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Anthony KERMAGORET - THESES ET MEMOIRES DE L'UDS

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Chapitre V<br />

[Ni(NOPON Me2 )Cl2]. 37 The presence of the CH3 substituents of the oxazoline function can be<br />

observed by the strong band at 1270 cm -1 for 7 which shifts to 1321 cm -1 for 8.<br />

2.3 Synthesis of the iron complexes<br />

The iron complexes 10-12 were prepared by reaction of one equiv of FeCl2·4H2O with<br />

ligands 1-3 , respectively, in CH2Cl2 at room temperature (Scheme 5).<br />

FeCl 2(H 2O) 4<br />

O<br />

O<br />

N<br />

Ph<br />

P<br />

1<br />

Ph<br />

P<br />

N<br />

N N<br />

2<br />

Ph<br />

P<br />

N N<br />

3<br />

O<br />

O<br />

CH 2Cl 2<br />

rt, 12 h<br />

CH 2Cl 2<br />

rt, 12 h<br />

CH 2Cl 2<br />

rt, 12 h<br />

O<br />

O<br />

N<br />

N<br />

N<br />

O N<br />

Scheme 5. Synthesis of iron complexes 10-12<br />

N<br />

Cl<br />

10<br />

P<br />

P<br />

Fe<br />

N<br />

Ph<br />

11<br />

Fe<br />

12<br />

N<br />

P<br />

Ph<br />

P<br />

N<br />

Fe<br />

N<br />

O<br />

N<br />

Cl<br />

Ph<br />

P Ph<br />

O<br />

2+<br />

(Fe 2OCl 6) 2-<br />

O<br />

2+<br />

(Fe 2OCl 6) 2-<br />

The iron complexes 10 and 11 precipitated instantaneously in CH2Cl2 and, after work-up, they<br />

were isolated as red powders in 62% and 58% yield, respectively. The IR spectrum of<br />

complex 10 was similar to that of the corresponding Ni complex 6. The strong IR band for the<br />

C=N vibration of 11 at 1639 cm -1 is shifted compared to that of its corresponding nickel<br />

complex 7 (1658 cm -1 ).<br />

8

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