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SYNTHESIS AND ANALYSIS OF COORDINATION COMBINATION OF
COPPER (II) CHLORIDE WITH MONOETHANOLAMINE AND P-
NITROBENZOIC ACID
a
Khudoyberganov O.I.,
b
Iskandarov D.F
a
Khorezm Mamun Academy
b
Urgench State University
Providing the population with a variety of food products at all stages of
human development has been one of the actual issues. One of the key factors in
this is the rational protection of plants from harmful organisms (pests, diseases and
weeds). In the
development of grain, potatoes, fruits, vegetables and other crops, as
well as livestock in the country, it is important to protect plants from pests.
Because the conditions of Uzbekistan (hot climate, its geographical location and
soil conditions) are very favorable for the growth of pests. They find abundant
food and a comfortable place in the fields, which in turn leads to more damage to
crops. One of the
main pests in cotton fields, spiders give 18-20 generations in
Uzbekistan, caradrina 4-6, caterpillars 3-4, plant lice 16-17 and Colorado beetle 3-
4 in potato growing areas. Therefore, in our conditions,
the development and
effective use of specific methods of pest control is one of the important measures
to increase productivity.
In this regard, in the fight against plant pests include simple monofilaments
of benzoic acid – all types of isomers of nitro-, amino- and hydroxybenzoic acids
(primary ligand), and as auxiliary ligands to obtain mono-, di- and tri-
ethanolamines with similar bioactivity and convert them into Cu, Co, It is
advisable to use complex compounds formed with biometals such as Mn, Mo and
Ni. Because these newly synthesized complexes
exhibit antimicrobial and
stimulatory properties.
37
This work is also devoted to the synthesis and study of complex compounds
of antimicrobial and stimulant substances: copper (II) chloride with
monoethanolamine and p-nitrobenzoic acid.
The purpose of the work: to develop a method for the synthesis of a complex
combination of Cu (II) chloride with para-nitrobenzoic acid, as well as to study the
composition and structure of the synthesized complex by modern physicochemical
methods.Complex synthesis was carried out according to the following method:
0.002 mol of p-nitrobenzoic acid was dissolved in 20 ml of hot methanol and 0.001
mol of copper (II) chloride solution in 30 ml of water was added at a rate of 5 ml
every 20 minutes. To this mixture was poured an alcoholic solution of
monoethanolamine in a ratio of 1:30. The solution was stirred at 55-60
о
С in a
magnetic stirrer of the MS-H280-Pro brand for 2 hours. The reaction mixture was
then left to crystallize at room temperature. After 5–6 days,
the blue complex
precipitate formed was separated, washed in methanol, and dried in the open air.
The amount of metals in the synthesized complex compounds was
determined on the Novaa 300 apparatus of Analytic Jena (Germany), and the
analysis
of carbon, hydrogen and nitrogen elements was determined on the EA
1108 apparatus of Carlo-Erba (Italy) (Table 1). KBr tablets with a diameter of 7
mm samples were prepared in the area of the IQ spectra 400-4000 cm
1
of the
compound on IRAffinity-1S spectrophotometer of Shimadzu (Japan). X-ray
structural analysis was obtained on an Xcalibur ROxford Diffraction automatic
diffractometer at a temperature of 293 K (Cu Karadiation, k = 1.54184 Å, xscan
mode, graphite monochromator).
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