نتایج جستجو برای: molybdenum vi

تعداد نتایج: 56345  

2008
Gino Georges Lavoie Richard R. Schrock Dietmar Seyferth Alan Davison Gregory C. Fu Julie Love

S Chapter 1 Study of Chiral Arylimido Molybdenum ROMP Catalysts. Molybdenum ROMP catalysts with a chiral ortho-(phenethyl)phenylimido ligand have been prepared. Mo(CHCMe2Ph)(N-2-C 6H4-CHMePh)(O-2,6-C 6H3-Ph2)2 (1la) and Mo(CHMe 2Ph)(N2-C6H4-CHMePh)[BIPHENO(Me) 2(t-Bu) 4] (11b) were isolated and shown to effect the polymerization of 2,3-dicarbomethoxynorbonadienes. Highly-trans syndiotactic poly...

Journal: :Bulletin of the Chemical Society of Japan 1967

Journal: :Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 2013
Hajime Katano Shu Taira Kohei Uematsu Hisashi Kimoto

A simple and convenient method of reducing monosaccharide assay is proposed. A Si(IV)-Mo(VI) solution (pH 4.9) was yellow due to the formation of the 11- and/or 12-molybdosilicate(VI) anions. By the addition of a reducing saccharide, glucosamine, the mixture turned to blue gradually, indicating that the Mo(VI) species was reduced by the saccharide to form a blue molybdosilicate anion. The molyb...

Journal: :Acta Crystallographica Section E Structure Reports Online 2008

Abbas Afkhami, Atousa Bahiraei Mahdi Moradi Tayyebeh Madrakian,

In this work a new chemically modified carbon paste electrode was constructed for accurate, simple, sensitive and selective determination of molybdenum (VI) ions. The results of modified electrode by an ion imprinted polymer were compared with those obtained with carbon paste electrode. The results showed the stripping peak currents had a dramatic increase at the modified electrode. Under the o...

Journal: :Dalton transactions 2016
Niklas Zwettler Martina E Judmaier Lara Strohmeier Ferdinand Belaj Nadia C Mösch-Zanetti

Synthesis of molybdenum(vi) dioxido complexes 1-3, coordinated by one or two functionalized iminophenolate ligands HL1 or HL2, bearing a donor atom side chain or a phenyl substituent, respectively, allowed for systematic investigation of the oxygen atom transfer (OAT) reactivity of such complexes towards phosphanes. Depending on stoichiometry and employed phosphane (PMe3 or PPh3), different mol...

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