Fullerene C60–Perylene-3,4:9,10-bis(dicarboximide) Light-Harvesting Dyads: Spacer-Length and Bay-Substituent Effects on Intramolecular Singlet and Triplet Energy Transfer

2008 ◽  
Vol 14 (16) ◽  
pp. 4974-4992 ◽  
Author(s):  
Jérôme Baffreau ◽  
Stéphanie Leroy-Lhez ◽  
Nguyên Vân Anh ◽  
René M. Williams ◽  
Piétrick Hudhomme
2007 ◽  
Vol 19 (15) ◽  
pp. 3673-3680 ◽  
Author(s):  
Tae-Hyuk Kwon ◽  
Myoung Ki Kim ◽  
Jongchul Kwon ◽  
Dae-Yup Shin ◽  
Su Jin Park ◽  
...  

2015 ◽  
Vol 6 (7) ◽  
pp. 3724-3737 ◽  
Author(s):  
Song Guo ◽  
Liang Xu ◽  
Kejing Xu ◽  
Jianzhang Zhao ◽  
Betül Küçüköz ◽  
...  

Hydrogen bonding-mediated supramolecular triplet photosensitizers with easily interchangeable visible light-harvesting Bodipy modules and the fullerene intersystem crossing module were devised.


Carotenoids are usually considered to perform two major functions in photosynthesis. They serve as accessory light harvesting pigments, extending the range of wavelengths over which light can drive photosynthesis, and they act to protect the chlorophyllous pigments from the harmful photodestructive reaction which occurs in the presence of oxygen. Drawing upon recent work with photosynthetic bacteria, evidence is presented as to how the carotenoids are organized within both portions of the photosynthetic unit (the light harvesting antenna and the reaction centre) and how they discharge both their functions. The accessory pigment role is a singlet-singlet energy transfer from the carotenoid to the bacteriochlorophyll, while the protective role is a triplet-triplet energy transfer from the bacteriochlorophyll to the carotenoid.


1994 ◽  
Vol 42 (2) ◽  
pp. 157-166 ◽  
Author(s):  
Roya Farhoosh ◽  
Veeradej Chynwat ◽  
Ronald Gebhard ◽  
Johan Lugtenburg ◽  
Harry A. Frank

2010 ◽  
Vol 1797 (10) ◽  
pp. 1759-1767 ◽  
Author(s):  
Marilena Di Valentin ◽  
Enrico Salvadori ◽  
Giancarlo Agostini ◽  
Federico Biasibetti ◽  
Stefano Ceola ◽  
...  

2020 ◽  
Author(s):  
Mauricio Lineros-Rosa ◽  
Antonio Francés-Monerris ◽  
Antonio Monari ◽  
Miguel Angél Miranda ◽  
Virginie Lhiaubet-Vallet

Interaction of nucleic acids with light is a scientific question of paramount relevance not only in the understanding of life functioning and evolution, but also in the insurgence of diseases such as malignant skin cancer and in the development of biomarkers and novel light-assisted therapeutic tools. This work shows that the UVA portion of sunlight, not absorbed by canonical DNA nucleobases, can be absorbed by 5-formyluracil (ForU) and 5-formylcytosine (ForC), two ubiquitous oxidative lesions and epigenetic intermediates present in living beings in natural conditions. We measure the strong propensity of these molecules to populate triplet excited states able to transfer the excitation energy to thymine-thymine dyads, inducing the formation of the highly toxic and mutagenic cyclobutane pyrimidine dimers (CPDs). By using steady-state and transient absorption spectroscopy, NMR, HPLC, and theoretical calculations, we quantify the differences in the triplet-triplet energy transfer mediated by ForU and ForC, revealing that the former is much more efficient in delivering the excitation energy and producing the CPD photoproduct. Although significantly slower than ForU, ForC is also able to harm DNA nucleobases and therefore this process has to be taken into account as a viable photosensitization mechanism. The present findings evidence a rich photochemistry crucial to understand DNA photodamage and of potential use in the development of biomarkers and non-conventional photodynamic therapy agents.


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