Molecule:100505: Difference between revisions
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molecule
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|trivialname=triethylamine | |trivialname=triethylamine | ||
|cid=8471 | |cid=8471 | ||
|iupacName= | |iupacName=N,N-diethylethanamine | ||
|molecularMass=101.120449483 | |molecularMass=101.120449483 | ||
|molecularFormula=C<sub>6</sub>H<sub>15</sub>N | |molecularFormula=C<sub>6</sub>H<sub>15</sub>N | ||
|logP=1.4 | |logP=1.4 | ||
|synonyms= | |synonyms=TRIETHYLAMINE$N,N-Diethylethanamine$Ethanamine, N,N-diethyl-$(Diethylamino)ethane$Triethylamin$triethyl amine$Triaethylamin$Trietilamina$N,N,N-Triethylamine$NEt3 | ||
|cas=121-44-8 | |cas=121-44-8 | ||
|hasVendors=true | |hasVendors=true | ||
|moleculeKey=ZMANZCXQSJIPKH-UHFFFAOYSA-N | |moleculeKey=ZMANZCXQSJIPKH-UHFFFAOYSA-N | ||
|molOrRxn= | |molOrRxn= | ||
-INDIGO- | -INDIGO-10172210542D | ||
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 18: | Line 18: | ||
M V30 COUNTS 7 6 0 0 0 | M V30 COUNTS 7 6 0 0 0 | ||
M V30 BEGIN ATOM | M V30 BEGIN ATOM | ||
M V30 1 | M V30 1 N 9.05997 -6.33177 0.0 0 | ||
M V30 2 C | M V30 2 C 8.35579 -5.63333 0.0 0 | ||
M V30 3 | M V30 3 C 7.39895 -5.89012 0.0 0 | ||
M V30 4 C | M V30 4 C 10.0472 -6.05249 0.0 0 | ||
M V30 5 C | M V30 5 C 10.7737 -6.74539 0.0 0 | ||
M V30 6 C | M V30 6 C 8.81579 -7.28361 0.0 0 | ||
M V30 7 C | M V30 7 C 9.54063 -7.97968 0.0 0 | ||
M V30 END ATOM | M V30 END ATOM | ||
M V30 BEGIN BOND | M V30 BEGIN BOND | ||
M V30 1 1 1 2 | M V30 1 1 1 2 | ||
M V30 2 1 2 3 | M V30 2 1 2 3 | ||
M V30 3 1 | M V30 3 1 1 4 | ||
M V30 4 1 4 5 | M V30 4 1 4 5 | ||
M V30 5 1 | M V30 5 1 1 6 | ||
M V30 6 1 6 7 | M V30 6 1 6 7 | ||
M V30 END BOND | M V30 END BOND | ||
M V30 END CTAB | M V30 END CTAB | ||
M END | M END | ||
|smiles= | |smiles=N(CC)(CC)CC | ||
|inchi=1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3 | |inchi=1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3 | ||
|inchikey=ZMANZCXQSJIPKH-UHFFFAOYSA-N | |inchikey=ZMANZCXQSJIPKH-UHFFFAOYSA-N | ||
|width=300px | |width=300px | ||
|height=200px | |height=200px | ||
|float= | |float=none | ||
|parent= | |parent= | ||
}} | }} | ||
Latest revision as of 14:11, 18 October 2024
| Properties | |
|---|---|
| CID | 8471 |
| CAS | 121-44-8 |
| IUPAC-Name | N,N-diethylethanamine |
| Abbreviation | TEA |
| Trivialname | triethylamine |
| Exact mass | 101.120449483 |
| Molecular formula | C6H15N |
| LogP | 1.4 |
| Has vendors | true |
| Molecular role | n/a |
| Synonyms | TRIETHYLAMINE, N,N-Diethylethanamine, Ethanamine, N,N-diethyl-, (Diethylamino)ethane, Triethylamin, triethyl amine, Triaethylamin, Trietilamina, N,N,N-Triethylamine, NEt3 |
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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
- Visible light driven reduction of CO2 catalyzed by an abundant manganese catalyst with zinc porphyrin photosensitizer
- 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
- Visible-Light Photoredox Catalysis: Selective Reduction of Carbon Dioxide to Carbon Monoxide by a Nickel N-Heterocyclic Carbene–Isoquinoline Complex
- Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers
- Water-Assisted Highly Efficient Photocatalytic Reduction of CO2 to CO with Noble Metal-Free Bis(terpyridine)iron(II) Complexes and an Organic Photosensitizer
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2
- Merging an organic TADF photosensitizer and a simple terpyridine–Fe(iii) complex for photocatalytic CO2 reduction
- Selective and Efficient Photocatalytic CO2 Reduction to CO Using Visible Light and an Iron-Based Homogeneous Catalyst
- Molecular Catalysis of the Electrochemical and Photochemical Reduction of CO2 with Earth-Abundant Metal Complexes. Selective Production of CO vs HCOOH by Switching of the Metal Center
- Visible-light-driven methane formation from CO2 with a molecular iron catalyst
- 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
- Toward Visible-Light Photochemical CO2‑to-CH4 Conversion in Aqueous Solutions Using Sensitized Molecular Catalysis
- 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
- Visible light driven reduction of CO2 catalyzed by an abundant manganese catalyst with zinc porphyrin photosensitizer/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
- Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers/Optimizations of the conditions
- Molecular Catalysis of the Electrochemical and Photochemical Reduction of CO2 with Earth-Abundant Metal Complexes. Selective Production of CO vs HCOOH by Switching of the Metal Center/Table 1
- Visible-Light Photoredox Catalysis: Selective Reduction of Carbon Dioxide to Carbon Monoxide by a Nickel N-Heterocyclic Carbene–Isoquinoline Complex/Table 1
- Visible-light-driven methane formation from CO2 with a molecular iron catalyst/Table 1
- Visible-light-driven methane formation from CO2 with a molecular iron catalyst/Table 2 CO gas
- Toward Visible-Light Photochemical CO2‑to-CH4 Conversion in Aqueous Solutions Using Sensitized Molecular Catalysis/Photocatalytic reduction of CO2: conditions optimization
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst/Photocatalytic reduction of CO2
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst/Photocatalytic reduction of CO
- Water-Assisted Highly Efficient Photocatalytic Reduction of CO2 to CO with Noble Metal-Free Bis(terpyridine)iron(II) Complexes and an Organic Photosensitizer/photocatalytic CO2 conversion
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Effect of proton donor
- Merging an organic TADF photosensitizer and a simple terpyridine–Fe(iii) complex for photocatalytic CO2 reduction/photocatalytic reduction of CO2 to CO
- Selective and Efficient Photocatalytic CO2 Reduction to CO Using Visible Light and an Iron-Based Homogeneous Catalyst/photocatalytic conversion of CO2 to CO
- 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/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
other
