Synthesis and 1H-, 15N-, 31P-, 183W-Multinuclear Magnetic Resonance Study of the Cyclotriphosphazenes [N3P3(dobp)2(OC5H4N-4)2] and [N3P3(dobp)(OC5H4N-4)4] and Their W(CO)5 Complexes (dobp = 2,2′-dioxybiphenyl)
✍ Scribed by Gabino A. Carriedo; Francisco J. García Alonso; José L. García; Rodrigo J. Carbajo; Fernando López Ortiz
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 269 KB
- Volume
- 1999
- Category
- Article
- ISSN
- 1434-1948
No coin nor oath required. For personal study only.
✦ Synopsis
The reactions of [N 3 P 3 (dobp) 2 Cl 2 ] and [N 3 P 3 (dobp)Cl 4 ] with revealed that the complexation of the N atom of one 4oxypyridine ligand by the W(CO) 5 fragment has a a mixture of HOC 5 H 4 N-4 and K 2 CO 3 in acetone give the cyclotriphosphazenes [N 3 P 3 (dobp) 2 (OC 5 H 4 N-4) 2 ] and [N 3 P 3 -measurable effect on other parts of the phosphazene molecule very far away from the coordination site. The (dobp)(OC 5 H 4 N-4) 4 ], respectively. These compounds react with [W(MeOH)(CO) 5 ] in methanol to give mixtures of the changes observed in δ 183 W have been used to identify the components in mixtures of compounds incorporating polymetallic complexes [N 3 P 3 (dobp) 2 (OC 5 H 4 N-4) 2 {W(CO) 5 } x ] (x = 1, 2) and [N 3 P 3 (dobp)(OC 5 H 4 N-4) 4 {W(CO) 5 } x ] (x = 1-4), different numbers of tungsten atoms in the molecule. The characterization of less sensitive nuclei has been which are unstable in solution, slowly undergoing loss of the pentacarbonyl moiety. A complete characterization by accomplished by means of indirect detection methods. multinuclear 1 H, 15 N, 31 P, 183 W magnetic resonance has probe for assessing structural and bonding effects of the
📜 SIMILAR VOLUMES
Tetraethylphosphonium azide, [P(C 2 H 5 ) 4 ] ם [N 3 ] מ , was prepared from tetraethyl phosphonium bromide and silver azide. Single crystals of [P(C 2 H 5 ) 4 ] ם [N 3 ] מ were grown from dichloromethane/THF (10:1) solution. The structure was determined by single-crystal X-ray diffraction a
Reaction of elemental antimony with sulfur under mild hydrothermal conditions yielded different polysulfidoclusters of antimony. These were isolated as tetraphenylphosphonium salts [P(C 6 H 5 ) 4 ] 3 Sb 3 S 25 and [P(C 6 H 5 ) 4 ] 2 Sb 2 S 15 2(C 3 N 2 H 6 ) and their crystal structures were determi