrophages - cytology | Zebrafish - embryology | Animals | Alkanesulfonates - chemistry | Mice | Molecular Structure | Hydrogen-Ion Concentration | Flow cytometry | Usage | Probes (Electronic instruments) | Superoxide | Chemical properties | Research | Chemical synthesis
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 03/2016, Volume 138, Issue 9, pp. 2893 - 2896
Despite significant developments in optical imaging of superoxide anion (O2 •–) as the preliminary reactive oxygen species, novel visualizing strategies that...
DOTS | STRESS | CHEMISTRY, MULTIDISCIPLINARY | DNA | BIOLOGY | PROBES | Pyrazines - chemistry | Animals | Imidazoles - chemistry | Superoxides - analysis | Superoxides - chemistry | Nanostructures - chemistry | Mice | Energy Transfer | Imidazoles - chemical synthesis | Luminescent Measurements - methods | Pyrazines - chemical synthesis | Energy transformation | Analysis | Chemiluminescence | Research | Chemical properties | Chemical synthesis | Chemical compounds
DOTS | STRESS | CHEMISTRY, MULTIDISCIPLINARY | DNA | BIOLOGY | PROBES | Pyrazines - chemistry | Animals | Imidazoles - chemistry | Superoxides - analysis | Superoxides - chemistry | Nanostructures - chemistry | Mice | Energy Transfer | Imidazoles - chemical synthesis | Luminescent Measurements - methods | Pyrazines - chemical synthesis | Energy transformation | Analysis | Chemiluminescence | Research | Chemical properties | Chemical synthesis | Chemical compounds
Journal Article
Journal of Photochemistry & Photobiology, B: Biology, ISSN 1011-1344, 06/2014, Volume 135, pp. 33 - 43
Three novel structure Ln(III) complexes (Ln = Sm, Eu and Tb) have been synthesized and characterized systematically. The ligand and Ln(III) complexes bind to...
DNA-binding property | Lanthanide(III) complex | Antioxidant activity | Bis(N-salicylidene)-3-oxapentane-1,5-diamine | Crystal structure | PROTEIN | COPPER(II) | BIOCHEMISTRY & MOLECULAR BIOLOGY | BENZOYL HYDRAZONE | ANTICANCER ACTIVITY | BIOPHYSICS | LIGANDS | AFFINITY | SCHIFF-BASES | MAGNETIC-PROPERTIES | COORDINATION POLYMERS | Viscosity | Free Radical Scavengers - chemistry | Molecular Conformation | Diamines - metabolism | Coordination Complexes - metabolism | Crystallography, X-Ray | Ethidium - metabolism | Salicylates - chemistry | Hydroxyl Radical - chemistry | Free Radical Scavengers - chemical synthesis | Salicylates - metabolism | Pentanes - metabolism | Binding, Competitive | Chemistry Techniques, Synthetic | Free Radical Scavengers - metabolism | Superoxides - chemistry | Models, Molecular | DNA - metabolism | Coordination Complexes - chemistry | Pentanes - chemistry | Lanthanoid Series Elements - chemistry | Schiff Bases - chemistry | Coordination Complexes - chemical synthesis | Diamines - chemistry | Ligands | Antioxidants | Genetic research | Chemical properties | Structure | DNA | Crystals
DNA-binding property | Lanthanide(III) complex | Antioxidant activity | Bis(N-salicylidene)-3-oxapentane-1,5-diamine | Crystal structure | PROTEIN | COPPER(II) | BIOCHEMISTRY & MOLECULAR BIOLOGY | BENZOYL HYDRAZONE | ANTICANCER ACTIVITY | BIOPHYSICS | LIGANDS | AFFINITY | SCHIFF-BASES | MAGNETIC-PROPERTIES | COORDINATION POLYMERS | Viscosity | Free Radical Scavengers - chemistry | Molecular Conformation | Diamines - metabolism | Coordination Complexes - metabolism | Crystallography, X-Ray | Ethidium - metabolism | Salicylates - chemistry | Hydroxyl Radical - chemistry | Free Radical Scavengers - chemical synthesis | Salicylates - metabolism | Pentanes - metabolism | Binding, Competitive | Chemistry Techniques, Synthetic | Free Radical Scavengers - metabolism | Superoxides - chemistry | Models, Molecular | DNA - metabolism | Coordination Complexes - chemistry | Pentanes - chemistry | Lanthanoid Series Elements - chemistry | Schiff Bases - chemistry | Coordination Complexes - chemical synthesis | Diamines - chemistry | Ligands | Antioxidants | Genetic research | Chemical properties | Structure | DNA | Crystals
Journal Article
Journal of Inorganic Biochemistry, ISSN 0162-0134, 02/2015, Volume 143, pp. 77 - 87
Two new Cu(II)–dipeptide complexes of 2-(4′-thiazolyl)benzimidazole, [Cu(Gly-Gly)(TBZ)(Cl)]·4H O ( ) and [Cu(Gly- -Leu)(TBZ)(Cl)]·H O ( ) (Gly-Gly =...
2-(4′-Thiazolyl)benzimidazole | Cytotoxicity | Metallopeptide complexes | Oxidative damage | Antioxidant activity | DNA binding | SUPEROXIDE | Metallopeptide complexes 2-(4'-Thiazolyl)benzimidazole | BIOCHEMISTRY & MOLECULAR BIOLOGY | TOPOISOMERASE-I | CLEAVAGE | MOLECULAR DOCKING | CHEMISTRY, INORGANIC & NUCLEAR | COPPER(II) COMPLEXES | RAY CRYSTAL-STRUCTURES | ETHIDIUM-BROMIDE | DINUCLEAR COMPLEXES | BINDING | ANTIMICROBIAL ACTIVITY | Antioxidants - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Anthelmintics - chemical synthesis | Copper - chemistry | Cytotoxins - pharmacology | Thiabendazole - chemical synthesis | Antineoplastic Agents - pharmacology | Dipeptides - chemical synthesis | Carcinoma - pathology | Carcinoma - drug therapy | Thiabendazole - chemistry | Thiabendazole - pharmacology | Cytotoxins - chemical synthesis | Dipeptides - pharmacology | Copper - pharmacology | Antioxidants - chemical synthesis | Antioxidants - pharmacology | DNA - metabolism | Anthelmintics - chemistry | Antineoplastic Agents - chemistry | Dipeptides - chemistry | Hep G2 Cells | DNA - chemistry | Anthelmintics - pharmacology | Cytotoxins - chemistry | Plasmids - chemistry | Carcinoma - metabolism | DNA Damage | HeLa Cells | Drug Screening Assays, Antitumor | Antioxidants | Chemotherapy | Ionization | Analysis | DNA | Glycine | Cancer
2-(4′-Thiazolyl)benzimidazole | Cytotoxicity | Metallopeptide complexes | Oxidative damage | Antioxidant activity | DNA binding | SUPEROXIDE | Metallopeptide complexes 2-(4'-Thiazolyl)benzimidazole | BIOCHEMISTRY & MOLECULAR BIOLOGY | TOPOISOMERASE-I | CLEAVAGE | MOLECULAR DOCKING | CHEMISTRY, INORGANIC & NUCLEAR | COPPER(II) COMPLEXES | RAY CRYSTAL-STRUCTURES | ETHIDIUM-BROMIDE | DINUCLEAR COMPLEXES | BINDING | ANTIMICROBIAL ACTIVITY | Antioxidants - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Anthelmintics - chemical synthesis | Copper - chemistry | Cytotoxins - pharmacology | Thiabendazole - chemical synthesis | Antineoplastic Agents - pharmacology | Dipeptides - chemical synthesis | Carcinoma - pathology | Carcinoma - drug therapy | Thiabendazole - chemistry | Thiabendazole - pharmacology | Cytotoxins - chemical synthesis | Dipeptides - pharmacology | Copper - pharmacology | Antioxidants - chemical synthesis | Antioxidants - pharmacology | DNA - metabolism | Anthelmintics - chemistry | Antineoplastic Agents - chemistry | Dipeptides - chemistry | Hep G2 Cells | DNA - chemistry | Anthelmintics - pharmacology | Cytotoxins - chemistry | Plasmids - chemistry | Carcinoma - metabolism | DNA Damage | HeLa Cells | Drug Screening Assays, Antitumor | Antioxidants | Chemotherapy | Ionization | Analysis | DNA | Glycine | Cancer
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 01/2011, Volume 133, Issue 1, pp. 131 - 140
The construction of a new class of compoundsthe hangman corrolesis provided efficiently by the modification of macrocyclic forming reactions from bilanes....
ARYL-SUBSTITUTED CORROLES | PI-CATION RADICALS | ELECTROCATALYTIC REDUCTION | O-O ACTIVATION | COUPLED ELECTRON-TRANSFER | X-RAY STRUCTURE | 1ST DIRECT SYNTHESIS | MICROWAVE-ASSISTED SYNTHESIS | WALLED CARBON NANOTUBES | CHEMISTRY, MULTIDISCIPLINARY | SPIN DELOCALIZATION | Protons | Electron Transport | Quantum Theory | Molecular Conformation | Porphyrins - chemistry | Oxygen - chemistry | Superoxides - chemistry | Models, Molecular | Porphyrins - chemical synthesis | Ligands | Spectrum Analysis | Cobalt - chemistry | Usage | Analysis | Organometallic compounds | Density functionals | Oxidation-reduction reaction | Catalysis | Chemical properties | Macrocycles | Structure | Cobalt
ARYL-SUBSTITUTED CORROLES | PI-CATION RADICALS | ELECTROCATALYTIC REDUCTION | O-O ACTIVATION | COUPLED ELECTRON-TRANSFER | X-RAY STRUCTURE | 1ST DIRECT SYNTHESIS | MICROWAVE-ASSISTED SYNTHESIS | WALLED CARBON NANOTUBES | CHEMISTRY, MULTIDISCIPLINARY | SPIN DELOCALIZATION | Protons | Electron Transport | Quantum Theory | Molecular Conformation | Porphyrins - chemistry | Oxygen - chemistry | Superoxides - chemistry | Models, Molecular | Porphyrins - chemical synthesis | Ligands | Spectrum Analysis | Cobalt - chemistry | Usage | Analysis | Organometallic compounds | Density functionals | Oxidation-reduction reaction | Catalysis | Chemical properties | Macrocycles | Structure | Cobalt
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 02/2017, Volume 139, Issue 5, pp. 2035 - 2044
The selectivity control toward aldehyde in the aromatic alcohol oxidation remains a grand challenge using molecular oxygen under mild conditions. In this work,...
ALCOHOLS | VISIBLE-LIGHT | NANOPARTICLES | CATALYSIS | SUPEROXIDE ANION | POROUS COORDINATION POLYMERS | COUPLING REACTIONS | METAL-ORGANIC FRAMEWORK | AEROBIC OXIDATION | CHEMISTRY, MULTIDISCIPLINARY | MOLECULAR-OXYGEN | Oxidation-reduction reaction | Usage | Catalysis | Chemical properties | Chemical synthesis | Platinum
ALCOHOLS | VISIBLE-LIGHT | NANOPARTICLES | CATALYSIS | SUPEROXIDE ANION | POROUS COORDINATION POLYMERS | COUPLING REACTIONS | METAL-ORGANIC FRAMEWORK | AEROBIC OXIDATION | CHEMISTRY, MULTIDISCIPLINARY | MOLECULAR-OXYGEN | Oxidation-reduction reaction | Usage | Catalysis | Chemical properties | Chemical synthesis | Platinum
Journal Article
Journal of Inorganic Biochemistry, ISSN 0162-0134, 2009, Volume 103, Issue 2, pp. 219 - 226
The coordination behavior of copper(II) with tricarballylic acid (H TCA) and imidazole (Imz) is described. Speciation in aqueous solution has been determined...
SOD activity | Cu(II) complexes | EPR | Speciation | Tricarballylic acid | TRANSITION-METAL IONS | ACID | BIOCHEMISTRY & MOLECULAR BIOLOGY | SALICYLGLYCINE | COORDINATION | CHEMISTRY, INORGANIC & NUCLEAR | COPPER(II) COMPLEXES | LIGANDS | CHEMISTRY | SUPEROXIDE-DISMUTASE | Superoxide Dismutase - chemistry | Copper - chemistry | Organometallic Compounds - chemical synthesis | Superoxide Dismutase - chemical synthesis | Imidazoles - chemistry | Organometallic Compounds - chemistry | Tricarboxylic Acids - chemistry | Copper compounds | Analysis | Superoxide
SOD activity | Cu(II) complexes | EPR | Speciation | Tricarballylic acid | TRANSITION-METAL IONS | ACID | BIOCHEMISTRY & MOLECULAR BIOLOGY | SALICYLGLYCINE | COORDINATION | CHEMISTRY, INORGANIC & NUCLEAR | COPPER(II) COMPLEXES | LIGANDS | CHEMISTRY | SUPEROXIDE-DISMUTASE | Superoxide Dismutase - chemistry | Copper - chemistry | Organometallic Compounds - chemical synthesis | Superoxide Dismutase - chemical synthesis | Imidazoles - chemistry | Organometallic Compounds - chemistry | Tricarboxylic Acids - chemistry | Copper compounds | Analysis | Superoxide
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 08/2007, Volume 129, Issue 34, pp. 10324 - 10325
We designed and synthesized fluorescent probes for the sensitive and selective detection of highly reactive oxygen species (hROS) in mitochondria of living...
SUPEROXIDE | OXIDATIVE DAMAGE | CANCER | CHEMISTRY, MULTIDISCIPLINARY | DNA | MODULATION | Fluorescent Dyes - chemical synthesis | Fluorescent Dyes - chemistry | Reactive Oxygen Species - chemistry | Reactive Oxygen Species - metabolism | Cell Survival | Heterocyclic Compounds, 3-Ring - chemistry | Humans | Drug Design | HL-60 Cells | Mitochondria - metabolism | Molecular Structure | Heterocyclic Compounds, 3-Ring - chemical synthesis | Oxides | Chemical properties | Chemical synthesis | Observations | Electric properties
SUPEROXIDE | OXIDATIVE DAMAGE | CANCER | CHEMISTRY, MULTIDISCIPLINARY | DNA | MODULATION | Fluorescent Dyes - chemical synthesis | Fluorescent Dyes - chemistry | Reactive Oxygen Species - chemistry | Reactive Oxygen Species - metabolism | Cell Survival | Heterocyclic Compounds, 3-Ring - chemistry | Humans | Drug Design | HL-60 Cells | Mitochondria - metabolism | Molecular Structure | Heterocyclic Compounds, 3-Ring - chemical synthesis | Oxides | Chemical properties | Chemical synthesis | Observations | Electric properties
Journal Article
Materials Research Bulletin, ISSN 0025-5408, 11/2016, Volume 83, p. 172
Display Omitted
Superoxide | Semiconductors | Chemical synthesis | Optical properties | Photoluminescence
Superoxide | Semiconductors | Chemical synthesis | Optical properties | Photoluminescence
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 10/2014, Volume 136, Issue 42, pp. 14896 - 14902
A combination of anionic and RAFT polymerization was used to synthesize an ABC triblock polymer...
BIODEGRADABLE HYDROGELS | AQUEOUS-SOLUTIONS | SUPEROXIDE | TEMPERATURE | FLUORESCENCE | NETWORKS | MICELLES | GELATION | CHEMISTRY, MULTIDISCIPLINARY | INJECTABLE HYDROGELS | POLY(N-ISOPROPYLACRYLAMIDE) | Biocompatible Materials - metabolism | NIH 3T3 Cells | Temperature | Reactive Oxygen Species - metabolism | Biocompatible Materials - chemistry | Molecular Conformation | Sulfides - chemistry | Hydrogels - chemical synthesis | Drug Carriers - chemistry | Biocompatible Materials - chemical synthesis | Micelles | Hydrogels - metabolism | Drug Carriers - metabolism | Rheology | Models, Molecular | Biocompatible Materials - pharmacology | Drug Carriers - chemical synthesis | Acrylic Resins - chemistry | Drug Carriers - pharmacology | Acrylamides - chemistry | Animals | Drug Liberation | Polymers - chemistry |
BIODEGRADABLE HYDROGELS | AQUEOUS-SOLUTIONS | SUPEROXIDE | TEMPERATURE | FLUORESCENCE | NETWORKS | MICELLES | GELATION | CHEMISTRY, MULTIDISCIPLINARY | INJECTABLE HYDROGELS | POLY(N-ISOPROPYLACRYLAMIDE) | Biocompatible Materials - metabolism | NIH 3T3 Cells | Temperature | Reactive Oxygen Species - metabolism | Biocompatible Materials - chemistry | Molecular Conformation | Sulfides - chemistry | Hydrogels - chemical synthesis | Drug Carriers - chemistry | Biocompatible Materials - chemical synthesis | Micelles | Hydrogels - metabolism | Drug Carriers - metabolism | Rheology | Models, Molecular | Biocompatible Materials - pharmacology | Drug Carriers - chemical synthesis | Acrylic Resins - chemistry | Drug Carriers - pharmacology | Acrylamides - chemistry | Animals | Drug Liberation | Polymers - chemistry |