Synthesis and photophysical properties of nitrated aza-BODIPYs

被引:6
|
作者
Zarcone, Samuel R. [1 ]
Yarbrough, Hana J. [1 ]
Neal, Martin J. [2 ]
Kelly, Jordan C. [2 ]
Kaczynski, Katie L. [2 ]
Bloomfield, Aaron J. [2 ]
Bowers, Geoffrey M. [1 ]
Montgomery, Thomas D. [2 ]
Chase, Daniel T. [1 ]
机构
[1] St Marys Coll Maryland, Dept Chem & Biochem, St Marys City, MD 20686 USA
[2] Duquesne Univ, Dept Chem & Biochem, Pittsburgh, PA 15282 USA
基金
美国国家科学基金会;
关键词
ORGANIC TRIPLET PHOTOSENSITIZERS; EXCITED-STATE; SEMICONDUCTING CHARACTERISTICS; HIGHLY FLUORESCENT; BF2; COMPLEXES; DYES; DIPYRROMETHENE; DESIGN; BORON; ABSORPTION;
D O I
10.1039/d1nj05976a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of ten electron deficient aza-BODIPYs were prepared through a facile nitration strategy where either one, two, or four nitro groups can be regioselectively attached which represents a novel synthetic transformation of the core structure. Installation of the highly withdrawing nitro group on the 2- and 6-positions was found to greatly impact the absorption and emission profiles of the aza-BODIPY core in comparison to their non-nitrated precursors as seen through unusually large negative solvatochromic effects and Stokes shifts, resulting in exceptional photophysical tunability. TD-DFT calculations also revealed that nitration on the 2- and 6-positions greatly stabilized both HOMO and LUMO energy levels by an average of 0.61 eV, resulting in average HOMO and LUMO energies of -4.46 eV and -6.44 eV, respectively. Moreover, preliminary studies suggested that nitrated aza-BODIPYs possess moderate to superior photostabilities when compared to their non-nitrated analogues. Combined, these data demonstrate that nitration of the 2- and 6-positions is a viable strategy in designing effective push-pull aza-BODIPYs with near-IR absorption and emission profiles.
引用
收藏
页码:4483 / 4496
页数:14
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