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Syntheses of ylidenbutenolide-modified derivatives of peridinin and their stereochemical and spectral characteristics. | LitMetric

Syntheses of ylidenbutenolide-modified derivatives of peridinin and their stereochemical and spectral characteristics.

Org Biomol Chem

Department of Chemistry and Open Research Center on Organic Tool Molecules, School of Science and Technology, Kwansei Gakuin University, Gakuen 2-1, Sanda, Hyogo 669-1337, Japan.

Published: June 2010

AI Article Synopsis

  • * Researchers have created two modified derivatives of peridinin to explore how its unique structure affects energy transfer capabilities.
  • * The study includes details about the synthesis of these derivatives and how their unique ylidenbutenolide group stabilizes the molecule while keeping it in a specific all-trans configuration.

Article Abstract

Peridinin is a light-harvesting carotenoid found in oceanic photosynthetic organisms. It possesses a unique gamma-ylidenbutenolide function and engages in energy transfer to chlorophyll a with very high (>90%) efficiency. In order to examine the relationship between the unique structure of peridinin and its facility in carrying out energy transfer, we have synthesized two different ylidenbutenolide-modified derivatives of peridinin. In this communication, the details of the syntheses are described as are the stereochemical and spectral characteristics of the derivatives; the novel ylidenbutenolide functional group stabilizes the molecule and maintains the conjugated pi-electron system in an all-trans configuration.

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Source
http://dx.doi.org/10.1039/c002006kDOI Listing

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