Photophysical Properties Controlled by Substituents with Lone-Pair Electrons at the Ortho- or Para-Positions of Fluoroquinolone Antibiotics-Reference-Cited by-同舟云学术

Photophysical Properties Controlled by Substituents with Lone-Pair Electrons at the Ortho- or Para-Positions of Fluoroquinolone Antibiotics

Published:2019-03-22 Issue:15 Volume:123 Page:3156-3162
ISSN:1520-6106
Container-title:The Journal of Physical Chemistry B
language:en
Short-container-title:J. Phys. Chem. B

Author:

Zhao Jianfeng¹,Zhang Xiting¹,Zhu Ruixue¹²,Su Tao³,Phillips David Lee¹^ORCID

Affiliation:

1. Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong 11111, P. R. China

2. School of Physical Science and Technology, Shanghai Tech University, Shanghai 201210, P. R. China

3. Department of Molten Salt Chemistry and Engineering, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, 2019, Jia Luo Road, Jiading District, Shanghai 201800, P. R. China

Funder

Research Grants Council, University Grants Committee

University Grants Committee

Publisher

American Chemical Society (ACS)

Subject

Materials Chemistry,Surfaces, Coatings and Films,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jpcb.8b10859

Reference40 articles.

1. Direct Observation of Photoinduced Ultrafast Generation of Singlet and Triplet Quinone Methides in Aqueous Solutions and Insight into the Roles of Acidic and Basic Sites in Quinone Methide Formation

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4. Efficient up-conversion of triplet excitons into a singlet state and its application for organic light emitting diodes

5. Triplet state dissolved organic matter in aquatic photochemistry: reaction mechanisms, substrate scope, and photophysical properties

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