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(2-Carbamoylethyl)bis(dimethylglyoximato-N, N')
1Department of Chemistry, Toho University School of Medicine, 5-21-16 Omorinishi, Ota-ku, Tokyo 143-8540, Japan. yohgo@med.toho-u.ac.jp.
Acta Crystallographica. Section C, Crystal Structure Communications
|September 15, 2000
Summary
Cobaloxime complexes undergo isomerization of carbamoylethyl groups when exposed to visible light in the solid state. This photochemical reaction occurs similarly despite differing crystal structures and hydrogen bonds.
Area of Science:
- Organometallic Chemistry
- Photochemistry
- Solid-State Chemistry
Background:
- Cobaloxime complexes are well-known for their structural versatility and photochemical reactivity.
- Isomerization reactions in organometallic compounds can be influenced by various factors, including light and crystal packing.
Purpose of the Study:
- To investigate the solid-state photochemical isomerization of specific cobaloxime complexes.
- To compare the reaction rates and mechanisms under varying crystalline environments.
Main Methods:
- Synthesis and characterization of cobaloxime complexes.
- Exposure of solid-state samples to visible light.
- Analysis of isomerized products using spectroscopic techniques.
- X-ray crystallography to determine crystal structures and intermolecular interactions.
Main Results:
- The 2-carbamoylethyl and 2-(methylcarbamoyl)ethyl groups in the cobaloxime complexes isomerized to 1-carbamoylethyl and 1-(methylcarbamoyl)ethyl groups, respectively.
- The isomerization proceeded efficiently upon exposure to visible light in the solid state.
- Similar reaction rates were observed for both complexes despite significant differences in their crystal structures and intermolecular hydrogen bonding.
Conclusions:
- Visible light can induce isomerization in cobaloxime complexes in the solid state.
- The photochemical isomerization process is robust and occurs at comparable rates even with distinct crystal packing and hydrogen bond networks.
- This suggests that the core photochemical mechanism is less sensitive to the solid-state environment than initially anticipated.