Related Experiment Video
Updated: Apr 13, 2026

Synthesis, Cellular Delivery and In vivo Application of Dendrimer-based pH Sensors
Published on: September 10, 2013
Polyimide dendrimers containing multiple electron donor-acceptor units and their unique photophysical properties
Francesca M Toma1, Fausto Puntoriero2, Toan V Pho1
1Department of Chemistry and Biochemistry, Department of Materials, Center for Polymers and Organic Solids, University of California, Santa Barbara, CA 93106 (USA).
Abstract:
A high-yielding synthesis of a series of polyimide dendrimers, including decacyclene- and perylene-containing dendrimer D6, in which two types of polyimide dyes are present, is reported. In these constructs, the branching unit is represented by trisphenylamine, and the solubilizing chains by N-9-heptadecanyl-substituted perylene diimides. The photophysical properties of the dendrimers have been studied by absorption, steady-state, and time-resolved emission spectroscopy and pump-probe transient absorption spectroscopy. Photoinduced charge-separated (CS) states are formed on the femtosecond timescale upon visible excitation. In particular, in D6, two different CS states can be formed, involving different subunits that decays independently with different lifetimes (ca. 10-100 ps).
More Related Videos
09:22Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
06:08Time-resolved Photophysical Characterization of Triplet-harvesting Organic Compounds at an Oxygen-free Environment Using an iCCD Camera
Published on: December 27, 2018
Related Concept Videos
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Structure of Conjugated Dienes
Conjugated dienes are compounds characterized by the presence of alternating double and single bonds. In a conjugated system like 1,3-butadiene, the unhybridized 2p orbital on each carbon overlaps continuously, allowing the π electrons to be delocalized across the entire molecule. In contrast, this type of overlap does not occur in cumulated and isolated dienes, such as 2,3-pentadiene and 1,4-pentadiene, respectively. Instead, the π electrons remain localized between the...