The absorption and fluorescence spectra of 2-styrylquinoline (2-StQ) indicate that two conformers exist in equilibrium in aprotic solvents, whereas only one conformer exists in protic solvents. The intermolecular hydrogen bonding between the solute and solvent plays an important role in changing the
Effect of pressure on the conformational equilibrium of 2-haloethanol in carbon disulfide
β Scribed by Seiji Sawamura; Keizo Suzuki; Yoshihiro Taniguchi
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 266 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
IR spectra of 2-baloethanoI.s (CH2XCH20H, X = CI, Br, and I) in carbon disulfide were measured at 25Β°C up to 2.5 kbar. The volume changes accompanying the transformation to the Gg conformer of the compounds were -12, eO.5, and +1.3 cm3 moT' for X = Cl, Br, and I, respectively.
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The relative energies and dipolar properties of two conformers of 2,2V-bipyridine (1) were calculated using AM1 and ab initio methods. Dipole moments of 1 and pyridine in many organic solvents were determined. On this basis, the Gibbs energy DG (s) for the conformational s-transWs-cis equilibrium of
## Abstract A conformational equilibrium exists in solution between two skew forms (__s__^+^ and __s__^β^) of [2.2]paracyclophane (1a). The vicinal coupling constants in the ^1^HβNMR spectra of the bridge protons in the six __ar__βmonosubstituted derivatives 1bβ1g (Rο£ΎCN, NO, Br, CH~3~, CHO, and NO~
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