Abstract: Xanthophylls are oxygenated carotenoids widely distributed in photosynthetic microorganisms, plants, algae, and certain invertebrates, where they function as key photoprotective and antioxidant pigments. Among them, xanthophylls containing vicinal 1,2-diol moieties exhibit unique chemical reactivity that enables reversible coordination with boron species naturally present in marine and terrestrial environments. The formation of cyclic borate esters between boron and diol-containing xanthophylls induces structural and electronic modifications that may enhance pigment stability and functional performance. Emerging evidence suggests that boron–xanthophyll complexes display improved resistance to photooxidative degradation, enhanced singlet oxygen quenching capacity, and increased radical-scavenging activity compared with their uncomplexed counterparts. In addition, boron coordination can influence molecular conformation, polarity, and supramolecular organization within lipid bilayers, thereby promoting membrane stabilization under conditions of high light exposure and oxidative stress. Together, these effects indicate a cooperative role of boron complexation in amplifying the intrinsic photoprotective and antioxidant properties of xanthophylls. A deeper understanding of the structural basis and biological implications of boron–xanthophyll interactions may provide new insights into adaptive stress tolerance in marine and photosynthetic organisms, as well as guide the development of advanced photoprotective systems for biomedical and technological applications.

Cite: Dembitsky V.M. , Terent’ev A.O.
Boron–Vicinal Diol Xanthophyll Complexes as Emerging Photoprotective Adjuvants
Photochem. 2026. V.6. N2. 22 . DOI: 10.3390/photochem6020022 OpenAlex

Dates:

Submitted:	Apr 7, 2026
Published online:	May 27, 2026

Identifiers:

≡ OpenAlex:

W7162530108

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