Molecule:100529: Difference between revisions
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{{Molecule | {{Molecule | ||
|abbrev=DMF | |abbrev=DMF | ||
|trivialname=N,N- | |trivialname=N,N-dimethylformamide | ||
|cid=6228 | |cid=6228 | ||
|iupacName=N,N-dimethylmethanamide | |iupacName=N,N-dimethylmethanamide | ||
| Line 11: | Line 11: | ||
|moleculeKey=ZMXDDKWLCZADIW-UHFFFAOYSA-N | |moleculeKey=ZMXDDKWLCZADIW-UHFFFAOYSA-N | ||
|molOrRxn= | |molOrRxn= | ||
-INDIGO- | -INDIGO-05222412212D | ||
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 17: | Line 17: | ||
M V30 COUNTS 5 4 0 0 0 | M V30 COUNTS 5 4 0 0 0 | ||
M V30 BEGIN ATOM | M V30 BEGIN ATOM | ||
M V30 1 C | M V30 1 C 5.375 -5.125 0.0 0 | ||
M V30 2 | M V30 2 O 5.375 -4.125 0.0 0 | ||
M V30 3 | M V30 3 N 6.24103 -5.625 0.0 0 | ||
M V30 4 C | M V30 4 C 6.24103 -6.625 0.0 0 | ||
M V30 5 | M V30 5 C 7.10705 -5.125 0.0 0 | ||
M V30 END ATOM | M V30 END ATOM | ||
M V30 BEGIN BOND | M V30 BEGIN BOND | ||
M V30 1 | M V30 1 2 1 2 | ||
M V30 2 1 | M V30 2 1 1 3 | ||
M V30 3 1 | M V30 3 1 3 4 | ||
M V30 4 | M V30 4 1 3 5 | ||
M V30 END BOND | M V30 END BOND | ||
M V30 END CTAB | M V30 END CTAB | ||
M END | M END | ||
|smiles= | |||
|smiles=C(N(C)C)=O | |||
|inchi=1S/C3H7NO/c1-4(2)3-5/h3H,1-2H3 | |inchi=1S/C3H7NO/c1-4(2)3-5/h3H,1-2H3 | ||
|inchikey=ZMXDDKWLCZADIW-UHFFFAOYSA-N | |inchikey=ZMXDDKWLCZADIW-UHFFFAOYSA-N | ||
| Line 38: | Line 39: | ||
|float=none | |float=none | ||
|molecularFormula=C<sub>3</sub>H<sub>7</sub>NO | |molecularFormula=C<sub>3</sub>H<sub>7</sub>NO | ||
}} | }} | ||
Latest revision as of 12:22, 22 May 2024
| Properties | |
|---|---|
| CID | 6228 |
| CAS | 68-12-2 |
| IUPAC-Name | N,N-dimethylmethanamide |
| Abbreviation | DMF |
| Trivialname | N,N-dimethylformamide |
| Exact mass | 73.052763847 |
| Molecular formula | C3H7NO |
| LogP | -1 |
| Has vendors | true |
| Molecular role | n/a |
| Synonyms | N,N-DIMETHYLFORMAMIDE, Dimethylformamide, N,N-Dimethylmethanamide, Dimethyl formamide, N-Formyldimethylamine, Formamide, N,N-dimethyl-, Dimethylformamid, DMF, Dimetilformamide, Dwumetyloformamid |
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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 Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst
- A molecular noble metal-free system for efficient visible light-driven reduction of CO2 to CO
- Photocatalytic CO2 reduction with aminoanthraquinone organic dyes
- Promoting photocatalytic CO2 reduction with a molecular copper purpurin chromophore
- Water-Assisted Highly Efficient Photocatalytic Reduction of CO2 to CO with Noble Metal-Free Bis(terpyridine)iron(II) Complexes and an Organic Photosensitizer
- Merging an organic TADF photosensitizer and a simple terpyridine–Fe(iii) complex for photocatalytic CO2 reduction
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production
- Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers
- Rhenium(I) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction
- Photocatalytic CO2 reduction using a Mn complex as a catalyst
- Nickel(II) pincer complexes demonstrate that the remote substituent controls catalytic carbon dioxide reduction
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes
- Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands
investigation
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Effect of proton donor
- 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
- A molecular noble metal-free system for efficient visible light-driven reduction of CO2 to CO/experiments
- 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
- Promoting photocatalytic CO2 reduction with a molecular copper purpurin chromophore/Control experiments
- Promoting photocatalytic CO2 reduction with a molecular copper purpurin chromophore/Photocatalytic CO2 reduction: best results
- 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
- Merging an organic TADF photosensitizer and a simple terpyridine–Fe(iii) complex for photocatalytic CO2 reduction/photocatalytic reduction of CO2 to CO
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production/Table 1
- Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers/Optimizations of the conditions
- Rhenium(I) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction/Table 2
- Rhenium(I) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction/Table 1
- Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH/Photocatalytic CO2 reduction with the Mn complexes under various conditions.
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3/Table 1: Summary of Catalytic Experiments for Photocatalysis.
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3/Table 2: Summary of Control Experiments for Photocatalysis.
- Photocatalytic CO2 reduction using a Mn complex as a catalyst/Photocatalytic CO2 reduction: conditions optimization
- Nickel(II) pincer complexes demonstrate that the remote substituent controls catalytic carbon dioxide reduction/Photocatalytic CO2 reduction under varied conditions
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Solvent effect study between DMA DMF and acetonitrile
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Time profile in DMF
- 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
- Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands/Table 1
other
Molecule roles
| Investigation type | Solvent |
|---|---|
| Photocatalytic CO2 conversion experiments |
|
| Cyclic Voltammetry experiments |  |
| Absorption Emission Spectroscopy experiments | |
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