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Titlebook: Supramolecular Photochemistry; Vincenzo Balzani Book 1987 D. Reidel Publishing Company, Dordrechet, Holland 1987 catalysis.colloid.metals.

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書目名稱Supramolecular Photochemistry
編輯Vincenzo Balzani
視頻videohttp://file.papertrans.cn/883/882202/882202.mp4
叢書名稱Nato Science Series C:
圖書封面Titlebook: Supramolecular Photochemistry;  Vincenzo Balzani Book 1987 D. Reidel Publishing Company, Dordrechet, Holland 1987 catalysis.colloid.metals.
描述The intellectual and utilitarian opportunities that lie at the frontiers of chemistry have been recently emphasized by the Pimentel Report. Such report recommends that in the field of chemical research priority should be given to "understanding chemical reactivity" and proposes initiatives aimed at the clarification of factors that control the rates of reaction and the development of new synthetic pathways for chemical change. In the broad field of chemical reactivity, a discipline that has grown with an extraordinary rate is photochemistry. Since the knowledge of the photochemical properties at the molecular level has made a substantial progress in the last few years, there is currently a trend to study more and more complex photochemical systems. In particular, an emerging and rapidly expanding branch of photochemistry is that concerning studies of assemblies of molecular components properly combined so as to obtain light-induced functions (supramolecular photochemistry). Although much of the current work in supramolecular photochemistry is fundamental in nature, it is clear that progress in this field will be most rewarding for several applications concerning the interaction of
出版日期Book 1987
關鍵詞catalysis; colloid; metals; photochemistry; polymer; structure; supramolecular chemistry; synthesis
版次1
doihttps://doi.org/10.1007/978-94-009-3979-0
isbn_softcover978-94-010-8265-5
isbn_ebook978-94-009-3979-0Series ISSN 1389-2185
issn_series 1389-2185
copyrightD. Reidel Publishing Company, Dordrechet, Holland 1987
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Energy Transfer in Synthetic Porphyrin Arrays,ng complex can be obtained. Here, efficient energy transfer occurs from antenna zinc porphyrins to a central free-base porphyrin, which retains sufficiently long-lived excited states to participate in bimolecular quenching reactions.
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