Binuclear cyclooctatetraene–iron carbonyl complexes: examples of fluxionality and valence tautomerism. (14th December 2015)

• Record Type: Journal Article
• Authors: Wang, Hongyan; Sun, Songsong; Wang, Hui; King, R. Bruce
• Is Part Of: New journal of chemistry. Volume 40:Number 2(2016:Feb.)
• Page Start: 1521
• Page End: 1528
• Publication Date: 2015-12-14
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c5nj02307f
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : Fluxionality and valence tautomerism are studied in the experimentally observed trans -(η 4, η 4 -C8 H8 )Fe2 (CO)6, cis -(η 3, η 3 -C8 H8 )Fe2 (CO)6, and cis -C8 H8 Fe2 (CO)4 (μ-CO) structures using density functional theory. Abstract : Reactions of cyclooctatetraene with iron carbonyls under various conditions give not only the monomeric (η 4 -C8 H8 )Fe(CO)3 but three C8 H8 Fe2 (CO)6 isomers and one C8 H8 Fe2 (CO)5 isomer. Density functional theory on the C8 H8 Fe2 (CO)6 system shows the trans -(η 4, η 4 -C8 H8 )Fe2 (CO)6 isomer to be the lowest energy isomer. The cis -(η 3, η 3 -C8 H8 )Fe2 (CO)6 isomer with an Fe–Fe bond and an uncomplexed CC double bond in the C8 H8 ring lying ∼11 kcal mol −1 in energy above trans -(η 4, η 4 -C8 H8 )Fe2 (CO)6 appears to correspond to one of the metastable C8 H8 Fe2 (CO)6 isomers obtained under relatively mild conditions. However, the cis -(η 4, η 4 -C8 H8 )Fe2 (CO)6 structure without an Fe–Fe bond suggested for the other metastable isomer appears to be a high-energy structure with a large imaginary vibrational frequency. Following the corresponding normal mode leads to cis -(η 3, η 3 -C8 H8 )Fe2 (CO)6 . For C8 H8 Fe2 (CO)5 the two lowest energy structures are singly bridged cis -C8 H8 Fe2 (CO)4 (μ-CO) structures differing only by a 22.5° rotation of the C8 H8 ring around the central Fe2 unit. One of these structures is the experimental C8 H8 Fe2 (CO)5 structure. The closeness in energy of these two C8 H8 Fe2 (CO)5 structures is consistent with the experimentally observed fluxionality of this molecule in the NMR spectrum at low temperatures. The unsaturated C8 H8 Fe2 (CO) n ( n = 4, 3) structures obtained by further decarbonylation of C8 H8 Fe2 (CO)5 retain the bridging bis(tetrahapto) or bis(pentahapto) C8 H8 rings of C8 H8 Fe2 (CO)5 and provide examples of structures with formal FeFe double bonds with the lowest energy such structures having triplet rather than singlet spin states. Viable carbonyl-rich (η 2, η 2 -C8 H8 )Fe2 (CO)8 and (η 4, η 2 -C8 H8 )Fe2 (CO)7 structures represent possible intermediates in the formation of the various C8 H8 Fe2 (CO) n ( n = 6, 5) species from cyclooctatetraene and iron carbonyls.