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  • 1
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An empirical method is suggested for estimating the NQR frequencies of substituted chloromethanes. The frequencies are given by the equation νCl = νo + ∑imi, where the parameters mi are characteristic of the substituent groups, with additive properties in the case of multiple substitution for substituted chloromethanes. The calculations reveal that (i) as in chlorobenzenes, the effect of substituent groups on the NQR frequencies is additive to a first order of approximation, (ii)the effect is much larger in chloromethanes than in chlorobenzenes, (iii) the relative effects of different substituent groups are similar in the two sets, (iv) where there is more than one substituent group their mutual interaction is of the same order of magnitude as the crystal field effects.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two NQR lines were observed for 35Cl in 2,5-dichloro-4-nitroaniline at room temperature, using a self-quenched super-regenerative spectrometer. Analysis of the Zeeman effect on the two lines using a cylindrical single crystal reveals that the crystal belongs to the monoclinic system. The principal field gradient Z axes enclose an angle of 35° and 28° in the cases of the low and high frequency resonance lines, respectively. The b axis is parallel to 81°, 280°. The unit cell contains either two or a multiple of two molecules. The molecules in the crystal can be arranged into two sets, with the molecular planes in each set being parallel among each other. The angle subtended between the two planes is 159° and each of the planes is inclined to the b axis at an angle of 79.5°. There is an in-plane bending of the two C—Cl bonds by 5.5°. The ionic, single bond and double bond characters of the C—Cl bonds for both chlorines are almost equal, and are in the ratio 24:73:3.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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