Porpholactone Chemistry: Shining New Light on an Old Cofactor

被引:4
作者
Jin, Guo-Qing [1 ]
Xue, Hao-Zong [1 ]
Zhang, Jun-Long [1 ]
机构
[1] Peking Univ, Coll Chem & Mol Engn, Beijing Natl Lab Mol Sci, State Key Lab Rare Earth Mat Chem & Applicat, Beijing 100871, Peoples R China
来源
CHEMPLUSCHEM | 2021年 / 86卷 / 01期
关键词
COUPLED ELECTRON-TRANSFER; C-H AMINATION; HYDROGEN-EVOLUTION; YTTERBIUM(III) COMPLEXES; BETA-LACTONIZATION; IN-VIVO; PORPHYRIN; OXIDATION; DESIGN; SUBSTITUENTS;
D O I
10.1002/cplu.202000494
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The emergence of porpholactone chemistry, discovered over 30 years ago, has significantly stimulated the development of biomimetic tetrapyrrole chemistry. It offers an opportunity, through modifications of non-pyrrolic building blocks, to clarify the relationship between chemical structure and excited-state properties, deciphering the structural code for the biological functions of life pigments. With intriguing photophysical properties in the red to near-infrared (NIR) regions, facile modulation of their electronic nature by fine-tuning chemical structures, and coordination ability with diverse metal ions, these novel porphyrinoids have favorable prospects in the fields of optical materials, bioimaging and therapy, and catalysis. In this Minireview, we summarize the brief history of porpholactone chemistry, and focus on the studies carried out in our group, particularly on the regioisomeric effect, NIR lanthanide luminescence, and metal catalysis. We outline the perspectives of these compounds in the construction of porpholactone-related biomedical applications and optical and energy materials, in order to inspire more interest and further advance bioinspired inorganic chemistry and lanthanide chemical biology.
引用
收藏
页码:71 / 81
页数:11
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