4.8 Article

Going beyond the borders: pyrrolo[3,2-b]pyrroles with deep red emission

期刊

CHEMICAL SCIENCE
卷 12, 期 48, 页码 15935-15946

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1sc05007a

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资金

  1. Polish National Science Centre, Poland [HARMONIA 2018/30/M/ST5/00460]
  2. Foundation for Polish Science [TEAM POIR.04.04.00-00-3CF4/16-00]
  3. EC (MSC ITN CHAIR)
  4. Ministry of Education and Research, Republic of Estonia [PRG661]
  5. National Science Foundation [CHE 2103628]

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A novel doubly B/N-doped ladder-type pyrrolo[3,2-b]pyrroles with strong absorption and efficient fluorescence properties have been developed. Structural modifications lead to significant variations in photophysical properties within the family of these ultrastable dyes. Theoretical calculations support experimental trends, including two-photon absorption, in a nearly quantitative manner.
A two-step route to strongly absorbing and efficiently orange to deep red fluorescent, doubly B/N-doped, ladder-type pyrrolo[3,2-b]pyrroles has been developed. We synthesize and study a series of derivatives of these four-coordinate boron-containing, nominally quadrupolar materials, which mostly exhibit one-photon absorption in the 500-600 nm range with the peak molar extinction coefficients reaching 150 000, and emission in the 520-670 nm range with the fluorescence quantum yields reaching 0.90. Within the family of these ultrastable dyes even small structural changes lead to significant variations of the photophysical properties, in some cases attributed to reversal of energy ordering of alternate-parity excited electronic states. Effective preservation of ground-state inversion symmetry was evidenced by very weak two-photon absorption (2PA) at excitation wavelengths corresponding to the lowest-energy, strongly one-photon allowed purely electronic transition. pi-Expanded derivatives and those possessing electron-donating groups showed the most red-shifted absorption- and emission spectra, while displaying remarkably high peak 2PA cross-section (sigma(2PA)) values reaching similar to 2400 GM at around 760 nm, corresponding to a two-photon allowed higher-energy excited state. At the same time, derivatives lacking pi-expansion were found to have a relatively weak 2PA peak centered at ca. 800-900 nm with the maximum sigma(2PA) similar to 50-250 GM. Our findings are augmented by theoretical calculations performed using TD-DFT method, which reproduce the main experimental trends, including the 2PA, in a nearly quantitative manner. Electrochemical studies revealed that the HOMO of the new dyes is located at ca. -5.35 eV making them relatively electron rich in spite of the presence of two B--N+ dative bonds. These dyes undergo a fully reversible first oxidation, located on the diphenylpyrrolo[3,2-b]pyrrole core, directly to the di(radical cation) stage.

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