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Dr. Zainab Mohammed Almarhoon

Associate Professor

Faculty

كلية العلوم
Building 5 Floor 3 Room no 252
المنشورات
مقال فى مجلة
2024

Structure-directing interactions in the crystals of tertiary butyl carbazate based imines: A combined experimental and theoretical investigation.

A convenient and facile synthesis of (E)-Tert-butyl 2-(4-methoxybenzylidine) hydrazine carboxylate(a), (E)Tert-butyl-2-benzylidene hydrazine carboxylate(b), (E)-Tert-butyl-2-(2-nitrobenzylidene) hydrazine carboxylate (c), (E)-Tert-butyl-2-(2-bromobenzylidene) hydrazine carboxylate(d), (E)-tert-butyl 2-(4-chorobenzylidene) hydrazine carboxylate(e) and (E)-Tert-butyl-2-(4-nitrobenzylidene) hydrazine carboxylate(f) were accomplished by refluxing t-butyl carbazate with an appropriate aldehyde in ethanol. In-depth spectroscopic methods combined with X-ray crystallography and theoretical calculations were used to characterize and identify interactions between and within different groups of t-butyl carbazate based imines(a-e). Compound a, b and e crystallizes in orthorhombic crystal system with Pca21space group, while as compound c, d and f crystallizes in monoclinic crystal system with P21/c space group. For compounds a-f the dominant structure-directing motif is a pairwise O & sdot;& sdot;& sdot;H interaction between carbonyl oxygens with hydrazine hydrogen and aromatic hydrogens in the form of NH...O = C and CH...O = C. In addition to this, Pi stacking interactions along with CH...Pi interactions and other short contacts are the defining aspect of crystal packing. Their solid-state behavior was also studied using Hirshfeld surfaces. Hirshfeld surface analysis was also applied to discern the intermolecular interactions, highlighting the significance of hydrogen bonding, van der Waals forces, and the influence of specific substituents. Crystal packing motifs were investigated with the aid of Hirshfeld surface fingerprint plots. Using the quantum theory of atoms in molecules and non-covalent interaction methods, hydrogen bonds and other weak interactions were examined. The key factor forming the hydrogen-bond system is the ability of hydrazine and carboxylate groups to donate and take protons, which ultimately leads to the establishment of interaction networks.

رقم المجلد
1305
مجلة/صحيفة
Journal of Molecular Structure
الصفحات
137724
مزيد من المنشورات
publications

In recent years, the use of natural compounds has gained much attention due to their low toxicity and wide availability. This work focused on using oleic acid (OA) as a widely available natural…

بواسطة Abdullah, Mahmood M.S.; Faqihi, Noorah A.; Al-Lohedan, Hamad A.; Almarhoon, Zainab M.; Karami, Abdulnasser Mahmoud.
2023
publications

A convenient and facile synthesis of (E)-Tert-butyl 2-(4-methoxybenzylidine) hydrazine carboxylate(a), (E)Tert-butyl-2-benzylidene hydrazine carboxylate(b), (E)-Tert-butyl-2-(2-nitrobenzylidene)…

بواسطة Bhat, MA ; Anis, I ; Almarhoon, ZM ; Bhat, SA ; Jan, M ; Dar, MA ; Butcher, RJ
2024
publications

Development of highly competent and stable electrocatalysts for electrochemical water splitting to attain oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is highly…

بواسطة Almarhoon, ZM ; Manzoor, I ; Shah, JH ; Ozcan, HG ; Abid, AG ; Allakhverdiev, SI
2024