Synthesis of d-galactose-substituted acylsilanes and acylgermanes. Model compounds for visible light photoinitiators with intriguing high solubility

7Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

A convenient synthetic method to obtain D-galactose-substituted acylsilanes and acylgermanes is described. These acyl group 14 compounds are easily accessible in good yields. Their structural properties were analyzed by a combination of NMR, single crystal X-ray crystallography, and UV/vis spectroscopy. A D-galactose-substituted tetraacylgermane represents a new interesting visible light photoinitiator based on its absorption properties as well as its high solubility.

Cite

CITATION STYLE

APA

Schuh, L., Müller, P., Torvisco, A., Stueger, H., Wrodnigg, T. M., & Haas, M. (2021). Synthesis of d-galactose-substituted acylsilanes and acylgermanes. Model compounds for visible light photoinitiators with intriguing high solubility. Organometallics, 40(9), 1185–1189. https://doi.org/10.1021/acs.organomet.0c00753

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free