2012
DOI: 10.3390/molecules17032877
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Key to Xenobiotic Carotenoids

Abstract: A listing of carotenoids with heteroatoms (X = F, Cl, Br, I, Si, N, S, Se, Fe) directly attached to the carotenoid carbon skeleton has been compiled. The 178 listed carotenoids with C,H,X atoms demonstrate that the classical division of carotenoids into hydrocarbon carotenoids (C,H) and xanthophylls (C,H,O) has become obsolete.

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Cited by 9 publications
(4 citation statements)
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“…Review articles have updated the synthetic efforts up to 2009 for general and specific carotenoids . A report on xenobiotic carotenoids described the design of extravagant polyenes inspired in the structure of the natural products …”
Section: Synthesis Of Carotenoidsmentioning
confidence: 99%
“…Review articles have updated the synthetic efforts up to 2009 for general and specific carotenoids . A report on xenobiotic carotenoids described the design of extravagant polyenes inspired in the structure of the natural products …”
Section: Synthesis Of Carotenoidsmentioning
confidence: 99%
“…The stability of chlorophylls can be increased by modification of the porphyrin ring, central metal ion substitution, addition or removal of peripheral substituents or aggregation [65,66]. The modification of carotenoids may include cyclisation of one or both ends, attachment of oxygen groups and heteroatoms, generation of aggregates [67]. Another possibility is a controlled assembly of photosynthetic structures by incorporation of desired pigments, polypeptides and other molecules (nanoparticles, nanowires) to the reconstituted complexes, or even use of genetically modified proteins with specifically altered properties.…”
Section: Open Issuesmentioning
confidence: 99%
“…40 Many synthetic carotenoids have been introduced in the past few decades including those having non-natural atoms such as sulfur, nitrogen, or phosphorus in their structure. 41 Yet, excited state dynamics of these carotenoids has not been studied, apart from two exceptions featuring nitrogen atoms in their structure. First, ultrafast dynamics of all- trans -7′,7′-dicyano-7′-apo-β-carotene, 42 demonstrating strong effect of the cyano groups on excited state lifetime.…”
Section: Introductionmentioning
confidence: 99%