Abstract

In this study, bis (1a, b) and tetrakis (2a, b) cyclotriphosphazenes containing aryl thio groups were reacted with n-butyl amine. Deprotonation reactions of the obtained mono amino bis phenylthio (3a, b) and bis naphthylthio (4a, b) cyclotriphosphazenes were carried out in the presence of NaH base. New N,N-spiro bridged biscyclotriphosphazenes containing bis geminal phenylthio (5a-I and 5a-II) and naphthythio (5b-I and 5b-II) groups were created. Characterization of the newly synthesized compounds was performed by MALDI-TOF, 31P and 1H NMR spectroscopy, and single-crystal X-Ray crystallography (5a-I and 5b-I). Photophysical properties of compounds 1a, b, 2a, b, 5a-I, and 5b-I were determined using UV/vis and fluorescence spectroscopies. At the same time, the structures of N,N-spiro bridged biscyclophosphazenes were comprehensively evaluated with the structures of previously synthesized biscyclophosphazenes containing different functional groups.

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