Diamond is a unique material with many exceptional properties. It has therefore been proven to be an important material for many applications. Moreover, the introduction of dopant species into the gas phase during the CVD growth process has been shown to strongly influence not only the properties and morphology of diamond, but also the growth rate. The purpose with the theoretical part of the present study has been to support and explain the experimental observations regarding the effect of various dopants (nitrogen, phosphorous, sulphur, and boron) on the diamond growth rate. Commonly observed H-terminated diamond surfaces [(111), (110) and (100)-2×1], were thereby carefully investigated using density functional theory under periodic boundary conditions. Based on the assumption that the hydrogen abstraction reaction is the growth rate-limiting step, both the thermodynamic and kinetic aspects of the diamond growth process were found to be severely affected by various dopants. More specifically, the results showed that nitrogen and phosphorous dopants (positioned within the 2nd, 3rd or 4th carbon layer) will cause an enhancement in the growth rate (as compared with non-doped situations). On the other hand, any growth rate improvement does only occur when positioning boron in the 2nd, and sulphur in the 4th, atomic carbon layer. With boron, and sulphur, positioned within the other atomic carbon layers, the growth rates were observed to decrease. In addition, the main purpose with the experimental part of the present study has been to investigate the effect of one specific dopant precursor (TMB) on the boron-doped diamond growth process. The result has shown that the increasing mass flow of TMB will not affect the mechanism of the HFCVD growth process of boron doped diamond. However, a linear boron carrier concentration in the diamond film vs. mass flow rate of TMB was observed.

The development of chiral organometallics for asymmetric synthesis is a topic of significant research in the recent past. The most studied in this class are the chiral organolithium reagents with many reported examples. The primary focus of our research is the development of C_α-chiral Grignard reagents, where the metal bearing α-carbon is the sole source of chirality. Examples of such Grignard reagents are rare owing to the problems associated with their synthesis, and their low configurational stability. We have studied these problems in three different modules of this project. Reactions of 1-magnesio-2,2-diphenyl-cyclopropylcarbonitrile with carbon electrophiles are first attempted in order to expand the utility of this configurationally stable C_α-chiral Grignard reagent in asymmetric synthesis. This reagent has been shown to be non-reactive towards carbon electrophiles at low temperatures. Consequently, we attempt to enhance the reactivity of this compound through two different approaches, Lewis-base activation and the "ate-complex" generation. The Magnesium/Halogen (Mg/X) exchange reactions have been shown to be extremely useful in the synthesis of complex Aryl, alkenyl (sp²) and alkynyl (sp) Grignard reagents. Examples of Mg/X exchange reactions of Alkyl (sp³) halides are, however, rare. Even more rare are such examples with secondary and tertiary alkyl halides, justifying the relative paucity of chiral Grignard reagents. In this module of our project, we study the Mg/X exchange reactions on secondary alkyl halides possessing a γ-hydroxyl group, as an internal activator for such Mg/X exchange reactions. Enantiomerization pathways of chiral organolithium compounds have been widely studied. However, few such studies have been performed on chiral Grignard reagents. In this module of the project, we studied the solvent assisted enantiomerization mechanism of the C_α-chiral 1-magnesio-2,2-diphenyl-cyclopropylcarbonitrile. Rate constant for the enantiomerization of this compound was measured in three different ethereal solvents to study the effect of solvent on the configurational stability. Finally, the order of the enantiomerization process with respect to [Et₂O] was studied in order to predict the mechanism of this process in Et₂O solvent. Our kinetic studies on the enantiomerization process provided us with a definitive picture for the enantiomerization of the C_α-chiral 1-magnesio-2,2-diphenyl-cyclopropylcarbonitrile, where solvation of the Grignard reagent preceded an ion-pair separation step which eventually lead to enantiomerization of the Grignard species. However, the precise structure of all the involved solvated intermediates could not be determined as kinetics was not able to distinguish between these intermediates. We next performed computational calculations to study the effect of solvation on the analogous 1-magnesio-cyclopropylcarbonitrile in order to address the unanswered questions from our kinetic studies. / Ph. D.

<p><strong>Apstrakt je obrađen tehnologijama za optičko prepoznavanje teksta (OCR).</strong></p><p>U radu je spektrofotometrijski ispitivana brzina oksidacije L-askorbinske kiseline. Tok reakcije je praćen snimanjem UV apsorpcionih spektara termostatiranih rastvora L-askorbinske kiseline u puferima različitih vrednosti rN: acetatnom (4-6). fosfatnom (5-8). fosfatno-citratnom (6-8), boratnom (8-11). glicinskom (9-11) i univerzalnom (4-11) !zveden je jednostavan oblik kinetičke jednačine reakcije vi&scaron;eg i razlomljenog reda. Dobijena jednačina je univerzalna, jer obuhvata jednačine nultog, prvog, drugog, trećeg i razlomljenog reda izračunate su vrednosti reda reakcije i one variraju sa promenom vrednosti rN unutar jednog puferskog sistema. Veza između vrednosti konstanti brzine oksidacije L-askorbinske kiseline i vrednosti rN ispitivanih pufera je linearna do vrednosti rN=10.00. Vrednosti koeficijenta pravca prave su različite za ispitivane pufere. Vrsta anjona prisutna u puferu kao i prisusutvo jona metala u kori&scaron;ćenim hemikalijama utiču na vrednosti konstante brzine oksidacije L-askorbinske kiseline i one su različite u raznim puferima istih vrednosti rN. Vrednosti konstante brzine oskidacije L-askorbinske kiseline su največe u univerzalnom puferu pri svim vrednostima rN. Prisutna sme&scaron;a anjona manje utiče na oksidaciju L-askorbinske kiseline nego pojedinačni anjoni, verovatno zbog među- sobnih interakcija.</p> / <p><strong>Abstract was processed by technology for Optical character recognition (OCR).</strong></p><p>The paper deats with the spectrophotometric study of L-ascorbic acid oxidation rate. The course of reaction has been observed by recording the UV absorption spectra of thermostated solution of L-ascorbic acid in buffers with different рН values: acetate (4-6), phosphate (5-8), phosphate-citrate (6-8), borate (8-11), glycine (9-11) and universal (4-11). A simple form of kinetic eguation of higher and fractional order reaction has been observed. The obtained eguation is universal as it comprises the eguations of zero, first, second, third and fractional order. The reaction order values have been calculated and they vary with change of рН values within each buffer system. The relation between the values of L-ascorbic acid oxidation rate constants and рН value of the studied buffers is linear up to рН value = 10.00. The straight line stopes are different for investigated buffers. The anion type present in a buffer as wett as the presence of metal ions in applied chemicals affect the values of L-ascorbic acid oxidation rate constant and they are different in different buffers with the same рН values. The values of L-ascorbic acid oxidation rate constant are the highest in the universal buffer at all рН values. The present anion mixture affects the L-ascorbtc acid oxidation to a tesser degree than single anions, presumabty due to mutuat interactions.</p>

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