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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 101 to 110 of 742 (0.031 seconds)Spelling suggestions: "subject:"molybdenum."" "subject:"olybdenum.""
| 101 |
Heteropolyoxo-and heteropolyperoxometalates as oxidation catalystsGresley, Nia Melanie January 1996 (has links)
No description available.
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| 102 |
Preparation and reactivity of cuboidal molybdenum (Mo4̲S4̲) and dimeric tungsten (V) (W2̲O4̲) aqua ionsSharp, C. January 1988 (has links)
No description available.
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| 103 |
Tungsten-substituted DMSO reductaseStewart, Lisa Joanne January 2001 (has links)
No description available.
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| 104 |
Experimental studies in the isomerism and structural variations in molybdenum and rhenium halo-compoundsAnderson, Ian Robert. January 1968 (has links) (PDF)
Includes bibliography.
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| 105 |
Growth and characterization of molybdenum disulfide, molybdenum diselenide, and molybdenum(sulfide, selenide) formed between molybdenum and copper indium(sulfide, selenide) during growthRickman, Sarah. January 2006 (has links)
Thesis (M.M.S.E.)--University of Delaware, 2006. / Principal faculty advisors: Robert L. Opila and Robert W. Birkmire, Dept. of Materials Science & Engineering. Includes bibliographical references.
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| 106 |
Guanidinates: a new class of ligands for dimetal units with multiple metal-metal bondsWilkinson, Chad C. 15 May 2009 (has links)
This dissertation concerns the discovery of the ability of the guanidinate ligand
hpp (hpp = anion of 1,3,4,6,7,8-hexahydropyrimido[1,2-a]pyrimidine) to stabilize high
oxidation states of dimetal units (particularly dimolybdenum species) and attempts to
control solubility and redox potential through modification of the ligand. Two general
strategies were used for the ligand modifications: alteration of the ring size, and addition
of alkyl substituents.
All of the dimetal complexes using these ligands show a significant shift in redox
potential compared to other commonly used classes of ligands (i.e. carboxylates and
formamidinates) allowing access to the Mo2
4+, Mo2
5+ and Mo2
6+ oxidation states. The
solubility of the complexes increases with increasing ring size, or with increasing length
of the alkyl substituent. The physical and chemical properties of the ligands and their
dimolybdenum complexes are described in detail.
|
| 107 |
The marine biogeochemistry of molybdenum /Tuit, Caroline Beth, January 1900 (has links)
Thesis (Ph. D.)--Joint Program in Marine Geology and Geophysics (Massachusetts Institute of Technology, Dept. of Earth, Atmospheric and Planetary Sciences, and the Woods Hole Oceanographic Institution), 2003. / Includes bibliographical references.
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| 108 |
Origin and distribution of molybdenum in the vicinity of the Glove Mine, Santa Cruz County, ArizonaSee, Joseph Melville, 1938- January 1964 (has links)
No description available.
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| 109 |
A study of the treatment of some Arizona molybdenite oresKelley, Mose Eggleston, 1910- January 1935 (has links)
No description available.
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| 110 |
Molybdenum-containing dyesMoss, Martha Cecil January 1960 (has links)
No description available.
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