4.6 Article

Revealing the sensing mechanism of a fluorescent pH probe based on a bichromophore approach

期刊

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 24, 期 43, 页码 26731-26737

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cp04339d

关键词

-

资金

  1. Lundbeck Foundation [R303-2018-3237]
  2. NSFC [22203085]
  3. Lundbeck Foundation [R303-2018-3237] Funding Source: researchfish

向作者/读者索取更多资源

Fluorescence sensing is important in biology and biomedicine. This study investigates the sensing mechanism of a pH probe using spectroscopy and calculations, and suggests that the bichromophore model is useful for understanding the probe's behavior.
Fluorescence sensing plays an increasingly important role in biology and biomedicine. For many practical applications of fluorescent probes, an off-on response is preferred. The question of how fluorescence quenching/enhancement occurs is fundamental and of high importance for application and design of new fluorescent probes. The sensing mechanism of an aminorhodamine (TMARh) pH probe is investigated using femtosecond transient absorption spectroscopy and quantum chemical calculations, showing that this probe is best understood using the bichromophore model rather than the more common models such as photoinduced electron transfer or intramolecular charge transfer. Under excitation in the main absorption band at 530 nm, a fast internal conversion to the first excited state (S-1) is observed for TMARh; meanwhile, no new transient components are obtained when TMARh is excited directly to S-1 in the weakly absorbing red tail at 630 nm. It is confirmed that the S-1 of TMARh is a dark off state. Theoretical calculations show that the S-1 off state is an intramolecular charge transfer state from an aminophenyl group to a rhodamine chromophore. After protonation of the aminophenyl group, to yield HTMARh, the transient S-2/S-1 internal conversion process that occurs in TMARh under 530 nm excitation is absent, suggesting that the charge transfer state becomes highly unfavorable. All calculations and spectral data confirm that HTMARh has localized transition in the rhodamine chromophore, in agreement with this being the bright on state of the pH probe. The current work not only provides a photophysical insight into the sensing mechanism of this specific probe, but also shows that the bichromophore model is useful and may be relevant for analyzing other probes or in the designing of new ones.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据