Abstract
New dioxomolybdenum(VI) complexes were prepared by reacting S-methyl/allyl-4-phenyl-thiosemicarbazones of 2-hydroxy-1-naphthaldehyde (L 1 H2 and L 2 H2) and [MoO 2(acac)2] in methyl, ethyl and propylalcohols. In the complexes the doubly deprotonated ligands are coordinated to molybdenum as tridentate ONN-donors through phenolic-oxygen, azomethine- and thioamide-nitrogen. The solid complexes of general formula [MoO 2L(ROH)] which contain an alcohol (ROH) as second ligand were characterized by physico-chemical and spectroscopic methods. The fluorescence emission intensities of the compounds were recorded in chloroform, and the intensity changes were evaluated depending on chelation and time. The structure of the S-allyl-4-phenyl-thiosemicarbazone complex has been determined by the single crystal X-ray diffraction method.
Original language | English |
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Pages (from-to) | 775-779 |
Number of pages | 5 |
Journal | Transition Metal Chemistry |
Volume | 33 |
Issue number | 6 |
DOIs | |
Publication status | Published - Sept 2008 |