Time-Resolved Electron Paramagnetic Resonance Investigation on the Quenching Reaction of Photo-Induced Excited Triplet Vitamin K3by Antioxidant Vitamin C in Homogeneous and Micelle Solutions-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Time-Resolved Electron Paramagnetic Resonance Investigation on the Quenching Reaction of Photo-Induced Excited Triplet Vitamin K3by Antioxidant Vitamin C in Homogeneous and Micelle Solutions

Published:2014-08-26 Issue:1 Volume:48 Page:32-39
ISSN:0038-7010
Container-title:Spectroscopy Letters
language:en
Short-container-title:Spectroscopy Letters

Author:

Wang Jian,Zheng Fei,Bian Weiwei,Zhu Guanglai,Xu Xinsheng

Funder

This work was supported by the National Natural Science Foundation of China (20903004 and 21173002) and the Natural Science Foundation of Anhui Province (1308085MB20). We are grateful to Professor Guozhong Wu for his help in obtaining transient absorption spectra.

Publisher

Informa UK Limited

Subject

Spectroscopy,Atomic and Molecular Physics, and Optics,Analytical Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00387010.2013.851088

Reference30 articles.

1. Solvent effects on singlet oxygen yield from n,.pi.* and .pi.,.pi.* triplet carbonyl compounds

2. BENZOPHENONE-SENSITIZED LIPID PEROXIDATION IN LINOLEATE MICELLES

3. Time-Resolved EPR Investigation of the Photo-initiated Intramolecular Antioxidant Reaction of Vitamin K−Vitamin E Linked Molecule

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Photosensitive damage of dipeptides: mechanism and influence of structure;Physical Chemistry Chemical Physics;2023

2. Study on Redox Mechanism of 2-Methyl-naphthoquinone in Dimethyl Sulfoxide and Acetonitrile;CHEM J CHINESE U;2018

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP