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The effect of bpy/phen on the structure, thermal stability and biological studies of some primary amine Ni(II) dithiocarbamate complexes
26th Global Congress on Biotechnology & 2nd World Biotechnology Congress
*Felicia F. Bobinihi and Damian C. Onwudiwe
Federal college of Education, P.M.B. 1026, Okene, Kogi-State, Nigeria
Department of Chemistry, School of Physical and Chemical Sciences, Faculty of Natural Science and Agriculture, North-West University,
Mafikeng Campus, Private Bag X2046, Mmabatho 2735, South Africa
The quest for new and effective compouds with pharmacological potentials can never be exhausted as there
continues to be the outbreak of new infectious diseases, new strains and drug resistance of the old ones are
also becoming concurrently rampant. Production of new antibiotics, anti inflamatories and anti-coagulants are
therefore necessary for the treatment and prevention of the spread of these micro-organisms.
Bipyridine(bpy) and phenanthroline(phen) are N donor atoms which can form complexes with almost all
the metals in the periodic table. They are Ï?- deficient and so are good Ï?- acceptors with their complexes
stabilized by back bonding into the Ï?* orbitals of the N ring. They are often incorporated into many bridging
ligands as classical bidentate chelating heterocyclic ligand to impart significant effects on the properties of their
metal complexes. They can expand the coordination numbers of metal dithiocarbamate complexes through
the interaction of metal complexes with various ligating Lewis bases. When combined with dithiocarbamates,
the adducts formation is influenced through the mesomeric effect of their â??NR2 group which help to impart
better physical properties and enhanced biological activities because of their resemblance with biomolecules.
Dithiocarbamates have proven to be relevant in the synthesis of new supramolecular structural compounds
because of their unique properties to stabilize both high and low oxidation states in transition metals, such
as to allow manipulations on their bonding and electronic properties through the incorporation of different
functionalities on their nitrogen atom. This has made their complexes to be widely studied because of the
rich and varied chemistry with diverse applications. Nickel plays an important role in the biochemistry of
organisms, since it is part of the active center of enzymes, its pharmacological activities can be enhanced
when bound to dithiocarbamate ligands through reaction of the dithiocarbamate with thiol groups. Nickel
complexes are capable of existing in higher coordination numbers which is achieved in the present case by
adducts formation with available ligands. They easily form adducts with nitrogen, oxygen, phosphorus and
sulphur donors and the adduct formation lead to reduction in the original polymeric structures to monomeric
adducts.
Primary amine complexes, the homoleptic compounds of phenyl and substituted phenyl dithiocarbamate
ligands of group 10 triads have been produced.To study further the effect of coordinating, flexibility and
easy kinetic tuning on the properties of this class of compounds, N donor atoms; 2, 2-bypiridine and 1,
10-phenanthroline have been incorporated into their ligand framework and utilizing the advantage of the free
Proton from the NH site which can promote the lipophilicity of the compounds for more active biological
properties. The spectral and thermal analyses show the influence of the positive inductive effect of the methyl
and ethyl substituents on the phenyl group on the dithiocarbamate. The effect of the N donor atoms of the
bipyridine and phenanthroline on the parent complexes also reflected with enhanced antimicrobial and
anticancer properties.
Biography
Felicia Bobinihi is a senior Lecturer at the Federal College of Education, Okene, Nigeria. She completed her PhD degree at the North West University, South Africa. She is working on inorganic synthesis for biological applications and material synthesis, their procecessing and applications in various fields. Some of her works have been published in international peer review journals.
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