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Photophysical Investigations on Photoinitiators with Covalently Linked Thioxanthone Sensitizer Moieties

✍ Scribed by Kurt Dietliker; Stephanie Broillet; Bruno Hellrung; Piotr Rzadek; Guenther Rist; Jakob Wirz; Dmytro Neshchadin; Georg Gescheidt


Book ID
102253785
Publisher
John Wiley and Sons
Year
2006
Tongue
German
Weight
252 KB
Volume
89
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The photophysical properties of three photoinitiators with a covalently linked thioxanthone sensitizer unit absorbing up to 410 nm were investigated by laser‐flash photolysis and CIDNP spectroscopy. These complementary techniques revealed two competing reaction pathways of the molecular dyads 13: i) triplet‐energy transfer from the sensitizer to the morpholine moiety followed by α‐cleavage to yield a radical pair, which initiates radical polymerization, and ii) bimolecular electron transfer from the morpholine to the thioxanthone subunit followed by proton transfer. The relative efficiency of these routes is determined by the triplet energy of the photoinitiator moiety relative to that of the sensitizer.