Raman and Infrared Spectra for All-trans-astaxanthin in Dimethyl Sulfoxide Solvent

• Published in: Chinese journal of chemical physics Vol. 30; no. 5; pp. 506 - 512
• Main Authors: Jiang, Li-lin, Liu, Wei-long, Yang, Yan-qiang
• Format: Journal Article
• Language: English
• Published: Teaching Affairs Office, Hezhou Ulniversity, Hezhou 542899, China%Department of Physics, Harbin Institute of Technology, Harbin 150001, China%National Key Laboratory of Shock Wave and Detonation Physics, Institute of Fluid Physics, China Academy of Engineering Physics, Mianyang 621900, China 27.10.2017
• Subjects: Resonance excitation; Intramolecular hydrogen bonding; Molecular structure; C=C stretching vibration
• ISSN: 1674-0068; 2327-2244
• DOI: 10.1063/1674-0068/30/cjcp1703054

The Raman and infrared spectra of all-trans-astaxanthin (AXT) in dimethyl sulfoxide (DMSO) solvent were investigated experimentally and theoretically. Density functional calculations of the Raman spectra predict the splitting of the ν1 band into ν1-1 and ν1-2 components. The absence of splitting in Raman experimental spectra is ascribed to the competition between the two symmetric C=C stretching vibrations of the backbone chain. The ν1 band is very sensitive to the excitation wavelength: resonance excitation stimulates the higher-frequency ν1-2 mode, and off-resonance excitation corresponds to the lower-frequency ν1-1 mode. Analyses of the intramolecular hydrogen bonding between C=O and O−H in the AXT/DMSO system reveal that the C4=O1⋯ H1−O3 and C4′=O2⋯ H2−O4 bonds are strengthened and weakened, respectively, in the electronically excited state compared with those in the ground state. This result reveals significant variations of the AXT molecular structure in different electronic states.