Quantifying Triplet State Formation in Zinc Dipyrrin Complexes

被引:7
作者
Alqahtani, Norah Z. [1 ]
Blevins, Toni G. [1 ]
McCusker, Catherine E. [1 ]
机构
[1] East Tennessee State Univ, Dept Chem, Johnson City, TN 37614 USA
关键词
SPECTRAL-LUMINESCENT PROPERTIES; INTRAMOLECULAR CHARGE-TRANSFER; VISIBLE-LIGHT; BODIPY DYES; PHOTOREDOX CATALYSIS; STRUCTURAL CONTROL; ZN(II) COMPLEXES; METAL-COMPLEXES; UP-CONVERSION; BASIS-SETS;
D O I
10.1021/acs.jpca.9b08682
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalysis is a promising method to harness solar energy and use it to form fuels and other high-value chemicals, but most sensitizers used in photo- catalytic reactions are complexes of rare and expensive metals a such as ruthenium and iridium. Zinc dipyrromethene a complexes have potential to be a more earth-abundant without heavy atoms, by transient absorption spectroscopy. Without heavy atoms, the triplet quantum yield was 16% in toluene and 27% in THF. With the addition of heavy I atoms, Wavelength (nm) the triplet quantum yield increased to 62-63% and was insensitive to solvent polarity. The fact that in the absence of heavy atoms the triplet yield is affected by solvent polarity and in the presence of heavy atoms it is not suggests that triplet formation occurs through different pathways in the two complexes. These triplet yields meet or exceed those of successful organic photosensitizers, illustrating the potential for zinc dipyrromethene complexes as photosensitizers.
引用
收藏
页码:10011 / 10018
页数:8
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