Diffusion influenced reactions at short times: breakdown of the Debye-Smoluchowski description
Fluorescence quenching studies were used to explore the validity of the Debye–Smoluchowski equation on the 0.5–200 ps time scale, using fluorescence upconversion. Complementary studies extending to 3.5 ns were carried out using time correlated single photon counting. We find, for the system rhodamin...
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Veröffentlicht in: | The Journal of chemical physics 1989-04, Vol.90 (7), p.3876-3878 |
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creator | EADS, D. D PERIASAMY, N FLEMING, G. R |
description | Fluorescence quenching studies were used to explore the validity of the Debye–Smoluchowski equation on the 0.5–200 ps time scale, using fluorescence upconversion. Complementary studies extending to 3.5 ns were carried out using time correlated single photon counting. We find, for the system rhodamine B quenched by ferrocyanide, that the fluorescence decay (i. e., reaction rate) is much faster at short times than implied by fits to the lower time resolution data. Possible reasons for the breakdown of the Debye–Smoluchowski equation at short times are briefly discussed. |
doi_str_mv | 10.1063/1.455794 |
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D</creatorcontrib><creatorcontrib>PERIASAMY, N</creatorcontrib><creatorcontrib>FLEMING, G. R</creatorcontrib><title>Diffusion influenced reactions at short times: breakdown of the Debye-Smoluchowski description</title><title>The Journal of chemical physics</title><description>Fluorescence quenching studies were used to explore the validity of the Debye–Smoluchowski equation on the 0.5–200 ps time scale, using fluorescence upconversion. Complementary studies extending to 3.5 ns were carried out using time correlated single photon counting. We find, for the system rhodamine B quenched by ferrocyanide, that the fluorescence decay (i. e., reaction rate) is much faster at short times than implied by fits to the lower time resolution data. Possible reasons for the breakdown of the Debye–Smoluchowski equation at short times are briefly discussed.</description><subject>Atomic and molecular physics</subject><subject>Exact sciences and technology</subject><subject>Fluorescence and phosphorescence; radiationless transitions, quenching (intersystem crossing, internal conversion)</subject><subject>Molecular properties and interactions with photons</subject><subject>Physics</subject><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LAzEYhIMoWKvgT8hF8LL1fTfZ7MabtPUDCh7Uq0uSTWjsdlOSXUr_vVsqeBqYeZiBIeQWYYYg2APOeFGUkp-RCUIls1JIOCcTgBwzKUBckquUfgAAy5xPyPfCOzckHzrqO9cOtjO2odEq049eoqqnaR1iT3u_temR6jHaNGHf0eBov7Z0YfXBZh_b0A5mHfZp42ljk4l-dyy4JhdOtcne_OmUfD0vP-ev2er95W3-tMoMy7HPlIaqAmmY0Q02WAlesAohFzpHzUqQrpBYKRTAlStycIxbUxgnhZFaNCWbkvtTr4khpWhdvYt-q-KhRqiPv9RYn34Z0bsTulPJqNZF1Rmf_nk5LgvB2S9I3WKF</recordid><startdate>19890401</startdate><enddate>19890401</enddate><creator>EADS, D. 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Complementary studies extending to 3.5 ns were carried out using time correlated single photon counting. We find, for the system rhodamine B quenched by ferrocyanide, that the fluorescence decay (i. e., reaction rate) is much faster at short times than implied by fits to the lower time resolution data. Possible reasons for the breakdown of the Debye–Smoluchowski equation at short times are briefly discussed.</abstract><cop>Woodbury, NY</cop><pub>American Institute of Physics</pub><doi>10.1063/1.455794</doi><tpages>3</tpages></addata></record> |
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subjects | Atomic and molecular physics Exact sciences and technology Fluorescence and phosphorescence radiationless transitions, quenching (intersystem crossing, internal conversion) Molecular properties and interactions with photons Physics |
title | Diffusion influenced reactions at short times: breakdown of the Debye-Smoluchowski description |
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