English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  Identification of the structure of triethanolamine oxygenation products in carbon nitride photocatalysis

Savateev, A., & Zou, Y. (2022). Identification of the structure of triethanolamine oxygenation products in carbon nitride photocatalysis. ChemistryOpen, 11(7): e202200095. doi:10.1002/open.202200095.

Item is

Files

show Files
hide Files
:
Article.pdf (Publisher version), 829KB
Name:
Article.pdf
Description:
-
OA-Status:
Hybrid
Visibility:
Public
MIME-Type / Checksum:
application/pdf / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-

Locators

show

Creators

show
hide
 Creators:
Savateev, Aleksandr1, Author           
Zou, Yajun1, Author           
Affiliations:
1Aleksandr Savateev, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_2421702              

Content

show
hide
Free keywords: carbon nitride; formamide; oxygenation; photocatalysis; triethanolamine
 Abstract: Triethanolamine (TEOA) is one of the most commonly used sacrificial agents in photocatalysis. Due to its more complex structure compared to, for example, ethanol, and its sacrificial role in photocatalysis, it gives a mixture of products. The structures of these molecules are not usually analyzed. Herein, we obtain and isolate the products of TEOA and N-tert-butyl diethanolamine oxygenation under photocatalytic conditions with ≈15 % yield, and followingly characterized them by NMR and mass spectroscopy. The reaction is mediated by potassium poly(heptazine imide) (K-PHI) in the presence of O2 and affords formyl esters of β-hydroxyethylene formamides from the corresponding ethanolamines.

Details

show
hide
Language(s): eng - English
 Dates: 2022-07-132022
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1002/open.202200095
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: ChemistryOpen
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 11 (7) Sequence Number: e202200095 Start / End Page: - Identifier: ISSN: 2191-1363