Journalartikel

Jahr der Veröffentlichung: 2016

Seiten: 16224-16227

Zeitschrift: Journal of the American Chemical Society

Bandnummer: 138

Heftnummer: 50

ISSN: 0002-7863

DOI Link: https://doi.org/10.1021/jacs.6b10738

Verlag: American Chemical Society

Abstract: 
Highly directional white-light generation was recently reported for the organotin sulfide cluster [(StySn)(4)S-6] (Sty = p-styryl). This effect was tentatively attributed to the amorphous nature of the material in combination with the specific combination of an inversion symmetry-free T/E cluster core (T = tetrel, E = chalcogen) with the attachment of ligands that allow pi delocalization of the electron density. Systematic variation of T and the organic ligand (R) that runs from T = Si through Ge to Sn and from R = methyl through phenyl and p-styryl to 1-naphthyl provides a more comprehensive view. According to powder X-ray data, only [(PhSi)(4)S-6] is single-crystalline among the named combinations. Here we demonstrate the fine-tuneability of the nonlinear response, i.e., changing from white-light generation to second harmonic generation as well as controlling the white light properties. These are investigated as a function of T, delocalization of the electron density within R, and the order within the molecular solids.

Harvard-Zitierstil: Rosemann, N., Eussner, J., Dornsiepen, E., Chatterjee, S. and Dehnen, S. (2016) Organotetrel Chalcogenide Clusters: Between Strong Second-Harmonic and White-Light Continuum Generation, Journal of the American Chemical Society, 138(50), pp. 16224-16227. https://doi.org/10.1021/jacs.6b10738

APA-Zitierstil: Rosemann, N., Eussner, J., Dornsiepen, E., Chatterjee, S., & Dehnen, S. (2016). Organotetrel Chalcogenide Clusters: Between Strong Second-Harmonic and White-Light Continuum Generation. Journal of the American Chemical Society. 138(50), 16224-16227. https://doi.org/10.1021/jacs.6b10738