No description available.

Single electron transfer (SET) mechanisms are becoming ubiquitous in modern organic chemistry. However, it is often difficult to distinguish SET mechanisms from polar mechanisms. Kinetics, products and product distributions, and response to perturbation in solvent and substituents are often identical between the two mechanisms. Detection techniques such as EPR, CIDNP, and UV absorption can often detect "blind" pathways and thus cannot provide unambiguous evidence regarding the true mechanism of interest. In recent years mechanistic probes have been developed which can test for single electron transfer in the mechanism of interest in a more unambiguous manner, although a given probe is often applicable to a narrower range of reactions. In this work 1,1-dimethyl-5,7-di-t-butylspiro[2.5]octa-4,7-dien-6-one (6) is presented as a new "hypersensitive" probe for single electron transfer to conjugated carbonyl compounds. This new probe functions in a rather unique fashion, allowing interpretation of the mechanism at work on the basis of the regiochemistry of spirocyclic ring opening. This "regiodifferentiation" based probe was studied with a variety of nucleophiles (particularly Grignard reagents) and has been found to be effective in differentiating SET from polar processes, although surprising results indicative of polar pathways in the case of reaction of 6 with Grignard reagents other than methyl Grignard were found. Additional insight into the mechanism of the reaction of Grignard reagents with conjugated ketones is also presented. / Master of Science

京都大学 / 0048 / 新制・課程博士 / 博士(理学) / 甲第19515号 / 理博第4175号 / 新制||理||1599(附属図書館) / 32551 / 京都大学大学院理学研究科化学専攻 / (主査)教授 丸岡 啓二, 教授 大須賀 篤弘, 教授 依光 英樹 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM

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The synthesis of five chiral DBFOX (dibenzofuran-oxazoline) ligands with either aryl or benzyl substituents will be presented. The requisite amino alcohols were obtained with high enantioselectivity either commercially (DBFOX/Bn), via Sharpless asymmetric aminohydroxylation (DBFOX/Nap, DBFOX/t-BuPh, DBFOX/Pip), or via phase-transfer catalyzed asymmetric alkylation (DBFOX/MeNap). These ligands, complexed with Mg(NTf2)2, were used as Lewis acid promoters of enantioselective radical conjugate additions to α/β-unsaturated nitro-amides/esters. A summary of these results is presented and discussed. These findings led us to believe that our initial binding model between metal, ligand, and substrate was flawed. Thus, we figured that if we started with a functionality known to bind to both nitro groups and carbonyls, and then introduced a chiral element for control, we may be able to improve the beta-carbon enantioselectivity. We have tried to accomplish this via hydrogen-bonding ligands (ureas and thioureas). Initial studies on achiral versions of this concept are discussed.

Lyconadin A is a pentacyclic Lycopodium alkaloid isolated from the club moss Lycopodium complanatum with antitumor properties. We have developed a novel 7-exo/6-exo acyl radical cascade cyclization as a method of making the bicyclo[5.4.0]undecane ring system of lyconadin A. The model products are trans-fused ring systems, while a cis-fused ring system is needed in lyconadin A. We have discovered a method to convert the trans-fused model cascade cyclization product into the desired cis isomer. Based on Donohoe's pyridone synthesis, we developed a method for the construction of 5-alkyl and 3,5-dialkyl-6-carbomethoxy-2-pyridones, the former of which is a subunit of lyconadin A. An intramolecular Reformatsky reaction is a key step in this process. We have proceeded with our total synthesis, in which we generated an epoxide by Shi asymmetric epoxidation and regioselectively opened epoxide rings. We have prepared carboxylic acid 197.

The oxidative degradation of organic materials typically operates through a radical-mediated chain mechanism known as autoxidation; a process that has severe consequences in both biological settings (i.e. accumulation of lipid peroxides) and non-living substrates (i.e. breakdown of petroleum-derived materials, such as lubricants/oils, plastics, polymers, rubbers, etc.). However, autoxidation can be retarded by radical-trapping antioxidants (RTAs); chemical species that capture chain-carrying radicals to break the chain of oxidation. A particular class of RTA, diarylamines, have proven especially effective at elevated temperatures due to a purported catalytic mechanism of inhibiting autoxidation, and thus, have found significant use as protective agents in engine lubricant oils. However, the current diarylamine technology struggles to manage the increased oxidative stress placed on it by modern internal combustion engines (ICEs), which burn fuel at higher temperatures in order to meet emission standards. Designing superior diarylamines is not straightforward, however, as the mechanisms by which they are forced from their catalytic cycle are not well understood. Herein, we report our investigations into the fate of an industrially-representative, isotopically-enriched diarylamine during hydrocarbon autoxidation at elevated temperatures using a novel 2D 1H – 15N heteronuclear multiple bond correlation (HMBC) spectroscopic technique. Synthesis of a small scope of oxidation products allowed for the identification of a previously unreported product of diarylamine autoxidation. Additionally, a consistent pattern of diarylamine speciation under varying conditions was observed spectroscopically. Use of the HMBC technique also confirmed previous reports of the regenerative ability of the diarylamine and the intermediates of its purported catalytic cycle. Quantification studies using ultra performance liquid chromatography (UPLC) during the early stages of autoxidation provided insight into the formation of initial diarylaminic intermediates. Additionally, we examined the fate of the diarylamine during autoxidations in the presence of nitrogen oxides (NOx), which are found in the blow-by gas of ICEs and have been shown to exacerbate hydrocarbon autoxidation. The performance of diarylamine was drastically reduced under such conditions, and HMBC spectroscopy illustrated its rapid conversion to a number of intermediates. The most prominent two intermediates were identified as mono- and di-nitrated analogues of the original diarylamine, and were demonstrated to possess no RTA activity; regardless of temperature or substrate. HMBC spectroscopy also illustrated the differences in product distribution under each set of conditions.

<p> The transient behaviour of a batch stirred-tank reactor (BSTR) for free radical polymerization of styrene in toluene has been studied experimentally and theoretically. A kinetic model applicable to high conversions was developed using data from measurements of monomer conversion and molecular weight distribution (MWD). Significant improvement over the conventional kinetic model is obtained when the viscosity or gel effect is accounted for. The termination rate constant and catalyst efficiency are allowed to vary with viscosity. The findings agree with the general theory of diffusion-controlled reaction which predicts that viscosity is the most important parameter.</p> / Thesis / Master of Engineering (MEngr)

<p> The Arrhenius equation for the ring opening isomerization of cyclopropylmethyl radicals (R•) to 3-buten-1-yl radicals (R•') for the 303-362 K temperature range was determined by thermolysis of cyclopropylmethyl [1-hydroxy-1-methylethyl] diazene in the presence of excess 1,1,3,3-tetra-methylisoindolin-2-yloxyl (Y•).</p> <p> Rate constants for coupling of R• with Y• were assumed to be proportional to diffusion controlled rate constants (kd) and rate constants (ki) for the isomerization were calculated from kd (corrected) and product ratios (RY/R'Y). The temperature dependence of ki, given by log(ki/s^-1) = (13.9 ± 0.4) - (7.6 ± 0.1)/θ, is significantly different from that determined by Ingold and co-workers by kinetic epr spectroscopy in the temperature range 128-153 K; log(ki/s^-1) = (11.34 ± 0.85) - (5.94 ± 0.57)/θ, where θ = 2.3 RT kcal mol^-1.</p> / Thesis / Master of Science (MSc)

<p> Aryl radical ring closures onto the azo functional group were investigated. A series of ortho-substituted aryl radicals (83a-f) have been generated by bromine abstraction from the corresponding 1-(orthobromophenyl)-1-methoxy-azoethanes (82a-f) by tributyltin radicals. The radicals generated underwent cyclization in the 5-endo sense, to ultimately afford the substituted indazoles (86a-f). There was also some evidence for cyclization to the other azo nitrogen (closure in the 4-exo sense) to form a 4-membered ring. The aryl radical also underwent hydrogen atom abstraction from tributyltin hydride in competition with cyclization. Since the rate constant for hydrogen atom abstraction from tributyltin hydride by aryl radicals is known, this makes it possible to estimate the rate constants for cyclization throughout the series.</p> / Thesis / Master of Science (MSc)