From mono- to tetraacylgermanes: extending the scope of visible light photoinitiators. Issue 1 (4th December 2017)

• Record Type: Journal Article
• Authors: Eibel, Anna; Radebner, Judith; Haas, Michael; Fast, David E.; Freißmuth, Hilde; Stadler, Eduard; Faschauner, Paul; Torvisco, Ana; Lamparth, Iris; Moszner, Norbert; Stueger, Harald; Gescheidt, Georg
• Is Part Of: Polymer chemistry. Volume 9:Issue 1(2018)
• Page Start: 38
• Page End: 47
• Publication Date: 2017-12-04
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/c7py01590a
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : We present a comparative study of the photoinitiating efficiency of selected acylgermanes, focusing on wavelength-dependent photobleaching, decomposition quantum yields and radical reactivity. Abstract : We have investigated the inititiaton efficiency of carefully selected germanium-based photointiators for radical polymerization. To establish a systematic relationship between structure and reactivity, we have developed a convenient synthetic protocol for the preparation of a trisacylgermane, closing the gap from mono- to tetraacylgermane photoinitiators. The studied acylgermanes display distinct, wavelength-dependent photobleaching upon irradiation up to 470 nm. In particular, tetraacylgermanes featuring ortho -alkyl substituents reveal red-shifted n–π* bands, in line with excellent photobleaching upon visible light irradiation. Quantum yields of decomposition (determined at 385 nm) have been found to be highest for bisacylgermanes. Germyl radicals produced upon triplet-state α-cleavage of the acylgermanes react remarkably fast with monomers. Addition rate constants to (meth)acrylates range from 0.4–4.5 × 10 8 M −1 s −1, depending on the substitution pattern. These values are clearly higher than those reported for related phosphorus-centered radicals derived from acylphosphane oxides. We have further established the nature of the products and side-products formed at initial stages of the polymerizations using chemically induced dynamic nuclear polarization (CIDNP) experiments.