ArticleTetrahedron letters2009
Energy transfer dyads based on Nile Red.
Article in Tetrahedron letters, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
4 citing papers in PubMed, 19 citations in OpenAlex.
- Bis-Rhodamines Bridged with a Diazoketone Linker: Synthesis, Structure, and Photolysis.The Journal of organic chemistry · 2022Article
- Dynamics of Photoinduced Energy Transfer in Fully and Partially Conjugated Polymers Bearing π-Extended Donor and Acceptor Monomers.Frontiers in chemistry · 2020Article
- Efficient deprotection of F-BODIPY derivatives: removal of BF2 using Brønsted acids.Beilstein journal of organic chemistry · 2015Article
- Development of UV-excitable red and near-infrared fluorescent labels and their application for simultaneous multicolor bioimaging by single-wavelength excitation.Journal of fluorescence · 2013Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors at 1 institution in 1 country.
Funding
Abstract
This project was initiated to develop energy transfer dyads emitting in the 600 - 700 nm region by using Nile Red acceptors. Thus fluorescein- and BODIPY-based donors were linked to these acceptors via alkynes or triazoles. The product dyads (1 - 5) have energy transfer efficiencies of 77 - 97% in organic media.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.