The main objective of this project is to synthesize the first family of polynuclear chromium pyrazolate complexes. Complexity in analysis of the experimental magnetic data of multinuclear complexes arises from their (2S +1)N microstates, where S is the spin of each metal center and N is the number of metal centers. For example, high-spin (HS)-FeIII3 has 216 microstates and HS-FeIII8 ≈ 1.7x106 microstates (S= 5/2). However, complexes with chromium(III) S = 3/2 will have a noticeable reduction of microstates. Mononuclear complexes with formula [mer-CrCl3(pzH*)3] (pz*H = pyrazole, 3-Me-pzH, 4-Me-pzH, 4-Cl-pzH, 4-I-pzH, 4-Br-pzH) and [trans-CrCl2(pzH*)4]Cl (pzH* = pyrazole and 3-Me-pzH) were synthesized and thoroughly characterized. Polynuclear iron pyrazolate complexes are prepared by the addition of base to [mer-FeCl3(pzH*)3] and [trans-FeCl2(pzH*)4]Cl complexes; the path is not paralleled by mononuclear chromium(III) pyrazole complexes. There is a challenging situation with these reactions, caused by the attainment of equilibrium, where the stable mononuclear complexes and traces of dinuclear species coexist in solution. Microwave assisted reaction of Cr(NO3)3·9H2O and pyrazole ligand in dimethylformamide (DMF) solution afforded redox inactive trinuclear formate-pyrazolate mixed-ligand complexes with formula [Cr3(μ3-O)(μ-O2CH)3(μ-4-R-pz)3(DMF)3]+ (pz = pyrazolate anion; R= H, Me, Cl). Thermally assisted synthesis with non-hydrolysable solvent yielded an electrochemically active all-pyrazolate complex. Complex with formula (Ph4P)2[Cr3(μ3-O)(μ-4-Cl-pz)6Cl3] and (Ph4P)2[Cr3(μ3-O)(μ-4-Cl-pz)6Br3] have an oxidation process at 0.502 V at 0.332 V, respectively. The latter has a second accessed oxidation process at 0.584 V. These systems are the first example of electrochemically amendable trinuclear pyrazolate complex with {Cr3O} core. The all-ferric complexes [Fe3(μ3-O)(μ-4-NO2-pz)6(L)3]2- (L = NCO-, N3) were synthesized from reaction of [Fe3(μ3-O)(μ-4-NO2-pz)6Cl3]2- with NaNCO and NaN3. Expected reversible reduction processes were observed for both complexes at more negative potential, -0.70 V, compared to the thiocyanate complex (-0.36 V). The 57Fe Mössbauer of the reduced [Fe3(μ3-O)(μ-4-NO2-pz)6(N3)3]3- is suggestive of a HS-to-LS electronic reorganization, as seen for the [Fe3(μ3-O)(μ-4-NO2-pz)6(SCN)3]3- complex. Furthermore, compound [Fe3(μ3-O)(μ-4-NO2-pz)6(N3)3]2-, shows a unique reversible oxidation process at 0.82 V (vs. Fc+/Fc) to a mixed-valent, formally Fe3+2/Fe4+ species.

京都大学 / 0048 / 新制・課程博士 / 博士(地球環境学) / 甲第19156号 / 地環博第131号 / 新制||地環||27(附属図書館) / 32107 / 京都大学大学院地球環境学舎地球環境学専攻 / (主査)准教授 森 晶寿, 教授 劉 徳強, 准教授 吉野 章 / 学位規則第4条第1項該当 / Doctor of Global Environmental Studies / Kyoto University / DFAM

No description available.

No description available.

No description available.

No description available.

No description available.

Polymer-derived ceramic (PDC) is the name for a class of materials synthesized by thermal decomposition of polymeric precursors which excellent thermomechanical properties, such as high thermal stability, high oxidation/corrosion resistance and high temperature multifunctionalities. Direct polymer-to-ceramic processing routes of PDCs allow easier fabrication into various components/devices with complex shapes/structures. Due to these unique properties, PDCs are considered as promising candidates for making high-temperature sensors for harsh environment applications, including high temperatures, high stress, corrosive species and/or radiation. The SiAlCN ceramics were synthesized using the liquid precursor of polysilazane (HTT1800) and aluminum-sec-tri-butoxide (ASB) as starting materials and dicumyl peroxide (DP) as thermal initiator. The as-received SiAlCN ceramics have very good thermal-mechanical properties and no detectable weight loss and large scale crystallization. Solid-state NMR indicates that SiAlCN ceramics have the SiN4, SiO4, SiCN3, and AlN5/AlN6 units. Raman spectra reveals that SiAlCN ceramics contain “free carbon” phase with two specific Raman peaks of “D” band and “G” band at 1350 cm1 and 1600 cm1 , respectively. The “free carbon” becomes more and more ordered with increasing the pyrolysis temperature. EPR results show that the defects in SiAlCN ceramics are carbon-related with a g-factor of 2.0016±0.0006. Meanwhile, the defect concentration decreases with increasing sintered temperature, which is consistent with the results obtained from Raman spectra. iv Electric and dielectric properties of SiAlCN ceramics were characterized. The D.C. conductivity of SiAlCN ceramics increases with increasing sintered temperature and the activation energy is about 5.1 eV which higher than that of SiCN ceramics due to the presence of oxygen. The temperature dependent conductivity indicates that the conducting mechanism is a semiconducting band-gap model and follows the Arrhenius equation with two different sections of activation energy of 0.57 eVand 0.23 eV, respectively. The temperature dependent conductivity makes SiAlCN ceramics suit able for high temperature sensor applications. The dielectric properties were carried out by the Agilent 4298A LRC meter. The results reveal an increase in both dielectric constant and loss with increasing temperature (both pyrolysis and tested). Dielectric loss is dominated by the increasing of conductivity of SiAlCN ceramics at high sintered temperatures. SiAlCN ceramic sensors were fabricated by using the micro-machining method. High temperature wire bonding issues were solved by the integrity embedded method (IEM). It’s found that the micro-machining method is a promising and cost-effective way to fabricate PDC high temperature sensors. Moreover IEM is a good method to solve the high temperature wire bonding problems with clear bonding interface between the SiAlCN sensor head and Pt wires. The Wheatstone bridge circuit is well designed by considering the resistance relationship between the matching resistor and the SiAlCN sensor resistor. It was found that the maximum sensitivity can be achieved when the resistance of matching resistor is equal to that of the SiAlCN v sensor. The as-received SiAlCN ceramic sensor was tested up to 600 C with the relative output voltage changing from -3.932 V to 1.153 V. The results indicate that the relationship between output voltage and test temperature is nonlinear. The tested sensor output voltage agrees well with the simulated results. The durability test was carried out at 510 C for more than two hours. It was found that the output voltage remained constant for the first 30 min and then decreased gradually afterward by 0.02, 0.04 and 0.07 V for 1, 1.5 and 2 hours.

Вещества, обладающие антирадикальной активностью (АРА) играют ведущую роль в системе защиты организма от свободных радикалов. Общие недостатки известных способов оценки АРА выражаются в том, что измерения проводятся непрямыми методами, что затрудняет количественно оценивать содержание веществ с антирадикальными свойствами. Результаты измерений представляются в относительных единицах, в качестве эталонных веществ чаще всего используются: тролокс, галловая и аскорбиновая кислоты, проявляющие разную АРА, что не позволяет сравнивать результаты между собой. Таким образом, существует необходимость в разработке прямого, безэталонного метода оценки антирадикальной активности. Одним из потенциально возможных решений данной проблемы является метод ЭПР-спектроскопии на модели 2,2-дифенил-1-пикрилгидразил. Цель и задачи исследования. Исследование безэталонным методом оценки антирадикальной активности природных и синтетических антиоксидантов на модели 2,2-дифенил-1-пикрилгидразил с использованием ЭПР-спектроскопии. Отработка методики определения антирадикальной активности на модели ДФПГ методом ЭПР-спектроскопии. Получение и анализ значений антирадикальной активности для ряда веществ с антирадикальными свойствами. Сравнение с результатами полученными методом потенциометрического определения антиоксидантной активности с использованием медиаторной системы. Полученные результаты. Установлены оптимальные условия для проведения анализа. Проведено исследование - новым, безэталонным методом оценки антирадикальной активности, ряда природных и синтетических антиоксидантов. Установлены значения антирадикальной активности ряда природных и синтетических антиоксидантов. Рассмотрены различные варианты механизмов ингибирования свободных радикалов и их зависимость от структуры антиоксиданта. / Substances with anti-radical activity (ARA) play a leading role in the body's defense system against free radicals. General disadvantages of the known methods of evaluating the APA expressed in the fact that measurements are carried out by indirect methods, making it difficult to quantify the content of substances with antiradical properties. The measurement results are presented in relative units, as reference substances are most often used: Trolox, ascorbic and gallic acid, exhibit different ARA, which does not allow to compare the results with each other. Thus, there is a need to develop direct, reference-free method of evaluating anti-radical activity. One possible solution to this potential problem is the method of EPR model 2,2-diphenyl-1-picrylhydrazyl. The purpose and objectives of the study. Study standardless method for assessing the antiradical activity of natural and synthetic antioxidants model 2,2-diphenyl-1-picrylhydrazyl using EPR spectroscopy. Testing methods for determining the anti-radical activity in the DPPH model EPR spectroscopy. Obtaining and analyzing anti-radical activity values for a number of substances with antiradical properties. Comparison with the results obtained by potentiometric determination of antioxidant activity using a mediator system Results. The optimum conditions for analysis. The research - the new reference-free method of evaluating anti-radical activity, a number of natural and synthetic antioxidants. Established values antiradical activity of natural and synthetic antioxidants. Various embodiments of the mechanisms of inhibition of free radicals and their antioxidant dependency structure.

The function of G protein-coupled receptors is intrinsically linked to their conformational dynamics. In conjugation with site-directed spin labeling, electron paramagnetic resonance (EPR) spectroscopy provides powerful tools to study the highly dynamic conformational states of these proteins. Here, we explored positions for nitroxide spin labeling coupled to single cysteines, introduced at transmembrane, intra- and extra-cellular sites of the human neuropeptide Y2 receptor. Receptor mutants were functionally analyzed in cell culture system, expressed in Escherichia coli fermentation with yields of up to 10 mg of purified protein per liter expression medium and functionally reconstituted into a lipid bicelle environment. Successful spin labeling was confirmed by a fluorescence assay and continuous wave EPR measurements. EPR spectra revealed mobile and immobile populations, indicating multiple dynamic conformational states of the receptor. We found that the singly mutated positions by MTSL ((1-oxyl-2,2,5,5-tetramethyl-2,5-dihydro-1H-pyrrol-3-yl) methyl methanesulfonothioate) have a water exposed immobilized conformation as their main conformation, while in case of the IDSL (bis(1-oxyl-2,2,5,5-tetramethyl-3-imidazolin-4-yl) disulfide) labeled positions, the main conformation are mainly of hydrophobic nature. Further, double cysteine mutants were generated and examined for potential applications of distance measurements by double electron–electron resonance (DEER) pulsed EPR technique on the receptor.