Kinetics and mechanism of the proton transfer to Cp*Fe(dppe)H: Absence of a direct protonation at the metal site

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[1] Belkova, Natalia V.

[2] Revin, Pavel O.

[3] Epstein, Lina M.

[4] Vorontsov, Evgenii V.

[5] 1,Bakhmutov, Vladimir I.

[6] Shubina, Elena S.

[7] Collange, Edmond

[8] Poli, Rinaldo

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Shubina, E.S. (poli@u-bourgogne.fr) | 1600年 / American Chemical Society卷 / 125期

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[31] OXYGEN ATOM TRANSFER-REACTIONS TO METAL-CARBONYLS - KINETICS AND MECHANISM OF CO SUBSTITUTION-REACTIONS OF FE3(CO)12,RU3(CO)12,OS3E(CO)12 IN THE PRESENCE OF (CH3)3NO
SHEN, JK
SHI, YL
GAO, YC
SHI, QZ
BASOLO, F
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (08) : 2414 - 2418
[32] REACTION OF THE METAL-SUBSTITUTED VINYLIDENE COMPLEX CP'(CO)2MN[=C=(H)-FP-ASTERISK] WITH EXCESS BULI, GIVING ACYLATED DINUCLEAR BRIDGING ALKENYL COMPLEXES, CP'MNCP-ASTERISK-FE[MU-CH=C(E)-C(=O)-BU] (MU-CO)(CO)2 (E=H, ME) - CONFIRMATION OF THE INTRAMOLECULAR 1,2-H SHIFT MECHANISM PROPOSED FOR THE FLUXIONAL PROCESS OF THE CATIONIC DIIRON MU-ETHYNYL COMPLEXES [((ETA(5)-C5R5)FE(CO)2)2(MU-C-EQUIVALENT-TO-C-H)]BF4
AKITA, M
TAKABUCHI, A
TERADA, M
ISHII, N
TANAKA, M
MOROOKA, Y
ORGANOMETALLICS, 1994, 13 (06) : 2516 - 2520
[33] Stereoselectivity in reactions of metal complexes Part XXI.: Kinetics and mechanism of electron transfer between rac-[Co(L)H2O]+ (L=N,N′-[(pyridine-2,6-diyl)-bis(methylene)]bis[amino acid]) and optically active iron(II) complexes
Bernauer, K
Hugi-Cleary, D
Hilgers, HJ
Abd-El-Khalek, H
Brugger, N
Kressl, C
INORGANICA CHIMICA ACTA, 1998, 276 (1-2) : 1 - 8
[34] Stereoselectivity in reactions of metal complexes part XXI. Kinetics and mechanism of electron transfer between rac-[Co(L)H2O]+ (L = N,N′-[(pyridine-2,6-diyl)-bis(methylene)]bis[amino acid]) and optically active iron(II) complexes
Bernauer, Klaus
Hugi-Cleary, Deirdre
Hilgers, Hermann Josef
Abd-El-Khalek, Habib
Brügger, Nadia
Kressl, Claudia
Inorganica Chimica Acta, 1998, 275-276 : 1 - 8
[35] MECHANISM OF HYDRIDE FLUXIONALITY AS INTRAMOLECULAR PROTON-TRANSFER BETWEEN METAL METAL BONDS - KINETICS OF HYDRIDE FLUXIONALITY FOR (MU-H)NRU3(MU-3-X)(CO)8L (N = 1, X = CH2SET, L = CO, N = 2, X = CHCO2ME, MEOC2ME, L = CO, N = 2, X = CHCO2ME, L = PPH3)
NEVINGER, LR
KEISTER, JB
ORGANOMETALLICS, 1990, 9 (08) : 2312 - 2321
[36] MECHANISM OF THE REACTION BETWEEN TRANS-[W(NNH2) (PARA-MEC6H4SO3)(PH2PCH2CH2PPH2)2]+ AND NET3 - THE INFLUENCE OF THE METAL ON THE RATES OF PROTON-TRANSFER OF HYDRAZIDO(2-)-LIGANDS
LANE, JD
HENDERSON, RA
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1987, (01): : 197 - 200
[37] Oxygen atom transfer reactions to metal carbonyls:: Kinetics and mechanism of CO substitution reactions of M2(CO)9L (M = Re, L = PPh3, PMePh2, PMe2Ph, C5H5N, or M = Mn, L = C5H5N) in the presence of (CH3)3NO
Peng, L
Gao, YC
SYNTHESIS AND REACTIVITY IN INORGANIC AND METAL-ORGANIC CHEMISTRY, 2004, 34 (07): : 1181 - 1190
[38] Structure expansion of the mixed-metal dicarbide cluster core in [(ae3-CtC-Fp)Ru3(ae-H)(CO9)] via direct radical and thermal coupling reactions leading to higher-nuclearity (ae-C2Hx)My cluster compounds (x = 0, 1; y = 7, 8), CpFeRu6(ae5-C2)(ae5-C2H)(CO)16, Cp2Fe2Ru5(ae5-C2)2(CO)17 and Cp2Fe2Ru6(ae6-C2)2(CO)17
Akita, M.
Hirakawa, H.
Tanaka, M.
Moro-oka, Y.
Journal of Organometallic Chemistry, 1995, 485 (1-2)
[39] STRUCTURE EXPANSION OF THE MIXED-METAL DICARBIDE CLUSTER CORE IN [(MU(3)-C-C-FP)RU-3(MU-H)(CO9)] VIA DIRECT RADICAL AND THERMAL COUPLING REACTIONS LEADING TO HIGHER-NUCLEARITY(MU-C2HX)M(Y) CLUSTER COMPOUNDS (X=0, 1, Y=7, 8), CPFERU(6)(MU(5)-C-2)(MU(5)-C2H)(CO)(16), CP(2)FE(2)RU(5)(MU(5)-C-2)(2)(CO)(17) AND CP(2)FE(2)RU(6)(MU(6)-C-2)(2)(CO)(17)
AKITA, M
HIRAKAWA, H
TANAKA, M
MOROOKA, Y
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1995, 485 (1-2) : C14 - C17

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