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Fluorenone

About: Fluorenone is a research topic. Over the lifetime, 1067 publications have been published within this topic receiving 17162 citations. The topic is also known as: Diphenylene ketone & 9-Oxofluorene.


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Journal ArticleDOI
TL;DR: In this article, a mechanism involving homolytic scission of the peroxidic bond of the substrate is proposed, which is much less effective when using free t-BuO. radicals.

18 citations

Journal ArticleDOI
TL;DR: In this article, the electrochemical and photochemical properties of the fluorenone analogues 9H-pyrrolo[1,2-a]indole-9-one (1), and 9Hpyrido[3,4,b] pyrrolizin-9one (2), which absorb in the visible region (e 400nm = 4711 mol −1 cm −1 for 1 and e 400m = 872 1 mol cm − 1 for 2 ), are described.

18 citations

Journal ArticleDOI
TL;DR: The Sc3N@Ih-C80˙– radical anions are dimerized in solution to form single-bonded Sc3n(C80–)2 dimers characterized by single-crystal X-ray diffraction.

18 citations

Journal ArticleDOI
TL;DR: The planarity of the fluorenone molecule disfavors the exploration of the configuration space where surface crossings would create high ISC probability, which occurs in benzophenone through surface crossings.
Abstract: Direct measurements of Single vibronic Level InterSystem Crossing (SLISC) have been performed on the fluorenone molecule in the gas phase, by time resolved photoelectron and photoion spectroscopy. Vibronic transitions above the S1 nπ* origin were excited in the 432–420 nm region and the decay of S1 and growth of T13ππ* could be observed within a 10 ns time domain. The ionization potential is measured as 8.33 ± 0.04 eV. The energy of the first excited triplet state of fluorenone, T1 has been characterized directly at 18640 ± 250 cm−1. The internal conversion of S1 to S0 is found to amount to ∼15% of the population decay, thus ISC is the dominant electronic relaxation process. ISC, although favored by the S11nπ*–T13ππ* coupling scheme, is 3 orders of magnitude less efficient than in the similar molecule benzophenone. Thus, the planarity of the fluorenone molecule disfavors the exploration of the configuration space where surface crossings would create high ISC probability, which occurs in benzophenone through surface crossings. The time evolution of S1 fluorenone is well accounted for by the statistical decay of individual levels into a quasi-continuum of T1 vibronic levels.

18 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202311
202221
202124
202026
201928
201822