Radical-Triggered Chemiluminescence of Phenanthroline Derivatives: An Insight into Radical–Aromatic Interaction-Reference-Cited by-同舟云学术

Radical-Triggered Chemiluminescence of Phenanthroline Derivatives: An Insight into Radical–Aromatic Interaction

Published:2019-08-30 Issue:12 Volume:4 Page:15004-15011
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Shah Syed Niaz Ali¹^ORCID,Shah Aamir Hassan²,Dou Xiangnan¹,Khan Mashooq¹^ORCID,Lin Ling²,Lin Jin-Ming¹^ORCID

Affiliation:

1. Beijing Key Laboratory of Microanalytical Methods and Instrumentation, MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing 100084, China

2. The National Center for Nanoscience and Technology (NCNST) of China, No. 11 ZhongGuanCun, 100190 Beijing, China

Funder

China Postdoctoral Science Foundation

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.9b01785

Reference35 articles.

1. Substituent effect on the N-oxidation of 1,10-phenanthroline derivatives by peroxomonosulfate ion

2. Formation of 1,10-Phenanthroline-N,N′-dioxide under Mild Conditions: The Kinetics and Mechanism of the Oxidation of 1,10-Phenanthroline by Peroxomonosulfate Ion (Oxone)

3. 1,10-Phenanthroline derivatives as mediators for glucose oxidase

4. Organic NLO material with H-bonded 1D helical self-assembly: synthesis, X-ray crystal structure, DFT calculations, SHG measurements and thermal studies of (5Z,6E)-1,10-phenanthroline-5,6-dione dioxime

5. tert-Butoxide-Mediated Arylation of Benzene with Aryl Halides in the Presence of a Catalytic 1,10-Phenanthroline Derivative

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