<?xml version="1.0" encoding="UTF-8"?>
<?xml-stylesheet type="text/xsl" media="screen" href="/~d/styles/rss2full.xsl"?><?xml-stylesheet type="text/css" media="screen" href="http://feeds.rsc.org/~d/styles/itemcontent.css"?><rss xmlns:a10="http://www.w3.org/2005/Atom" xmlns:feedburner="http://rssnamespace.org/feedburner/ext/1.0" version="2.0"><channel><title>RSC - Photochem. Photobiol. Sci. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/PP</link><description>RSC - Photochem. Photobiol. Sci. latest articles</description><copyright>Copyright (c)  The Royal Society of Chemistry</copyright><lastBuildDate>Tue, 14 Feb 2012 03:05:42 Z</lastBuildDate><category>RSC - Photochem. Photobiol. Sci. latest articles</category><image><url>http://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gif</url><title>RSC - Photochem. Photobiol. Sci. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/PP</link></image><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" type="application/rss+xml" href="http://feeds.rsc.org/rss/PP" /><feedburner:info uri="rss/pp" /><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="hub" href="http://pubsubhubbub.appspot.com/" /><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05382A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05382A</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/_xzHiR5ezOA/C2PP05382A</link><title>Photochemistry and photophysics of the endoperoxide of mesodiphenylhelianthrene: a contribution to the localization of the S1([small pi]*[sigma]*) state of aromatic endoperoxides</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05382A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05382A, Paper&lt;/div&gt;&lt;div&gt;Reinhard Schmidt&lt;br/&gt;Excitation of the S&lt;small&gt;&lt;sub&gt;1&lt;/sub&gt;&lt;/small&gt;([small pi]*[sigma]*) state of the non-fluorescent endoperoxide MDHPO produces quantitatively by O-O bond rupture a biradical, the precursor of the strongly fluorescent diepoxide MDHDO and of ground state MDHPO.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/_xzHiR5ezOA" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Reinhard Schmidt</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05382A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05295D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05295D</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/OjMVAEAqhQk/C2PP05295D</link><title>A computational model for previtamin D3 production in skin</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05295D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05295D, Paper&lt;/div&gt;&lt;div&gt;Merve Meinhardt-Wollweber, Ronald Krebs&lt;br/&gt;We introduce a computational model predicting UV derived vitamin D production in human skin. The effect of variations in the different input parameters are shown and discussed to give an idea of the capabilities of the model.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/OjMVAEAqhQk" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Merve Meinhardt-Wollweber</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ronald Krebs</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05295D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05379A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05379A</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/HICGj4c0qgI/C2PP05379A</link><title>Oxidatively generated damage to DNA at 5-methylcytosine mispairs</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05379A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05379A, Paper&lt;/div&gt;&lt;div&gt;Joshy Joseph, Gary B. Schuster&lt;br/&gt;5-Methylcytosine (C&lt;small&gt;&lt;sub&gt;m&lt;/sub&gt;&lt;/small&gt;) in DNA sequences containing C&lt;small&gt;&lt;sub&gt;m&lt;/sub&gt;&lt;/small&gt;-A or C&lt;small&gt;&lt;sub&gt;m&lt;/sub&gt;&lt;/small&gt;-T mismatches behaves like "thymine" in one electron oxidation induced modifications. The reactivity of C&lt;small&gt;&lt;sub&gt;m&lt;/sub&gt;&lt;/small&gt; is attributed to the efficient generation of the 5-methyl radical by a Proton Coupled Electron Transfer (PCET) mechanism.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/HICGj4c0qgI" height="1" width="1"/&gt;</description><a10:updated>2012-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Joshy Joseph</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gary B. Schuster</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05379A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05352G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05352G</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/N129DvayHrc/C2PP05352G</link><title>Small change in structure leads to large difference in protein photocleavage: two porphyrins bearing rhodanine-based pendants</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05352G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05352G, Paper&lt;/div&gt;&lt;div&gt;Guo-Yu Jiang, Wan-Hua Lei, Qian-Xiong Zhou, Yuan-Jun Hou, Xue-Song Wang&lt;br/&gt;The presence of a COOH group renders RhDCOOH-TPP less hydrophobic in character and leads to additional interactions toward BSA, which leads to a significant increase of the &lt;small&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/small&gt;O&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; quantum yield upon BSA binding and effective BSA photocleavage. In contrast, RhD-TPP is inactive in the photocleavage of BSA.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/N129DvayHrc" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guo-Yu Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wan-Hua Lei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qian-Xiong Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuan-Jun Hou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xue-Song Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05352G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05360H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05360H</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/WwlsZyWrH7E/C2PP05360H</link><title>The donor-acceptor biphenyl platform: A versatile chromophore for the engineering of highly efficient two-photon sensitive photoremovable protecting groups</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05360H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05360H, Paper&lt;/div&gt;&lt;div&gt;Alexandre Specht, Frederic Bolze, Loic Donato, Cyril Herbivo, Sebastien Charon, David Warther, Sylvestre Gug, Jean-Francois Nicoud, Maurice Goeldner&lt;br/&gt;Different photoremovable protecting groups in the &lt;i&gt;o&lt;/i&gt;-nitrobenzyl, phenacyl, and 2-(&lt;i&gt;o&lt;/i&gt;-nitrophenyl)propyl series with a donor-acceptor biphenyl backbone were investigated in order to develop efficient two-photon sensitive photoremovable protecting groups.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/WwlsZyWrH7E" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alexandre Specht</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Frederic Bolze</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Loic Donato</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cyril Herbivo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastien Charon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Warther</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sylvestre Gug</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Francois Nicoud</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Maurice Goeldner</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05360H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05286E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05286E</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/vrz5uE_5acQ/C2PP05286E</link><title>Aromatic aldols and 1,5-diketones as optimized fragrance photocages</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05286E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05286E, Paper&lt;/div&gt;&lt;div&gt;Axel G. Griesbeck, Olga Hinze, Helmut Gorner, Ursula Huchel, Christian Kropf, Uta Sundermeier, Thomas Gerke&lt;br/&gt;Aromatic aldols and 1,5-diketones with abstractable [gamma]-hydrogen atoms are highly photoactive cage molecules for the release of fragrance compounds (aldehydes and Michael ketones, respectively). By tuning the properties of the chromophores, [small delta]-damascone cages were developed for selective release of fragrances under air and solar irradiation. The intermediates of the Norrish II process were observed by laser transient absorption spectroscopy.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/vrz5uE_5acQ" height="1" width="1"/&gt;</description><a10:updated>2012-02-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Axel G. Griesbeck</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olga Hinze</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Helmut Gorner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ursula Huchel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christian Kropf</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Uta Sundermeier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas Gerke</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05286E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05350K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05350K</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/GNADAYtfU4g/C2PP05350K</link><title>Photochemical investigation of the IR absorption bands of molecular oxygen in organic and aqueous environment</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05350K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05350K, Paper&lt;/div&gt;&lt;div&gt;A. A Krasnovsky, A. S. Kozlov, Ya. V. Roumbal&lt;br/&gt;Absorbance of dissolved oxygen molecules corresponding to the weak IR absorption maxima at 765, 1073 and 1273 nm has been estimated in air-saturated solvents using the photooxygenation rates of the &lt;small&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/small&gt;O&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; traps upon direct excitation of O&lt;small&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;/small&gt; by IR diode lasers.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/GNADAYtfU4g" height="1" width="1"/&gt;</description><a10:updated>2012-02-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">A. A Krasnovsky</creator><creator xmlns="http://purl.org/dc/elements/1.1/">A. S. Kozlov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ya. V. Roumbal</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05350K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05354C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05354C</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/UyIp0yjDQfs/C2PP05354C</link><title>Reaction of the m-THPC triplet state with the antioxidant Trolox and the anesthetic Propofol: Modulation of photosensitization mechanisms relevant to photodynamic therapy?</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05354C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05354C, Paper&lt;/div&gt;&lt;div&gt;O. Friaa, P. Maillard, D. Brault&lt;br/&gt;Antioxidants may affect the outcome of photodynamic therapy (PDT) through the inactivation of reactive oxygen species or reaction with the photosensitizer triplet state.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/UyIp0yjDQfs" height="1" width="1"/&gt;</description><a10:updated>2012-02-06T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">O. Friaa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">P. Maillard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">D. Brault</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05354C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05275J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05275J</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/6mDOv69pk0Q/C2PP05275J</link><title>Effects of visible and UV light on the characteristics and properties of crude oil-in-water (O/W) emulsions</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05275J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05275J, Paper&lt;/div&gt;&lt;div&gt;Homer C. Genuino, Dayton T. Horvath, Cecil K. King'ondu, George E. Hoag, John B. Collins, Steven L. Suib&lt;br/&gt;Prudhoe Bay and South Louisiana crude oil-in-water emulsions were prepared, characterized, and exposed to both visible and UV light irradiation. The unique changes in physico-chemical properties of these emulsions as a result of photodegradation were investigated.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/6mDOv69pk0Q" height="1" width="1"/&gt;</description><a10:updated>2012-02-02T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Homer C. Genuino</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dayton T. Horvath</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cecil K. King'ondu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">George E. Hoag</creator><creator xmlns="http://purl.org/dc/elements/1.1/">John B. Collins</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Steven L. Suib</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05275J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05387J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05387J</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/TZPVXal35QU/C2PP05387J</link><title>Direct aerobic photo-oxidative syntheses of aromatic methyl esters from methyl aromatics using anthraquinone-2,3-dicarboxylic acid as organophotocatalyst</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05387J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05387J, Communication&lt;/div&gt;&lt;div&gt;Norihiro Tada, Yuki Ikebata, Tomoya Nobuta, Shin-ichi Hirashima, Tsuyoshi Miura, Akichika Itoh&lt;br/&gt;This paper reports a useful method for facile direct syntheses of aromatic methyl esters from methyl aromatics by aerobic photo-oxidation using anthraquinone-2,3-dicarboxylic acid as an organophotocatalyst.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/TZPVXal35QU" height="1" width="1"/&gt;</description><a10:updated>2012-02-01T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Norihiro Tada</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuki Ikebata</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tomoya Nobuta</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shin-ichi Hirashima</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tsuyoshi Miura</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Akichika Itoh</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05387J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05363B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05363B</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/LdauG4pYyXU/C2PP05363B</link><title>Characterization and reactivity of photodimers of dihydroneopterin and dihydrobiopterin</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05363B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05363B, Paper&lt;/div&gt;&lt;div&gt;Mariana Vignoni, Carolina Lorente, Franco M. Cabrerizo, Rosa Erra-Balsells, Esther Oliveros, Andres H. Thomas&lt;br/&gt;The photodimerization of 7,8-dihydrobiopterin and 7,8-dihydroneopterin upon UV-A irradiation yields two main isomeric dimers containing an azacyclobutane ring. The dimers undergo a retro [2 + 2]-cycloaddition in the dark.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/LdauG4pYyXU" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mariana Vignoni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carolina Lorente</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Franco M. Cabrerizo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rosa Erra-Balsells</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Esther Oliveros</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andres H. Thomas</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05363B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05348A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05348A</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/_Unh-ZqU5k8/C2PP05348A</link><title>Spectral, photophysical and photochemical properties of tetra- and octaglycosylated zinc phthalocyanines</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05348A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05348A, Paper&lt;/div&gt;&lt;div&gt;Zafar Iqbal, Nkosiphile Masilela, Tebello Nyokong, Alexey Lyubimtsev, Michael Hanack, Thomas Ziegler&lt;br/&gt;Zinc phthalocyanines substituted with glucose and galactose moieties show high triplet quantum yields ranging from 0.68 to 0.88 and long triplet lifetimes which range from 100 to 430 [small mu ]s.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/_Unh-ZqU5k8" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zafar Iqbal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nkosiphile Masilela</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tebello Nyokong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexey Lyubimtsev</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Hanack</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas Ziegler</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05348A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05368C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05368C</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/hQpg0-4eHNE/C2PP05368C</link><title>Structural volume changes upon triplet formation of water-soluble porphyrins depend on the resonant effect of the substituents</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05368C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05368C, Paper&lt;/div&gt;&lt;div&gt;Mikalai M. Kruk, Silvia E. Braslavsky&lt;br/&gt;The contractions determined upon production of the triplet state in water-soluble porphyrins with &lt;i&gt;para&lt;/i&gt; substituents in the &lt;i&gt;meso&lt;/i&gt; phenyl groups correlate with the substituent Hammett resonant &lt;i&gt;[sigma]&lt;/i&gt;&lt;small&gt;&lt;sub&gt;R&lt;/sub&gt;&lt;/small&gt; constants.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/hQpg0-4eHNE" height="1" width="1"/&gt;</description><a10:updated>2012-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mikalai M. Kruk</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Silvia E. Braslavsky</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05368C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05369A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05369A</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/1MPsi7fxVD0/C2PP05369A</link><title>Ketonization of enols in aqueous solution: is carbon protonation always rate-determining?</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05369A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05369A, Paper&lt;/div&gt;&lt;div&gt;Anna Paola Pelliccioli, Peter Sebej, Jakob Wirz&lt;br/&gt;The answer to the title question is: No! The rate-determining step for ketonization of the (&lt;i&gt;E&lt;/i&gt;)-enol of &lt;i&gt;o&lt;/i&gt;-methylacetophenone up to pH 11 is ionization of the hydroxyl group.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/1MPsi7fxVD0" height="1" width="1"/&gt;</description><a10:updated>2012-01-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anna Paola Pelliccioli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peter Sebej</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jakob Wirz</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05369A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05337C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05337C</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/YlvTb96TBz0/C2PP05337C</link><title>Environmental polarity estimation in living cells by use of quinoxaline-based full-colored solvatochromic fluorophore PQX and its derivatives</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05337C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05337C, Paper&lt;/div&gt;&lt;div&gt;Kentaro Kudo, Atsuya Momotake, Junko K. Tanaka, Yoshihiro Miwa, Tatsuo Arai&lt;br/&gt;Site-dependent fluorescence spectra were observed in HEp-2 cells after staining with PQX, which indicated less polarity at the Golgi body and more polarity around the cell periphery.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/YlvTb96TBz0" height="1" width="1"/&gt;</description><a10:updated>2012-01-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kentaro Kudo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Atsuya Momotake</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junko K. Tanaka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yoshihiro Miwa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tatsuo Arai</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05337C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05341A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05341A</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/GSGmOj9jmdE/C2PP05341A</link><title>[small pi]-Cation interactions as the origin of the weak absorption at 532 nm observed in tryptophan-containing polypeptides</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05341A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05341A, Paper&lt;/div&gt;&lt;div&gt;O. A. Roveri, S. E. Braslavsky&lt;br/&gt;A weak light absorption at 532 nm, well detected by LIOAS, was observed with acid solutions of tryptophan and neutral solution of tryptophan containing polypeptides and proteins: this is a spectral manifestation of [small pi]-cation interactions.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/GSGmOj9jmdE" height="1" width="1"/&gt;</description><a10:updated>2012-01-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">O. A. Roveri</creator><creator xmlns="http://purl.org/dc/elements/1.1/">S. E. Braslavsky</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05341A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05378K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05378K</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/k3-iU7PpRQA/C2PP05378K</link><title>Bis-semiquinone (bi-radical) formation by photoinduced proton coupled electron transfer in covalently linked catechol-quinone systems: Aviram's hemiquinones revisited</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05378K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05378K, Paper&lt;/div&gt;&lt;div&gt;Nguyen Van Anh, Rene M. Williams&lt;br/&gt;"Bi-radical state caught in the act". Transient absorption spectroscopy of the hydrogen-bonded donor (blue)-acceptor (red) system shows the fingerprint of a long-lived (300 ns to 18 [small mu ]s) bi-radical state. Charge transfer interactions and two conformations are present. These molecules played a role in the genesis of molecular electronics.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/k3-iU7PpRQA" height="1" width="1"/&gt;</description><a10:updated>2012-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nguyen Van Anh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rene M. Williams</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05378K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05346B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05346B</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/mL6PDT81G64/C2PP05346B</link><title>Differential interactions of a biological photosensitizer with liposome membranes having varying surface charges</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05346B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05346B, Paper&lt;/div&gt;&lt;div&gt;Bijan Kumar Paul, Nikhil Guchhait&lt;br/&gt;Electrostatic interactions plays a key role in the differential interaction of the potent cancer cell photosensitizer harmane (HM) with liposome membranes of varying surface charges. Photophysics, prototropic transformation equilibrium and dynamics of the drug are differentially modulated within the two lipids DMPC and DMPG.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/mL6PDT81G64" height="1" width="1"/&gt;</description><a10:updated>2012-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Bijan Kumar Paul</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nikhil Guchhait</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05346B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05237G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05237G</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/oJ5mStAw6jc/C2PP05237G</link><title>Cobalt bis(dicarbollide) versus closo-dodecaborate in boronated chlorin e6 conjugates: implications for photodynamic and boron-neutron capture therapy</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05237G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05237G, Paper&lt;/div&gt;&lt;div&gt;Anastasija V. Efremenko, Anastasija A. Ignatova, Alena A. Borsheva, Mikhail A. Grin, Vladimir I. Bregadze, Igor B. Sivaev, Andrey F. Mironov, Alexey V. Feofanov&lt;br/&gt;A conjugate with cobalt bis(dicarbollide) is promising for BNCT and fluorescence diagnostics of cancer. A conjugate with &lt;i&gt;closo&lt;/i&gt;-dodecaborate is suitable for PDT and BNCT.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/oJ5mStAw6jc" height="1" width="1"/&gt;</description><a10:updated>2012-01-20T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anastasija V. Efremenko</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anastasija A. Ignatova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alena A. Borsheva</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mikhail A. Grin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vladimir I. Bregadze</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Igor B. Sivaev</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrey F. Mironov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexey V. Feofanov</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05237G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05326H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05326H</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/U5CCbcmILTU/C2PP05326H</link><title>Externally sensitized deprotection of PPG-masked carbonyls as a spatial proximity probe in photoamplified detection of binding events</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05326H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05326H, Paper&lt;/div&gt;&lt;div&gt;Tiffany P. Gustafson, Greg A. Metzel, Andrei G. Kutateladze&lt;br/&gt;Externally sensitized fragmentation in dithiane PPG-protected carbonyls is adopted for detection and amplification of binding events, which trigger massive self-amplified release of benzophenone from its masked state, simultaneously quenching the fluorescence.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/U5CCbcmILTU" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tiffany P. Gustafson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Greg A. Metzel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrei G. Kutateladze</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05326H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C1PP05238A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C1PP05238A</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/GuwHG-6HQug/C1PP05238A</link><title>Multi-domain GFP-like proteins from two species of marine hydrozoans</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C1PP05238A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C1PP05238A, Paper&lt;/div&gt;&lt;div&gt;Marguerite E. Hunt, Chintan K. Modi, Galina V. Aglyamova, D. V. S. Ravikant, Eli Meyer, Mikhail V. Matz&lt;br/&gt;Jellyfish on fire: the fiery orange fluorescence of this anthoathecate jellyfish is due to a protein named Ember, which consists of four concatenated GFP-like domains.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/GuwHG-6HQug" height="1" width="1"/&gt;</description><a10:updated>2012-01-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Marguerite E. Hunt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chintan K. Modi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Galina V. Aglyamova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">D. V. S. Ravikant</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eli Meyer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mikhail V. Matz</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C1PP05238A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05342J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05342J</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/18aNphcHENM/C2PP05342J</link><title>Photoactivatable fluorophores and techniques for biological imaging applications</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05342J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05342J, Perspective&lt;/div&gt;&lt;div&gt;Wen-hong Li, Genhua Zheng&lt;br/&gt;Photoactivatable fluorophores (PAFs) are powerful imaging probes for biological research. We review recent developments in this field, emphasizing on a novel class of caged coumarins with numerous outstanding properties ideally suitable for live cell imaging.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/18aNphcHENM" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wen-hong Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Genhua Zheng</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05342J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05320A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05320A</guid><link>http://feeds.rsc.org/~r/rss/PP/~3/kRpFniz5ATw/C2PP05320A</link><title>Photorelease of tyrosine from [small alpha]-carboxy-6-nitroveratryl ([small alpha]CNV) derivatives</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2PP05320A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Photochem. Photobiol. Sci.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2PP05320A, Paper&lt;/div&gt;&lt;div&gt;Alexander G. Russell, Matthew J. Sadler, Helen J. Laidlaw, Agustin Gutierrez-Loriente, Christopher W. Wharton, David Carteau, Dario M. Bassani, John S. Snaith&lt;br/&gt;[small alpha]-Carboxy-6-nitroveratryl ([small alpha]CNV) tyrosine ethers undergo rapid photolysis above 300 nm to release the free phenol. &lt;i&gt;N&lt;/i&gt;-Fmoc derivatives suitable for incorporation of caged tyrosine into peptides are described.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/PP/~4/kRpFniz5ATw" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alexander G. Russell</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthew J. Sadler</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Helen J. Laidlaw</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Agustin Gutierrez-Loriente</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher W. Wharton</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David Carteau</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dario M. Bassani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">John S. Snaith</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/PP/C2PP05320A</feedburner:origLink></item></channel></rss>

