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一种短π电子共轭多甲藻素类似物的激发态性质

Excited state properties of a short π-electron conjugated peridinin analogue.

作者信息

Magdaong Nikki M, Niedzwiedzki Dariusz M, Greco Jordan A, Liu Hongbin, Yano Koki, Kajikawa Takayuki, Sakaguchi Kazuhiko, Katsumura Shigeo, Birge Robert R, Frank Harry A

机构信息

Department of Chemistry, University of Connecticut, Storrs, CT, 06269-3060, USA.

Photosynthetic Antenna Research Center, Washington University in St Louis, MO 63130, USA.

出版信息

Chem Phys Lett. 2014 Feb 11;593:132-139. doi: 10.1016/j.cplett.2014.01.002.

DOI:10.1016/j.cplett.2014.01.002
PMID:24678069
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3963168/
Abstract

C-peridinin is a synthetic analogue of the important, naturally-occurring carotenoid, peridinin, found in several marine algal species. C-peridinin has five conjugated carbon-carbon double bonds compared to eight possessed by peridinin and also lacks the methyl group functionalities typically present along the polyene chain of carotenoids. These structural modifications lead to unique excited state properties and important insights regarding the factors controlling the photophysics of peridinin and other carbonyl-containing carotenoids, which are critical components of the light-harvesting systems of many photosynthetic organisms.

摘要

C-多甲藻素是一种重要的天然类胡萝卜素——多甲藻素的合成类似物,多甲藻素存在于多种海洋藻类物种中。与多甲藻素拥有的八个共轭碳-碳双键相比,C-多甲藻素具有五个共轭碳-碳双键,并且还缺少通常存在于类胡萝卜素多烯链上的甲基官能团。这些结构修饰导致了独特的激发态性质,并为控制多甲藻素和其他含羰基类胡萝卜素光物理性质的因素提供了重要见解,而这些类胡萝卜素是许多光合生物光捕获系统的关键组成部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/d078bd831259/nihms560564f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/b1e3a899556a/nihms560564f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/4170046a4558/nihms560564f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/38d48db33c0f/nihms560564f3a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/ea08490ce868/nihms560564f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/72c83b42ff51/nihms560564f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/d078bd831259/nihms560564f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/b1e3a899556a/nihms560564f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/4170046a4558/nihms560564f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/38d48db33c0f/nihms560564f3a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/ea08490ce868/nihms560564f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/72c83b42ff51/nihms560564f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cc/3963168/d078bd831259/nihms560564f6.jpg

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本文引用的文献

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J Phys Chem B. 2013 Jun 13;117(23):6874-87. doi: 10.1021/jp400038k. Epub 2013 May 30.
2
The nature of the intramolecular charge transfer state in peridinin.关于甲藻黄素分子内电荷转移态的本质。
Biophys J. 2013 Mar 19;104(6):1314-25. doi: 10.1016/j.bpj.2013.01.045.
3
Energy transfer in an LH4-like light harvesting complex from the aerobic purple photosynthetic bacterium Roseobacter denitrificans.来自好氧紫色光合细菌反硝化红杆菌的类LH4光捕获复合物中的能量转移。
Biochim Biophys Acta. 2011 May;1807(5):518-28. doi: 10.1016/j.bbabio.2011.03.004. Epub 2011 Mar 16.
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The intramolecular charge transfer state in carbonyl-containing polyenes and carotenoids.含羰基多烯和类胡萝卜素中的分子内电荷转移态。
J Phys Chem B. 2010 Sep 30;114(38):12416-26. doi: 10.1021/jp106113h.
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Effect of carotenoid structure on excited-state dynamics of carbonyl carotenoids.类胡萝卜素结构对羰基类胡萝卜素激发态动力学的影响。
Phys Chem Chem Phys. 2009 Oct 21;11(39):8795-803. doi: 10.1039/b909924g. Epub 2009 Jul 31.
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Triplet state spectra and dynamics of peridinin analogs having different extents of pi-electron conjugation.具有不同程度π电子共轭的拟叶黄素类似物的三重态光谱和动力学。
Photosynth Res. 2010 Mar;103(3):167-74. doi: 10.1007/s11120-010-9535-y. Epub 2010 Feb 18.
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Syntheses of C33-, C35-, and C39-peridinin and their spectral characteristics.C33-、C35-和C39-多甲藻素的合成及其光谱特征。
Org Lett. 2009 Nov 5;11(21):5006-9. doi: 10.1021/ol901940g.
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