Phosphorus-nitrogen compounds. Part 52. The reactions of octachlorocyclotetraphosphazene with sodium 3-(N-ferrocenylmethylamino)-1-propanoxide: Investigations of spectroscopic, crystallographic and stereogenic properties

Elmas G., Okumuş A., Hökelek T., Kilic Z.

INORGANICA CHIMICA ACTA, cilt.497, 2019 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 497
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1016/j.ica.2019.119106
  • Dergi Adı: INORGANICA CHIMICA ACTA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Anahtar Kelimeler: Bis-ferrocenyl-cyclotetraphosphazenes, Spectroscopy, Crystallography, Stereogenism, DNA INTERACTIONS, SPIRO-ANSA, SPIROCYCLIC CYCLOTRIPHOSPHAZENES, ANTIMICROBIAL ACTIVITIES, CHIRAL CONFIGURATIONS, BIOLOGICAL-ACTIVITIES, CYTOTOXIC ACTIVITIES, CRYSTAL-STRUCTURES, CYCLOTETRAPHOSPHAZENE, ANTITUBERCULOSIS
  • Ankara Üniversitesi Adresli: Evet

Özet

The reaction of octachlorocyclotetraphosphazene (tetramer, N4P4Cl8, 1) with two mole equivalents of sodium 3( N-ferrocenylmethylamino)-1-propanoxide (2) gave the novel ansa-spiro (3), 2-trans-6-dispiro (4), 2-cis-6-dispiro (5), 2-trans-4-dispiro (6) and 2-cis-4-dispiro (7) cyclotetraphosphazenes. However, when the reaction was carried out with 1 and three mole equivalents of 2, seven products observed with respect to the P-31 NMR spectrum of the reaction mixture. Five of these products were identified as 3, 4, 5, 6 and 7, and the other two products are expected to be 2-trans-4-trans-6-trispiro (8) derived from 4 and/or 6, and 2-trans-4-cis-6-trispiro (9) derived from 5 and/or 7. Both of the trispiro products (8 and 9) were not isolated using column chromatography. Besides, when the reaction was made with 1 and excess amount of 2, the tetraspiro products were not observed by TLC and P-31 NMR spectrum of the reaction mixture. The structures of cyclotetraphosphazene derivatives were verified by ESI-MS, FTIR, H-1, C-13 and P-31 NMR spectral data. The molecular and solid state structures of 3, 5 and 6 were established by X-ray diffraction method. The X-Ray crystallographic data indicate that compounds 3 and 6 have three-different and two equivalent chiral P centers, respectively. The absolute configurations of 3 and 6 were also found to be as SS'S'' and RR.