Previous Page  20 / 25 Next Page
Information
Show Menu
Previous Page 20 / 25 Next Page
Page Background

Page 73

Industrial Chemistry | ISSN: 2469-9764 | Volume 4

17

th

International Conference on

May 21-22, 2018 | New York, USA

Industrial Chemistry and Water Treatment

Ind Chem 2018, Volume 4

DOI: 10.4172/2469-9764-C1-009

Kinetics and mechanism of periodate oxidation of two ternary nitrilotriacetate chromium (III)

complexes involving histidine and aspartate co-ligands

Mohamed A Habib

Sirte University, Libya

T

he oxidation of [Cr

III

(HNTA)(Hist) (H

2

O)]- and [Cr

III

(HNTA)(Asp)(H

2

O)]- (NTA=nitrilotriacetate, Hist=L-histidine and

Asp=DL-aspartate) by periodate in aqueous medium has been studied spectrophotometrically between 15.0 and 35.0°C

under pseudo-first-order conditions, [IO

4

]- [complex]. The rate increases over the pH range 3.40-4.45 in both cases, but the

two complexes give different rate laws, in aqueous solutions, [Cr

III

(HNTA)(Hist)(H

2

O)]- is oxidized by IO

4

- according to the

following rate law: d[CrV

I

]/dt =(k

1

K

2

+k

2

K3K

1

/[H+])[IO

4

-][Cr

III

]T/{1+ (K

1

/[H+]) +(K

2

+K

1

K3/[H+])[IO

4

-]}. The other case

is [Cr

III

(HNTA)(Asp)(H

2

O)]- the derived rate law is given by equation: Rate=k

1

K

2

[Cr

III

]T[I

VII

]T/{1+ ([H+]/K

1

) + K

2

[I

VII

]T}.

Electron transfer, outer-sphere and inner-sphere mechanisms have been discussed. The nature, properties, chemical behavior

and different species in aqueous solutions of periodate have been reported. A literature survey on the oxidation of organic

and inorganic compound in aqueous solutions and in aqueous organic solvent was reported. The nature of α-amino acids and

their metal complexes have been briefly discussed, it is clear that [Cr

III

(NTA)(Asp)(OH)]

2

- may be the reactive species, an

inner-sphere process may be still accommodating through replacement of coordinated H

2

O in two species by IO4-. The rate of

reaction increases with the increasing of complex concentration and ionic strength. The thermodynamic activation parameters

were calculated, and we propose that electron transfer proceeds through an inner-sphere mechanism, via coordination of IO4-

to chromium (III). A common mechanism for the oxidation of some to chromium(III) complexes by periodate is proposed by

an excellent isokinetic relationship between and values for these reactions.

MohamedHabib952@gmail.com