| Literature DB >> 28156043 |
Judith Radebner1, Anna Eibel2, Mario Leypold1, Christian Gorsche3, Lukas Schuh1, Roland Fischer1, Ana Torvisco1, Dmytro Neshchadin2, Roman Geier2, Norbert Moszner4, Robert Liska3, Georg Gescheidt2, Michael Haas1, Harald Stueger1.
Abstract
In this contribution a convenient synthetic method to obtain tetraacylgermanes Ge[C(O)R]4 (R=mesityl (1 a), phenyl (1 b)), a previously unknown class of highly efficient Ge-based photoinitiators, is described. Tetraacylgermanes are easily accessible via a one-pot synthetic protocol in >85 % yield, as confirmed by NMR spectroscopy, mass spectrometry, and X-ray crystallography. The efficiency of 1 a,b as photoinitiators is demonstrated in photobleaching (UV/Vis), time-resolved EPR (CIDEP), and NMR/CIDNP investigations as well as by photo-DSC studies. Remarkably, the tetraacylgermanes exceed the performance of currently known long-wavelength visible-light photoinitiators for free-radical polymerization.Entities:
Keywords: acylgermanes; photochemistry; photoinitiators; radical polymerization; reaction mechanisms
Year: 2017 PMID: 28156043 DOI: 10.1002/anie.201611686
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336