Molecule:100530: Difference between revisions
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{{Molecule | {{Molecule | ||
|abbrev=MeCN | |abbrev=MeCN | ||
|trivialname= | |trivialname=ACETONITRILE | ||
|cid=6342 | |cid=6342 | ||
|iupacName=ethanenitrile | |iupacName=ethanenitrile | ||
|molecularMass=41.026549100 | |molecularMass=41.026549100 | ||
|synonyms=acetonitrile, | |synonyms=ACETONITRILE$Cyanomethane$Methyl cyanide$Ethanenitrile$Ethyl nitrile$Methanecarbonitrile$Methane, cyano-$Acetonitril$Cyanure de methyl$Methylkyanid$MeCN$Methylkyanid [Czech]$USAF EK-488$RCRA waste number U003$Cyanure de methyl [French]$Acetonitril [German, Dutch]$Acetonitrile, anhydrous$CH3CN$NCI-C60822$NCMe$Acetonitrile, dimer$CH3-C#N$CHEBI:38472$Z072SB282N$ACETONITRILE WITH 0.1per cent AMMONIUM ACETATE$MFCD00001878$Acetonitrile with 0.1% ammonium acetate$Acetonitrile [UN1648] [Flammable liquid]$Acetonitril (GERMAN, DUTCH)$Acetonitrile, for DNA synthesis$acetnitrile$Ethanonitrile$CCN$HSDB 42$CCRIS 1628$NSC 7593$Acetonitrile, for HPLC, gradient grade, >=99.9%$EINECS 200-835-2$UN1648$RCRA waste no. U003$acetonitile$acetonitnle$acetonitriie$acteonitril$acteonitrile$actonitrile$methylcyanide$methylnitrile$ace-tonitrile$aceto-nitrile$acetonitrile-$UNII-Z072SB282N$AI3-00327$Acetonitrile ACS$CC.equiv.N$Acetonitrile LC-MS$Acetonitrile,homopolymer$Cyanomethylidyne radical$DSSTox_CID_9$Acetonitrile HPLC grade$H3CCN$Acetonitrile, LCMS grade$bmse000826$bmse000896$EC 200-835-2$WLN: NC1$Acetonitrile, >=99.5%$DSSTox_RID_75320$DSSTox_GSID_20009$Acetonitrile with formic acid$Acetonitrile, puriss., 95%$CHEMBL45211$Acetonitrile, for chromatography$DTXSID7020009$Acetonitrile UV/HPLC ACS grade$Acetonitrile, analytical standard$Acetonitrile for preparative HPLC$Acetonitrile, AR, >=99.5%$Acetonitrile, Environmental Grade$NSC7593$Acetonitrile, anhydrous, 99.8%$Acetonitrile, >=99.5% (GC)$Acetonitrile, HPLC gradient Grade$Amidite Diluent, for DNA synthesis$NSC-7593$STR02933$Acetonitrile, far UV/gradient grade$Tox21_202481$Acetonitrile, HPLC Grade (Far UV)$Acetonitrile, p.a., dry, 99.9%$Acetonitrile, ReagentPlus(R), 99%$c1151$STL283937$Acetonitrile, Spectrophotometric Grade$Acetonitrile, >=99.8%, for HPLC$Acetonitrile, for HPLC, >=99.9%$AKOS000269067$Acetonitrile, HPLC Plus, >=99.9%$NA 1648$UN 1648$Acetonitrile, >=99.5%, ACS reagent$Acetonitrile, ACS reagent, >=99.5%$Acetonitrile, AldraSORB(TM), 99.8%$Acetonitrile, purum, >=99.0% (GC)$CAS-75-05-8$Acetonitrile (for HPLC) isocratic grade$Acetonitrile, HPLC grade, >=99.93%$NCGC00091552-01$NCGC00260030-01$Acetonitrile 1000 microg/mL in Methanol$Acetonitrile, purification grade, 99.8%$Ultrapure Acetonitrile, for DNA synthesis$Acetonitrile with 0.1% Formic Acid (v/v)$Acetonitrile, biotech. grade, >=99.93%$Acetonitrile, p.a., ACS reagent, 99.8%$Acetonitrile, SAJ first grade, >=99.0%$A0060$A0293$A0793$Acetonitrile, JIS special grade, >=99.5%$FT-0621807$FT-0621808$Acetonitrile, anhydrous, ZerO2(TM), 99.8%$Acetonitrile, for HPLC-GC, >=99.8% (GC)$Acetonitrile, for UHPLC, for mass spectrometry$Acetonitrile, Supergradient HPLC Grade (Far UV)$Acetonitrile, spectrophotometric grade, >=99.5%$Q408047$Acetonitrile, for HPLC, for UV, >=99.9% (GC)$Acetonitrile, puriss. p.a., ACS reagent, 99.8%$J-008497$Acetonitrile, for preparative HPLC, >=99.8% (GC)$Acetonitrile, for synthesis of DNA, >=99.9% (GC)$Acetonitrile, HPLC Plus, >=99.9%, poly-coated bottles$Acetonitrile solution, contains 0.035 % (v/v) acetic acid$Acetonitrile solution, contains 0.05 % (v/v) acetic acid$Acetonitrile solution, contains 0.1 % (v/v) acetic acid$Acetonitrile, electronic grade, 99.999% trace metals basis$Acetonitrile, for HPLC, gradient grade, >=99.9% (GC)$Acetonitrile, for HPLC, gradient grade, >=99.90% (GC)$Acetonitrile, puriss. p.a., ACS reagent, >=99.5% (GC)$Acetonitrile solution, contains 0.1 % (v/v) ammonium hydroxide$Acetonitrile with 0.1% ammonium acetate, tested for UHPLC-MS$Acetonitrile, for protein sequence analysis, >=99.8% (GC)$Acetonitrile, for residue analysis, suitable for 5000 per JIS$Acetonitrile, Vetec(TM) reagent grade, anhydrous, >=99.8%$Acetonitrile solution, ~20% in H2O, for protein sequence analysis$Acetonitrile solution, contains 0.05 % (v/v) trifluoroacetic acid$Acetonitrile solution, contains 0.1 % (v/v) formic acid, for HPLC$Acetonitrile, Preparateur, >=99.9% (GC), Customized plastic drum$Acetonitrile solution, contains 0.1 % (v/v) trifluoroacetic acid, for HPLC$Acetonitrile solution, for HPLC, acetonitrile:water 56 : 44% (w/w)$Acetonitrile, >=99.8%, for residue analysis, suitable for 1000 per JIS$Acetonitrile, >=99.8%, for residue analysis, suitable for 300 per JIS$Acetonitrile, puriss. p.a., ACS reagent, reag. Ph. Eur., >=99.5% (GC)$Acetonitrile solution, contains 0.035 % (v/v) trifluoroacetic acid, for HPLC$Acetonitrile solution, contains 0.1 % (v/v) formic acid, for UHPLC, for mass spectrometry$Acetonitrile solution, contains 0.10 % (v/v) trifluoroacetic acid, 10.0 % (v/v) water$Acetonitrile solution, contains 10.0% acetone, 40.0% 2-propanol, 0.05% formic acid$Acetonitrile, configured for PerkinElmer 8900, configured for Polygen, for DNA synthesis$Acetonitrile, Pharmaceutical Secondary Standard; Certified Reference Material$Acetonitrile, Preparateur, >=99.9% (GC), One-time steel-plastic (SP) drum$Alcohol Determination - Acetonitrile, United States Pharmacopeia (USP) Reference Standard$Acetonitrile solution, contains 5 % (v/v) water, 0.05 % (w/v) ammonium formate, 0.1 % (v/v) formic acid, for HPLC$Acetonitrile solution, for HPLC, acetonitrile:water 5:95% (v/v), 10 mM Ammoniumbicarbonate, pH 10,0$Acetonitrile solution, NMR reference standard, 0.23 wt. % in D2O (99.9 atom % D), water 0.05 wt. %, NMR tube size 6.5 mm x 8 in.$Residual Solvent - Acetonitrile, Pharmaceutical Secondary Standard; Certified Reference Material$Residual Solvent Class 2 - Acetonitrile, United States Pharmacopeia (USP) Reference Standard | ||
|cas=75-05-8 | |cas=75-05-8 | ||
|hasVendors=true | |hasVendors=true |
Revision as of 17:01, 3 May 2024
Properties | |
---|---|
CID | 6342 |
CAS | 75-05-8 |
IUPAC-Name | ethanenitrile |
Abbreviation | MeCN |
Trivialname | ACETONITRILE |
Exact mass | 41.026549100 |
Molecular formula | C2H3N |
LogP | n/a |
Has vendors | true |
Molecular role | n/a |
Synonyms | ACETONITRILE, Cyanomethane, Methyl cyanide, Ethanenitrile, Ethyl nitrile, Methanecarbonitrile, Methane, cyano-, Acetonitril, Cyanure de methyl, Methylkyanid, MeCN, [[Synonym::Methylkyanid [Czech]]], USAF EK-488, RCRA waste number U003, [[Synonym::Cyanure de methyl [French]]], [[Synonym::Acetonitril [German, Dutch]]], Acetonitrile, anhydrous, CH3CN, NCI-C60822, NCMe, Acetonitrile, dimer, CH3-C#N, CHEBI:38472, Z072SB282N, ACETONITRILE WITH 0.1per cent AMMONIUM ACETATE, MFCD00001878, Acetonitrile with 0.1% ammonium acetate, [[Synonym::Acetonitrile [UN1648] [Flammable liquid]]], Acetonitril (GERMAN, DUTCH), Acetonitrile, for DNA synthesis, acetnitrile, Ethanonitrile, CCN, HSDB 42, CCRIS 1628, NSC 7593, Acetonitrile, for HPLC, gradient grade, >=99.9%, EINECS 200-835-2, UN1648, RCRA waste no. U003, acetonitile, acetonitnle, acetonitriie, acteonitril, acteonitrile, actonitrile, methylcyanide, methylnitrile, ace-tonitrile, aceto-nitrile, acetonitrile-, UNII-Z072SB282N, AI3-00327, Acetonitrile ACS, CC.equiv.N, Acetonitrile LC-MS, Acetonitrile,homopolymer, Cyanomethylidyne radical, DSSTox_CID_9, Acetonitrile HPLC grade, H3CCN, Acetonitrile, LCMS grade, bmse000826, bmse000896, EC 200-835-2, WLN: NC1, Acetonitrile, >=99.5%, DSSTox_RID_75320, DSSTox_GSID_20009, Acetonitrile with formic acid, Acetonitrile, puriss., 95%, CHEMBL45211, Acetonitrile, for chromatography, DTXSID7020009, Acetonitrile UV/HPLC ACS grade, Acetonitrile, analytical standard, Acetonitrile for preparative HPLC, Acetonitrile, AR, >=99.5%, Acetonitrile, Environmental Grade, NSC7593, Acetonitrile, anhydrous, 99.8%, Acetonitrile, >=99.5% (GC), Acetonitrile, HPLC gradient Grade, Amidite Diluent, for DNA synthesis, NSC-7593, STR02933, Acetonitrile, far UV/gradient grade, Tox21_202481, Acetonitrile, HPLC Grade (Far UV), Acetonitrile, p.a., dry, 99.9%, Acetonitrile, ReagentPlus(R), 99%, c1151, STL283937, Acetonitrile, Spectrophotometric Grade, Acetonitrile, >=99.8%, for HPLC, Acetonitrile, for HPLC, >=99.9%, AKOS000269067, Acetonitrile, HPLC Plus, >=99.9%, NA 1648, UN 1648, Acetonitrile, >=99.5%, ACS reagent, Acetonitrile, ACS reagent, >=99.5%, Acetonitrile, AldraSORB(TM), 99.8%, Acetonitrile, purum, >=99.0% (GC), CAS-75-05-8, Acetonitrile (for HPLC) isocratic grade, Acetonitrile, HPLC grade, >=99.93%, NCGC00091552-01, NCGC00260030-01, Acetonitrile 1000 microg/mL in Methanol, Acetonitrile, purification grade, 99.8%, Ultrapure Acetonitrile, for DNA synthesis, Acetonitrile with 0.1% Formic Acid (v/v), Acetonitrile, biotech. grade, >=99.93%, Acetonitrile, p.a., ACS reagent, 99.8%, Acetonitrile, SAJ first grade, >=99.0%, A0060, A0293, A0793, Acetonitrile, JIS special grade, >=99.5%, FT-0621807, FT-0621808, Acetonitrile, anhydrous, ZerO2(TM), 99.8%, Acetonitrile, for HPLC-GC, >=99.8% (GC), Acetonitrile, for UHPLC, for mass spectrometry, Acetonitrile, Supergradient HPLC Grade (Far UV), Acetonitrile, spectrophotometric grade, >=99.5%, Q408047, Acetonitrile, for HPLC, for UV, >=99.9% (GC), Acetonitrile, puriss. p.a., ACS reagent, 99.8%, J-008497, Acetonitrile, for preparative HPLC, >=99.8% (GC), Acetonitrile, for synthesis of DNA, >=99.9% (GC), Acetonitrile, HPLC Plus, >=99.9%, poly-coated bottles, Acetonitrile solution, contains 0.035 % (v/v) acetic acid, Acetonitrile solution, contains 0.05 % (v/v) acetic acid, Acetonitrile solution, contains 0.1 % (v/v) acetic acid, Acetonitrile, electronic grade, 99.999% trace metals basis, Acetonitrile, for HPLC, gradient grade, >=99.9% (GC), Acetonitrile, for HPLC, gradient grade, >=99.90% (GC), Acetonitrile, puriss. p.a., ACS reagent, >=99.5% (GC), Acetonitrile solution, contains 0.1 % (v/v) ammonium hydroxide, Acetonitrile with 0.1% ammonium acetate, tested for UHPLC-MS, Acetonitrile, for protein sequence analysis, >=99.8% (GC), Acetonitrile, for residue analysis, suitable for 5000 per JIS, Acetonitrile, Vetec(TM) reagent grade, anhydrous, >=99.8%, Acetonitrile solution, ~20% in H2O, for protein sequence analysis, Acetonitrile solution, contains 0.05 % (v/v) trifluoroacetic acid, Acetonitrile solution, contains 0.1 % (v/v) formic acid, for HPLC, Acetonitrile, Preparateur, >=99.9% (GC), Customized plastic drum, Acetonitrile solution, contains 0.1 % (v/v) trifluoroacetic acid, for HPLC, Acetonitrile solution, for HPLC, acetonitrile:water 56 : 44% (w/w), Acetonitrile, >=99.8%, for residue analysis, suitable for 1000 per JIS, Acetonitrile, >=99.8%, for residue analysis, suitable for 300 per JIS, Acetonitrile, puriss. p.a., ACS reagent, reag. Ph. Eur., >=99.5% (GC), Acetonitrile solution, contains 0.035 % (v/v) trifluoroacetic acid, for HPLC, Acetonitrile solution, contains 0.1 % (v/v) formic acid, for UHPLC, for mass spectrometry, Acetonitrile solution, contains 0.10 % (v/v) trifluoroacetic acid, 10.0 % (v/v) water, Acetonitrile solution, contains 10.0% acetone, 40.0% 2-propanol, 0.05% formic acid, Acetonitrile, configured for PerkinElmer 8900, configured for Polygen, for DNA synthesis, Acetonitrile, Pharmaceutical Secondary Standard; Certified Reference Material, Acetonitrile, Preparateur, >=99.9% (GC), One-time steel-plastic (SP) drum, Alcohol Determination - Acetonitrile, United States Pharmacopeia (USP) Reference Standard, Acetonitrile solution, contains 5 % (v/v) water, 0.05 % (w/v) ammonium formate, 0.1 % (v/v) formic acid, for HPLC, Acetonitrile solution, for HPLC, acetonitrile:water 5:95% (v/v), 10 mM Ammoniumbicarbonate, pH 10,0, Acetonitrile solution, NMR reference standard, 0.23 wt. % in D2O (99.9 atom % D), water 0.05 wt. %, NMR tube size 6.5 mm x 8 in., Residual Solvent - Acetonitrile, Pharmaceutical Secondary Standard; Certified Reference Material, Residual Solvent Class 2 - Acetonitrile, United States Pharmacopeia (USP) Reference Standard |
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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
- Carbon dioxide reduction via light activation of a ruthenium–Ni(cyclam) complex
- 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
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3
- 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
- Visible-Light Photoredox Catalysis: Selective Reduction of Carbon Dioxide to Carbon Monoxide by a Nickel N-Heterocyclic Carbene–Isoquinoline Complex
- 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
- Ir(tpy)(bpy)Cl as a Photocatalyst for CO2 Reduction under Visible-Light Irradiation
- Water-Assisted Highly Efficient Photocatalytic Reduction of CO2 to CO with Noble Metal-Free Bis(terpyridine)iron(II) Complexes and an Organic Photosensitizer
- Highly efficient and selective visible-light driven CO2-to-CO conversion by a Co-based cryptate in H2O-CH3CN solution
- Photocatalytic CO2 reduction using a Mn complex as a catalyst
- Metal-free reduction of CO2 to formate using a photochemical organohydride-catalyst recycling strategy
- A Dinuclear Cobalt Cryptate as a Homogeneous Photocatalyst for Highly Selective and Efficient Visible-Light Driven CO2 Reduction to CO in CH3CN-H2O Solution
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction
- Selective and Efficient Photocatalytic CO2 Reduction to CO Using Visible Light and an Iron-Based Homogeneous Catalyst
- A Cu(I) Co(II) cryptate for the visible light-driven reduction of CO2
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes
- 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
- Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH
- Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light
- 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
- Phenoxazine-Sensitized CO2-to-CO Reduction with an Iron Porphyrin Catalyst: A Redox Properties-Catalytic Performance Study/Table 1
- 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
- Pyranopterin Related Dithiolene Molybdenum Complexes as Homogeneous Catalysts for CO2 Photoreduction/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/Table 1
- Photocatalytic CO2 reduction using a Mn complex as a catalyst/Photocatalytic CO2 reduction: conditions optimization
- 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
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3/Table 1
- Carbon dioxide reduction via light activation of a ruthenium–Ni(cyclam) complex/Photoreduction of CO2 result
- 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
- Nickel(II) pincer complexes demonstrate that the remote substituent controls catalytic carbon dioxide reduction/Photocatalytic CO2 reduction under varied conditions
- 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
- Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts/Durability test
- Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light/Table 3 - CV
- Toward Visible-Light Photochemical CO2‑to-CH4 Conversion in Aqueous Solutions Using Sensitized Molecular Catalysis/Photocatalytic reduction of CO2: conditions optimization
- Ir(tpy)(bpy)Cl as a Photocatalyst for CO2 Reduction under Visible-Light Irradiation/Photoreduction of CO2
- A Cu(I) Co(II) cryptate for the visible light-driven reduction of CO2/Photocatalytic reduction of CO2
- New Photosensitizers Based on Heteroleptic Cu(I) Complexes and CO2 Photocatalytic Reduction with (Ni(II)(cyclam))Cl2/Photocatalytic CO2 reduction and control experiments
- 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
- 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
- Highly efficient and selective visible-light driven CO2-to-CO conversion by a Co-based cryptate in H2O-CH3CN solution/photocatalytic CO2 conversion under different conditions
- Metal-free reduction of CO2 to formate using a photochemical organohydride-catalyst recycling strategy/photocatalytic CO2 conversion under different conditions
- A Dinuclear Cobalt Cryptate as a Homogeneous Photocatalyst for Highly Selective and Efficient Visible-Light Driven CO2 Reduction to CO in CH3CN-H2O Solution/Best result and control experiments
- 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
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Concentration and solvent effect
- 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
- 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
- Toward Visible-Light Photochemical CO2‑to-CH4 Conversion in Aqueous Solutions Using Sensitized Molecular Catalysis/Cyclic voltammetry in various conditions
- 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 obtained in a reaction 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