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Relevant bibliographies by topics / Radical pairs; Recombination

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Academic literature on the topic 'Radical pairs; Recombination'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Radical pairs; Recombination"

1

Hansen, Martin J., and J. Boiden Pedersen. "Recombination yield of initially separated geminate radical pairs." Chemical Physics Letters 360, no. 5-6 (July 2002): 453–58. http://dx.doi.org/10.1016/s0009-2614(02)00726-1.

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2

Scott, T. W., and S. N. Liu. "Picosecond geminate recombination of phenylthiyl free-radical pairs." Journal of Physical Chemistry 93, no. 4 (February 1989): 1393–96. http://dx.doi.org/10.1021/j100341a042.

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3

Roth, Heinz D. "Recombination of radical ion pairs of triplet multiplicity." Journal of Photochemistry and Photobiology C: Photochemistry Reviews 2, no. 2 (December 2001): 93–116. http://dx.doi.org/10.1016/s1389-5567(01)00013-2.

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Roth, Heinz D. "Biradicals by triplet recombination of radical ion pairs." Photochemical & Photobiological Sciences 7, no. 5 (2008): 540. http://dx.doi.org/10.1039/b800524a.

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5

Benniston, Andrew C., Anthony Harriman, Douglas Philp, and J. Fraser Stoddart. "Charge recombination in cyclophane-derived, intimate radical ion pairs." Journal of the American Chemical Society 115, no. 12 (June 1993): 5298–99. http://dx.doi.org/10.1021/ja00065a052.

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6

Delbaere, Stephanie, Maylis Orio, Jerome Berthet, Michel Sliwa, Sayaka Hatano, and Jiro Abe. "Insights into the recombination of radical pairs in hexaarylbiimidazoles." Chemical Communications 49, no. 52 (2013): 5841. http://dx.doi.org/10.1039/c3cc43037e.

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7

Popov, A. V., P. A. Purtov, and A. B. Doktorov. "The CIDNP kinetics in recombination of successive radical pairs." Applied Magnetic Resonance 23, no. 2 (December 2002): 149–70. http://dx.doi.org/10.1007/bf03166192.

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8

Hansen, Martin J., and J. Boiden Pedersen. "Recombination yield of geminate radical pairs in low magnetic fields." Chemical Physics Letters 361, no. 3-4 (July 2002): 219–25. http://dx.doi.org/10.1016/s0009-2614(02)00724-8.

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9

Serelis, AK, DH Solomon, and PJ Steel. "Stereospecificity in the Geminate Recombination of 1,3-Diphenylpropyl Radical Pairs." Australian Journal of Chemistry 42, no. 3 (1989): 395. http://dx.doi.org/10.1071/ch9890395.

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1,3,4,6-Tetraphenylhexanes (3m) and (3r), formed by the geminate recombination of 1,3- diphenylpropyl (1) radical pairs generated at 90� from diastereomerically pure meso - and rac-1,1′,3,3'-tetraphenylazopropane (2m) and (2r), are obtained with substantial retention (up to 46% d.e .) of precursor stereochemistry. The stable nitroxyls 1,1,3,3-tetramethylisoindolin-2-yloxyl (4) and 2,2,6,6-tetramethylpiperidin-1-yloxyl (5) were used as scavengers to isolate the geminate reaction (30-35% cage effect). A slight selectivity (64% d.e .) in favour of meso-l,3,4,6-tetraphenylhexane (3m) is found in the encounter reaction of (1). The nature of the molecular motions associated with the partial loss of stereochemistry during the reaction (2) → (1) →(3) is discussed. n.m.r. spectroscopy, particularly 13C, was used for correlating product and precursor stereochemistries and for diastereomer identification. The structural assignments were confirmed by single-crystal X-ray diffraction analysis of (3r).

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10

van Dijk, B., J. K. H. Carpenter, A. J. Hoff, and P. J. Hore. "Magnetic Field Effects on the Recombination Kinetics of Radical Pairs." Journal of Physical Chemistry B 102, no. 2 (January 1998): 464–72. http://dx.doi.org/10.1021/jp9721816.

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Dissertations / Theses on the topic "Radical pairs; Recombination"

1

Till, Ulrike. "Recombination kinetics of radical pairs." Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267949.

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Carpenter, Joanna Katharine Hicks. "Magnetic field effects on electron transfer reactions in photosynthetic bacteria." Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390466.

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Wedge, Christopher J. "Radiofrequency Magnetic Field Effects on Radical Pair Recombination Reactions." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.515011.

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Books on the topic "Radical pairs; Recombination"

1

Wu, Jie Qiang. Spin relaxation mechanisms controlling magnetic-field dependent radical pair recombination kinetics in nanoscopic reactors. Konstanz: Hartung-Gorre Verlag, 1993.

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Book chapters on the topic "Radical pairs; Recombination"

1

Korolenko, E. C., K. M. Salikhov, and N. V. Shokhirev. "Low-Field CIDNP Manifestation of the Minor Recombination Channel Via Triplet State of Radical Pairs." In Organic Free Radicals, 177–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73963-7_88.

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2

Schlodder, E., and K. Brettel. "Recombination Kinetics of the Radical Pair, P680+I‒, in Closed Reaction centers of PS II as Function of Temperature." In Current Research in Photosynthesis, 447–50. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0511-5_100.

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3

Atkins, Peter. "Divorce and Reconciliation: Radical Recombination." In Reactions. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199695126.003.0016.

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Abstract:

In Reaction 3 you saw that a radical is a species with at least one unpaired electron. An ‘unpaired electron’ is a single electron that is present in the molecule but not playing a role in bonding. The French word celebataire conveys the sense of the electron’s forlorn loneliness very well. However, it is capable of joining forces with another unpaired electron on another radical to form a bond. Two examples of radicals are ·OH (1, a hydroxyl radical), and ·CH3 (2, a methyl radical). The dot denotes the unpaired electron. In most cases, radicals are highly reactive and aggressively attack other species in order to use their unpaired electron to pair with an electron on the second species and so form a bond. The most primitive type of radical reaction is simply the clunking together of two radicals, each donating its unpaired electron to the formation of an electron-pair bond, as in the combination of two ·CH3 radicals to form ethane, CH3–CH3, 3. Some species might have more than one unpaired electron that they can use for biting into other molecules. If they are double-fanged, the most common case after ordinary single-fanged radicals, then the species is known as a ‘biradical’. To continue the partnering analogy: the two electrons cohabit but are platonic in their relationship. A very important example is an oxygen atom, O, which is a biradical. For the purposes of this section I shall write it ·O· with two dots for its two relevant electrons. An O2 molecule is also a sort of biradical, so when I want to emphasize its radical nature I shall denote it ·O–O·. There are a lot of reasons why you should be interested in radical reactions. One is that, as I explained in Reaction 3, they take part in the combustion reactions of the everyday world. Combustion reactions include the reactions that take place inside internal combustion and jet engines and move us around the world. Radical reactions occur wherever there is fire. Because fire is sometimes unintended, if the reactions that contribute to it are understood, then better ways to control and quench it can be devised.

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