Angewandte Chemie - International Edition, ISSN 1433-7851, 08/2010, Volume 49, Issue 36, pp. 6405 - 6408
Journal Article
Current Opinion in Chemical Biology, ISSN 1367-5931, 08/2013, Volume 17, Issue 4, pp. 699 - 707
Recent advances in the development of the phosphorescent Ir(III) complexes have made it possible to implement the phosphorescence modality in bioimaging...
POLYPYRIDINE COMPLEXES | HOMOCYSTEINE | NANOPARTICLES | LUMINESCENT IRIDIUM(III) | BIOPHYSICS | IRIDIUM(III) COMPLEXES | RU(II) COMPLEXES | BIOCHEMISTRY & MOLECULAR BIOLOGY | CYSTEINE | SENSOR | ENERGY-TRANSFER | LIVING CELLS | Iridium - analysis | Animals | Cyclization | Luminescence | Biosensing Techniques - methods | Iridium - chemistry | Oxygen - analysis | Photochemical Processes
POLYPYRIDINE COMPLEXES | HOMOCYSTEINE | NANOPARTICLES | LUMINESCENT IRIDIUM(III) | BIOPHYSICS | IRIDIUM(III) COMPLEXES | RU(II) COMPLEXES | BIOCHEMISTRY & MOLECULAR BIOLOGY | CYSTEINE | SENSOR | ENERGY-TRANSFER | LIVING CELLS | Iridium - analysis | Animals | Cyclization | Luminescence | Biosensing Techniques - methods | Iridium - chemistry | Oxygen - analysis | Photochemical Processes
Journal Article
Accounts of Chemical Research, ISSN 0001-4842, 04/2014, Volume 47, Issue 4, pp. 1174 - 1185
Iridium is a relatively rare precious heavy metal, only slightly less dense than osmium. Researchers have long recognized the catalytic properties of...
IR(III) COMPLEXES | RHODIUM(III) | IRIDIUM(III) COMPLEXES | MOLECULAR-STRUCTURE | REACTIVITY | RUTHENIUM | DNA-BINDING PROPERTIES | MECHANISMS | CANCER-CELL CYTOTOXICITY | CHEMISTRY, MULTIDISCIPLINARY | CATHEPSIN-B | NAD - chemistry | Iridium - pharmacology | Pyridines - chemistry | Humans | Ligands | Organometallic Compounds - chemistry | Antineoplastic Agents - pharmacology | Structure-Activity Relationship | Catalysis | Antineoplastic Agents - chemistry | Iridium - chemistry | Organometallic Compounds - pharmacology | Catalysts | Inert | Oxidation | Coordination compounds | Anticancer properties | Cancer
IR(III) COMPLEXES | RHODIUM(III) | IRIDIUM(III) COMPLEXES | MOLECULAR-STRUCTURE | REACTIVITY | RUTHENIUM | DNA-BINDING PROPERTIES | MECHANISMS | CANCER-CELL CYTOTOXICITY | CHEMISTRY, MULTIDISCIPLINARY | CATHEPSIN-B | NAD - chemistry | Iridium - pharmacology | Pyridines - chemistry | Humans | Ligands | Organometallic Compounds - chemistry | Antineoplastic Agents - pharmacology | Structure-Activity Relationship | Catalysis | Antineoplastic Agents - chemistry | Iridium - chemistry | Organometallic Compounds - pharmacology | Catalysts | Inert | Oxidation | Coordination compounds | Anticancer properties | Cancer
Journal Article
Applied Catalysis A: General, ISSN 0926-860X, 08/2012, Volume 433-434, pp. 128 - 134
Hydrogenolysis of aqueous glycerol was conducted with Ir-ReO /SiO catalyst and solid acid co-catalyst. Considering the reusability and activity, H-ZSM-5 is the...
Hydrogenolysis | Glycerol | Iridium | Rhenium | Zeolite
Hydrogenolysis | Glycerol | Iridium | Rhenium | Zeolite
Journal Article
1984, Volume no. 3030.
Book
Cancer Letters, ISSN 0304-3835, 2017, Volume 396, pp. 76 - 84
Abstract Four benzofuran-conjugated iridium(III) or rhodium (III)-based metal complexes are synthesized to screen as an inhibitor of STAT3 activity in prostate...
Hematology, Oncology and Palliative Medicine | NF-κB | Benzofuran-conjugated iridium(III) complex | Dual inhibitors | Prostate cells | STAT3 | APOPTOSIS | ACTIVATION | SURVIVIN | KINASE | NECROSIS-FACTOR-ALPHA | IDENTIFICATION | SUPPRESSION | NF-kappa B | ONCOLOGY | GENE-EXPRESSION | DERIVATIVES | EPIDEMIOLOGY | Prostatic Neoplasms - metabolism | Iridium - pharmacology | NF-kappa B - antagonists & inhibitors | Humans | Mice, Inbred C57BL | Benzofurans - pharmacology | Male | NF-kappa B - metabolism | Random Allocation | Benzofurans - chemistry | Xenograft Model Antitumor Assays | Animals | HEK293 Cells | Cell Line, Tumor | Mice | STAT3 Transcription Factor - antagonists & inhibitors | Iridium - chemistry | Prostatic Neoplasms - drug therapy | STAT3 Transcription Factor - metabolism | Translocation | Transcription | Stat3 protein | Kinases | Gene expression | Cancer therapies | Experiments | Iridium compounds | Proteins | Side effects | Inhibitors | Rhodium | Benzofuran | Cell cycle | Xenografts | Tumor necrosis factor-TNF | Iridium | Coordination compounds | Prostate cancer | Metal complexes | Prostate | Cancer | Apoptosis
Hematology, Oncology and Palliative Medicine | NF-κB | Benzofuran-conjugated iridium(III) complex | Dual inhibitors | Prostate cells | STAT3 | APOPTOSIS | ACTIVATION | SURVIVIN | KINASE | NECROSIS-FACTOR-ALPHA | IDENTIFICATION | SUPPRESSION | NF-kappa B | ONCOLOGY | GENE-EXPRESSION | DERIVATIVES | EPIDEMIOLOGY | Prostatic Neoplasms - metabolism | Iridium - pharmacology | NF-kappa B - antagonists & inhibitors | Humans | Mice, Inbred C57BL | Benzofurans - pharmacology | Male | NF-kappa B - metabolism | Random Allocation | Benzofurans - chemistry | Xenograft Model Antitumor Assays | Animals | HEK293 Cells | Cell Line, Tumor | Mice | STAT3 Transcription Factor - antagonists & inhibitors | Iridium - chemistry | Prostatic Neoplasms - drug therapy | STAT3 Transcription Factor - metabolism | Translocation | Transcription | Stat3 protein | Kinases | Gene expression | Cancer therapies | Experiments | Iridium compounds | Proteins | Side effects | Inhibitors | Rhodium | Benzofuran | Cell cycle | Xenografts | Tumor necrosis factor-TNF | Iridium | Coordination compounds | Prostate cancer | Metal complexes | Prostate | Cancer | Apoptosis
Journal Article
Book
Book
Angewandte Chemie - International Edition, ISSN 1433-7851, 10/2010, Volume 49, Issue 41, pp. 7548 - 7552
Journal Article
Advanced Functional Materials, ISSN 1616-301X, 10/2018, Volume 28, Issue 44, pp. 1804714 - n/a
Three new highly efficient green‐emitting heteroleptic phosphorescent iridium(III) complexes are designed and synthesized for the fabrication of...
green iridium complexes | very low efficiency roll‐off | organic light‐emitting diodes | high current efficiency | solubilizing group | very low efficiency roll-off | organic light-emitting diodes | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | HOST DENDRONS | MATERIALS SCIENCE, MULTIDISCIPLINARY | SUBSTITUTED LIGANDS | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | LIGHT-EMITTING-DIODES | CARBAZOLE | EXTERNAL QUANTUM EFFICIENCY | DRIVING VOLTAGE | IRIDIUM(III) COMPLEXES | DEVICES | LAYER | PHOSPHORESCENT OLEDS | Light-emitting diodes | Iridium compounds | Quantum efficiency | Efficiency | Photoluminescence | Organic light emitting diodes | Current efficiency | Ligands | Electroluminescence | Phosphorescence | Cascade chemical reactions | Iridium | Diodes
green iridium complexes | very low efficiency roll‐off | organic light‐emitting diodes | high current efficiency | solubilizing group | very low efficiency roll-off | organic light-emitting diodes | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | HOST DENDRONS | MATERIALS SCIENCE, MULTIDISCIPLINARY | SUBSTITUTED LIGANDS | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | LIGHT-EMITTING-DIODES | CARBAZOLE | EXTERNAL QUANTUM EFFICIENCY | DRIVING VOLTAGE | IRIDIUM(III) COMPLEXES | DEVICES | LAYER | PHOSPHORESCENT OLEDS | Light-emitting diodes | Iridium compounds | Quantum efficiency | Efficiency | Photoluminescence | Organic light emitting diodes | Current efficiency | Ligands | Electroluminescence | Phosphorescence | Cascade chemical reactions | Iridium | Diodes
Journal Article
Topics in Catalysis, ISSN 1022-5528, 6/2019, Volume 62, Issue 5, pp. 429 - 438
A novel route for obtaining iridium-based electrocatalysts supported on sub-stoichiometric titanium oxides for catalytic applications is presented....
Chemistry | Titanium oxide synthesis | Physical Chemistry | Pharmacy | Electrocatalysts | Characterization and Evaluation of Materials | Water electrolysis | Catalysis | Oxygen evolution reaction | Industrial Chemistry/Chemical Engineering | Iridium/iridium oxide | OXIDATION | STABILITY | PERFORMANCE | CHEMISTRY, PHYSICAL | FILMS | iridium oxide | Iridium | CHEMISTRY, APPLIED | CATALYSTS | Nanoparticles | Electrical conductivity | Electrolysis | Catalysts | Analysis | Oxides | Electrolytes | Combustion | Investigations | Electric properties
Chemistry | Titanium oxide synthesis | Physical Chemistry | Pharmacy | Electrocatalysts | Characterization and Evaluation of Materials | Water electrolysis | Catalysis | Oxygen evolution reaction | Industrial Chemistry/Chemical Engineering | Iridium/iridium oxide | OXIDATION | STABILITY | PERFORMANCE | CHEMISTRY, PHYSICAL | FILMS | iridium oxide | Iridium | CHEMISTRY, APPLIED | CATALYSTS | Nanoparticles | Electrical conductivity | Electrolysis | Catalysts | Analysis | Oxides | Electrolytes | Combustion | Investigations | Electric properties
Journal Article
Chemical Communications : Chem Comm, ISSN 1359-7345, 4/2018, Volume 54, Issue 32, pp. 461 - 461
Correction for 'A luminescent bimetallic iridium( iii ) complex for ratiometric tracking intracellular viscosity' by Fengyu Liu et al. , Chem. Commun. , 2018,...
Viscosity | Iridium compounds | Bimetals | Tracking | Iridium
Viscosity | Iridium compounds | Bimetals | Tracking | Iridium
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 04/2010, Volume 352, Issue 6, pp. 1055 - 1062
The use of a chiral iridium catalyst generated in situ from the (cyclooctadiene)iridium chloride dimer, [Ir(COD)Cl]2, the P‐Phos ligand...
iridium catalysis | pyridines | asymmetric hydrogenation | quinolines | P‐Phos | Iridium catal-ysis | Quinolines | Asymmetric hydrogenation | Pyridines | P-Phos | N-IMINOPYRIDINIUM YLIDES | CHEMISTRY, ORGANIC | HETEROAROMATIC-COMPOUNDS | HOMOGENEOUS HYDROGENATION | LIGANDS | PIPERIDINE | IRIDIUM COMPLEXES | ENHANCEMENT | CHEMISTRY, APPLIED | QUINOXALINES | ALKALOIDS | Additives | Asymmetry | Catalysts | Quinoline | Derivatives | Conversion | Hydrogenation
iridium catalysis | pyridines | asymmetric hydrogenation | quinolines | P‐Phos | Iridium catal-ysis | Quinolines | Asymmetric hydrogenation | Pyridines | P-Phos | N-IMINOPYRIDINIUM YLIDES | CHEMISTRY, ORGANIC | HETEROAROMATIC-COMPOUNDS | HOMOGENEOUS HYDROGENATION | LIGANDS | PIPERIDINE | IRIDIUM COMPLEXES | ENHANCEMENT | CHEMISTRY, APPLIED | QUINOXALINES | ALKALOIDS | Additives | Asymmetry | Catalysts | Quinoline | Derivatives | Conversion | Hydrogenation
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2013, Volume 52, Issue 7, pp. 2046 - 2050
The salt makes the difference: In the presence of a chiral iridium catalyst, 1‐ and 3‐substituted as well as 1,3‐disubstituted isoquinolinium salts can be...
iridium | tetrahydroisoquinolines | isoquinolines | asymmetric synthesis | hydrogenation | DIFLUORPHOS | PYRIDINE-DERIVATIVES | QUINOLINES | CHEMISTRY, MULTIDISCIPLINARY | ACID-DERIVATIVES | HIGHLY ENANTIOSELECTIVE HYDROGENATION | LIGANDS | QUINOXALINES | EFFICIENT | ACCESS | ALKALOIDS | Tetrahydroisoquinolines - chemistry | Stereoisomerism | Catalysis | Tetrahydroisoquinolines - chemical synthesis | Coordination Complexes - chemistry | Hydrogenation | Iridium - chemistry | Synthesis | Universities and colleges | Evolutionary biology | Organic compounds | Drugs | Asymmetry | Catalysts | Optical activity | Iridium
iridium | tetrahydroisoquinolines | isoquinolines | asymmetric synthesis | hydrogenation | DIFLUORPHOS | PYRIDINE-DERIVATIVES | QUINOLINES | CHEMISTRY, MULTIDISCIPLINARY | ACID-DERIVATIVES | HIGHLY ENANTIOSELECTIVE HYDROGENATION | LIGANDS | QUINOXALINES | EFFICIENT | ACCESS | ALKALOIDS | Tetrahydroisoquinolines - chemistry | Stereoisomerism | Catalysis | Tetrahydroisoquinolines - chemical synthesis | Coordination Complexes - chemistry | Hydrogenation | Iridium - chemistry | Synthesis | Universities and colleges | Evolutionary biology | Organic compounds | Drugs | Asymmetry | Catalysts | Optical activity | Iridium
Journal Article
Advanced Materials, ISSN 0935-9648, 01/2017, Volume 29, Issue 3, pp. 1603253 - n/a
Ionic iridium(III) complexes are emerging with great promise for organic electronic devices, owing to their unique features such as ease of molecular design...
ionic iridium(III) complexes | luminescence | organic light‐emitting diodes | data record storage | light‐emitting electrochemical cells | light-emitting electrochemical cells | organic light-emitting diodes | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | CYCLOMETALATED IR(III) COMPLEXES | NEAR-INFRARED POLYMER | TRANSITION-METAL-COMPLEXES | EMITTING ELECTROCHEMICAL-CELLS | MATERIALS SCIENCE, MULTIDISCIPLINARY | WHITE-LIGHT EMISSION | CHEMISTRY, PHYSICAL | CU-I COMPLEXES | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | HIGHLY EFFICIENT | EXTERNAL QUANTUM EFFICIENCY | LAYER ELECTROLUMINESCENT DEVICES | TURN-ON TIMES | Electrochemistry | Iridium compounds | Electronic materials | Electronic devices | Electroluminescence | Phosphorescence | Evaporation | Chemical synthesis | Vacuum evaporation | Synthesis (chemistry) | Colors (materials) | Cationic | Lighting | Illumination | Devices
ionic iridium(III) complexes | luminescence | organic light‐emitting diodes | data record storage | light‐emitting electrochemical cells | light-emitting electrochemical cells | organic light-emitting diodes | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | CYCLOMETALATED IR(III) COMPLEXES | NEAR-INFRARED POLYMER | TRANSITION-METAL-COMPLEXES | EMITTING ELECTROCHEMICAL-CELLS | MATERIALS SCIENCE, MULTIDISCIPLINARY | WHITE-LIGHT EMISSION | CHEMISTRY, PHYSICAL | CU-I COMPLEXES | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | HIGHLY EFFICIENT | EXTERNAL QUANTUM EFFICIENCY | LAYER ELECTROLUMINESCENT DEVICES | TURN-ON TIMES | Electrochemistry | Iridium compounds | Electronic materials | Electronic devices | Electroluminescence | Phosphorescence | Evaporation | Chemical synthesis | Vacuum evaporation | Synthesis (chemistry) | Colors (materials) | Cationic | Lighting | Illumination | Devices
Journal Article