Issue 29, 2024

Synthesis and spectroscopic properties of carotenoid bis-phenylhydrazone astaxanthin: extending conjugation to a C[double bond, length as m-dash]N group

Abstract

We report on the synthesis and detailed spectroscopic characterization of bis-phenylhydrazone astaxanthin (BPH-Asx), a derivative of astaxanthin (Asx), in which the conjugated carbonyl group of Asx is replaced by a conjugated C[double bond, length as m-dash]N bond. BPH-Asx was successfully synthesized and characterized using various spectroscopic techniques, revealing subtle changes in absorption spectra and significant alterations in excited-state dynamics compared to Asx. The results reveal a shortened S1 lifetime, 1.4 ps for BPH-Asx compared to 5 ps for Asx, indicating a significant impact on its excited-state dynamics. Since no polarity-induced effect was observed for BPH-Asx, the changes induced by the conjugated C[double bond, length as m-dash]N group are due to prolongation of effective conjugation. Moreover, the identification of a distinctive S* signal with a 3 ps lifetime in BPH-Asx underscores the relation between effective conjugation and presence of the S* signal that is not detected in Asx.

Graphical abstract: Synthesis and spectroscopic properties of carotenoid bis-phenylhydrazone astaxanthin: extending conjugation to a C [[double bond, length as m-dash]] N group

Supplementary files

Article information

Article type
Paper
Submitted
15 May 2024
Accepted
30 Jun 2024
First published
01 Jul 2024

New J. Chem., 2024,48, 12919-12928

Synthesis and spectroscopic properties of carotenoid bis-phenylhydrazone astaxanthin: extending conjugation to a C[double bond, length as m-dash]N group

E. Özcan, G. Keşan, P. Chábera, R. Litvín and T. Polívka, New J. Chem., 2024, 48, 12919 DOI: 10.1039/D4NJ02282C

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