Issue 7, 2017

Substituent effects on the aggregation-induced emission and two-photon absorption properties of triphenylamine–dibenzo[a,c]phenazine adducts

Abstract

Exploration of high-performance fluorescent materials, especially those with two-photon absorption and aggregation-induced emission (AIE) properties, is of great significance to both fundamental research and practical applications. In the present work, a series of triphenylamine–dibenzo[a,c]phenazine adducts (Q1–Q5) with triphenylamine (TPA) moieties decorated by substituents ranging from nil to alkyl (methyl/octyl) and finally to alkoxy (methoxyl/octyloxy) groups were elaborately designed and facilely synthesized. Their photophysical properties including one- and two-photon absorption properties have been systematically investigated to clarify the relationships between their structures and properties and to see how a small change in the structure makes big differences in their performances. The proterotype triphenylamine–dibenzo[a,c]phenazine (TPA–DBP) adduct Q1 and the alkyl-substituted TPA–DBP adducts (Q2 and Q3) show intramolecular charge transfer (ICT) plus aggregation-enhanced emission (AEE) features while the alkoxy-decorated TPA–DBP adducts, i.e., Q4 and Q5, exhibit typical AIE behaviors. The differences in their photophysical properties can be mainly ascribed to the substituent effects, which are closely associated with the RIM (restriction of intramolecular motion) mechanism. Moreover, the AIE-active red luminogen Q5 with the largest two-photon absorption cross-section (σ = 801 GM) and high brightness has been further fabricated into nanoparticles via a simple and well-established method to satisfy the requirements of in vivo two-photon fluorescence imaging of blood vessels. The water-dispersible and biocompatible PEG-modified nanoparticles of Q5 performed well as an effective contrast agent for the visualization of blood vasculature with high signal-to-noise ratios, low photodamage and deep-tissue penetration capability (100 μm).

Graphical abstract: Substituent effects on the aggregation-induced emission and two-photon absorption properties of triphenylamine–dibenzo[a,c]phenazine adducts

Supplementary files

Article information

Article type
Research Article
Submitted
18 Qun 2017
Accepted
24 Nah 2017
First published
28 Nah 2017

Mater. Chem. Front., 2017,1, 1396-1405

Substituent effects on the aggregation-induced emission and two-photon absorption properties of triphenylamine–dibenzo[a,c]phenazine adducts

J. Yang, Y. Gao, T. Jiang, W. Liu, C. Liu, N. Lu, B. Li, J. Mei, Q. Peng and J. Hua, Mater. Chem. Front., 2017, 1, 1396 DOI: 10.1039/C7QM00024C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements