Other — Constructing a Redox-Active Cu(I)-Pyridyltriazine Framework for Catalytic Photoreduction of Nitrobenzenes and Carboxylic Cyclization of Alkynol with CO2

Measurement evidence

Other

Constructing a Redox-Active Cu(I)-Pyridyltriazine Framework for Catalytic Photoreduction of Nitrobenzenes and Carboxylic Cyclization of Alkynol with CO2 · Zhang T., Si C., Guo K. et al. · Inorganic Chemistry · 2022 · 20657-20665

3 measurement groups · 15 results

Reported values remain attached to the sample, method, conditions, extraction quality and source location that produced them.

Carboxylic cyclization of alkynol with CO2

As-synthesised Cu(I)-TPT catalyst powder · Powder

1 mmol substrate, 15 mg Cu(I)-TPT, 1 mL CH3CN, 20 uL TEA, 0.5 MPa CO2, 50 C, 24 h.

Temperature
323
Atmosphere
0.5 MPa CO2
Geometry
25 mL autoclave
Context
pristine framework catalyst
Measurement source
p006 / 20662 · Catalysis of Carboxyl Cyclization · Table 2
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
2-methyl-3-butyn-2-ol carboxylic cyclization TOFMarked as a best value within this paper1.79 h-11.79 h-1Table
Exact Reported
p006 / 20662 · Catalysis of Carboxyl Cyclization · Table 2
2-methyl-3-butyn-2-ol carboxylic cyclization TONMarked as a best value within this paper43.0443.04 TONTable
Exact Reported
p006 / 20662 · Catalysis of Carboxyl Cyclization · Table 2
2-methyl-3-butyn-2-ol carboxylic cyclization yieldMarked as a best value within this paper99%99 %Table
Exact Reported
p006 / 20662 · Catalysis of Carboxyl Cyclization · Table 2
3-methyl-1-pentyn-3-ol carboxylic cyclization yield94%94 %Table
Exact Reported
p006 / 20662 · Catalysis of Carboxyl Cyclization · Table 2
Carboxylic cyclization yield without Cu(I)-TPTtraceSI Table
Qualitative
S31 · Section 3 Catalysis Details · Table S4
Carboxylic cyclization yield using Cu-TPT without TEAtraceSI Table
Qualitative
S31 · Section 3 Catalysis Details · Table S4

Photocatalytic reduction of nitroarenes

As-synthesised Cu(I)-TPT catalyst powder · Powder

0.5 mmol substrate, 10 mg Cu(I)-TPT, 2 mmol N2H4.H2O, CH3CN/H2O 4:1 v/v, 2.5 mL total, N2 1 atm, 10 W 365 nm LED, room temperature, 8 h unless otherwise noted.

Temperature
room temperature
Atmosphere
N2
Geometry
quartz tube / WATTCAS parallel light reactor
Context
pristine framework catalyst
Measurement source
p005 / 20661 · Photocatalysis Reduction of Nitroaromatic Compounds · Table 1
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Cu leaching efficiency after cycle experiments0.11%0.11 %Text
Exact Reported
p005 / 20661 · Photocatalysis Reduction of Nitroaromatic Compounds · Figure S11
Nitrobenzene reduction yield after three runs93%93 %Text
Exact Reported
p005 / 20661 · Photocatalysis Reduction of Nitroaromatic Compounds · Figure S10
Nitrobenzene-to-aniline selectivityMarked as a best value within this paper99%99 %Table
Exact Reported
p005 / 20661 · Photocatalysis Reduction of Nitroaromatic Compounds · Table 1
Nitrobenzene-to-aniline yieldMarked as a best value within this paper99% after 8 h99 %Table
Exact Reported
p005 / 20661 · Photocatalysis Reduction of Nitroaromatic Compounds · Table 1
Nitrobenzene reduction yield under dark conditionstraceSI Table
Qualitative
S14 · Section 3 Catalysis Details · Table S3
Nitrobenzene reduction yield without catalyst11%11 %SI Table
Exact Reported
S14 · Section 3 Catalysis Details · Table S3
Nitrobenzene reduction yield under white light10%10 %SI Table
Exact Reported
S14 · Section 3 Catalysis Details · Table S3

Thermogravimetric analysis / DTA

As-synthesised Cu(I)-TPT orange rhombus single crystals · Single Crystal

TGA/SDTA heated from 35 to 1000 C at 10 C min-1 under dynamic N2 atmosphere.

Atmosphere
dynamic N2
Geometry
powder/crystal sample
Context
pristine framework
Measurement source
S2 and S10 · 1.1 Materials and Characterizations · Figure S5
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Complete CH3CN loss temperatureabout 317 C590.15 KText
Approximate
p003 / 20659 · Characterizations · Figure S5
Total weight loss from 25 to 500 C68.8% (calculated 71.25%)68.8 %Text
Exact Reported
p003 / 20659 · Characterizations · Figure S5