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Abstract
The condensation reaction of { N-[(2-hydroxyphenylmethyl)amino]-4,6-dimethylpyridine} ( 2), which is a reduction product of 1, with trimer N 3P 3Cl 6 affords partially a substituted spiro-cyclic phosphazene derivative ( 3). The fully substituted phosphazenes ( 4 and 5) have also been obtained from the reactions of 3 with the excess of pyrrolidine and morpholine. The characterizations and spectral investigations of these compounds have been made by elemental analyses, FTIR, 1H-, 13C-, 31P NMR, correlation spectroscopy (COSY), heteronuclear chemical shift correlation (HETCOR), heteronuclear multiple-bond correlation (HMBC) and mass spectroscopy (MS). The salient features of spectral data of these compounds have been discussed.
Published Version
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Schedule a callMore From: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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