Nickel(II) interactions with chlorophylls in solution: impact to degradation induced by UV-irradiation

J. Zvezdanović, S. Petrović, Aleksandar Lazarević
{"title":"Nickel(II) interactions with chlorophylls in solution: impact to degradation induced by UV-irradiation","authors":"J. Zvezdanović, S. Petrović, Aleksandar Lazarević","doi":"10.46793/chemn5.2.01z","DOIUrl":null,"url":null,"abstract":"Chlorophylls and metal substituted complexes of chlorophylls with known photosensitizing abilities can be used in many types of biological and solar energy applications; thus, it is important to analyze their basic properties when they are treated by visible light and/or UV radiation. Nickel(II) can replace central magnesium from chlorophyll (Chl) molecule to form a metal substituted, “central” Ni-Chl complex. So, the possible formation of nickel-chlorophyll complexes in 95% ethanol at 40 °C was studied by UHPLC-DAD chromatography (UltraHigh Performance Liquid Chromatography–Diode Array Detector). Nickel(II)-chlorophylls interactions in the reaction solutions at 40 °C lead not only to the formation of the Ni-related Chls, Ni-Chl complexes but several oxidation and demetalation products of chlorophylls. On the other hand, the influence of nickel(II) – chlorophyll interactions on chlorophylls solutions stability under continual UV-A, -B, and -C irradiation in 95% ethanol, was followed by UV-Vis spectrophotometry. Chlorophylls as well as their reaction solutions with nickel(II) undergo photochemical degradation obeying first- order kinetics. In general, the degradation is “energy-dependent”, i.e. proportional to the UV photons energy input. Chlorophylls are less stable than their reaction solutions with nickel(II), probably due to the higher stability of Ni-chlorophylls complexes, to all three subranges of UV- irradiation.","PeriodicalId":351621,"journal":{"name":"Chemia Naissensis","volume":"124 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemia Naissensis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46793/chemn5.2.01z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Chlorophylls and metal substituted complexes of chlorophylls with known photosensitizing abilities can be used in many types of biological and solar energy applications; thus, it is important to analyze their basic properties when they are treated by visible light and/or UV radiation. Nickel(II) can replace central magnesium from chlorophyll (Chl) molecule to form a metal substituted, “central” Ni-Chl complex. So, the possible formation of nickel-chlorophyll complexes in 95% ethanol at 40 °C was studied by UHPLC-DAD chromatography (UltraHigh Performance Liquid Chromatography–Diode Array Detector). Nickel(II)-chlorophylls interactions in the reaction solutions at 40 °C lead not only to the formation of the Ni-related Chls, Ni-Chl complexes but several oxidation and demetalation products of chlorophylls. On the other hand, the influence of nickel(II) – chlorophyll interactions on chlorophylls solutions stability under continual UV-A, -B, and -C irradiation in 95% ethanol, was followed by UV-Vis spectrophotometry. Chlorophylls as well as their reaction solutions with nickel(II) undergo photochemical degradation obeying first- order kinetics. In general, the degradation is “energy-dependent”, i.e. proportional to the UV photons energy input. Chlorophylls are less stable than their reaction solutions with nickel(II), probably due to the higher stability of Ni-chlorophylls complexes, to all three subranges of UV- irradiation.
镍(II)与溶液中叶绿素的相互作用:对紫外线照射诱导的降解的影响
叶绿素和已知光敏能力的叶绿素金属取代配合物可用于许多类型的生物和太阳能应用;因此,当它们被可见光和/或紫外线辐射处理时,分析它们的基本特性是很重要的。镍(II)可以取代叶绿素(Chl)分子中的中心镁,形成金属取代的“中心”镍-Chl配合物。因此,采用UHPLC-DAD色谱(超高高效液相色谱-二极管阵列检测器)研究了在40°C下95%乙醇中镍-叶绿素复合物的可能形成。在40°C的反应溶液中,镍(II)-叶绿素相互作用不仅形成了镍相关的chl、Ni-Chl配合物,还形成了多种叶绿素的氧化和脱金属产物。另一方面,采用紫外可见分光光度法研究了在95%乙醇连续UV-A、- b和- c照射下,镍(II) -叶绿素相互作用对叶绿素溶液稳定性的影响。叶绿素及其与镍(II)的反应溶液遵循一级动力学进行光化学降解。一般来说,降解是“能量依赖”的,即与输入的紫外光子能量成正比。叶绿素的稳定性低于与镍(II)的反应溶液,这可能是由于ni -叶绿素配合物在紫外线照射下具有较高的稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信