Evidence for dual La and L b emission in 5-methylindole.

J Fluoresc

Department of Chemistry, University of Mississippi, 38677, University, Mississippi.

Published: June 1994

The steady-state fluorescence anisotropy of 5-methylindole is shown to depend on both excitation and emission wavelengths, at room temperature in glycerol. A simulation is presented that shows that this emission wavelength dependence of the anisotropy can be explained in terms of dual emission from both the La and the Lb transition moments of the indole ring. For such dual emission to occur, the lowest excited-state energy level of both of these oscillators must be very similar.

Download full-text PDF

Source
http://dx.doi.org/10.1007/BF01881884DOI Listing

Publication Analysis

Top Keywords

dual emission
12
emission
5
evidence dual
4
emission 5-methylindole
4
5-methylindole steady-state
4
steady-state fluorescence
4
fluorescence anisotropy
4
anisotropy 5-methylindole
4
5-methylindole depend
4
depend excitation
4

Similar Publications

Luminescent materials doped with rare-earth (RE) ions have emerged as powerful tools in thermometry, offering high sensitivity and accuracy. However, challenges remain, particularly in maintaining efficient luminescence at elevated temperatures. This study investigates the thermometric properties of BiVO: Yb/Er (BVO: Er/Yb) nanophosphors synthesized the sol-gel method.

View Article and Find Full Text PDF

Cytosine-rich and poly(adenine)-tailed tetrahedral DNA framework (TDF) is designed as template (A-TDF) for anchoring silver nanoclusters (AgNCs) and igniting the dual-color fluorescence of AgNCs. The resultant DNA-AgNCs simultaneously emits red and green fluorescence, and the quantum yield of red fluorescence is as high as 44.8%.

View Article and Find Full Text PDF

In this paper, a dual-parameter liquid level and refractive index (R.I.) sensor is fabricated using three pieces of bare polymer optical fibers (POFs), which can independently and simultaneously sense the liquid level and R.

View Article and Find Full Text PDF

Developing donor-acceptor [n]cycloparaphenylenes (D-A [n]CPPs) with multiple emissions from different emissive states remains challenging yet crucial for achieving white-light emission in single-molecule. Here, we report our explorations into acceptor engineering of quinone-based D-A [10]CPPs (Nq/Aq/Tq[10]CPPs) via a post-lateral annulation using Diels-Alder reactions of oxTh[10]CPP. X-ray analysis reveals that Nq[10]CPP displays a side by side packing via naphthoquione stacking while Aq[10]CPP adopts an intercalated conformation through anthraquinone interaction.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!