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Trichloro-fluoro-methane

Subsequent to the 1982 compilation of Lounila and Jokisaari [237], a large number of studies report chemical shift anisotropies for various nuclei in liquid crystalline solvents. Representative examples include ACTh in dichloromethylphosphine [243], methylisothiocyanide [244], and norborna-diene [141] A(Tc in chloro- and bromoform [245], bis(trimethylsilyl)diacetylene [246], and pyridine, pyrazine, pyridazine, and pyrimidine [247] ACTh and ACq in butyne [248], fluoro- [245,249], bromo- [245], and iodomethane [244, 245, 250], ethylene [251], methylisocyanide [252], dimethyl-mercury [253], benzene [250, 254, 255], 1,3,5-trichloro- [99, 256], 1,3,5-tribromo-[244], and 1,3,5-trinitrobenzene [244] Afluoro-methane [249] Aa in dimethylmercury [253] AcTsein carbon diselenide [258] AcTje in tellurophene [259] and AOxe [260]. [Pg.875]

See other pages where Trichloro-fluoro-methane is mentioned: [Pg.369]    [Pg.997]    [Pg.12]    [Pg.10]    [Pg.429]    [Pg.369]    [Pg.997]    [Pg.12]    [Pg.10]    [Pg.429]    [Pg.574]    [Pg.86]   


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