N-H···O hydrogen bonding: An FT-IR, NIR study of N-methylformamide-ether systems
Branislav Jović, Aleksandar S. Nikolić, Erna Davidovic, Slobodan D. Petrovic
Abstract
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Branislav Jović, Aleksandar S. Nikolić, Erna Davidovic, Slobodan D. Petrovic
Abstract
Open-access reader
This paper reports the results of an FT-IR and NIR study of N-methylformamide in carbon tetrachloride solution in presence of ethers as the O-electron donors, i.e., diethyl ether (DEE), diisopropyl ether (DiPE), methyl t- -butyl ether (MtBE), dibutyl ether (DBE), dipentyl ether (DPE), tetrahydrofuran (THF) and tetrahydropyran (THP). The spectroscopic characteristics of the N-H???O hydrogen bonded complexes are given. In addition, the equilibrium constants for 1:1 complex formation were determined at 25?C using Mid-IR and NIR measurements.
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This paper reports the results of an FT-IR and NIR study of N-methylformamide in carbon tetrachloride solution in presence of ethers as the O-electron donors, i.e., diethyl ether (DEE), diisopropyl ether (DiPE), methyl t- -butyl ether (MtBE), dibutyl ether (DBE), dipentyl ether (DPE), tetrahydrofuran (THF) and tetrahydropyran (THP). The spectroscopic characteristics of the N-H???O hydrogen bonded complexes are given. In addition, the equilibrium constants for 1:1 complex formation were determined at 25?C using Mid-IR and NIR measurements.
Key concepts: Tetrahydrofuran, Chemistry, Diisopropyl ether, Ether, Tetrahydropyran, Diethyl ether, Hydrogen bond, Medicinal chemistry