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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Synthesis of chlorophyll-a derivatives possessing (un)substituted 13~1-exo-methylene moiety and their optical properties
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Synthesis of chlorophyll-a derivatives possessing (un)substituted 13~1-exo-methylene moiety and their optical properties

机译:具有(未)取代的13〜1-exo-亚甲基部分的叶绿素-a衍生物的合成及其光学性质

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摘要

Chlorophyll-a derivatives possessing an un/mono/disubstituted methylene moiety at the 13~1-position were prepared by (un)substituted methylation of the 13-carbonyl group and successive dehydration. Substitution of the 13~1oxo to the methylene group slightly blue-shifted electronic absorption and emission bands in a solution and decreased chemical stability to give an oxidation product cleaved at the E-ring. Further mono/disubstitution at the methylene terminal increased wavelengths of absorption and emission maxima as well as oxidative tolerance.
机译:通过13-羰基的(未)取代甲基化和连续脱水制得在13-1位具有未/单/二取代的亚甲基部分的叶绿素-a衍生物。 13〜1氧代取代亚甲基会使溶液中的电子吸收和发射带发生蓝移,并降低化学稳定性,从而使氧化产物在E环处裂解。在亚甲基末端的进一步单/二取代增加了最大吸收和发射波长以及氧化耐受性。

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