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ChemicalBook--->CAS DataBase List--->2243590-42-1

2243590-42-1

2243590-42-1 Structure

2243590-42-1 Structure
IdentificationBack Directory
[Name]

BTT
[CAS]

2243590-42-1
[Synonyms]

BTT22
benzo[1,2-b:3,4-b':5,6-b'']trithiophene-2,5,8-tricarbaldehyde
[Molecular Formula]

C15H6O3S3
[MOL File]

2243590-42-1.mol
[Molecular Weight]

330.4
Chemical PropertiesBack Directory
[Boiling point ]

642.4±50.0 °C(Predicted)
[density ]

1.692±0.06 g/cm3(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H315-H302
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Uses]

Benzo[1,2-b:3,4-b':5,6-b'']trithiophene-2,5,8-tricarbaldehyde (BTT) is a porous organic material with a conjugated backbone, highly dispersed π-π conjugation, and stabilized chemical bonding, which has the ability to act as a visible light photocatalyst. Starting from BTT, two porous organic materials linked to ethylene and imine were synthesized respectively with 1,4-phenylenediacetonitrile (PDAN) and 1,4-phenylenediamine (PDA) structural units. The less reversible ethylene can only form conjugated microporous polymers (CMPs), i.e., BTT-PDAN-CMP, while on the contrary, the more reversible imine can build covalent organic frameworks (COFs), i.e., BTT-PDA-COF.Although BTT-PDAN-CMP is amorphous, it shows better photovoltaic properties than BTT-PDA-COF, due to the enhanced electron transfer from ethylene. better photoelectric properties. BTT-PDAN-CMP proved to be an efficient photocatalyst. In fact, BTT-PDAN-CMP, as a visible light photocatalyst, showed higher efficiency than BTT-PDA-COF in selective aerobic sulfur oxidation. Driven by green light on BTT-PDAN-CMP, molecular oxygen was converted into superoxide and single-linear state oxygen, which contributed to the highly selective formation of organic sulfur oxides.
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