Novel truxene-based dipyrromethanes (DPMs): synthesis, spectroscopic characterization and photophysical properties

For the first time, herein, we report the synthetic part of the truxene-centred mono-, di- and tri-substituted dipyromethanes (DPMs) in good yields (60-80%) along with their preliminary photophysical (absorption, emission and time resolved fluorescence lifetime) properties. The condensation reaction for assembling the required DPMs were catalyzed with trifluoroacetic acid (TFA) at 0 °C to room temperature (rt), and the stable dipyrromethanes were purified through silica-gel column chromatography. After successfully synthesizing these easy-to-make yet interesting molecules, they were fully characterized by means of the standard spectroscopic techniques (<sup>1</sup>H NMR, <sup>13</sup>C NMR and HRMS). We are of the opinion that these truxene-based systems will be useful for diverse applications in future studies.

Authors

Institutions

Publication Details

Journal
Beilstein Journal of Organic Chemistry
Published
2024-08-29
DOI
https://doi.org/10.3762/bjoc.20.186
Citations
1
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
0.12

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Novel truxene-based dipyrromethanes (DPMs): synthesis, spectroscopic characterization and photophysical properties

Rashid Ali, Shakeel Alvi
1 citations
Beilstein Journal of Organic Chemistry
Luminescence and Fluorescent Materials
0.12
article

Novel truxene-based dipyrromethanes (DPMs): synthesis, spectroscopic characterization and photophysical properties

Rashid Ali, Shakeel Alvi
article en
1 citations

Abstract

For the first time, herein, we report the synthetic part of the truxene-centred mono-, di- and tri-substituted dipyromethanes (DPMs) in good yields (60-80%) along with their preliminary photophysical (absorption, emission and time resolved fluorescence lifetime) properties. The condensation reaction for assembling the required DPMs were catalyzed with trifluoroacetic acid (TFA) at 0 °C to room temperature (rt), and the stable dipyrromethanes were purified through silica-gel column chromatography. After successfully synthesizing these easy-to-make yet interesting molecules, they were fully characterized by means of the standard spectroscopic techniques (<sup>1</sup>H NMR, <sup>13</sup>C NMR and HRMS). We are of the opinion that these truxene-based systems will be useful for diverse applications in future studies.

Beilstein Journal of Organic ChemistryVol. 20
Jamia Millia Islamia (IN)
Jamia Millia Islamia, Department of Science and Technology, Ministry of Science and Technology, India, Science and Engineering Research Board
Openalex Percentile: Top 60%
Luminescence and Fluorescent Materials
0.12
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.