Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9769863 | Journal of Molecular Structure | 2005 | 8 Pages |
Abstract
The condensation reactions of {N-[(2-hydroxyphenylmethyl)amino]-methylpyridines (5-8) with trimer, N3P3Cl6, have been afforded partially substituted novel spiro-cyclic phosphazene derivatives (9-12) (Scheme 1). Compounds (9-12) have been characterized by elemental analyses, FTIR, 1H-, 13C-, 31P-NMR, HETCOR, and MS. The structure of the spiro-cyclic phosphazene (9) has been examined crystallographically. It crystallizes in the P21/n space group with a=10.7906(10)Â Ã
, b=8.5625(17)Â Ã
, c=21.187(5)Â Ã
, β=91.298(12)°, V=1957.1(6) Ã
3, Z=4 and Dx=1.660 g cmâ3. The structure consists of a non-planar phosphazene ring with a bulky methylpyridinyl and a benzo-fused spiro-cyclic side group. The six-membered spiro-cyclic ring has a twist-boat conformation.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hakan Dal, Serap Safran, Yasemin Süzen, Tuncer Hökelek, Zeynel Kılıç,