Issue 18, 2019

Study on a polymerizable visible light initiator for fabrication of biosafety materials

Abstract

Developing low-mobility visible light photoinitiators (PIs) will open new application fields for photopolymerization. In this paper, a polymerizable visible light PI (PBDA) containing acryloyl groups based on a benzylidene cyclopentanone moiety was synthesized and characterized by 1H-NMR, 13C-NMR, UV-Vis spectrum and HR-MS. Its linear absorption appears in the visible region (400–530 nm) and overlaps very well with the emission spectrum of a common blue light source. Under the irradiation of a 473 nm diode laser, the polymerization of commercial acrylate monomers can be induced directly by PBDA. Due to the existence of acryloyl groups, PBDA can be linked into the polymer networks, which decreases its migration in the matrix and improves the biosafety of the end-products. Furthermore, PBDA presents a large two-photon absorption cross-section around 800 nm based on its D–π–A–π–D conjugated structure. 3D microstructures were fabricated using the formulation containing PBDA as PI by two-photon photopolymerization.

Graphical abstract: Study on a polymerizable visible light initiator for fabrication of biosafety materials

Supplementary files

Article information

Article type
Paper
Submitted
02 Feb 2019
Accepted
25 Mar 2019
First published
27 Mar 2019

Polym. Chem., 2019,10, 2273-2281

Study on a polymerizable visible light initiator for fabrication of biosafety materials

X. Huang, Y. Zhang, M. Shi, Y. Zhang and Y. Zhao, Polym. Chem., 2019, 10, 2273 DOI: 10.1039/C9PY00173E

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