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Spectroscopic study of solvent effects on the electronic absorption spectra of morpholine and its complexes Masoud, Mamdouh Saad Ali, Alaa Eldin Elasala, Gehan Shaaban Elwardany, Rehab Elsaid UV spectra Absorption Dipole moment Solvent polarity Solvatochromic Morpholine complexes The electronic absorption spectra of morpholine and its five morpholine complexes have been studied in different solvents of various polarities. The regression and correlation coefficients have been calculated with the SPSS program. Solvation energy relationships were deduced from spectral shifts and correlated with solvent parameters α (solvent hydrogen bond donor acidity), β (solvent hydrogen bond acceptor basicity), and π* (dipolarity/polarizability). The percentage contributions of the calculated solvatochromic parameters show that classic solvation effects play a major role in explaining the spectral shifts in all investigated complexes. The blue shift of [Fe(MOR)3Cl3]·4H2O, [Ni(MOR)4Cl2]·4H2O, and [Cu(MOR)4Cl2]·6H2O complexes is due to the formation of hydrogen bonds, which suggests the stabilization of the ground electronic state compared with the excited state. [CuNi(MOR)2Cl4]·4H2O and [CuZn(MOR)3Cl4]·2H2O are mixed metal complexes that suffer a red shift due to the solute-solvent interactions, which causes stabilization of the excited solute state with increasing solvent polarity. The bands are affected by specific solute-solvent interactions including hydrogen bond donor ability (acidity) and hydrogen bond acceptor ability (basicity) and nonspecific solute-solvent interactions including electromagnetic interaction between the dipole moments of solute and polar solvents. Atlanta Publishing House LLC 2023-03-31 info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion application/pdf https://www.eurjchem.com/index.php/eurjchem/article/view/2365 10.5155/eurjchem.14.1.53-64.2365 European Journal of Chemistry; Vol. 14 No. 1 (2023): March 2023; 53-64 2153-2257 2153-2249 eng https://www.eurjchem.com/index.php/eurjchem/article/view/2365/pdf_2365 Copyright (c) 2023 Authors