6965-62-4Relevant articles and documents
Tandem dinucleophilic cyclization of cyclohexane-1,3-diones with pyridinium salts
Kiamehr, Mostafa,Moghaddam, Firouz Matloubi,Mkrtchyan, Satenik,Semeniuchenko, Volodymyr,Supe, Linda,Villinger, Alexander,Langer, Peter,Laroshenko, Viktor O.
supporting information, p. 1119 - 1126 (2013/07/19)
The cyclization of cyclohexane-1,3-diones with various substituted pyridinium salts afforded functionalized 8-oxa-10-aza-tricyclo[7.3.1.0 2,7]trideca-2(7),11-dienes. The reaction proceeds by regioselective attack of the central carbon atom of t
Substantial formation of hydrates and hemiacetals from pyridinium ketones
Huang, Sha,Miller, Amanda K.,Wu, Weiming
scheme or table, p. 6584 - 6585 (2011/02/24)
Pyridinium ketones have been found to exist as hydrates and hemiacetals in considerable amount in aqueous and alcoholic solutions, respectively. The relative position of the pyridinium positive charge has a large effect on the equilibrium constants. The polar substituent constants, σ,* of the pyridinium group substituted at different positions can be estimated from the hydration constants.
Substituent effects on formation of cation dimers by weak hydrogen bonds in crystals of carbonyl pyridinium salts of ni(dmit)2
Tomono, Kazuaki,Koyano, Ayako,Morita, Takashi,Miyamura, Kazuo
experimental part, p. 1152 - 1159 (2009/12/25)
Five 1:1 salts of 3-X-1-methylpyridinium (X = benzoyl, acetyl, methoxycarbonyl, carboxy, and aminocarbonyl; abbreviated as Ben, Ace, Met, Car, and Ami, respectively) cations with a [Ni(dmit)2]- anion ([Ben]+[Ni(dmit)2]- (1), Ace] +[Ni(dmit)2]- (2), [Met]+[Ni(dmit) 2]- (3), [Car]+[Ni(dmit)2] - (4), and [Ami]+[Ni(dmit)2]- (5)) have been synthesized and characterized by single-crystal X-ray analysis and conductivity measurements. In the crystals, three cations 1-3 were found to form dimers by weak C-H...O hydrogen bonds, and the arrangements of cations had a strong relation with the electronic effect of the substituents. The cations of 1-3 formed similar centrosymmetrically associated dimers constructed by weak C-H...O hydrogen bonds, whose geometric parameters had a correlation with the electronic effect of the substituents. A cation of 4 also formed centrosymmetrically associated dimer, but it was made by an O-H...O hydrogen bond as usually observed in the case of carboxylic acid. In contrast with other complex salts, cations of 5 formed one-dimensional structure by C-H...O hydrogen bonding. The conductivities of salts 1, 2, 3, 4, and 5 at room temperature were 1.00 × 10-6, 1.10 × 10-6, 2.86 × 10-6, 9.77 × 10-6, and 8.75 × 10 -7Scm-1, respectively.