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The Global ETD Search service is a free service for researchers
to find electronic theses and dissertations. This service is
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Networked Digital Library of Theses and Dissertations.
Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
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Showing 1 to 8 of 8 (0.082 seconds)Spelling suggestions: "subject:"antimony compounds""
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Organoantimony coordination chemistryMeinema, Harmen Anne, January 1971 (has links)
Proefschrift--Utrecht. / Vita. Includes bibliographical references.
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Organic compounds of antimonyDunning, Fitzgerald, January 1927 (has links)
Thesis (Ph. D.)--Johns Hopkins University, 1927. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 33-34).
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The influence of the stibino [sic]-group on the reactivity of nuclear chlorine,Biswell, Charles Bedford. January 1934 (has links)
Thesis (Ph. D.)--University of Nebraska, 1934. / eContent provider-neutral record in process. Description based on print version record. Bibliography: p. 22.
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The influence of the stibino [sic]-group on the reactivity of nuclear chlorine,Biswell, Charles Bedford. January 1934 (has links)
Thesis (Ph. D.)--University of Nebraska, 1934. / eContent provider-neutral record in process. Description based on print version record. Bibliography: p. 22.
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Organic derivaties of arsenic, antimony and bismuth Part I. Distibyls.--Tetraphenyldistibyl. Attempts to obtain tetraphenyldibismuthyl. Tetra-p-bromotetrapheny- and tetra-p-tolyldistibyl. Di-alpha-naphthyliodostibine. Part II. The interaction of diarylarsyl iodides, diarylstibyl iodides and phenyldihaloarsines with the piperidine salt of N-pentamethylenedithiocarbamic acid ...Oakdale, Urban Oscar, January 1933 (has links)
Thesis (Ph. D.)--University of Michigan, 1929.
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Organic derivaties of arsenic, antimony and bismuth. Part I. Distibyls.--Tetraphenyldistibyl. Attempts to obtain tetraphenyldibismuthyl. Tetra-p-bromotetrapheny- and tetra-p-tolyldistibyl. Di-alpha-naphthyliodostibine. Part II. The interaction of diarylarsyl iodides, diarylstibyl iodides and phenyldihaloarsines with the piperidine salt of N-pentamethylenedithiocarbamic acid ...Oakdale, Urban Oscar, January 1933 (has links)
Thesis (PH. D.)--University of Michigan, 1929.
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Hypervalent diorganoantimony(III) fluorides via diorganoantimony(III) cations – a general method of synthesisPreda, Ana Maria, Raţ, Ciprian I., Silvestru, Cristian, Lang, Heinrich, Rüffer, Tobias, Mehring, Michael 18 February 2016 (has links) (PDF)
Novel diorganoantimony(III) fluorides containing ligands with pendant arms, R2SbF (5), (R)PhSbF (6) [R = 2-(2′,6′-iPr2C6H3N[double bond, length as m-dash]CH)C6H4], R′′2SbF (7) and (R′′)PhSbF (8) [R′′ = 2-(Me2NCH2)C6H4], were prepared via the ionic derivatives [R2Sb]+[PF6]− (1), [(R)PhSb]+[PF6]− (2), [R′′2Sb]+[SbF6]− (4) and [(R′′)PhSb]+[SbF6]− (obtained in situ) by treatment with [Bu4N]F·3H2O. The ionic species used as starting materials as well as [R′2Sb]+[PF6]− (3) [R′ = 2-(2′,4′,6′-Me3C6H2N[double bond, length as m-dash]CH)C6H4] were obtained from the corresponding bromides or chlorides and Tl[PF6] or Ag[SbF6]. The compounds were investigated by multinuclear NMR spectroscopy in solution, MS and IR spectroscopy in the solid state. The molecular structures of the ionic species 1·2CH2Cl2 and 3·2CHCl3 as well as of the fluorides 5–8 were determined by single-crystal X-ray diffraction. / Dieser Beitrag ist aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
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Hypervalent diorganoantimony(III) fluorides via diorganoantimony(III) cations – a general method of synthesisPreda, Ana Maria, Raţ, Ciprian I., Silvestru, Cristian, Lang, Heinrich, Rüffer, Tobias, Mehring, Michael 18 February 2016 (has links)
Novel diorganoantimony(III) fluorides containing ligands with pendant arms, R2SbF (5), (R)PhSbF (6) [R = 2-(2′,6′-iPr2C6H3N[double bond, length as m-dash]CH)C6H4], R′′2SbF (7) and (R′′)PhSbF (8) [R′′ = 2-(Me2NCH2)C6H4], were prepared via the ionic derivatives [R2Sb]+[PF6]− (1), [(R)PhSb]+[PF6]− (2), [R′′2Sb]+[SbF6]− (4) and [(R′′)PhSb]+[SbF6]− (obtained in situ) by treatment with [Bu4N]F·3H2O. The ionic species used as starting materials as well as [R′2Sb]+[PF6]− (3) [R′ = 2-(2′,4′,6′-Me3C6H2N[double bond, length as m-dash]CH)C6H4] were obtained from the corresponding bromides or chlorides and Tl[PF6] or Ag[SbF6]. The compounds were investigated by multinuclear NMR spectroscopy in solution, MS and IR spectroscopy in the solid state. The molecular structures of the ionic species 1·2CH2Cl2 and 3·2CHCl3 as well as of the fluorides 5–8 were determined by single-crystal X-ray diffraction. / Dieser Beitrag ist aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
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