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Reactivity of Ferriophosphaalkene [(η5-C5Me5)(CO)2Fe–P=C(NMe2)2] and Ferrioarsaalkene [(η5-C5Me5)(CO)2Fe–As=C(NMe2)2] Towards Trimethylaluminium, -gallium and -indium

✍ Scribed by Lothar Weber; Matthias H. Scheffer; Hans-Georg Stammler; Anja Stammler


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
308 KB
Volume
1999
Category
Article
ISSN
1434-1948

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✦ Synopsis


Reaction of equimolar amounts of the ferriophosphaalkene P; M = Al (2a), Ga (3a), In (4a) and E = As; M = Al (2b), Ga (3b), and In (4b). These compounds feature η 1 -coordination [(η 5 -C 5 Me 5 )(CO) 2 FeP=C(NMe 2 ) 2 ] (1a) or the ferrioarsaalkene [(η 5 -C 5 Me 5 )(CO) 2 FeAs=C(NMe 2 ) 2 ] (1b) with trimethyl-of the phosphaalkene or the arsaalkene ligand towards the Lewis acid via the pnictogen atom. The molecular structures aluminium, trimethylgallium and trimethylindium afforded the adducts [(η 5 -C 5 Me 5 )(CO) 2 FeE{MMe 3 }C(NMe 2 ) 2 ] with E = of 2a and 3a were elucidated by X-ray diffraction analyses.


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Metalloarsaalkene [(η5-C5Me5)(CO)2FeAs=C
✍ Lothar Weber; Matthias H. Scheffer; Hans-Georg Stammler; Beate Neumann 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 487 KB 👁 1 views

Reaction of equimolar amounts of the metalloarsaalkene [(η 5 -[Fe(CO) 4 ] (3), and [Cr(CO) 5 ] (4). These feature η 1 coordination of the arsaalkene ligand via the arsenic atom. The mo-C 5 Me 5 )(CO) 2 FeAs=C(NMe 2 ) 2 ] (1) with the carbonyl complexes [Ni(CO) 4 ], [Fe 2 (CO) 9 ], and [{(Z)-cyclooct