Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Photoluminescence: Applications01:14

Photoluminescence: Applications

1.2K
Photoluminescence offers a wide range of applications due to its inherent sensitivity and selectivity. This technique allows for both direct and indirect analyses of the analyte. Direct quantitative analysis is possible when the analyte exhibits a favorable quantum yield for fluorescence or phosphorescence. However, an indirect analysis may be feasible if the analyte is not fluorescent or phosphorescent, or if the quantum yield is unfavorable. Indirect methods include reacting the analyte with...
1.2K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Transient Activation Windows Program Adaptive Photochemical Responses.

Angewandte Chemie (International ed. in English)·2026
Same author

Red-light-excited dynamic near-infrared organic afterglow materials for in vivo bioimaging.

Light, science & applications·2026
Same author

Single-molecule electrical characterization of photoinduced aggregation evolution.

Nature communications·2026
Same author

Copper-Catalyzed Remote Asymmetric Three-Component Sulfonylation Using SO<sub>2</sub> as the Sulfur Source to Access Chiral Allylic Sulfones.

Organic letters·2026
Same author

Chronic myelomonocytic leukemia without increased classical monocyte subsets exhibits a distinct genetic profile, including frequent CBL mutations.

American journal of clinical pathology·2026
Same author

Biomimetic Supramolecular Assemblies With Programmable Structural and Chiroptical Dynamics.

Angewandte Chemie (International ed. in English)·2026
Same journal

Efficient Syngas Photoproduction Enabled by Electronic Engineering of Co-Immobilized Imine COFs.

Angewandte Chemie (International ed. in English)·2026
Same journal

Pathway Controlled Phase Separation of Minimal Building Blocks Utilizing a Dissociative Chemical Transformation.

Angewandte Chemie (International ed. in English)·2026
Same journal

Interaction Hierarchy and Polymorphic Structure-Property Dynamics in Luminescent Molecular Crystals.

Angewandte Chemie (International ed. in English)·2026
Same journal

The Role of Zn-Hf Site Proximity and Oxygen Vacancies for Methanol Formation Over ZnHfO<sub>x</sub> Catalysts Under CO<sub>2</sub> Hydrogenation Conditions.

Angewandte Chemie (International ed. in English)·2026
Same journal

Breaking the Linear Scaling Relationship: Bioinspired Electronic Coupling in S-Bridged Fe-Fe Dual Sites for Efficient Oxygen Reduction.

Angewandte Chemie (International ed. in English)·2026
Same journal

Programming Bio-Bio Electronic Interfaces for Light-Driven Interspecies Electron Transfer.

Angewandte Chemie (International ed. in English)·2026
See all related articles

Related Experiment Video

Updated: Mar 19, 2026

Author Spotlight: Advancing Bioimaging and Therapy with Functional Nanomaterials
07:12

Author Spotlight: Advancing Bioimaging and Therapy with Functional Nanomaterials

Published on: September 13, 2024

3.1K

Pseudo-Homologue Doping Strategy for Afterglow Materials.

Jiayu Wang1, Liangwei Ma1, Bingbing Ding1

  • 1Key Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center For Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, China.

Angewandte Chemie (International Ed. in English)
|March 18, 2026
PubMed
Summary
This summary is machine-generated.

Trace impurities, identified as biphenyl carboxylic acid derivatives, are responsible for the afterglow in benzene-carboxylic acid (BCA) materials. A new pseudo-homologues strategy significantly improves the success rate of creating these dual-component afterglow materials.

Keywords:
impurityisomersphosphorescencephotochemistrypseudo‐homologues

More Related Videos

Synthesis of Wavelength-shifting DNA Hybridization Probes by Using Photostable Cyanine Dyes
07:44

Synthesis of Wavelength-shifting DNA Hybridization Probes by Using Photostable Cyanine Dyes

Published on: July 6, 2016

11.7K
High Resolution Phonon-assisted Quasi-resonance Fluorescence Spectroscopy
10:40

High Resolution Phonon-assisted Quasi-resonance Fluorescence Spectroscopy

Published on: June 28, 2016

8.0K

Related Experiment Videos

Last Updated: Mar 19, 2026

Author Spotlight: Advancing Bioimaging and Therapy with Functional Nanomaterials
07:12

Author Spotlight: Advancing Bioimaging and Therapy with Functional Nanomaterials

Published on: September 13, 2024

3.1K
Synthesis of Wavelength-shifting DNA Hybridization Probes by Using Photostable Cyanine Dyes
07:44

Synthesis of Wavelength-shifting DNA Hybridization Probes by Using Photostable Cyanine Dyes

Published on: July 6, 2016

11.7K
High Resolution Phonon-assisted Quasi-resonance Fluorescence Spectroscopy
10:40

High Resolution Phonon-assisted Quasi-resonance Fluorescence Spectroscopy

Published on: June 28, 2016

8.0K

Area of Science:

  • Organic Chemistry
  • Materials Science
  • Photophysics

Background:

  • Impurities in organic phosphorescent materials are a subject of recent scientific interest.
  • The afterglow properties of commercial benzene-carboxylic acid (BCA) derivatives have been observed but not fully understood.

Purpose of the Study:

  • To identify the specific impurities responsible for the afterglow in BCA derivatives.
  • To develop a novel strategy for constructing efficient dual-component afterglow materials based on structural similarities.

Main Methods:

  • Chemical analysis to identify trace impurities in BCA derivatives.
  • Synthesis and characterization of 275 doped samples using a pseudo-homologues strategy.
  • Evaluation of phosphorescence and afterglow properties of the synthesized materials.

Main Results:

  • Trace amounts of biphenyl carboxylic acid derivatives were identified as the source of afterglow in BCA materials.
  • One impurity induced phosphorescence at doping levels as low as 0.1 ppm.
  • The pseudo-homologues strategy achieved a 73.3% success rate for afterglow materials, significantly higher than other samples (6.5%).

Conclusions:

  • The study elucidates the role of specific impurities in enabling afterglow in organic materials.
  • A pseudo-homologues strategy provides a new framework for designing dual-component afterglow materials.
  • This approach offers valuable insights for the development of advanced luminescent materials.