A master's thesis at the University of Basrah discusses (preparing some implicit complexes of Schiff bases with betacyclodextrin and studying their physical properties)

The College of Education for Pure Sciences at the University of Basrah  discussed a master’s thesis entitled (Preparation of some implicit complexes of Schiff bases with β-cyclodexrin and the study of their physical properties)
The letter presented by the researcher (Tawfiq Kazem Mahdi) included
It is a group of natural products formed during the bacterial decomposition of starch. Which can split and rearrange the polymer chain of starch leading to the formation of various cyclodextrins. Therefore, dextrins are non-reducing cyclic sugars that are crystalline and homogeneous consisting of glucose units.
The most common cyclodextrins are (α-cyclodextrains, β-cyclodextrains, γ-cyclodextrains) containing different numbers of glucose units (8, 7, 6), respectively, these units are linked by α-(1→4) glycosidic bonds.
These bonds that are formed between glucose units form ring structures where the three cyclodextrins are equal in length and different in width depending on the number of glucose units forming the ring, where the inner cavity of the cyclodextrins is hydrophobic and lipophilic.
Aim of the study
Study of the physical properties of some implicit complexes of Schiff bases derived from some sulfa drugs with
Betacyclodextrin prepared by freeze-drying method, and comparison of physical properties with Schiff bases
The free physical and spectroscopic methods are infrared, FT-IR, scanning electron microscopy (SEM), 1HNMR, X-ray diffraction, and UV-UV
The study concluded
It is derived from infrared spectra, nuclear magnetic resonance, and diffraction
X-rays and ultraviolet rays show that the link between the guest and betacyclodextrin is in a proportion
1:1 for all prepared complexes.
The binding between the compounds and betacyclodextrin is in two directions, the first being on the one hand
The aldehyde and the other from the sulfa side
The solubility of the prepared bases is improved when they form implicit complexes with betacyclodextrin
Study recommended
Compounds used in the study Schiff bases derived from some sulfa drugs were used
As anti-bacterial and anti-inflammatory, but because it is less soluble in water, this is what limited
of use as a treatment. Therefore, these compounds were complexed with betacyclodextrin and became

The College of Education for Pure Sciences at the University of Basra discussed the preparation of some implicit complexes of Schiff bases with β-cyclodexrin and the study of their physical properties)
cyclodextrins
The letter presented by the researcher (Tawfiq Kazem Mahdi) included
It is a group of natural products formed during the bacterial decomposition of starch. Which can split and rearrange the polymer chain of starch leading to the formation of various cyclodextrins. Therefore, dextrins are non-reducing cyclic sugars that are crystalline and homogeneous consisting of glucose units.
The most common cyclodextrins are (α-cyclodextrains, β-cyclodextrains, γ-cyclodextrains) containing different numbers of glucose units (8, 7, 6), respectively, these units are linked by α-(1→4) glycosidic bonds.
These bonds that are formed between glucose units form ring structures where the three cyclodextrins are equal in length and different in width depending on the number of glucose units forming the ring, where the inner cavity of the cyclodextrins is hydrophobic and lipophilic.
Aim of the study
Study of the physical properties of some implicit complexes of Schiff bases derived from some sulfa drugs with
Betacyclodextrin prepared by freeze-drying method, and comparison of physical properties with Schiff bases
The free physical and spectroscopic methods are infrared, FT-IR, scanning electron microscopy (SEM), 1HNMR, X-ray diffraction, and UV-UV
The study concluded
It is derived from infrared spectra, nuclear magnetic resonance, and diffraction
X-rays and ultraviolet rays show that the link between the guest and betacyclodextrin is in a proportion
1:1 for all prepared complexes.
The binding between the compounds and betacyclodextrin is in two directions, the first being on the one hand
The aldehyde and the other from the sulfa side
The solubility of the prepared bases is improved when they form implicit complexes with betacyclodextrin
Study recommended
Compounds used in the study Schiff bases derived from some sulfa drugs were used
As anti-bacterial and anti-inflammatory, but because it is less soluble in water, this is what limited
of use as a treatment. Therefore, these compounds were complexed with betacyclodextrin