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- W2000975777 abstract "Abstract The possibilities of intermolecular hydrogen bonding interactions were studied between 2-phenyl-3(2′-furyl)propenoic acid and 2-phenyl-3(3′-furyl)propenoic acid stereoisomers (α-phenyl furylcinnamic acids) by semiempirical quantum chemical method. Calculations revealed that long-range ordering was only possible between the hydrogen-bonded dimers of the Z isomers. Then, the chain-like structures were held together by (phenyl)C–H⋯(furyl)O close contacts. However, the chain length could not be increased infinitely, it was limited to the pentamer of dimers. If the propenoic acid held two furyl substituents, the dimers of both stereoisomers, due to steric congestion, lost the possibility of intermolecular hydrogen bonding." @default.
- W2000975777 created "2016-06-24" @default.
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- W2000975777 date "2003-01-01" @default.
- W2000975777 modified "2023-10-15" @default.
- W2000975777 title "Intermolecular hydrogen bonding interactions between α-phenyl furylcinnamic acid stereoisomers studied by semiempirical quantum chemical method" @default.
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- W2000975777 doi "https://doi.org/10.1016/s0166-1280(02)00582-1" @default.
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