Category: OTHER PAPERS

F. An et al., J. Hazardous Materials 2009, 168, 352-357: Adsorption mechanism and property of a novel adsorption material PAM/SiO2 towards 2,4,6-trinitrotoluene.

S. Taubert et al., J Org Chem. 2009, 74, 6495-6502: Magnetically induced currents in bianthraquinodimethane-stabilized Moebius and and Huckel [16]annulenes.

A. Pawlukojc et al., Spectrochim. Acta, A 2006, 63, 766-773: Low frequency internal modes of 1,2,4,5-tetramethylbenzene, tetramethylpyrazine and tetramethyl-1,4-benzoquinone: INS, Raman, infrared and theoretical DFT studies.

H.-M. Huang et al., J. Colloid and Interface Science, 2003, 263, 23-28: Microcalorimetric studies of the mechanism of interaction between designed peptides and hydrophobic adsorbents.

A. Tsuge, et al., J. Chem. Res.-S, 2001, 250-252: Synthesis and electrochemical properties of bis([2.2]metacyclophane) bipyridinium.

S. Sundararajan et al., Spectrochimica Acta, A 2000, 56, 1855-1867: Trimethylphosphate-acetylene interaction: a matrix-isolation infrared and ab initio study.

H. Abe, K. Miyamura, Inorg. Chim. Acta 2000, 298, 90-93: Monolayer formation and aggregation of nickel(II) complexes coordinated with salen substituted by non-linear alkyl side chains.

T. Fujii, K. Miyamura, Bull. Chem. Soc. Jpn. 2000, 73, 365-368: Observation of molecular alignments and dimer formation of bis(5-alkylsalicylidene)ethylenediaminatonickel(II) in a monolayer.

V. Tsukanova et al., Chem. Phys. 1999, 250, 207-215: Compression of the dye monolayer at the air/water interface studied by second harmonic generation.

J. Otsuki et al., Tetrahedron Lett. 1993, 34, 1945-48: Oligosaccharide-peptide interaction. Binding of maltodextrin to Trp-Trp via sugar-bisindole intercalation.

M. Hirota, M. Nishio, Kagaku 1991, 46, 592-595: The CH/pi hypothesis. Phenyl and t-butyl groups come close to each other [REVIEW]. (in Japanese)

M. Hirota et al., Tetrahedron 1983, 39, 3091-3099: Theoretical description of the preference of vicinal alkyl/phenyl gauche conformation by molecularmechanics. An alternative interpretation for the CH-pi attractive interaction.

M. Nishio, Kagaku no Ryoiki 1979, 33, 422-432: CH/pi hypothesis and weak chemical interactions [REVIEW]. (in Japanese)

M. Nishio, Kagaku no Ryoiki 1977, 31, 834-841; 998-1006: Stereochemistry and interactions between groups - Conformation and reaction specificity [REVIEW]. (in Japanese)

Z. Yoshida, E. Osawa, Nippon Kagaku Zasshi 1966, 87, 509-535: Intermolecular hydrogen bond involving a pi-base as the proton acceptor. (in Japanese)

J. C. D. Brand et al., J. Chem. Soc. 1965, 5914-5919: The ethynyl hydrogen bond. Part II. The association of benzoylacetylene with aromatic hydrocarbons and with n-butyl ether studied by infrared and proton resonance spectroscopy and by calorimetry.

R. West, C. S. Kraihanzel, J. Am. Chem. Soc. 1961, 83, 765-768: Hydrogen bonding studies. VI. The hydrogen bonding properties of acetylenes.

N. Nakagawa, Nippon Kagaku Zasshi 1961, 82, 141-147: Solvent shifts in NMR spectra of organic compounds. I. The solvation shift of the methyl group. (in Japanese)

N. Nakagawa, S. Fujiwara, Bull. Chem. Soc. Jpn. 1961, 34, 143-146: Solvent shift of methyl proton nuclear magnetic resonance.

J. V. Hatton, R. E. Richards, Trans. Faraday Soc. 1961, 57, 28-33: Solvent effects in the high resolution resonance spectra of some acetylenes.

H. Shimizu, Nippon Kagaku Zasshi 1960, 81, 1025-1028: Solvent effect in the NMR spectra of fatty acids with aromatic compounds. (in Japanese)

N. Nakagawa, S. Fujiwara, Bull. Chem. Soc. Jpn. 1960, 33, 1634: Association shifts of NMR spectra of phenylacetylene.

L. W. Reeves, W. G. Schneider, Can. J. Chem. 1957, 35, 251-261: Nuclear magnetic resonance measurements of complexes of chloroform with aromatic molecules and olefins.

C. M. Huggins, G. C. Pimentel, J. Phys. Chem. 1956, 60, 1615-1619: Systematics of the infrared spectral properties of hydrogen bonding systems: Frequence shift, half width and intensity.

C. M. Huggins, G. C. Pimentel, J. Chem. Phys. 1955, 23, 896-898: Infrared intensity of the C-D stretch of chloroform-d in various solvents.

M. Tamres, J. Am. Chem. Soc. 1952, 74, 3375-3378: Aromatic compounds as donor molecules in hydrogen bonding.