Synthesis and Photophysical Properties of [3]Cyclo-1,8-pyrenes via [4 + 2] Cycloaddition Reaction.
Huiqing LiuGui-Lin ZhuangShengda WangPingsen HuangMuqing ChenShangfeng YangPingwu DuPublished in: The Journal of organic chemistry (2021)
Herein, we report the synthesis, characterization, and photophysical properties of the crown-like structure of [3]cyclo-1,8-pyrenes (compounds 9 and 10). Planar pyrenyl arylene-ethynylene macrocycles are used as the precursors to synthesize these pyrene-based cycloarenes by [4 + 2] cycloaddition reaction with good yields. These molecules are confirmed by nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry. The structure of 9 was unambiguously determined by single-crystal X-ray diffraction. Their photophysical properties are investigated by steady-state absorption, fluorescence, and time-resolved fluorescence spectroscopies, combined with theoretical calculations.
Keyphrases
- high resolution mass spectrometry
- single molecule
- liquid chromatography
- high resolution
- density functional theory
- energy transfer
- magnetic resonance imaging
- molecular dynamics
- molecular dynamics simulations
- ultra high performance liquid chromatography
- magnetic resonance
- atomic force microscopy
- mass spectrometry
- electron microscopy