436162-62-8Relevant articles and documents
Activation and functionalization of vinylic C-F bonds by transition metal compounds: The factors determining reactions between nucleophiles and a (Perfluorovinyl)diiron(I) complex; syntheses of diiron derivatives containing new C-N, C-S, C-H and C-O bonds
Guennou De Cadenet, Karine,Rumin, Rene,Petillon, Francois Y.,Yufit, Dmitri S.,Muir, Kenneth W.
, p. 639 - 657 (2008/10/08)
The reactions between alcohols ROH (R = Me, Et) and RR(OH)2 (RR = CH2-CH2) and the [perfluoro(sulfanyl)vinyl]- diiron complex [{Fe(CO)3}2{μ-C(SMe) (CF3)CβCαF2}] (1) in THF at room temperature involve substitution at the Cα atom to give new (alkoxymethylene)thiaferracyclobutadiene compounds [{Fe(CO)3}2{μ-S(Me)C (CF3)CβCα(OR)2}] [R = Me (2a), Et (2b); RR = CH2CH2 (2c)]. Treatment of 1 with aniline and (methoxycarbonyl)hydrazine, bases of intermediate strength according to Pearson, produces α,β-substituted thiaferracyclopentadiene [{Fe(CO)3}2{μ-S(Me)C (CF3)Cβ(NHR)Cα-(NHR)}] [R = Ph (5a), NHC(O)OMe (5b)] complexes. It is suggested that these compounds form through initial nucleophilic attack at Cα to give the zwitterionic intermediate [{Fe(CO)3}2{μ-S(Me)C (CF3)CC(NRH)2}] (f). Thermally induced C-F bond activation is a feature of these reactions. When 1 reacts with thioamides containing three hard competitive primary and secondary amine functions and one soft thione function, the nucleophile first attacks at Cα through a secondary amine and, in a second step, at Cβ through the thiol function to give α,β adducts [{Fe(CO)3}2{μ-S(Me)C (CF3)CβSC(=NR2)N (R1)Cα(Cβ-Cα)] [R1 = NH2, R2 = CH3 (6a); R1 = CH3, R2 = H (6b); R1 = R2 = CH3 (6c)l possessing novel iminothiazolidine systems fused to the five-membered metallacyclic ring. Treatment of 1 with acetylhydrazine, which has three hard nucleophilic functions, results in the formation of the compound [{Fe(CO)3}2{μ-S(Me)C (CF3)C(H)C(10)NNC(Me)O(C(10)-O)}] (7a), in which an oxadiazole function is fused to the thiaazaferracyclohexene ring. The position of the fluorine substituent on the CαCβCγ(CF3)S(Me) ring of ferracyclopentadiene complexes has been found to be the essential factor determining the specific activation of the C-F bond. A single fluoro substituent attached to the β-carbon atom of the chain can be activated by nucleophiles to give α,β adducts [{Fe(CO)3}2{μ-S(Me)C (CF3)Cβ(X)Cα(NRR′)}] [X = OR″, R = R′ = R″ = Me (3a); X = OR″, R = R″ = Me, R″ = C(O)NMe2 (3b); X = SR″ (4)]. In contrast, complexes in which a single fluorine atom is linked to the α-carbon atom do not undergo C-F bond cleavage reactions. X-ray structures of compounds 2a, 3b, 5a, 5b, 6a and 7a are reported.
