4.7 Article

Two hydrogen donor-containing naphthalimide benzyl thioether photoinitiators for LED photopolymerization

Journal

PROGRESS IN ORGANIC COATINGS
Volume 162, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.porgcoat.2021.106562

Keywords

Naphthalimide; Carbon-Sulphur bond; Photoinitiator; Hydrogen donor; Oxygen inhibition; LED photopolymerization

Funding

  1. National Natural Science Foundation of China [52073018]

Ask authors/readers for more resources

This study introduces two novel photoinitiators for LED photopolymerization, with good absorption and initiating ability. Among them, NBT-HD2 with acryloyl group shows excellent capability in reducing oxygen inhibition and outstanding migration stability in polymer film.
This work reports two hydrogen donor-containing naphthalimide benzyl thioether photoinitiators (NBT-HD1 and NBT-HD2), combining characters of one-component and two-component photoinitiators, for LED photopolymerization. They have good absorptions at emission wavelengths of LED and their epsilon max are more than or close to 1 x 104 M-1 cm-1. Both photoinitiators can generate radicals having initiating ability through not only the cleavage of C-S bonds, but also intermolecular hydrogen abstractions themselves under 405 nm LED irradiation. NBT-HD2 with acryloyl group presents an excellent capability of reducing oxygen inhibition. Moreover, NBT-HD1 or NBT-HD2/iodonium salt can trigger the cationic photopolymerization of the epoxide under 405 nm LED irradiation. More significantly, NBT-HD2 with acryloyl group exhibits a prominent migration stability in the polymer film and has broad application prospects in the field of food packaging and biomaterials.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available