Tetraacylstannanes as Long-Wavelength Visible-Light Photoinitiators with Intriguing Low Toxicity.
Judith RadebnerAnna EibelMario LeypoldNina JungwirthThomas PicklAna TorviscoRoland FischerUrs Karl FischerNorbert MosznerGeorg GescheidtHarald StuegerMichael HaasPublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2018)
The first tetraacylstannanes Sn[(CO)R]4 (R=2,4,6-trimethylphenyl (1 a) and 2,6-dimethylphenyl (1 b)), a class of highly efficient Sn-based photoinitiators, were synthesized. The formation of these derivatives was confirmed by NMR spectroscopy, mass spectrometry, and X-ray crystallography. The UV/Vis absorption spectra of 1 a, b reveal a significant redshift of the longest wavelength absorption compared to the corresponding germanium compounds. In contrast to the known toxicity of organotin derivatives, the AMES test and cytotoxicity studies reveal intriguing low toxicity. The excellent performance of 1 as photoinitiators is demonstrated by photobleaching (UV/Vis) and NMR/CIDNP investigations, as well as photo-DSC studies.
Keyphrases
- highly efficient
- visible light
- high resolution
- mass spectrometry
- oxidative stress
- magnetic resonance
- genome wide
- oxide nanoparticles
- single cell
- case control
- liquid chromatography
- magnetic resonance imaging
- computed tomography
- structure activity relationship
- gas chromatography
- high performance liquid chromatography
- gene expression
- solid state
- dual energy
- aqueous solution
- molecular dynamics