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1,2,3-Dithiazolyl and 1,2,35-Dithiadiazolyl Radicals as Spin-Bearing ...

1,2,3-Dithiazolyl and 1,2,35-Dithiadiazolyl Radicals as Spin-Bearing ...

1,2,3-Dithiazolyl and 1,2,35-Dithiadiazolyl Radicals as Spin-Bearing ...

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some effect on several of the bond lengths which would therefore impact frequency of the<br />

absorption <strong>as</strong>sociated with the stretches of the bonds that are most affected by the<br />

presence of the extra electron. The peak <strong>as</strong>sociated with the N-S bond within the new<br />

1,2,3-DTA ring w<strong>as</strong> at 721 cm -1 <strong>and</strong> h<strong>as</strong> shifted substantially to 680 cm -1 . The weak<br />

intensity peak at 1261 cm -1 <strong>as</strong>sociated with the N-S stretches of the 1,2,5-TDA ring is not<br />

shifted substantially, however the medium intensity peaks at 936 <strong>and</strong> 584 cm -1 in V-3<br />

have shifted to 913 <strong>and</strong> 575 cm -1 in V-1 respectively, both lower than in the precursor<br />

salt. Similarly, the C-N stretches have shifted form 1482 <strong>and</strong> 15<strong>35</strong> cm -1 in V-3 to 1493<br />

<strong>and</strong> 1544 cm -1 respectively in V-1. The C-Cl stretch h<strong>as</strong> also shifted from an absorption<br />

at 861 cm -1 in V-3 to 814 cm -1 in V-1.<br />

Figure 5-4. Infrared spectra of V-1 <strong>and</strong> overlaid with V-3. Peaks labelled for V-1 only.<br />

5.2.4 X-ray Crystallography<br />

The only compound for which X-ray crystallography quality crystals were obtained<br />

w<strong>as</strong> V-4. They were grown from a combination of acetonitrile <strong>and</strong> chlorobenzene <strong>as</strong><br />

145

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