Reactions of monoazadienes with metal carbonyl complexes III. Thermal conversion of n-alkyl-(e)-crotonaldimine with ru3(co)12 to σ-n,μ2-η3-allyl and μ2-η3-azaallyl bonded six electron fragments coordinated to a hexacarbonyl diruthenium unit. X-ray single crystal structure determinations of ru2(co)6{σ-n,μ2-η3-ch2cc(h)c(h)nc4h9-t} and ru2(co)6{μ2-η3-c2h5cc(h)nc4h9−}

Autor: Cornelis J. Elsevier, L.H. Polm, Wilhelmus P. Mul, F. Muller, Kees Vrieze, Casper H. Stam, Martin J. N. Christophersen
Rok vydání: 1988
Předmět:
Zdroj: Polyhedron. 7:2521-2530
ISSN: 0277-5387
DOI: 10.1016/s0277-5387(00)83868-1
Popis: Two complexes Ru 2 (CO) 6 L that arise from thermal reactions of monoazadienes ( E )-CH 3 C(H)C(H)C(H)NR ( 1 ); (R = t−C 4 H 9 , i−C 3 H 7 , c− C 6 H 11 ) with Ru 3 (CO) 12 are reported. The bonding of the six-electron donating organic fragments in the complexes Ru 2 (CO) 6 {σ-N,μ 2 -η 3 -CH 2 CC(H)C(H)NC 4 H 9 −t } ( 4a ) and Ru 2 (CO) 6 {C 2 H 5 CC(H) NC 4 H 9 −t } ( 5a ) is described on the basis of their X-ray single crystal structure determinations. In compound 4a the organic ligand is σ-N,μ 2 -η 3 -coordinated and contains a distorted η 3 -allyl fragment bridging the two Ru(CO) 3 moieties. Compound 5a features a μ 2 -η 3 -azaallyl dianion which bridges the Ru centres in the Ru 2 (CO) 6 core. Possible pathways for the formation of 4a and 5a , involving dehydrogenation and a 1,2-H shift, respectively, are discussed.
Databáze: OpenAIRE