Relevant bibliographies by topics / Photochemistry. Solution (Chemistry)

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters

Academic literature on the topic 'Photochemistry. Solution (Chemistry)'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Photochemistry. Solution (Chemistry)"

1

Selco, J. I., T. Brooks, M. Chang, M. T. Trieu, J. K. McDonald, and S. P. McManus. "Solution photochemistry of azulene." Journal of Organic Chemistry 59, no. 2 (1994): 429–33. http://dx.doi.org/10.1021/jo00081a024.

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Clark, K. Brady, and William J. Leigh. "Cyclobutene photochemistry. Involvement of carbene intermediates in the photochemistry of alkylcyclobutenes." Canadian Journal of Chemistry 66, no. 7 (1988): 1571–78. http://dx.doi.org/10.1139/v88-255.

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The photochemistry of 1,3,3,4- and 1,3,4,4-tetramethylcyclobutene has been investigated in pentane solution with monochromatic far ultraviolet (185, 193, and 214 nm) light sources, as well as in methanol solution with 214-nm excitation. Photolysis of each of the two isomeric cyclobutene derivatives results in competitive electrocyclic ring opening (yielding mixtures of stereoisomeric dienes in each case), fragmentation to yield propyne and methyl-2-butene, and isomerization to the other cyclobutene isomer. Quantum yields for product formation with 185-nm excitation have been measured in each c
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3

Belov, D. G., B. G. Rogachev, L. I. Tkachenko, V. A. Smirnov, and S. M. Aldoshin. "Photochemistry of arylhydrazides in solution." Russian Chemical Bulletin 49, no. 4 (2000): 666–68. http://dx.doi.org/10.1007/bf02495478.

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Leigh, William J., and J. Alberto Postigo. "Cyclobutene photochemistry. Substituent effects on the photochemistry of 1-phenylcyclobutene." Canadian Journal of Chemistry 73, no. 2 (1995): 191–203. http://dx.doi.org/10.1139/v95-028.

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The photochemistry and photophysics of 1-phenylcyclobutene and five aryl-substituted derivatives have been studied in various solvents at room temperature. All six compounds fluoresce with quantum yields in the 0.2–0.3 range in cyclohexane and acetonitrile solution. 1-Phenylcyclobutene undergoes [2+2]-cycloreversion [Formula: see text] to yield phenylacetylene upon photolysis in either hydrocarbon or acetonitrile solution, and undergoes (Markovnikov) solvent addition upon irradiation in methanol solution [Formula: see text] in addition to cycloreversion. Triplet sensitization and quenching exp
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5

Vignoni, Mariana, Franco M. Cabrerizo, Carolina Lorente, Catherine Claparols, Esther Oliveros, and Andrés H. Thomas. "Photochemistry of dihydrobiopterin in aqueous solution." Org. Biomol. Chem. 8, no. 4 (2010): 800–810. http://dx.doi.org/10.1039/b913095k.

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6

Hill, Roger R., John D. Coyle, David Birch, et al. "Photochemistry of dipeptides in aqueous solution." Journal of the American Chemical Society 113, no. 5 (1991): 1805–17. http://dx.doi.org/10.1021/ja00005a053.

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7

Gonzalez, M. Micaela, M. Laura Salum, Yousef Gholipour, Franco M. Cabrerizo, and Rosa Erra-Balsells. "Photochemistry of norharmane in aqueous solution." Photochemical & Photobiological Sciences 8, no. 8 (2009): 1139. http://dx.doi.org/10.1039/b822173a.

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8

Nguyen, N., B. E. Harris, K. B. Clark, and W. J. Leigh. "The solution-phase photochemistry of 2-trifluoromethylnorbornene." Canadian Journal of Chemistry 68, no. 11 (1990): 1961–66. http://dx.doi.org/10.1139/v90-301.

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The photochemistry of 2-trifluoromethylnorbornene in pentane solution has been investigated. Direct photolysis with 193 nm light yields 1-trifluoromethyl-2-norcarene in 90% yield, due to formal [1,3]-sigmatropic rearrangement, in addition to three other minor products. Chlorobenzene-sensitized photolysis affords photoreduction products, principally exo- and endo-2-trifluoromethylnorbornane and decane isomers, in addition to several products of higher molecular weight. On the basis of comparisons of the photochemistry of this compound to that previously reported for norbornene and 2-cyanonorbor
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9

Fahie, Brian J., and William J. Leigh. "The far-ultraviolet photochemistry of alkylcyclopropenes in solution." Canadian Journal of Chemistry 67, no. 11 (1989): 1859–67. http://dx.doi.org/10.1139/v89-289.

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The photochemistry of 1,3,3-trimethylcyclopropene and 1-tert-butyl-3,3-dimethylcyclopropene has been investigated in hydrocarbon, methanol, and 1-hexene solution with far-ultraviolet (185–228 nm) light. Direct photolysis of the two compounds affords allene, alkyne, and 1,3-diene derivatives, formally as a result of initial bond cleavage to yield vinylcarbene intermediates. Products derived from cleavage of the most substituted (C1—C3) cyclopropene bond account for 60–80% of the observed mixture in each case. Results from the photolysis of 1,3,3-trimethylcyclopropene-1-13C suggest a second path
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10

Wan, Peter, Darryl W. Brousmiche, Christy Z. Chen, John Cole, Matthew Lukeman, and Musheng Xu. "Quinone methide intermediates in organic photochemistry." Pure and Applied Chemistry 73, no. 3 (2001): 529–34. http://dx.doi.org/10.1351/pac200173030529.

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Quinone methides are widely encountered reactive intermediates in the chemistry of phenols and related compounds. This paper summarizes our recent progress in uncovering new and general photochemical methods for forming quinone methides of various structural types in aqueous solution. Their mechanism of formation and subsequent chemistry are also discussed. New examples of excited-state intramolecular proton transfer (ESIPT) have been uncovered in these studies. We have also discovered that appropriately designed biphenyls and terphenyls display photochemistry that is best rationalized by high
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Dissertations / Theses on the topic "Photochemistry. Solution (Chemistry)"

1

Haward, Mark T. "Spectroscopy and photochemistry in liquid xenon solution." Thesis, University of Nottingham, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334777.

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2

Murray, S. G. "Solution and polymer photochemistry of azo dyes." Thesis, University of Leeds, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.371437.

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3

Harrington, Cameron Robert Leigh William J. "Time-resolved spectroscopic studies of the chemistry of transient germylenes and digermenes in solution." *McMaster only, 2006.

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4

Mousa, Souad Abd. "Photochemistry of β-carbolines and azine dyes in solution and colloidal systems". Thesis, Swansea University, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.678433.

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5

Cosson, Herve. "Photodecomposition of chlorine dioxide and sodium chlorite in aqueous solution by irradiation with ultraviolet light." Thesis, Georgia Institute of Technology, 1993. http://hdl.handle.net/1853/11177.

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6

Shields, Dylan J. "Photochemistry of Organic Azides, Quinones, and Peroxides in Solution, Crystals, Super Molecular Complexes and Cryogenic Matrices." University of Cincinnati / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin157441745178423.

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7

Mereshchenko, Andrey S. "ULTRAFAST PHOTOCHEMISTRY OF POLYATOMIC MOLECULES CONTAINING LABILE HALOGEN ATOMS IN SOLUTION." Bowling Green State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1369774991.

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8

Pokkuluri, Phani Raj. "Solution and solid state photochemistry of some bridgehead substituted dibenzobarrelene diesters : x-ray crystallography of starting materials and photoproducts." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/31154.

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The solid state and solution phase photochemistry of three bridgehead-substituted dibenzobarrelene-11,12-diesters and a 2,3-naphthobarrelene diester derivative were investigated. These compounds were expected to undergo the di-π-methane rearrangement via their triplet excited states, and a rearrangement to a cyclooctatetraene (COT) derivative via their singlet excited states. All compounds investigated underwent smooth photoreactions in the solid state to produce the same products as observed in the corresponding solution phase photolyses. One exception to this was a bridgehead dimethyl- sub
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9

El-Khoury, Patrick Z. "Femtosecond Dynamics of Small Polyatomic Molecules in Solution: A Combined Experimental and Computational Approach." Bowling Green State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1272899005.

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10

Banerjee, Upasana. "Mechanistic Investigations into the Photoreactivity of Organic Azides in Solution, Crystals and Cryogenic Matrices." University of Cincinnati / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1623250627543686.

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Books on the topic "Photochemistry. Solution (Chemistry)"

1

Françoise, Lahmani, and Castex M. C, eds. Photophysics and photochemistry above 6eV: Proceedings of the 38th International Meeting of the Société de chimie physique, Bombannes, 17-21 September 1984. Elsevier, 1985.

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Françoise, Lahmani, ed. Photophysics and photochemistry above 6 eV: Proceedings of the 38th International Meeting of the Société de chimie physique, Bombannes, 17-21 September 1984. Elsevier, 1985.

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3

Noz, Marilyn E. Radiation protection in the health sciences: With problem solutions manual. 2nd ed. World Scientific, 2007.

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Radiation Protection in the Health Sciences: With Problem Solutions Manual. 2nd ed. World Scientific Publishing Company, 2007.

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Book chapters on the topic "Photochemistry. Solution (Chemistry)"

1

Khatouri, J., M. Mostafavi, and J. Belloni. "Kinetics of Electron Transfer in Solution Catalyzed by Metal Clusters." In Photochemistry and Radiation Chemistry. American Chemical Society, 1998. http://dx.doi.org/10.1021/ba-1998-0254.ch018.

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2

Pollum, Marvin, Lara Martínez-Fernández, and Carlos E. Crespo-Hernández. "Photochemistry of Nucleic Acid Bases and Their Thio- and Aza-Analogues in Solution." In Topics in Current Chemistry. Springer International Publishing, 2014. http://dx.doi.org/10.1007/128_2014_554.

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3

Gauduel, Y., and H. Gelabert. "Ultrafast Electron Transfer and Short-Lived Prereactive Steps in Solutions." In Photochemistry and Radiation Chemistry. American Chemical Society, 1998. http://dx.doi.org/10.1021/ba-1998-0254.ch020.

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You might also be interested in the extended bibliographies on the topic 'Photochemistry. Solution (Chemistry)' for particular source types:
Journal articles Dissertations / Theses
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