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Reactions of fluorinated functions and synthesis of fluorinated paraffins /Groth, Richard Henry January 1956 (has links)
No description available.
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The synthesis of some isomeric polyalkylcycloparaffins /Otto, Bruce Michael January 1963 (has links)
No description available.
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The metabolism of cycloalkanes by different species of XanthobacterWarburton, Elizabeth Jean January 1989 (has links)
No description available.
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The oxidation of trans-2-butene and propene between 400 and 520 degree CStothard, Nigel David January 1990 (has links)
No description available.
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Selective oxidation of adamantane by metal complexesRaviJayaKumar, K., University of Western Sydney, Faculty of Science and Technology January 1997 (has links)
A series of tri-substituted iron and cobalt complexes of the form [M(A)3]n+ were synthesized, and were characterised by UV/Visible absorption and 1H-NMR spectroscopy. The complexes [Co(phen)2(en)]3+ and [Co(bipy)2(en)]3+ have been reported in the literature but 1H-NMR spectroscopy showed that the material produced in both syntheses is [Co(en)3]3+. Spectroscopy further showed that these species cannot be prepared by the literature methods. The complexes were tested in the oxidation of adamantane in the solvents, acetic acid and trifluoroacetic acid and they all oxidised adamantane to a mixture of 1-adamantanol, 1-adamantanol and 2-adamantanone both in the presence and the absence of the oxidant, O2. In all the reactions, however, the yield of conversion was very low. The mechanism for this oxidation was different depending on the presence or absence of O2. In the presence of O2 a catalytic cycle was produced for the oxidation of adamantine. In the oxidation in the presence and absence of O2 there was little variation in activity between the tri-substituted iron and cobalt complexes of 1,10-phenanthroline when compared with the analgous 2,2’-bipyridine complexes. However, the substitution of an ethylenediamine ligand into the co-ordination sphere of cobalt produced significant increase in the activity, although the change was not constant. / Master of Science (Hons)
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Investigation of poly(pyrrolone-imide) materials for the olefin/paraffin separationBurns, Ryan Lance. January 2002 (has links) (PDF)
Thesis (Ph. D.)--University of Texas at Austin, 2002. / Vita. Includes bibliographical references. Available also from UMI Company.
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Synthetic and biodegradation studies of some sedimentary isoprenoid hydrocarbonsRobson, John Nicholas January 1987 (has links)
No description available.
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Kinetic and mechanistic studies of reactions of atomic chlorine with haloalkanesPiety, Charles Andrew 08 1900 (has links)
No description available.
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Scope of microporous and mesoporous molecular sieves in the oxidation of higher alkanes with ozonePullabhotla, V. S. R. Rajasekhar. January 2008 (has links)
Alkane-rich fractions including n-paraffins are the most important chemical feedstock used in the / Thesis (Ph.D.)-University of KwaZulu-Natal, Westville, 2008.
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The synthesis and reactions of functionalised transition metal substituted paraffins.Onani, Martin Opiyo. January 2002 (has links)
The compounds [Cp(CO)3W{(CH2)nX}] (X = Br, I; n = 3 - 6) were prepared in high yield by the reaction ofNa[Cp(CO)3W ] with Br(CH2)nBr. The bromoalkyl compounds were subsequently reacted with NaI to give the corresponding iodoalkyl complexes. The crystal structures of [Cp(CO)3W{(CH2)sI}] and [Cp(CO)3W{(CH2)3Br}] are reported for the first time. The former compound forms orthorhombic crystals in the space group P21nb and the latter forms triclinic crystals in the space group PI. Both have W-C bond lengths of2.35 A. The C-I bond length is 2.12 A; the C-Br bond length is 1.94 A. In a similar manner to the above, the compounds [Cp(CO)2(PPhiMe3 - i)Mo{(CH2)nBr}] (Cp = TJs-CsHs, n = 3, 4; i = 0 3) and [Cp*(CO)3Mo{(CH2)nBr}] (Cp* = TJs-CS(CH3)s,n = 3, 4) were prepared in medium to high yield by the reaction of the corresponding anion [Cp(CO)2(PPhjMe3-i)Mor or [Cp*(CO)3Mor with Br(CH2)nBr. The bromoalkyl compounds were subsequently reacted with NaI to give the corresponding iodoalkyl compounds [Cp(CO)2(PPhiMe3 _i)Mo{( CH2)nI}] (n = 3, 4; i = 0 - 3) and [Cp*(CO)3Mo{(CH2)nI}] (n = 3, 4) respectively. The iodoalkyl compounds were also prepared by the reaction of the corresponding anion and a,O)diiodoalkane in much lower yields. These compounds have been fully characterised and their properties are discussed. The crystal and molecular structure of [Cp(CO)2(PPh3)Mo{(CH2)3I}] is also reported, again for the first time. The compound forms crystals in the monoclinic space group P21/n; with a Mo-C bond length of 2.40 Aand a C-I bond length of 2.13 A These halogenoalkyl compounds were used as precursors to the new heterobimetallic complexes [Cp(CO)3W(CH2)nMo(CO)3Cp] n = 3 - 6; [Cp(CO)3W(CH2)nMo(COhCp*] n = 3,4; [Cp(CO)3W(CH2)nMo(CO)2(PPhiMe3_i)Cp] n = 3,4; i = 0 - 3 and [Cp(CO)2Fe(CH2)nMo(CO)2(PPhiMe3_i)Cp] n = 3,4; i = 0 - 3. The heterobimetallic complexes were prepared by the direct displacement of the iodide of a metallo-iodoalkyl complex with the appropriate anion. The complexes have been fully characterised by IR, IH NMR, 13C NMR, COSY, HETCOR or HSQC and elemental analyses. X-ray diffraction studies are for the first time reported for the complexes [Cp(CO)3W(CH2)3Mo(CO)2(PPh3)Cp] and [Cp(CO)2( PPh3)Mo(CH2)3Fe(CO)2Cp]. Both compounds form monoclinic crystals in the space group P 2I/c. The former, with a W-C bond length of2.32 Aand Mo-C bond length of2.35 Aand the latter with a Mo-C bond length of2.37 A and Fe-C bond length of2.08 A. The reactions of some of the above halogenoalkyl compounds with some simple inorganic molecules were investigated. The reactions of [Cp(CO)3W{CH2)4Br}] and [Cp(CO)2(PPhMe2)Mo{(CH2)3Br}] with silver nitrate in acetonitrile formed orange products, [Cp(CO)3W{(CH2)40N02}] and [Cp(CO)2(PPhMe2)Mo{(CH2)30N02}] respectively. The compounds [Cp(CO)3W{(CH2)sCN}], [Cp(CO)3W{(CH2)4CN}], [Cp(CO)2(PPhMe2)Mo{(CH2)3CN}], [Cp(CO)3W{(CH2)4N3}], [Cp(CO)3W{(CH2)sN3}], [Cp(CO)2(PPhMe2)Mo{(CH2)3N3}] were also obtained from various reactions using the reagents; AgCN, KCN, NaCN and NaN3. Similar reactions with molybdenum analogs gave cyclic carbene compounds. Reaction studies were also done on some of the above heterobimetallic compounds with tertiary phosphines; carbon monoxide gas and trityl salt, and thermolyses were also investigated. The reactions of PPh3 with [Cp(CO)3W{(CH2)3}MLy] {MLy = MO(CO)3Cp, MO(CO)3Cp* and MO(CO)2(PMe3)Cp} were found to be totally metalloselective, with the phosphines always attacking the expected metal site predicted by the reactions ofthe corresponding monometallic or homodinuclear alkyl species. A similar reaction involving CO with [Cp(CO)3W(CH2)3Mo(CO)3Cp] and [Cp(COhFe(CH2)3Mo(CO)2(PMe3)Cp] was also metalloselective. The reaction of [Cp(COhFe(CH2)4Mo(CO)3)Cp*] with trityl salt gave the expected complex [Cp(CO)2Fe(C4H7)Mo(CO)3)Cp*]PF6. It is believed that the structure of the trityl salt complex has the iron atom n-bonded whilst the molybdenum is cr-bonded to the butyl chain. The compounds [Cp(CO)3W(CH2)3Mo(CO)3Cp*] and [Cp(CO)2Fe(CH2)3Ru(CO)2Cp] both gave cyclopropane on thermolysis, indicating a ~elimination and reductive processes taking place. The crystal structure of [Cp(CO)3W{(CH2)3COOH}], which was obtained in one of the reaction studies, where the compound [Cp(CO)3W(CH2)3Mo(CO)2(PMe3)Cp] was reacted with excess PPh3in acetonitrile, is reported. / Thesis (Ph.D.)-University of Natal, Durban, 2002.
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