## Abstract Biliverdin dimethyl ester (**2**) in freshly prepared ethanolic solution showed fluorescence maxima at 710 and 770 nm which were shifted to 725 and 806 nm on monoprotonation. ฮฆ~F~ for **2** and 2 H ^+^ was similar at room temperature (1.1 ยท 10^โ4^ and 2.7 ยท 10^โ4^, respectively), and it
The fluorescence of biliverdin dimethyl ester
โ Scribed by Silvia E. Braslavsky; Alfred R. Holzwarth; Harald Lehner; Kurt Schaffner
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- German
- Weight
- 201 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
Freshly prepared solutions of biliverdin dimethyl ester (2) in ethanol showed fluorescence maxima at 710 and 770 nm [ฮฆ~F~ = 1.1. 10^โ4^ (room temperature) and 5.0 10^โ4^ (77 K)]. The maxima of monoprotonated 2 at 77 K were shifted to 725 and 806 nm and the quantum yield was increased to 2.6. 10^โ2^. This acid effect was reversible by neutralization with base. When a neutral solution was kept standing in the dark at room temperature, or when an acidic solution was neutralized by base, an additional fluorescence maximum at 500 nm with a mirror image excitation spectrum with ฮป~max~ = 470 nm developed, which disappeared on addition of acid and which is attributed to a chemical change of 2.
๐ SIMILAR VOLUMES
## Abstract Biliverdin dimethyl ester (**1b;** IXฮฑ) and its XIIIฮฑ isomer **2b** have been isolated on a preparative scale after esterification of an isomeric mixture obtained by oxidation of bilirubin. Both isomers readily form solid solutions. The substitution patterns and the predominant helical