Charge transfer associations are a well-established phenomena and a rather extensively investigated one also. Since the acceptor component of such complexes normally does not exist as a liquid under standard conditions, they wish to report on two organic liquids which function as acceptor components with suitable complimentary molecules. As indicated in Figure 1 (the presence of an extended shoulder in the spectra of the mixture), pentafluorobenzonitrile (PFBN) complexes with N,N,N{prime},N{prime}-tetramethyl-p-phenylenediamine (TMPD), with N,N-dimethylaniline (DMA), and with phenothiazine in cyclohexane. In addition, crystalline complexes of TMPN-PFBN and DMA-PFBN are obtained when the pure materials are mixed. These two organic bases also form solid complexes with hexafluorobenzene (HFB) when the materials are mixed in the pure state in a ratio of 1:1. However, new absorption bands are not detected in the spectra (in cyclohexane solutions) of mixtures of TMPD or DMA with HFB. When HFB is used as a solvent for TMPD or DMA, the solutions are visibly yellow. However, with time a reaction occurs as evident by the formation of a black precipitate. The solid complex formed between TMPD-PFBN, which is orange, was analyzed by a combination extraction and spectroscopic method and by vapor phase chromatography and found to contain a …

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The presence of several homologous series of porphyrins have been demonstrated in some oil shale rocks, shale oils, and petroleums. However, the application of microanalytical techniques (i.e., mass spectrometry and gas chromatography) to structure determination has been limited due to the low volatility of the porphyrin components. The authors report the synthesis of several novel Si(IV) etioporphyrin I derivatives and the effects that their various additional silicon ligands have on porphyrin volatility as measured by gas chromatography at normal pressure.