Binuclear cyclooctatetraene-iron carbonyl complexes: examples of fluxionality and valence tautomerism

被引:7
|
作者
Wang, Hongyan [1 ,2 ,3 ,4 ]
Sun, Songsong [1 ,2 ]
Wang, Hui [1 ,2 ]
King, R. Bruce [3 ,4 ]
机构
[1] Southwest Jiaotong Univ, Sch Phys Sci & Technol, Chengdu 610031, Peoples R China
[2] Minist Educ China, Key Lab Adv Technol Mat, Chengdu 610031, Peoples R China
[3] Univ Georgia, Dept Chem, Athens, GA 30602 USA
[4] Univ Georgia, Ctr Computat Quantum Chem, Athens, GA 30602 USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
DENSITY-FUNCTIONAL THEORY; MOLECULAR-STRUCTURE; CORRELATION-ENERGY; BASIS SETS; TRICARBONYL; CYTOCHROME-P450; THERMOCHEMISTRY; PHOTOCHEMISTRY; APPROXIMATION; TRANSITION;
D O I
10.1039/c5nj02307f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reactions of cyclooctatetraene with iron carbonyls under various conditions give not only the monomeric (eta(4)-C8H8)Fe(CO)(3) but three C8H8Fe2(CO)(6) isomers and one C8H8Fe2(CO)(5) isomer. Density functional theory on the C8H8Fe2(CO)(6) system shows the trans-(eta(4),eta(4)-C8H8)Fe-2(CO)(6) isomer to be the lowest energy isomer. The cis-(eta(3),eta(3)-C8H8)Fe-2(CO)(6) isomer with an Fe-Fe bond and an uncomplexed C=C double bond in the C8H8 ring lying similar to 11 kcal mol(-1) in energy above trans-(eta(4),eta(4)-C8H8)Fe-2(CO)(6) appears to correspond to one of the metastable C8H8Fe2(CO)(6) isomers obtained under relatively mild conditions. However, the cis-(eta(4),eta(4)-C8H8)Fe-2(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-(eta(3),eta(3)-C8H8)Fe-2(CO)(6). For C8H8Fe2(CO)(5) the two lowest energy structures are singly bridged cis-C8H8Fe2(CO)(4)(mu-CO) structures differing only by a 22.5 degrees rotation of the C8H8 ring around the central Fe-2 unit. One of these structures is the experimental C8H8Fe2(CO)(5) structure. The closeness in energy of these two C8H8Fe2(CO)(5) structures is consistent with the experimentally observed fluxionality of this molecule in the NMR spectrum at tow temperatures. The unsaturated C8H8Fe2(CO)(n) (n = 4, 3) structures obtained by further decarbonylation of C8H8Fe2(CO)(5) retain the bridging bis(tetrahapto) or bis(pentahapto) C8H8 rings of C8H8Fe2(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 (eta(2),eta(2)-C8H8)Fe-2(CO)(8) and (eta(4),eta(2)-C8H8)Fe-2(CO)(7) structures represent possible intermediates in the formation of the various C8H8Fe2(CO)(n) (n = 6, 5) species from cyclooctatetraene and iron carbonyls.
引用
收藏
页码:1521 / 1528
页数:8
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