subject:(Photochemistry)

University of Georgia

1. Green, Joanna Louise. Linking photochemical carbon transformations and microbial responses in the Amazon River plume.

Degree: MS, Marine Sciences, 2013, University of Georgia

URL: http://purl.galileo.usg.edu/uga_etd/green_joanna_l_201305_ms

► This work focuses on the interplay between sunlight-driven and microbe-driven transformation of dissolved organic matter (DOM) from a dynamic system, the Amazon River plume. To… (more)

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Green, J. L. (2013). Linking photochemical carbon transformations and microbial responses in the Amazon River plume. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/green_joanna_l_201305_ms

Chicago Manual of Style (16^th Edition):

Green, Joanna Louise. “Linking photochemical carbon transformations and microbial responses in the Amazon River plume.” 2013. Masters Thesis, University of Georgia. Accessed February 18, 2020. http://purl.galileo.usg.edu/uga_etd/green_joanna_l_201305_ms.

MLA Handbook (7^th Edition):

Green, Joanna Louise. “Linking photochemical carbon transformations and microbial responses in the Amazon River plume.” 2013. Web. 18 Feb 2020.

Vancouver:

Green JL. Linking photochemical carbon transformations and microbial responses in the Amazon River plume. [Internet] [Masters thesis]. University of Georgia; 2013. [cited 2020 Feb 18]. Available from: http://purl.galileo.usg.edu/uga_etd/green_joanna_l_201305_ms.

Council of Science Editors:

Green JL. Linking photochemical carbon transformations and microbial responses in the Amazon River plume. [Masters Thesis]. University of Georgia; 2013. Available from: http://purl.galileo.usg.edu/uga_etd/green_joanna_l_201305_ms

University of Georgia

2. Reader, Heather Erin. Smouldering oceans: on the photochemically mediated oxidation of dissolved organic matter in coastal waters.

Degree: PhD, Marine Sciences, 2011, University of Georgia

URL: http://purl.galileo.usg.edu/uga_etd/reader_heather_e_201105_phd

► Marine dissolved organic carbon (DOC) is one of the largest and most dynamic pools of reduced carbon on earth. Photochemical processes have the potential to… (more)

▼ Marine dissolved organic carbon (DOC) is one of the largest and most dynamic pools of reduced carbon on earth. Photochemical processes have the potential to significantly affect the content of this DOC pool. Photochemical oxidation to carbon monoxide and carbon dioxide are two direct pathways for the removal of DOC from the marine system. Indirectly, photochemical processes can lead to the removal of DOC through the alteration of chemical structures rendering them more biologically labile. In order to assess the influence of photochemistry on the coastal carbon cycle the variability of these processes must be well constrained. To calculate photochemical production in marine waters, it is crucial to know how light is absorbed by chromophoric dissolved organic matter (CDOM), as well as the spectral efficiency of the resulting photochemical reactions (i.e. the apparent quantum yield (AQY) spectra). The challenges of using visible wavelength CDOM absorption data to model ultraviolet absorption data are investigated. Direct measurements of ultraviolet absorption data model photochemical processes best. When this is not possible, visible data can be used with an accuracy of +/- 10% in coastal waters. Either a hyperbolic absorption model or one using correction factors applied to a traditional exponential model will allow for similar accuracy in the ultraviolet portion of the absorption spectrum. The variability of photochemical oxidation of dissolved organic carbon in a coastal system was studied in order to constrain remote sensing calculations. The variability of CO and CO2 AQY spectra were relatively well constrained in three estuaries of Georgia, USA. The AQY for CO varied within +/- 12.7% year-round while CO2 varied within +/- 33.6% year-round. Hyperspectral remote sensing reveals finescale hydrodynamic structure in estuarine systems and is readily adaptable to photochemical modeling applications. Defining the variability of photochemistry’s influence on the biological lability of DOC is a complex undertaking. Unlike direct photochemical oxidation of DOC to CO and CO2, the biologically labile products (BLPs) of incomplete oxidation can themselves be photochemically reactive. Competition between production and destruction of BLPs during irradiation is a significant consideration when determining the quantitative influence of photochemistry on marine systems. Advisors/Committee Members: William L. Miller.

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Reader, H. E. (2011). Smouldering oceans: on the photochemically mediated oxidation of dissolved organic matter in coastal waters. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/reader_heather_e_201105_phd

Chicago Manual of Style (16^th Edition):

Reader, Heather Erin. “Smouldering oceans: on the photochemically mediated oxidation of dissolved organic matter in coastal waters.” 2011. Doctoral Dissertation, University of Georgia. Accessed February 18, 2020. http://purl.galileo.usg.edu/uga_etd/reader_heather_e_201105_phd.

MLA Handbook (7^th Edition):

Reader, Heather Erin. “Smouldering oceans: on the photochemically mediated oxidation of dissolved organic matter in coastal waters.” 2011. Web. 18 Feb 2020.

Vancouver:

Reader HE. Smouldering oceans: on the photochemically mediated oxidation of dissolved organic matter in coastal waters. [Internet] [Doctoral dissertation]. University of Georgia; 2011. [cited 2020 Feb 18]. Available from: http://purl.galileo.usg.edu/uga_etd/reader_heather_e_201105_phd.

Council of Science Editors:

Reader HE. Smouldering oceans: on the photochemically mediated oxidation of dissolved organic matter in coastal waters. [Doctoral Dissertation]. University of Georgia; 2011. Available from: http://purl.galileo.usg.edu/uga_etd/reader_heather_e_201105_phd

University of Victoria

3. Hou, Yunyan. Formal intramolecular photoredox reactions of anthraquinones mediated by water.

Degree: Dept. of Chemistry, 2011, University of Victoria

URL: http://hdl.handle.net/1828/3319

► The formal intramolecular photoredox reaction initially discovered for the parent 2- (hydroxymethyl)-9,10-anthraquinone (HMAQ) in aqueous solution was extended to a variety of anthraquinone derivatives 2.1-2.9,… (more)

Subjects/Keywords: photochemistry

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APA (6^th Edition):

Hou, Y. (2011). Formal intramolecular photoredox reactions of anthraquinones mediated by water. (Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/3319

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Hou, Yunyan. “Formal intramolecular photoredox reactions of anthraquinones mediated by water.” 2011. Thesis, University of Victoria. Accessed February 18, 2020. http://hdl.handle.net/1828/3319.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Hou, Yunyan. “Formal intramolecular photoredox reactions of anthraquinones mediated by water.” 2011. Web. 18 Feb 2020.

Vancouver:

Hou Y. Formal intramolecular photoredox reactions of anthraquinones mediated by water. [Internet] [Thesis]. University of Victoria; 2011. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1828/3319.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hou Y. Formal intramolecular photoredox reactions of anthraquinones mediated by water. [Thesis]. University of Victoria; 2011. Available from: http://hdl.handle.net/1828/3319

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Victoria

4. Wang, Yunxia. The syntheses and photochromic properties of several substituted and condensed benzo[e]dimethyl-dihydropyrenes.

Degree: Department of Chemistry, 2017, University of Victoria

URL: http://hdl.handle.net/1828/8044

► The symmetric multistate photo-switchable molecule 72, which contains two DHP units with a dibenzocyclophane as a spacer, was successfully synthesized by different routes using aryne-furan… (more)

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Wang, Y. (2017). The syntheses and photochromic properties of several substituted and condensed benzo[e]dimethyl-dihydropyrenes. (Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/8044

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Wang, Yunxia. “The syntheses and photochromic properties of several substituted and condensed benzo[e]dimethyl-dihydropyrenes.” 2017. Thesis, University of Victoria. Accessed February 18, 2020. http://hdl.handle.net/1828/8044.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Wang, Yunxia. “The syntheses and photochromic properties of several substituted and condensed benzo[e]dimethyl-dihydropyrenes.” 2017. Web. 18 Feb 2020.

Vancouver:

Wang Y. The syntheses and photochromic properties of several substituted and condensed benzo[e]dimethyl-dihydropyrenes. [Internet] [Thesis]. University of Victoria; 2017. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1828/8044.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wang Y. The syntheses and photochromic properties of several substituted and condensed benzo[e]dimethyl-dihydropyrenes. [Thesis]. University of Victoria; 2017. Available from: http://hdl.handle.net/1828/8044

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Victoria

5. Kleinman, Mark Howard. The Dynamics of benzylic radical pairs in organized media : binding and mobility.

Degree: Department of Chemistry, 2017, University of Victoria

URL: http://hdl.handle.net/1828/8298

► Through the use of laser flash photolysis and product studies, the photochemistry of dibenzyl ketone and its derivatives in SDS micelles shows that these aggregates… (more)

Subjects/Keywords: Flash photolysis; Photochemistry; Laser Photochemistry

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APA (6^th Edition):

Kleinman, M. H. (2017). The Dynamics of benzylic radical pairs in organized media : binding and mobility. (Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/8298

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Kleinman, Mark Howard. “The Dynamics of benzylic radical pairs in organized media : binding and mobility.” 2017. Thesis, University of Victoria. Accessed February 18, 2020. http://hdl.handle.net/1828/8298.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Kleinman, Mark Howard. “The Dynamics of benzylic radical pairs in organized media : binding and mobility.” 2017. Web. 18 Feb 2020.

Vancouver:

Kleinman MH. The Dynamics of benzylic radical pairs in organized media : binding and mobility. [Internet] [Thesis]. University of Victoria; 2017. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1828/8298.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kleinman MH. The Dynamics of benzylic radical pairs in organized media : binding and mobility. [Thesis]. University of Victoria; 2017. Available from: http://hdl.handle.net/1828/8298

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Texas A&M University

6. Kim, Hahkjoon. Imaging studies of photochemistry of the stratospheric bromine and chlorine compounds.

Degree: 2006, Texas A&M University

URL: http://hdl.handle.net/1969.1/3726

► This dissertation focuses on the photodissociation dynamics of stratospheric bromine and chlorine radical intermediates (BrO, ClO) along with reservoir species (ClONO2), which are known to… (more)

Subjects/Keywords: photochemistry

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APA (6^th Edition):

Kim, H. (2006). Imaging studies of photochemistry of the stratospheric bromine and chlorine compounds. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/3726

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Kim, Hahkjoon. “Imaging studies of photochemistry of the stratospheric bromine and chlorine compounds.” 2006. Thesis, Texas A&M University. Accessed February 18, 2020. http://hdl.handle.net/1969.1/3726.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Kim, Hahkjoon. “Imaging studies of photochemistry of the stratospheric bromine and chlorine compounds.” 2006. Web. 18 Feb 2020.

Vancouver:

Kim H. Imaging studies of photochemistry of the stratospheric bromine and chlorine compounds. [Internet] [Thesis]. Texas A&M University; 2006. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1969.1/3726.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kim H. Imaging studies of photochemistry of the stratospheric bromine and chlorine compounds. [Thesis]. Texas A&M University; 2006. Available from: http://hdl.handle.net/1969.1/3726

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Oregon State University

7. Staible, Thomas Fredrick. The reaction between O-ions and F centers.

Degree: MS, Chemistry, 1972, Oregon State University

URL: http://hdl.handle.net/1957/46103

► The photochemical reaction between O⁻ ions and F centers was investigated. The activation energy was determined by the Arrhenius law to be 0.10 + 0.04… (more)

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Staible, T. F. (1972). The reaction between O-ions and F centers. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/46103

Chicago Manual of Style (16^th Edition):

Staible, Thomas Fredrick. “The reaction between O-ions and F centers.” 1972. Masters Thesis, Oregon State University. Accessed February 18, 2020. http://hdl.handle.net/1957/46103.

MLA Handbook (7^th Edition):

Staible, Thomas Fredrick. “The reaction between O-ions and F centers.” 1972. Web. 18 Feb 2020.

Vancouver:

Staible TF. The reaction between O-ions and F centers. [Internet] [Masters thesis]. Oregon State University; 1972. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1957/46103.

Council of Science Editors:

Staible TF. The reaction between O-ions and F centers. [Masters Thesis]. Oregon State University; 1972. Available from: http://hdl.handle.net/1957/46103

Oregon State University

8. Siggel, Lorenz. The photochemistry of some insect juvenile hormone analogs.

Degree: PhD, Chemistry, 1986, Oregon State University

URL: http://hdl.handle.net/1957/40126

► The photochemistry of some analogs of insect growth regulators (IGR's) was studied. Methyl geranate, TY, was synthesized and the mechanisms of its photochemical reaction pathways… (more)

▼ The photochemistry of some analogs of insect growth regulators (IGR's) was studied. Methyl geranate, TY, was synthesized and the mechanisms of its photochemical reaction pathways were studied by a variety of techniques. Direct irradiation of 71 in ether leads to the formation of five new products: 98, the product of a [1,3] sigmatropic shift; 72, a bicyclo[2.1.1]hexane derivative; 73, a cylclopentane derivative; 100, the product of in-chain deconjugation to the Z isomer; and 97, the product of isomerization about the C-2 bond. Irradiation in the presence of propiophenone as a triplet sensitizer lead to the formation of only 72, 73 and 97, identifying them as arising from the triplet excited state. Irradiation of 71 in ether with varying amounts of base lead to the formation of (in addition to products already mentioned) 99 and 100, the other two possible deconjugation products. Examination of Scheme 29 leads to the derivation of the kinetic rate expressions in Scheme 31, and plotting the ratios of 99/73, 100/73 and 101/73 yields values for the relative rate of [1,5] sigmatropic shift of hydrogen from a photodienol species (119, 121, 123) to regenerate starting esters (71, 97) rather than going on to deconjugation products (99, 100, 101). It was found that the relative rates of sigmatropic shift for 119 and 123 were nearly identical but 121 was about 75 times slower. This decrease in the relative rate for 121 is ascribed to the extra steric repulsion in 121, causing it to adopt the unreactive s-trans conformation and thus slowing the reaction. Insect juvenile hormone, 74, was synthesized and irradiated in ether and was found to undergo photochemical processes similar to that of 71. The primary photoprocess is isomerizatrion about the C-2 and C-6 double bonds. Isomerization about the C-6 bond was unexpected and indicated the intermediacy of an exciplex. To study the role of exciplexes in the E/Z isomerizartion of isolated double bonds in the juvenile hormone, 74, the unsymmetrically terminated analog 92 and the dihydro analog 93 were synthesized. Irradiation of 92 and 93 in solvents of varying polarity (ET) lead to an increase of the quantum yield of E/Z isomerization for both 92 and 93, indicating the intermediacy of an intermolecular exciplex. to study the role of intramolecular exciplexes 92 and 93 were irradiated in ether at increasing dilution (0.1 M - 0.0008 M). It was found that the intermolecular exciplex is the major contributor in the concentration range studied without any evidence for an intramolecular exciplex. Advisors/Committee Members: Freeman, Peter K. (advisor).

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Siggel, L. (1986). The photochemistry of some insect juvenile hormone analogs. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/40126

Chicago Manual of Style (16^th Edition):

Siggel, Lorenz. “The photochemistry of some insect juvenile hormone analogs.” 1986. Doctoral Dissertation, Oregon State University. Accessed February 18, 2020. http://hdl.handle.net/1957/40126.

MLA Handbook (7^th Edition):

Siggel, Lorenz. “The photochemistry of some insect juvenile hormone analogs.” 1986. Web. 18 Feb 2020.

Vancouver:

Siggel L. The photochemistry of some insect juvenile hormone analogs. [Internet] [Doctoral dissertation]. Oregon State University; 1986. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1957/40126.

Council of Science Editors:

Siggel L. The photochemistry of some insect juvenile hormone analogs. [Doctoral Dissertation]. Oregon State University; 1986. Available from: http://hdl.handle.net/1957/40126

Oregon State University

9. Huang, Yo-hsin. The photochemistry of some polyhalobenzenes.

Degree: MS, Chemistry, 1986, Oregon State University

URL: http://hdl.handle.net/1957/40412

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Huang, Y. (1986). The photochemistry of some polyhalobenzenes. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/40412

Chicago Manual of Style (16^th Edition):

Huang, Yo-hsin. “The photochemistry of some polyhalobenzenes.” 1986. Masters Thesis, Oregon State University. Accessed February 18, 2020. http://hdl.handle.net/1957/40412.

MLA Handbook (7^th Edition):

Huang, Yo-hsin. “The photochemistry of some polyhalobenzenes.” 1986. Web. 18 Feb 2020.

Vancouver:

Huang Y. The photochemistry of some polyhalobenzenes. [Internet] [Masters thesis]. Oregon State University; 1986. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1957/40412.

Council of Science Editors:

Huang Y. The photochemistry of some polyhalobenzenes. [Masters Thesis]. Oregon State University; 1986. Available from: http://hdl.handle.net/1957/40412

University of Hawaii – Manoa

10. Fenstemacher, Roland John. Polyene photochemistry : solvent controlled state ordering.

Degree: PhD, 2009, University of Hawaii – Manoa

URL: http://hdl.handle.net/10125/9492

►

Bibliography: leaves [130]-138.

Microfiche.

ix, 138 leaves, bound ill. 29 cm

Four nitrile retinoids were synthesized: 1,1-didemethyl- β-ionylidenacetonitrile; 5,6,7,8,9, 10,11,12-octahydroretinonitrile; 5,6,7,8-tetrahydroretinonitrile; and retinonitrile. These four… (more)

Subjects/Keywords: Photochemistry; Retinonitrile

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APA (6^th Edition):

Fenstemacher, R. J. (2009). Polyene photochemistry : solvent controlled state ordering. (Doctoral Dissertation). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/9492

Chicago Manual of Style (16^th Edition):

Fenstemacher, Roland John. “Polyene photochemistry : solvent controlled state ordering.” 2009. Doctoral Dissertation, University of Hawaii – Manoa. Accessed February 18, 2020. http://hdl.handle.net/10125/9492.

MLA Handbook (7^th Edition):

Fenstemacher, Roland John. “Polyene photochemistry : solvent controlled state ordering.” 2009. Web. 18 Feb 2020.

Vancouver:

Fenstemacher RJ. Polyene photochemistry : solvent controlled state ordering. [Internet] [Doctoral dissertation]. University of Hawaii – Manoa; 2009. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/10125/9492.

Council of Science Editors:

Fenstemacher RJ. Polyene photochemistry : solvent controlled state ordering. [Doctoral Dissertation]. University of Hawaii – Manoa; 2009. Available from: http://hdl.handle.net/10125/9492

University of Hawaii

11. Chen, Rongliang. Synthesis of 7-cis containing 3-dehydroretinal isomers and their binding properties with bovine opsin: Synthesis and properties of a series of lower homologs of β-carotene.

Degree: PhD, 2009, University of Hawaii

URL: http://hdl.handle.net/10125/9525

►

At head of first title: "Part 1"; at head of second title: "Part 2."

Title of second work on added title page: Preparation and properties… (more)

▼

At head of first title: "Part 1"; at head of second title: "Part 2."

Title of second work on added title page: Preparation and properties of a series of lower homologs of β-carotene.

"December 1995."

Typescript.

Microfiche.

167 leaves ill. 28 cm

Part I: A new synthetic route, starting from 3-hydroxy-B-ionone, was developed for the synthesis of hindered 7-cis isomers of 3-dehydroretinal which led to six 7-cis isomers of 3dehydroretinal and four 7-cis isomers of 3-hydroxyretinal. The structures of these isomers were characterized with UV-Vis and 1H-NMR. HyperChem program was used to calculate structural data such as dihedral angels, charge density, total energy of the 3-dehydroretinal isomers and synthetic intermediates to account for the observed UV properties and photochemistry. The 7-cis isomers were found to have a C5-C6-C7-C8 dihedral angel in the range of 60 -70° while the 7-trans isomers have the corresponding dihedral angles in the range of 40-50° . The binding of these new isomers with bovine opsin was investigated. While the 7-cis and 7,9-dicis isomers of 3-dehydroretinal and 3-hydroxyretinal formed pigments with opsin without isomerization, the 7,13-dicis, 7,9, 13-tricis, 7,1l-dicis and 7,9,1l-tricis isomers of 3-dehydroretinal all showed instability in the binding media and isomerized during the binding process. The Spectra Calc software package was employed to analyze the pattern of isomerization and the likely configuration of the chromophore in the pigments formed. 7,13-Dicis and 7,9,13-tricis 3-dehydroretinal have been shown to isomerize to 7cis and 7,9-dicis during the binding process and the newly formed pigments are of 7-cis and 7,9-dicis configuration. The analysis of binding curves of 7,ll-dicis 3-dehydroretinal indicates that two pigments were likely formed during the binding process, one with 7,11dicis configuration, the other with 7-cis configuration. 7,9,1l-Tricis 3-dehydroretinal was shown to form a pigment of the 7,9-dicis configuration. Part II. A series of lower B-carotene homologs (dubbed mini-carotenes) were prepared and their properties and photostationary states were investigated. The cis isomer of the mini-3, lowest member of this series, showed dynamic NMR behavior at much lower temperature than the 7-cis compounds in the retinal series. It also showed thermall,7-H-shift reaction, which was rarely observed in the retinal series. The unusual red-shifted UV absorption of cis-mini-S has been attributed to the secondary orbital overlap in its spiral structure. Photochemistry of both cis-mini-S and trans-mini-S was studied. The cis-trans isomerization was found to be accompanied by other irreversible sigmatropic 1,5-H-shift and electrocyclization reactions to give complex mixtures. Photostationary state of mini-5 consists of about 60% 9-cis isomer and 40% all trans isomers. No7-cis isomers were detected. Preliminary work with mini-7 indicated that it is relatively inactive toward light.

Subjects/Keywords: Isomerization; Photochemistry

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APA (6^th Edition):

Chen, R. (2009). Synthesis of 7-cis containing 3-dehydroretinal isomers and their binding properties with bovine opsin: Synthesis and properties of a series of lower homologs of β-carotene. (Doctoral Dissertation). University of Hawaii. Retrieved from http://hdl.handle.net/10125/9525

Chicago Manual of Style (16^th Edition):

Chen, Rongliang. “Synthesis of 7-cis containing 3-dehydroretinal isomers and their binding properties with bovine opsin: Synthesis and properties of a series of lower homologs of β-carotene.” 2009. Doctoral Dissertation, University of Hawaii. Accessed February 18, 2020. http://hdl.handle.net/10125/9525.

MLA Handbook (7^th Edition):

Chen, Rongliang. “Synthesis of 7-cis containing 3-dehydroretinal isomers and their binding properties with bovine opsin: Synthesis and properties of a series of lower homologs of β-carotene.” 2009. Web. 18 Feb 2020.

Vancouver:

Chen R. Synthesis of 7-cis containing 3-dehydroretinal isomers and their binding properties with bovine opsin: Synthesis and properties of a series of lower homologs of β-carotene. [Internet] [Doctoral dissertation]. University of Hawaii; 2009. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/10125/9525.

Council of Science Editors:

Chen R. Synthesis of 7-cis containing 3-dehydroretinal isomers and their binding properties with bovine opsin: Synthesis and properties of a series of lower homologs of β-carotene. [Doctoral Dissertation]. University of Hawaii; 2009. Available from: http://hdl.handle.net/10125/9525

University of Victoria

12. Zhou, Xiaobing. Phosphinoorganosilane synthesis and Bis(phosphinoorgano)silyl complexes of ruthenium.

Degree: Department of Chemistry, 2017, University of Victoria

URL: https://dspace.library.uvic.ca//handle/1828/8451

► Hydrozirconation and subsequent phosphination have been developed into a versatile synthetic methodology leading to formation of phosphorus-carbon bonds. A family of phosphinoalkylsilane ligand precursors SiHMen(CH₂CH₂CH₂PPh₂)₃₋n… (more)

▼ Hydrozirconation and subsequent phosphination have been developed into a versatile synthetic methodology leading to formation of phosphorus-carbon bonds. A family of phosphinoalkylsilane ligand precursors SiHMen(CH₂CH₂CH₂PPh₂)₃₋n (ChelH, I: n = 2; biPSiH, II: n = 1; triPSiH, III: n = 0) previously prepared via a photo-chemical route were synthesized in this way and the phosphination step has been shown to be dependent on steric factors. Similar methods have been used to obtain a group of new ligand precursors, the poly(silaalkyl)phosphines PPhn(CH₂CH₂CH₂PR₂)₃₋n (12: n = 1; 13: n = 0), which have been isolated and fully characterized. Analogues PPhn(o-C₆H₄SiMe₂H)₃₋n (21 : n = 1; 22: n = 0) containing more rigid benzylic backbones have been prepared from the corresponding (o-tolyl)phosphines via polylithiation and shown to exhibit temperature dependent NMR behavior. Poly(silaalkyl)phosphine coordination chemistry has been explored, yielding an unprecedented trans-bis(silyl) Pt(II) complex Pt[PhP(o-C₆H₄CH₂SiMe₂)₂]PPh₃ (25 ) which was isolated and characterized by using spectroscopic methods. The chemistry of [bis(diphenylphosphinopropyl)silyl] hydrido dicarbonyl ruthenium(II), RuH (biPSi)(CO)₂ (26), has been investigated in detail. The two diastereomers, syn and anti, were observed to exchange slowly with the two CO groups also scrambling at a comparable rate. A kinetic study of these two intramolecular isomerization processes suggests the involvement of dissociation and re-association of the chelate (biPSi) phosphines. Oxygen atom insertion into the Ru-Si bond of 26 occurs both in a hydrolysis process and direct oxidation by dioxygen. A labeling experiment suggests the former may involve a molecular dihydrogen intermediate, while the latter leads to insertion of oxygen atoms into both Ru-Si and Si-C bonds. Chlorination of 26 and subsequent thermal loss of a CO group afforded a novel l6e five coordinate Ru(II) species RuCl(biPSi)(CO) (42). Reaction of 42 with NaBH₄ or LiAlH₄ gave a mononuclear borohydride complex Ru(biPSi)(CO)(μ-η²-H₂BH₂) (43) or a rare hydrido anionic complex [fac-Ru(H)₂biPSi)(CO)]⁻ (44), both of which are extremely sensitive and have been identified in situ by using solution NMR spectroscopy. The silyl group in 26 was found to exert a stronger trans effect than hydride. Advisors/Committee Members: Stobart, Stephen R. (supervisor).

Subjects/Keywords: Phosphorus; Photochemistry

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APA (6^th Edition):

Zhou, X. (2017). Phosphinoorganosilane synthesis and Bis(phosphinoorgano)silyl complexes of ruthenium. (Thesis). University of Victoria. Retrieved from https://dspace.library.uvic.ca//handle/1828/8451

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Zhou, Xiaobing. “Phosphinoorganosilane synthesis and Bis(phosphinoorgano)silyl complexes of ruthenium.” 2017. Thesis, University of Victoria. Accessed February 18, 2020. https://dspace.library.uvic.ca//handle/1828/8451.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Zhou, Xiaobing. “Phosphinoorganosilane synthesis and Bis(phosphinoorgano)silyl complexes of ruthenium.” 2017. Web. 18 Feb 2020.

Vancouver:

Zhou X. Phosphinoorganosilane synthesis and Bis(phosphinoorgano)silyl complexes of ruthenium. [Internet] [Thesis]. University of Victoria; 2017. [cited 2020 Feb 18]. Available from: https://dspace.library.uvic.ca//handle/1828/8451.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zhou X. Phosphinoorganosilane synthesis and Bis(phosphinoorgano)silyl complexes of ruthenium. [Thesis]. University of Victoria; 2017. Available from: https://dspace.library.uvic.ca//handle/1828/8451

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Victoria

13. Shukla, Deepak. Exploratory studies and chemistry of photogenerated carbanions and carbocations from dibenzannelated systems.

Degree: Department of Chemistry, 2018, University of Victoria

URL: https://dspace.library.uvic.ca//handle/1828/9678

► Photochemical reactivity of several dibenzannelated systems has been investigated to demonstrate that the driving force inherent in many of their reactions is the attainment of… (more)

▼ Photochemical reactivity of several dibenzannelated systems has been investigated to demonstrate that the driving force inherent in many of their reactions is the attainment of a 4n π-electron system or intermediate in S1. It has been shown that the inherent driving force for the benzylic C-H bond ionization in 9H-xanthene (125) and 9H-thioxanthene (136) is the formation of 8π-electron cyclically conjugated carbanion intermediates 130 and 137, respectively, in S1. Formation of deuterium incorporated products when 125 and 136 are photolyzed in NaOD-EtOD solutions and protium incorporation in products when photolysis of 123 and 134 is carried out in NaOH-EtOH is consistent with the intermediacy of carbanions in these reactions. Fluorescence quenching of 123 and 125 by ethanolamine in CH3CN gave linear Stern-Volmer plots, with kq = (2.16 ± 0.05) x [special characters omitted] for 125 and (1.12 ± 0.05) x [special characters omitted] for 123, which corresponds to an isotope effect for quenching by ethanolamine, of [special characters omitted] = 1.92 ± 0.04. Enhanced stability of 8π carbanions in S1 is further evidenced in the photodecarboxylation of xanthene-9-carboxylic acids (142 and 145) and thioxanthene-9-carboxylic acids (147 and 148) in aqueous solution. The intermediacy of carbanions has been demonstrated in the product studies carried out in 80% [special characters omitted] solution. A mechanism has been proposed which involves heterolytic bond cleavage of the carboxylate ion in S1 to give intermediate carbanions. Additional support for the excited state stability of 4n systems comes from the studies of 155. Photoexcitation of bent 155 results in its planarization to give planar 155 in S1. The driving force for this change of conformation of 155 is believed to be the attainment of a conjugated 8π-electron internal cyclic array in S1. Photolysis of substituted suberenes in aqueous [special characters omitted] results in benzylic C-H bond cleavage in these systems in S1 the efficiency of which is greatly affected by the nature of substituent present. Results obtained in this study are consistent with benzylic C-H bond cleavage, with H2C acting as the base, to give intermediate carbanions in S1. Quantum yields of exchange in [special characters omitted] (L = H or D) and in a variety of other solvent mixtures have been measured. The photochemistry of xanthenium (99 and 114) and thioxanthenium (219) cations has been studied in aqueous [special characters omitted] in the presence of di- and trimethoxybenzenes. It has been shown that the primary photochemical step is electron transfer from methoxybenzenes to singlet excited 99 and 114. The radical intermediates thus generated subsequently react with 02 to give peroxy compounds as final products. These and other results of the photochemistry of dibenzannelated systems show that there is much interesting photochemistry to be discovered in these molecules. Advisors/Committee Members: Wan, Peter (supervisor).

Subjects/Keywords: Carbanions; Photochemistry

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APA (6^th Edition):

Shukla, D. (2018). Exploratory studies and chemistry of photogenerated carbanions and carbocations from dibenzannelated systems. (Thesis). University of Victoria. Retrieved from https://dspace.library.uvic.ca//handle/1828/9678

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Shukla, Deepak. “Exploratory studies and chemistry of photogenerated carbanions and carbocations from dibenzannelated systems.” 2018. Thesis, University of Victoria. Accessed February 18, 2020. https://dspace.library.uvic.ca//handle/1828/9678.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Shukla, Deepak. “Exploratory studies and chemistry of photogenerated carbanions and carbocations from dibenzannelated systems.” 2018. Web. 18 Feb 2020.

Vancouver:

Shukla D. Exploratory studies and chemistry of photogenerated carbanions and carbocations from dibenzannelated systems. [Internet] [Thesis]. University of Victoria; 2018. [cited 2020 Feb 18]. Available from: https://dspace.library.uvic.ca//handle/1828/9678.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Shukla D. Exploratory studies and chemistry of photogenerated carbanions and carbocations from dibenzannelated systems. [Thesis]. University of Victoria; 2018. Available from: https://dspace.library.uvic.ca//handle/1828/9678

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Montana State University

14. Pagenkopf, Brian L. Substrate and reagent control of diastereoselectivity in transition metal mediated processes : development of a catalytic photopromoted Pauson-Khand reaction.

Degree: College of Letters & Science, 1996, Montana State University

URL: https://scholarworks.montana.edu/xmlui/handle/1/7445

Subjects/Keywords: Photochemistry.

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APA (6^th Edition):

Pagenkopf, B. L. (1996). Substrate and reagent control of diastereoselectivity in transition metal mediated processes : development of a catalytic photopromoted Pauson-Khand reaction. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/7445

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Pagenkopf, Brian L. “Substrate and reagent control of diastereoselectivity in transition metal mediated processes : development of a catalytic photopromoted Pauson-Khand reaction.” 1996. Thesis, Montana State University. Accessed February 18, 2020. https://scholarworks.montana.edu/xmlui/handle/1/7445.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Pagenkopf, Brian L. “Substrate and reagent control of diastereoselectivity in transition metal mediated processes : development of a catalytic photopromoted Pauson-Khand reaction.” 1996. Web. 18 Feb 2020.

Vancouver:

Pagenkopf BL. Substrate and reagent control of diastereoselectivity in transition metal mediated processes : development of a catalytic photopromoted Pauson-Khand reaction. [Internet] [Thesis]. Montana State University; 1996. [cited 2020 Feb 18]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/7445.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Pagenkopf BL. Substrate and reagent control of diastereoselectivity in transition metal mediated processes : development of a catalytic photopromoted Pauson-Khand reaction. [Thesis]. Montana State University; 1996. Available from: https://scholarworks.montana.edu/xmlui/handle/1/7445

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Victoria

15. Diao, Li. Photogeneration and chemistry of quinone methides from hydroxybenzyl alcohols.

Degree: Department of Chemistry, 2017, University of Victoria

URL: https://dspace.library.uvic.ca//handle/1828/8729

► The photosolvolysis of a series of hydroxy-substituted benzyl alcohols (ArCH₂OH) has been studied. Photomethanolysis of these alcohols showed exceptionally higher efficiencies for methyl ether formation… (more)

▼ The photosolvolysis of a series of hydroxy-substituted benzyl alcohols (ArCH₂OH) has been studied. Photomethanolysis of these alcohols showed exceptionally higher efficiencies for methyl ether formation (in 1:1 H₂O-MeOH) than the corresponding methoxybenzyl alcohols. UV-Vis absorption spectra of photogenerated transients were recorded in aqueous solution and had similar appearance to the carbocations that are observable from the methoxybenzyl alcohols, but with much longer lifetimes. These transients were also observable in neat organic solution for the ortho isomers. The yields of all these transients increased with increasing water content. The highest yields were observed in basic aqueous solution when pH > pKₐ(S₀) (of the phenol moiety). In addition, photolysis of the appropriate coumaranones gave the same transient absorption as that from the corresponding o-hydroxybenzyl alcohols. Since photolysis of coumaranones are known to give o-quinone methide, (o-QM) intermediates (via loss of CO), the transients observed for the o-hydroxybenzyl alcohols are assigned to o-QMs. The transients observed for the m and p-isomers are assigned to the corresponding m and p-QMs. The quantum efficiencies for QMs generation from hydroxybenzyl alcohols are in the order as o > m >> p, in agreement with Zimmerman's orthoctivation theory. The mechanism proposed at pH < pKₐ(S₀) involves adiabatic deprotonation of the ArOH moiety in the first excited singlet state (S₁) followed by heterolytic cleavage of the C-O bond of the hydroxymethyl group. In basic media, direct excitation of the phenolate ion results in the loss of hydroxide ion to generate QMs. Subsequent nucleophilic trapping of these QMs by solvent results in the observed solvolysis product. o-QMs were also generated in neat organic solution. The proposed mechanism involves adiabatic deprotonation of phenol moiety facilitated by either intermolecular or intramolecular hydrogen bonding with a benzylic OH group. This Thesis has demonstrated that a simple and general method is available for the photogeneration of all the QM isomers. Notably, the method is applicable to m-QMs, which have previously required more elaborate methods for their generation. A polymerization reaction of m-QMs has been discovered in basic media during investigations of their chemistry. Advisors/Committee Members: Wan, Peter (supervisor).

Subjects/Keywords: Quinone; Photochemistry

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APA (6^th Edition):

Diao, L. (2017). Photogeneration and chemistry of quinone methides from hydroxybenzyl alcohols. (Thesis). University of Victoria. Retrieved from https://dspace.library.uvic.ca//handle/1828/8729

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Diao, Li. “Photogeneration and chemistry of quinone methides from hydroxybenzyl alcohols.” 2017. Thesis, University of Victoria. Accessed February 18, 2020. https://dspace.library.uvic.ca//handle/1828/8729.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Diao, Li. “Photogeneration and chemistry of quinone methides from hydroxybenzyl alcohols.” 2017. Web. 18 Feb 2020.

Vancouver:

Diao L. Photogeneration and chemistry of quinone methides from hydroxybenzyl alcohols. [Internet] [Thesis]. University of Victoria; 2017. [cited 2020 Feb 18]. Available from: https://dspace.library.uvic.ca//handle/1828/8729.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Diao L. Photogeneration and chemistry of quinone methides from hydroxybenzyl alcohols. [Thesis]. University of Victoria; 2017. Available from: https://dspace.library.uvic.ca//handle/1828/8729

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

16. Ruiji Li. Highly Photosensitive 6π-Electrocyclization and Self-Contained Photoacid Generators Based on Terarylene Backbone : ターアリーレン誘導体における高感度6π-電子環状反応と自己完結型光酸発生剤の開発; ターアリーレンユウドウタイニオケルコウカンド 6π デンシカンジョウハンノウトジコカンケツガタコウサンハッセイザイノカイハツ.

Degree: 博士（工学）, 2017, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

URL: http://hdl.handle.net/10061/11709

Subjects/Keywords: photochemistry

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APA (6^th Edition):

Li, R. (2017). Highly Photosensitive 6π-Electrocyclization and Self-Contained Photoacid Generators Based on Terarylene Backbone : ターアリーレン誘導体における高感度6π-電子環状反応と自己完結型光酸発生剤の開発; ターアリーレンユウドウタイニオケルコウカンド 6π デンシカンジョウハンノウトジコカンケツガタコウサンハッセイザイノカイハツ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/11709

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Li, Ruiji. “Highly Photosensitive 6π-Electrocyclization and Self-Contained Photoacid Generators Based on Terarylene Backbone : ターアリーレン誘導体における高感度6π-電子環状反応と自己完結型光酸発生剤の開発; ターアリーレンユウドウタイニオケルコウカンド 6π デンシカンジョウハンノウトジコカンケツガタコウサンハッセイザイノカイハツ.” 2017. Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed February 18, 2020. http://hdl.handle.net/10061/11709.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Li, Ruiji. “Highly Photosensitive 6π-Electrocyclization and Self-Contained Photoacid Generators Based on Terarylene Backbone : ターアリーレン誘導体における高感度6π-電子環状反応と自己完結型光酸発生剤の開発; ターアリーレンユウドウタイニオケルコウカンド 6π デンシカンジョウハンノウトジコカンケツガタコウサンハッセイザイノカイハツ.” 2017. Web. 18 Feb 2020.

Vancouver:

Li R. Highly Photosensitive 6π-Electrocyclization and Self-Contained Photoacid Generators Based on Terarylene Backbone : ターアリーレン誘導体における高感度6π-電子環状反応と自己完結型光酸発生剤の開発; ターアリーレンユウドウタイニオケルコウカンド 6π デンシカンジョウハンノウトジコカンケツガタコウサンハッセイザイノカイハツ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; 2017. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/10061/11709.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Li R. Highly Photosensitive 6π-Electrocyclization and Self-Contained Photoacid Generators Based on Terarylene Backbone : ターアリーレン誘導体における高感度6π-電子環状反応と自己完結型光酸発生剤の開発; ターアリーレンユウドウタイニオケルコウカンド 6π デンシカンジョウハンノウトジコカンケツガタコウサンハッセイザイノカイハツ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; 2017. Available from: http://hdl.handle.net/10061/11709

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

17. Powers, Leanne. Probing the photochemical reactivity of oceanic dissolved organic carbon.

Degree: PhD, Marine Sciences, 2014, University of Georgia

URL: http://purl.galileo.usg.edu/uga_etd/powers_leanne_201412_phd

► After 20 years of research in aquatic photochemistry, there remains a need to identify and constrain many photochemical reactions involving colored dissolved organic matter (CDOM).… (more)

▼ After 20 years of research in aquatic photochemistry, there remains a need to identify and constrain many photochemical reactions involving colored dissolved organic matter (CDOM). This thesis uses laboratory and field studies in diverse marine systems to examine the photochemical efficiency and reaction rates for carbon monoxide (CO), carbon dioxide (CO2), superoxide (O2-) and hydrogen peroxide (H2O2), all important photoproducts, and improves quantitative understanding of photochemistry’s significance in biogeochemical cycles. Input of these results to ocean color-based models allowed estimation of photochemical rates on regional and global scales. Direct photo-oxidation of dissolved organic carbon (DOC) to CO2 and CO is a significant, albeit poorly constrained, DOC removal mechanism. Working in the Northern Gulf of Mexico, we amassed the largest cohesive CO apparent quantum yield (AQY) data set for any marine region (n=99; 18 paired with CO2), defining distinct inshore and offshore AQY spectra for improved regional photochemical rate models. Analytical limitations for determining CO2 AQY spectra forced the use of ill-defined coastal CO2:CO ratios (~6 − 66) for blue water CO2 calculations, highlighting the need for new direct methods or better proxies to quantify CO2 photochemistry in marine waters. Significant photochemical removal of biologically refractory DOC (RDOC), well-mixed in the ocean but isolated at depth, is not compatible with its 14C age. Reevaluation of RDOC photochemical reactivity using paired O2- and H2O2 photoproduction studies for abyssal Gulf of Alaska samples showed declining O2- steady-state concentrations during long-term exposure, with little or no H2O2 accumulation past ~6 − 12 hours. This is consistent with a loss of O2- source, a shift to oxidative pathways for O2 decay, and a lack of long-term photochemical reactivity for RDOC. Because H2O2 formation is a thermal reaction involving O¬2-, blending remotely sensed sea surface temperature and color allowed correction of H2O2 AQY spectra and production of the first global H¬2O2 and O2 photoproduction rate maps from remotely sensed data. Further analysis of paired H2O2 and CO2 photoproduction experiments indicated that H2O2 is a far better proxy for CO2 photoproduction than CO (CO2:H2O2 ratio = 6.89 ± 1.64), and will lead to constrained estimates for global CO2 photochemical fluxes. Advisors/Committee Members: William L. Miller.

Subjects/Keywords: Photochemistry

…1 1.1 CDOM and Marine Photochemistry… …1 1.2 Photochemistry and Coastal Carbon Cycling ........................................ 8… …1.3 Photochemistry as a Sink for Marine Dissolved Organic Carbon ....... 11 1.4… …CHALLENGES FOR QUANTIFYING THE IMPACT OF PHOTOCHEMISTRY ON CARBON CYCLES… …282 xii CHAPTER 1 INTRODUCTION AND LITERATURE REVIEW 1.1 CDOM and Marine Photochemistry…

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APA (6^th Edition):

Powers, L. (2014). Probing the photochemical reactivity of oceanic dissolved organic carbon. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/powers_leanne_201412_phd

Chicago Manual of Style (16^th Edition):

Powers, Leanne. “Probing the photochemical reactivity of oceanic dissolved organic carbon.” 2014. Doctoral Dissertation, University of Georgia. Accessed February 18, 2020. http://purl.galileo.usg.edu/uga_etd/powers_leanne_201412_phd.

MLA Handbook (7^th Edition):

Powers, Leanne. “Probing the photochemical reactivity of oceanic dissolved organic carbon.” 2014. Web. 18 Feb 2020.

Vancouver:

Powers L. Probing the photochemical reactivity of oceanic dissolved organic carbon. [Internet] [Doctoral dissertation]. University of Georgia; 2014. [cited 2020 Feb 18]. Available from: http://purl.galileo.usg.edu/uga_etd/powers_leanne_201412_phd.

Council of Science Editors:

Powers L. Probing the photochemical reactivity of oceanic dissolved organic carbon. [Doctoral Dissertation]. University of Georgia; 2014. Available from: http://purl.galileo.usg.edu/uga_etd/powers_leanne_201412_phd

University of British Columbia

18. Morse, Robert Donald. Flash photolysis of NO2 and SO2.

Degree: 1969, University of British Columbia

URL: http://hdl.handle.net/2429/34722

► Vibrationally excited oxygen with up to 15 quanta of energy has been produced in the flash photolysis of NO₂ . When the NO₂ was selectively… (more)

▼ Vibrationally excited oxygen with up to 15 quanta of energy has been produced in the flash photolysis of NO₂ . When the NO₂ was selectively photolysed such that only radiation below 4000 A° was admitted to the reaction vessel the highest level observed was reduced to v" = 11 which in terms of vibrational energy corresponds to the exothermicity of the reaction O + NO₂ —> NO + O₂ Relative population ratios for the successive vibrational levels v" = 6 to 11 were calculated for both the filtered and unfiltered photolysis of NO₂ using two independently calculated arrays of Franck-Condon Factors. In both cases the ratios showed that the population distribution was definitely non Boltzmann. in that the levels were almost equally populated. The distribution for the unfiltered experiments gave a pronounced dip at v" =11 indicating that the levels 12 ≤ v" ≤ 15 are formed by a second reaction. This reaction has been shown to be Q+ NO*₂—> O*₂ v" ≥12 +NO where the NO₂ is probably electronically excited. The adiabatic flash photolysis of both NO₂ and SO₂ has been investigated. These spectra show weakening of their banded structure up to 100 microseconds after the flash and then gradual strengthening until back to normal by 10 milliseconds. This effect is well known for SO₂ and has been postulated to be the result of the formation of a high temperature isomer of SO₂. Subsequently the postulated isomer had a transient spectrum in the vacuum ultraviolet assigned to it. We have found that the weakening of both the NO₂ and SO₂ banded structure is the result of temperature broadening. The spectrum assigned to the SO₂ isomer has been extended. It has also been produced from the flash photolysis of SO₂ under isothermal conditions showing that its assignment to a high temperature isomer is incorrect. From kinetic data this spectrum in the 1800 A° region and another the 1400 A° region has been tentatively identified as two triplet systems of SO.

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Morse, R. D. (1969). Flash photolysis of NO2 and SO2. (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/34722

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Morse, Robert Donald. “Flash photolysis of NO2 and SO2. ” 1969. Thesis, University of British Columbia. Accessed February 18, 2020. http://hdl.handle.net/2429/34722.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Morse, Robert Donald. “Flash photolysis of NO2 and SO2. ” 1969. Web. 18 Feb 2020.

Vancouver:

Morse RD. Flash photolysis of NO2 and SO2. [Internet] [Thesis]. University of British Columbia; 1969. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/2429/34722.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Morse RD. Flash photolysis of NO2 and SO2. [Thesis]. University of British Columbia; 1969. Available from: http://hdl.handle.net/2429/34722

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of British Columbia

19. Lungle, Melvin Leroy. Photochemistry of cis, cis-cyclodeca-3,8-diene-1,6-dione .

Degree: 1969, University of British Columbia

URL: http://hdl.handle.net/2429/35072

► In order to extend the study of medium-sized ring compounds, cis,cis-cyclodeca-3,8-diene-l,6-dione was synthesized by known methods and photolyzed. By monitoring the photolysis by glpc and… (more)

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Lungle, M. L. (1969). Photochemistry of cis, cis-cyclodeca-3,8-diene-1,6-dione . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/35072

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Lungle, Melvin Leroy. “Photochemistry of cis, cis-cyclodeca-3,8-diene-1,6-dione .” 1969. Thesis, University of British Columbia. Accessed February 18, 2020. http://hdl.handle.net/2429/35072.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Lungle, Melvin Leroy. “Photochemistry of cis, cis-cyclodeca-3,8-diene-1,6-dione .” 1969. Web. 18 Feb 2020.

Vancouver:

Lungle ML. Photochemistry of cis, cis-cyclodeca-3,8-diene-1,6-dione . [Internet] [Thesis]. University of British Columbia; 1969. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/2429/35072.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lungle ML. Photochemistry of cis, cis-cyclodeca-3,8-diene-1,6-dione . [Thesis]. University of British Columbia; 1969. Available from: http://hdl.handle.net/2429/35072

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Oregon State University

20. Castle, Karen J. Photochemistry of molecules oriented with a uniform electric field.

Degree: PhD, Chemistry, 2000, Oregon State University

URL: http://hdl.handle.net/1957/33351

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Castle, K. J. (2000). Photochemistry of molecules oriented with a uniform electric field. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/33351

Chicago Manual of Style (16^th Edition):

Castle, Karen J. “Photochemistry of molecules oriented with a uniform electric field.” 2000. Doctoral Dissertation, Oregon State University. Accessed February 18, 2020. http://hdl.handle.net/1957/33351.

MLA Handbook (7^th Edition):

Castle, Karen J. “Photochemistry of molecules oriented with a uniform electric field.” 2000. Web. 18 Feb 2020.

Vancouver:

Castle KJ. Photochemistry of molecules oriented with a uniform electric field. [Internet] [Doctoral dissertation]. Oregon State University; 2000. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1957/33351.

Council of Science Editors:

Castle KJ. Photochemistry of molecules oriented with a uniform electric field. [Doctoral Dissertation]. Oregon State University; 2000. Available from: http://hdl.handle.net/1957/33351

Oregon State University

21. Murray, John Sutherland. Transient optical absorptivity of nitrogen dioxide following pulsed illumination.

Degree: MS, Physics, 1966, Oregon State University

URL: http://hdl.handle.net/1957/47816

► A knowledge of the time rates for intermediate reactions during the photolysis of nitrogen dioxide enables one to deduce the possible intermediate reactions which are… (more)

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Murray, J. S. (1966). Transient optical absorptivity of nitrogen dioxide following pulsed illumination. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/47816

Chicago Manual of Style (16^th Edition):

Murray, John Sutherland. “Transient optical absorptivity of nitrogen dioxide following pulsed illumination.” 1966. Masters Thesis, Oregon State University. Accessed February 18, 2020. http://hdl.handle.net/1957/47816.

MLA Handbook (7^th Edition):

Murray, John Sutherland. “Transient optical absorptivity of nitrogen dioxide following pulsed illumination.” 1966. Web. 18 Feb 2020.

Vancouver:

Murray JS. Transient optical absorptivity of nitrogen dioxide following pulsed illumination. [Internet] [Masters thesis]. Oregon State University; 1966. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1957/47816.

Council of Science Editors:

Murray JS. Transient optical absorptivity of nitrogen dioxide following pulsed illumination. [Masters Thesis]. Oregon State University; 1966. Available from: http://hdl.handle.net/1957/47816

Oregon State University

22. McRitchie, Donna Louise. The photodecomposition of t-butyl bicyclo [7.1.0] decane-2-percarboxylate.

Degree: MS, Chemistry, 1972, Oregon State University

URL: http://hdl.handle.net/1957/45302

► This paper describes the synthesis of t-butyl bicyclo[7.1.0] decane-2-percarboxylate and its photolytic decomposition. The title compound was found to undergo simple homolytic cleavage when exposed… (more)

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

McRitchie, D. L. (1972). The photodecomposition of t-butyl bicyclo [7.1.0] decane-2-percarboxylate. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/45302

Chicago Manual of Style (16^th Edition):

McRitchie, Donna Louise. “The photodecomposition of t-butyl bicyclo [7.1.0] decane-2-percarboxylate.” 1972. Masters Thesis, Oregon State University. Accessed February 18, 2020. http://hdl.handle.net/1957/45302.

MLA Handbook (7^th Edition):

McRitchie, Donna Louise. “The photodecomposition of t-butyl bicyclo [7.1.0] decane-2-percarboxylate.” 1972. Web. 18 Feb 2020.

Vancouver:

McRitchie DL. The photodecomposition of t-butyl bicyclo [7.1.0] decane-2-percarboxylate. [Internet] [Masters thesis]. Oregon State University; 1972. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1957/45302.

Council of Science Editors:

McRitchie DL. The photodecomposition of t-butyl bicyclo [7.1.0] decane-2-percarboxylate. [Masters Thesis]. Oregon State University; 1972. Available from: http://hdl.handle.net/1957/45302

Oregon State University

23. Lee, Youn-Sik. The photochemistry of polychlorobenzenes in micellar media.

Degree: MS, Chemistry, 1987, Oregon State University

URL: http://hdl.handle.net/1957/40026

► Photolysis of pentachlorobenzene was carried out in the absence of an electron donor species at 254 nm in cetyltrimethylammonium bromide surfactant solution. The results are… (more)

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Lee, Y. (1987). The photochemistry of polychlorobenzenes in micellar media. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/40026

Chicago Manual of Style (16^th Edition):

Lee, Youn-Sik. “The photochemistry of polychlorobenzenes in micellar media.” 1987. Masters Thesis, Oregon State University. Accessed February 18, 2020. http://hdl.handle.net/1957/40026.

MLA Handbook (7^th Edition):

Lee, Youn-Sik. “The photochemistry of polychlorobenzenes in micellar media.” 1987. Web. 18 Feb 2020.

Vancouver:

Lee Y. The photochemistry of polychlorobenzenes in micellar media. [Internet] [Masters thesis]. Oregon State University; 1987. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1957/40026.

Council of Science Editors:

Lee Y. The photochemistry of polychlorobenzenes in micellar media. [Masters Thesis]. Oregon State University; 1987. Available from: http://hdl.handle.net/1957/40026

University of Arizona

24. Stout, Edward Irvin, 1939-. Photolysis of some carbohydrate dithiobis (thioformates) .

Degree: 1973, University of Arizona

URL: http://hdl.handle.net/10150/565281

Subjects/Keywords: Photochemistry.

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APA (6^th Edition):

Stout, Edward Irvin, 1. (1973). Photolysis of some carbohydrate dithiobis (thioformates) . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/565281

Chicago Manual of Style (16^th Edition):

Stout, Edward Irvin, 1939-. “Photolysis of some carbohydrate dithiobis (thioformates) .” 1973. Doctoral Dissertation, University of Arizona. Accessed February 18, 2020. http://hdl.handle.net/10150/565281.

MLA Handbook (7^th Edition):

Stout, Edward Irvin, 1939-. “Photolysis of some carbohydrate dithiobis (thioformates) .” 1973. Web. 18 Feb 2020.

Vancouver:

Stout, Edward Irvin 1. Photolysis of some carbohydrate dithiobis (thioformates) . [Internet] [Doctoral dissertation]. University of Arizona; 1973. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/10150/565281.

Council of Science Editors:

Stout, Edward Irvin 1. Photolysis of some carbohydrate dithiobis (thioformates) . [Doctoral Dissertation]. University of Arizona; 1973. Available from: http://hdl.handle.net/10150/565281

Simon Fraser University

25. Lee, Antonio Chun Hung. Photolyses of N-nitrosamides in acidic and neutral media.

Degree: 1967, Simon Fraser University

URL: http://summit.sfu.ca/item/618

► Photolyses of several N-nitrosamides in acidic and neutral media were studied. The photochemical decomposition of II-nitrosanides was found to involve exclusively nitrogen-nitrogen bond cleavage of… (more)

Subjects/Keywords: Photochemistry.

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APA (6^th Edition):

Lee, A. C. H. (1967). Photolyses of N-nitrosamides in acidic and neutral media. (Thesis). Simon Fraser University. Retrieved from http://summit.sfu.ca/item/618

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Lee, Antonio Chun Hung. “Photolyses of N-nitrosamides in acidic and neutral media.” 1967. Thesis, Simon Fraser University. Accessed February 18, 2020. http://summit.sfu.ca/item/618.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Lee, Antonio Chun Hung. “Photolyses of N-nitrosamides in acidic and neutral media.” 1967. Web. 18 Feb 2020.

Vancouver:

Lee ACH. Photolyses of N-nitrosamides in acidic and neutral media. [Internet] [Thesis]. Simon Fraser University; 1967. [cited 2020 Feb 18]. Available from: http://summit.sfu.ca/item/618.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lee ACH. Photolyses of N-nitrosamides in acidic and neutral media. [Thesis]. Simon Fraser University; 1967. Available from: http://summit.sfu.ca/item/618

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of British Columbia

26. Doering, Juergen Gerhard Walter. The photolysis of potassium cobaltioxalate in dilute acid solution .

Degree: 1961, University of British Columbia

URL: http://hdl.handle.net/2429/40088

► A new sensitive spectrophotometric method for the direct determination of Co²⁺ ion in the presence of excess Co(III) was developed. Using this method the primary… (more)

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Doering, J. G. W. (1961). The photolysis of potassium cobaltioxalate in dilute acid solution . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/40088

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Doering, Juergen Gerhard Walter. “The photolysis of potassium cobaltioxalate in dilute acid solution .” 1961. Thesis, University of British Columbia. Accessed February 18, 2020. http://hdl.handle.net/2429/40088.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Doering, Juergen Gerhard Walter. “The photolysis of potassium cobaltioxalate in dilute acid solution .” 1961. Web. 18 Feb 2020.

Vancouver:

Doering JGW. The photolysis of potassium cobaltioxalate in dilute acid solution . [Internet] [Thesis]. University of British Columbia; 1961. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/2429/40088.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Doering JGW. The photolysis of potassium cobaltioxalate in dilute acid solution . [Thesis]. University of British Columbia; 1961. Available from: http://hdl.handle.net/2429/40088

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of British Columbia

27. Connelly, Barry Thomas. Photolyses of ketene at 3130 A and 3340 A .

Degree: 1958, University of British Columbia

URL: http://hdl.handle.net/2429/40150

► Previous research on the photolyses of ketene at 2700 A and 3650 A has shown that considerably different mechanisms are necessary to explain the experimental… (more)

▼ Previous research on the photolyses of ketene at 2700 A and 3650 A has shown that considerably different mechanisms are necessary to explain the experimental results. Exactly how the process of deactivation of the excited ketene molecule was affected by change in wavelength was not fully understood. It was felt that investigations of the primary quantum yields at intermediate wavelengths would be fruitful in obtaining a better understanding of the variation of reaction mechanism with wavelength. At 2700 A, using pure ketene, the only primary process is dissociation and therefore the primary quantum yield is unity, while at 3650 A dissociation occurs by way of an excited state which has a finite lifetime during which the excited ketene molecule may undergo collisional deactivation and internal conversion. At 3650 A therefore the primary quantum yield is much less than unity even at low pressure, and decreases with increasing pressure. This research has shown that in the case of ketene at 3130 A the primary quantum yield is approximately unity at low pressures, 20 mm., and decreases to 0.6 at one atmosphere. At 3340 A the primary quantum yield is approximately 0.7 at 26 mm. and 0.2 at 400 mm. and increases with increasing temperature. The dependence of primary quantum yield on pressure at 3130 A and 3340 A was anticipated and can be explained by almost the same mechanism as that proposed for 3650 A radiation. The amount of radiation absorbed during each run was very accurately measured and it was therefore possible to determine quantum yields to within ± 2% at 3130 A, and within ± 10% at 3340 A. For the photolysis at 3650 A the ratios of the rate constants of collisional deactivation and product formation and of internal conversion and product formation at 26° C are 4.6 x 10⁴ litres/mole and 28 respectively. At 3130 A and 37°C this research has shown these ratios to be 16.8 litres/mole and zero respectively, while at 3340 A the ratios are 1.64 x 10² litres/mole and 0.25 at 37°C and 0.99 x 10² and 0.1 at 100°C.

Subjects/Keywords: Photochemistry

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APA (6^th Edition):

Connelly, B. T. (1958). Photolyses of ketene at 3130 A and 3340 A . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/40150

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Connelly, Barry Thomas. “Photolyses of ketene at 3130 A and 3340 A .” 1958. Thesis, University of British Columbia. Accessed February 18, 2020. http://hdl.handle.net/2429/40150.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Connelly, Barry Thomas. “Photolyses of ketene at 3130 A and 3340 A .” 1958. Web. 18 Feb 2020.

Vancouver:

Connelly BT. Photolyses of ketene at 3130 A and 3340 A . [Internet] [Thesis]. University of British Columbia; 1958. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/2429/40150.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Connelly BT. Photolyses of ketene at 3130 A and 3340 A . [Thesis]. University of British Columbia; 1958. Available from: http://hdl.handle.net/2429/40150

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Simon Fraser University

28. Chang, David Wen-lung. A study of N-nitrosamine photoaddition. – .

Degree: 1970, Simon Fraser University

URL: http://summit.sfu.ca/item/4258

Subjects/Keywords: Photochemistry.

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APA (6^th Edition):

Chang, D. W. (1970). A study of N-nitrosamine photoaddition. – . (Thesis). Simon Fraser University. Retrieved from http://summit.sfu.ca/item/4258

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Chang, David Wen-lung. “A study of N-nitrosamine photoaddition. – .” 1970. Thesis, Simon Fraser University. Accessed February 18, 2020. http://summit.sfu.ca/item/4258.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Chang, David Wen-lung. “A study of N-nitrosamine photoaddition. – .” 1970. Web. 18 Feb 2020.

Vancouver:

Chang DW. A study of N-nitrosamine photoaddition. – . [Internet] [Thesis]. Simon Fraser University; 1970. [cited 2020 Feb 18]. Available from: http://summit.sfu.ca/item/4258.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chang DW. A study of N-nitrosamine photoaddition. – . [Thesis]. Simon Fraser University; 1970. Available from: http://summit.sfu.ca/item/4258

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Simon Fraser University

29. Lee, Antonio Chun Hung. Photolyses of N-nitrosamides in acidic and neutral media. -.

Degree: 1967, Simon Fraser University

URL: http://summit.sfu.ca/item/4364

Subjects/Keywords: Photochemistry.

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APA (6^th Edition):

Lee, A. C. H. (1967). Photolyses of N-nitrosamides in acidic and neutral media. -. (Thesis). Simon Fraser University. Retrieved from http://summit.sfu.ca/item/4364

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Lee, Antonio Chun Hung. “Photolyses of N-nitrosamides in acidic and neutral media. -.” 1967. Thesis, Simon Fraser University. Accessed February 18, 2020. http://summit.sfu.ca/item/4364.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Lee, Antonio Chun Hung. “Photolyses of N-nitrosamides in acidic and neutral media. -.” 1967. Web. 18 Feb 2020.

Vancouver:

Lee ACH. Photolyses of N-nitrosamides in acidic and neutral media. -. [Internet] [Thesis]. Simon Fraser University; 1967. [cited 2020 Feb 18]. Available from: http://summit.sfu.ca/item/4364.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lee ACH. Photolyses of N-nitrosamides in acidic and neutral media. -. [Thesis]. Simon Fraser University; 1967. Available from: http://summit.sfu.ca/item/4364

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Michigan State University

30. Lankin, David Charles. The preparation and photochemistry of spiro [1,2,3,4,5,6,7,8,9,10-decahydroanthracence 10-one-9,1'-cyclopentane].

Degree: MS, Dept. of Chemistry, 1967, Michigan State University

URL: http://etd.lib.msu.edu/islandora/object/etd:11365

Subjects/Keywords: Photochemistry

Record Details Similar Records Cite « Share

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APA (6^th Edition):

Lankin, D. C. (1967). The preparation and photochemistry of spiro [1,2,3,4,5,6,7,8,9,10-decahydroanthracence 10-one-9,1'-cyclopentane]. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:11365

Chicago Manual of Style (16^th Edition):

Lankin, David Charles. “The preparation and photochemistry of spiro [1,2,3,4,5,6,7,8,9,10-decahydroanthracence 10-one-9,1'-cyclopentane].” 1967. Masters Thesis, Michigan State University. Accessed February 18, 2020. http://etd.lib.msu.edu/islandora/object/etd:11365.

MLA Handbook (7^th Edition):

Lankin, David Charles. “The preparation and photochemistry of spiro [1,2,3,4,5,6,7,8,9,10-decahydroanthracence 10-one-9,1'-cyclopentane].” 1967. Web. 18 Feb 2020.

Vancouver:

Lankin DC. The preparation and photochemistry of spiro [1,2,3,4,5,6,7,8,9,10-decahydroanthracence 10-one-9,1'-cyclopentane]. [Internet] [Masters thesis]. Michigan State University; 1967. [cited 2020 Feb 18]. Available from: http://etd.lib.msu.edu/islandora/object/etd:11365.

Council of Science Editors:

Lankin DC. The preparation and photochemistry of spiro [1,2,3,4,5,6,7,8,9,10-decahydroanthracence 10-one-9,1'-cyclopentane]. [Masters Thesis]. Michigan State University; 1967. Available from: http://etd.lib.msu.edu/islandora/object/etd:11365

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