Molecule:100508: Difference between revisions
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{{Molecule | {{Molecule | ||
|abbrev=BIH | |||
|trivialname=13-dimethyl-2-phenylbenzimidazoline | |||
|cid=199049 | |cid=199049 | ||
|iupacName=1,3-dimethyl-2-phenyl-2h-benzimidazole | |iupacName=1,3-dimethyl-2-phenyl-2h-benzimidazole | ||
|molecularMass=224.131348519 | |molecularMass=224.131348519 | ||
|molecularFormula=C<sub>15</sub>H<sub>16</sub>N<sub>2</sub> | |molecularFormula=C<sub>15</sub>H<sub>16</sub>N<sub>2</sub> | ||
|synonyms=13-dimethyl-2-phenylbenzimidazoline,13-dimethyl-2-phenyl-23-dihydro-1h-benzodimidazole,13-dimethyl-2-phenyl-2h-benzimidazole,benzimidazoline 13-dimethyl-2-phenyl-,13-dimethyl-13-dihydro-2-phenyl-2h-benzimidazole,chemdiv3_000319,schembl993337,dtxsid90190025,hms1473o11,zinc225668 | |synonyms=13-dimethyl-2-phenylbenzimidazoline,13-dimethyl-2-phenyl-23-dihydro-1h-benzodimidazole,13-dimethyl-2-phenyl-2h-benzimidazole,benzimidazoline 13-dimethyl-2-phenyl-,13-dimethyl-13-dihydro-2-phenyl-2h-benzimidazole,chemdiv3_000319,schembl993337,dtxsid90190025,hms1473o11,zinc225668 | ||
|cas=3652-92-4 | |cas=3652-92-4 | ||
|hasVendors=true | |hasVendors=true | ||
|moleculeKey=VDFIVJSRRJXMAU-UHFFFAOYSA-N | |moleculeKey=VDFIVJSRRJXMAU-UHFFFAOYSA-N | ||
|molOrRxn= | |molOrRxn=-INDIGO-10172211072D | ||
0 0 0 0 0 0 0 0 0 0 0 V3000 | 0 0 0 0 0 0 0 0 0 0 0 V3000 | ||
| Line 65: | Line 63: | ||
|height=VDFIVJSRRJXMAU-UHFFFAOYSA-N | |height=VDFIVJSRRJXMAU-UHFFFAOYSA-N | ||
|float=none | |float=none | ||
}} | }} | ||
Revision as of 11:41, 13 December 2022
| Properties | |
|---|---|
| CID | 199049 |
| CAS | 3652-92-4 |
| IUPAC-Name | 1,3-dimethyl-2-phenyl-2h-benzimidazole |
| Abbreviation | BIH |
| Trivialname | 13-dimethyl-2-phenylbenzimidazoline |
| Exact mass | 224.131348519 |
| Molecular formula | C15H16N2 |
| LogP | n/a |
| Has vendors | true |
| Molecular role | n/a |
| Synonyms | 13-dimethyl-2-phenylbenzimidazoline,13-dimethyl-2-phenyl-23-dihydro-1h-benzodimidazole,13-dimethyl-2-phenyl-2h-benzimidazole,benzimidazoline 13-dimethyl-2-phenyl-,13-dimethyl-13-dihydro-2-phenyl-2h-benzimidazole,chemdiv3_000319,schembl993337,dtxsid90190025,hms1473o11,zinc225668 |
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Molecule is used on following pages
topic
- Photocatalytic CO2 conversion to CO
- Homogeneous photocatalytic CO2 conversion
- Photocatalytic CO2 conversion to HCOOH
- Photocatalytic CO2 conversion to CH4
publication
- Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts
- Phenoxazine-Sensitized CO2-to-CO Reduction with an Iron Porphyrin Catalyst: A Redox Properties-Catalytic Performance Study
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production
- Nickel(II) pincer complexes demonstrate that the remote substituent controls catalytic carbon dioxide reduction
- Photocatalytic CO2 Reduction Using a Robust Multifunctional Iridium Complex toward the Selective Formation of Formic Acid
- Pyranopterin Related Dithiolene Molybdenum Complexes as Homogeneous Catalysts for CO2 Photoreduction
- New Photosensitizers Based on Heteroleptic Cu(I) Complexes and CO2 Photocatalytic Reduction with (Ni(II)(cyclam))Cl2
- Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers
- Metal-free reduction of CO2 to formate using a photochemical organohydride-catalyst recycling strategy
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction
- Photocatalytic CO2 Reduction Mediated by Electron Transfer via the Excited Triplet State of Zn(II) Porphyrin
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes
- Light-Driven Reduction of CO2 to CO in Water with a Cobalt Molecular Catalyst and an Organic Sensitizer
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst
- Durable Solar-Powered Systems with Ni-Catalysts for Conversion of CO2 or CO to CH4
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction
investigation
- Photocatalytic CO2 Reduction Using a Robust Multifunctional Iridium Complex toward the Selective Formation of Formic Acid/Photocatalytic reduction of CO2, best TON
- Phenoxazine-Sensitized CO2-to-CO Reduction with an Iron Porphyrin Catalyst: A Redox Properties-Catalytic Performance Study/Table 1
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production/Table 1
- Light-Driven Reduction of CO2 to CO in Water with a Cobalt Molecular Catalyst and an Organic Sensitizer/Photocatalytic CO2 Reduction by 1 (2 μM) in CO2-Saturated Aqueous CH3CN Solutions
- Pyranopterin Related Dithiolene Molybdenum Complexes as Homogeneous Catalysts for CO2 Photoreduction/Table 1
- Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts/Results for photocatalytic reduction of CO2
- Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers/Optimizations of the conditions
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Control experiments
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Presence of water effect
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Hg poisoning
- Nickel(II) pincer complexes demonstrate that the remote substituent controls catalytic carbon dioxide reduction/Photocatalytic CO2 reduction under varied conditions
- Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts/Durability test
- Promoting photocatalytic CO2 reduction with a molecular copper purpurin chromophore/Photocatalytic CO2 reduction: best results
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst/Photocatalytic reduction of CO
- Promoting photocatalytic CO2 reduction with a molecular copper purpurin chromophore/Control experiments
- New Photosensitizers Based on Heteroleptic Cu(I) Complexes and CO2 Photocatalytic Reduction with (Ni(II)(cyclam))Cl2/Photocatalytic CO2 reduction and control experiments
- Photocatalytic Reduction of CO2 by Highly Efficient Homogeneous FeII Catalyst based on 2,6-Bis(1’,2’,3’-triazolyl-methyl)pyridine. Comparison with Analogues./CO2 reduction experiments testing different catalysts
- Photocatalytic Reduction of CO2 by Highly Efficient Homogeneous FeII Catalyst based on 2,6-Bis(1’,2’,3’-triazolyl-methyl)pyridine. Comparison with Analogues./Optimization of CO2 reduction conditions
- Photocatalytic CO2 reduction with aminoanthraquinone organic dyes/Photocatalytic reduction of CO2 with different photosensitizers
- Photocatalytic CO2 reduction with aminoanthraquinone organic dyes/Photocatalytic CO2 reduction with varying concentrations of cat and PS
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Concentration and solvent effect
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Maximum TON
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes/Optimizations of conditions for Co(qpy)(H2O)2(ClO4)2 and Ru(bpy)3Cl2
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes/Optimizations of conditions for Fe(qpy)(H2O)2(ClO4)2 and Ru(bpy)3Cl2
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes/Optimizations of conditions for Co(qpy)(H2O)2(ClO4)2 and purpurin
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes/Optimizations of conditions for Fe(qpy)(H2O)2(ClO4)2
- Photocatalytic CO2 Reduction Mediated by Electron Transfer via the Excited Triplet State of Zn(II) Porphyrin/photocatalytic CO2 conversion
- Durable Solar-Powered Systems with Ni-Catalysts for Conversion of CO2 or CO to CH4/Results for different electron donors and proton donors
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Iron-Catalyzed Photochemical CO2 Reduction under diverse conditions
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Iron-Catalyzed Photochemical CO2 Reduction under diverse conditions error
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 Conversion with Co catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 conversion with Co catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 Co catalyst testing
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/testtest2
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Results obtained with Co2+ catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/results CO2+ experiments
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/CO2+ results from SI
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Results Co2+ experiments taken from SI
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/CO2 Reduction under diverse conditions with diverse sensitizers
other
