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Journal ArticleDOI

Spectral and thermogravimetric studies of oxohalobis(4-morpholinyldithiocarbamato)molybdenum(V) complexes

01 Oct 1984-Transition Metal Chemistry (Kluwer Academic Publishers)-Vol. 9, Iss: 10, pp 382-384

TL;DR: In this article, a six coordinate structure around Mo with an oxo, halo and two dithiocarbamate groups is proposed and the magnetic moment values at 1.65 B.p.m. and e.r.

AbstractMolybdenum(V) complexes [MoOX(4-Morphdtc)2] (X=F, Cl, Br or I; 4-Morphdtc = 4-morpholinyldithiocarbamate) have been prepared from molybdenum trioxide using hydrazine hydrohalides as reducing agents. The magnetic moment values atca. 1.65 B.M. and e.p.r. studies indicated that the complexes are mononuclear and that molybdenum is in + 5 oxidation state. The i.r. spectral bands at 1500 and 960 cm−1 suggest that the dithiocarbamate acts as a univalent bidentate ligand and the bands at 930 cm−1 confirms the presence of a MoO3+ moiety in the complex. The low conductivity values for the complexes inN, N-dimethylformamide indicate that the complexes are non-ionic. The [MoOX(4-Morphdtc)2] complexes (X=F, Cl or Br) decompose in the first step by the loss of one dithiocarbamate group, whereas in [MoOI(4-Morphdtc)2] the iodine atom is lost in the first step. The second and third steps lead to the formation of MoS3 and MoO3, respectively. A six coordinate structure around Mo with an oxo, halo and two dithiocarbamate groups is proposed.

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Citations
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4 citations

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TL;DR: In this paper, four dioxomolybdenum (VI) complexes of a polydentate ligand derived from Isatin and o-Phenylene Diamine (PDAI) were synthesized and characterized on the basis of different physico chemical methods.
Abstract: Four dioxomolybdenum (VI) complexes of a polydentate ligand derived from Isatin and o-Phenylene Diamine (PDAI) were synthesized and characterized on the basis of different physico chemical methods. Thermal stability of one of the complexes was revealed from its thermal study. Antibacterial activities of the ligand, PDAI and one of its complexes were measured at different concentrations and none of them was found to be active towards S. aureus ATCC 25923 and E. coli ATCC 25922. On the basis of the various physico chemical studies, a distorted octahedral geometry is suggested for all the dioxomolybdenum (VI) complexes.

References
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1,247 citations

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TL;DR: The biological role of molybdenum, biophysical studies of the molybordenum atoms, and aspects of coordination chemistry that bear on the understanding of Molybdo-enzymes are discussed in this paper.
Abstract: The biological role of molybdenum, biophysical studies of the molybdenum atoms in molybdo-enzymes, and aspects of coordination chemistry that bear on the understanding of molybdo-enzymes.

27 citations

Journal ArticleDOI
TL;DR: The complexes OMoX 2 L 2 (L = S 2 )CNEt 2 ) 2 and OMoXL 2 (X = Cl, Br) as mentioned in this paper showed the lack of atom transfer ability of tungsten(VI) relative to its molybdenum analog.
Abstract: The complexes OMoX 2 L 2 (L = S 2 )CNEt 2 ) 2 react with Na 2 S 2 O 4 to yield OMoL 2 (X = Cl), with PhNCO to yield (PhN)MoX 2 L 2 (X = Cl), with PPh 2 Et to give MoX 2 (PPh 2 Et)L 2 (X = Cl, Br), and with OMol 2 to produce OMoXL 2 (X = Cl, Br). The epr spectra of OMoXL 2 display halogen superhyperfine splitting [A( 35,37 Cl) = ∼3 gauss; A(bb]79,81Br) = 12.3 gauss). Reaction of WCl 6 with NaL in MeOH yields the new complex OWCl 2 L 2 which either does not react at all or gives no characterizable products with the above reagents. The results demonstrate the lack of atom transfer ability of tungsten(VI) relative to its molybdenum analog.

10 citations


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