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Boletín de la Sociedad Chilena de Química

Print version ISSN 0366-1644

Bol. Soc. Chil. Quím. vol.47 no.3 Concepción Sept. 2002

http://dx.doi.org/10.4067/S0366-16442002000300003 

Bol. Soc. Chil. Quím., 47, 213-220 (2002) ISSN 0366-1644

NEW ENTRY TO PIANO -STOOL ELECTRON RICH
(PENTAMETHYL CYCLOPENTADIENYL) IRON COMPLEXES

C. DIAZ* ,N. CABEZAS ,F. MENDIZABAL

Departamento de Quimica, Facultad de Ciencias, Universidad de Chile
Casilla 653,Santiago Chile

(Received: October 29, 2001 - Accepted: April 8, 2002)

ABSTRACT

A new route to the electron rich pentamethylcyclopetadienyl iron complexes (n5-C5Me5)=Cp*) starting from the commercially available dimer [Cp*Fe(CO)2]2 ,is presented. Reaction of the dimer with I2 in CH2Cl2, affords the mononuclear carbonyl complex Cp*Fe(CO)2I which in turn reacts with bis(diphenylphosphinoethane) in toluene under Uv irradiation to give Cp*Fe(dppe)I. Treatment of Cp*Fe(dppe)I with the neutral ligands L (L = CH3CN, PPh3, SEt2) in the presence of TlPF6 affords the cationic derivatives [Cp*Fe(dppe)L]PF6 ,while that the reaction with S2(CH2C6H5 )2 in CH3OH yields the thiolate complex [Cp*Fe(dppe)S-CH2C6H5 ] PF6 .The unusual magnetic properties of these complexes are discussed. Extended Hückel OM calculation confirmed the most electron rich character of the Cp*Fe(dppe)+ derivatives than their unsustituted CpFe(dppe)+ .Electrochemical as well as Mösbauer data are in agree with this.

Keywords: pentamethylcyclopentadienyl iron, electron rich fragments, OM calculation, organometallic

RESUMEN

Se presenta una nueva ruta de síntesis para compuestos complejos pentametilociclopentadienilo-hierro(II) usando como precursor el dímero [Cp*Fe(CO)2]2.

La reacción de este dímero con I2 in CH2Cl2, produce el compuesto Cp*Fe(CO)2I el cual a su vez reacciona con bis(difenifosfinoetano) en tolueno para dar el complejo Cp*Fe(dppe)I.

La reacción de éste con ligandos neutros L (L = CH3CN, PPh3, SEt2) en presencia de TlPF6 produce los derivados cationicos [Cp*Fe(dppe)L]PF6 mientras que la reacción con S2(CH2C6H5 )2 en CH3OH genera el complejo thiolato [Cp*Fe(dppe)S-CH2C6H5 ] PF6. Se discuten las propiedades inusuales paramagnéticas de los complejos. Cálculos de orbitales moleculares Hückel extendido confirman la más alta densidad electrónica de los derivados Cp*Fe(dppe)+ respecto de los correspondientes no sustituidos CpFe(dppe)+ .Estudios electroquimicos y de espectometria Mösbauer están de acuerdo con estos resultados.

Palabras Claves: pentametilciclopentadienilo-hierro(II), fragmentos con alta densidad electrónica, cálculos de OM ,organometalico

INTRODUCTION

Whereas the cyclopentadienyl iron dicarbonyl series is one of the most widely studied organometallic families, [1] pentamethyl cyclopetadienyl (n5-C5Me5)=Cp*) homologues have been less studied [2] Green et al. reported the first synthetic route to this series by metal vapor synthesis [2c]. Subsequently Lehmkuhl [1f] et al. proposed another entry to bis(monophosphine) iron complexes of the type Cp* Fe [(P(CH3))n(C6H 5)3-n] 2Cl n = 0-3. More recently Astrucs [2a,b] and Bercaws [2e] proposed a new route to pentamethyl cyclopentadienyl complexes starting from CpFe(acac), which can be obtained from Fe(acac)2 and Cp*Li [2d]. The last reported method to the series Cp*Fe(dppe)X involves the reaction of Fe (dppe)Cl2 with Cp*Li [2a] or with C5Me5H [2g] to give Cp*Fe(dppe)Cl. Here we report a new synthetic entry to iron pentamethylcyclopentadienyl compounds and a general discussion about the influence of the methyl substitution ring using experimental and OM calculations .

RESULTS AND DISCUSSION

We have previously reported [3] the synthesis of CpFe(dppe)I from CpFe(CO)2I and dppe under Uv - radiation in toluene as solvent and also of their cationic [CpFe(dppe) L]PF6 from treatment with L in CH2Cl2, in presence of TlPF6 [4]. An analogous treatment of Cp* Fe(CO)2I (1) with dppe in toluene under Uv - irradiation affords Cp*Fe(dppe)I [2a] (2) which was conveniently isolated in 72 %, see Scheme 1.


The precursor (2) in spite of that has been used previously as starting reactive for to introduce the Cp*Fe(CO)2 fragment [5], surprisingly its has been poorly characterized [6]. The original cite of their synthesis by Moro- Oko Akita et al. [6] does not include an adequate characterization of this complex. Treatment of the commercially available [Cp*Fe(CO)2]2 with a excess of I2 in CH2Cl2 at room temperature followed by elimination of excess of I2 with Na2S2O3 affords (2) as a black - red powder, which was recrystallized from a n-hexane/CH2Cl2 solution as dark red crystals in a 91%. As expected two carbonyl bands were observed in their Ir spectrum, at 2000 and 1953 cm-1. The 13C-NMR exhibit the Cp* signal at 97.9 ppm while that the carbonyl signal was clearly observed at 217 ppm. The signal methyl group of Cp* ligand signal appears at 11.15 ppm.

The complex Cp*Fe(dppe)I react with neutral ligand L (L = CH3CN, PPh3, SEt2) in CH2Cl2 and in presence of Tl PF6 to give the series of complexes [Cp*Fe(dppe)L]PF6. The complex [Cp*Fe(dppe) NCCH3] PF6 have been previously prepared by reaction of [Cp*Fe (CH3CN)3]+ with dppe [2b] and starting from Cp*Fe(dppe)Cl [2a].

On the other hand the reaction of Cp*Fe(dppe)I with S2(CH2C6H5 )2 in CH3OH and in presence of NH4PF6 yield the new iron(III)-thiolate [Cp*Fe (dppe) S-CH2C6H5] PF6.

The new complexes [Cp*Fe(dppe)SEt2]PF6 , [Cp*Fe(dppe) PPh3]PF6 are paramagnetic and were characterized by elemental analysis, Ir, Uv-visible and magnetic method. 31P and 1H NMR spectra of the complexes give rise to broad (almost missing in some cases) and/or shifted signal. As example in figure 1

Figure 1. 1H - NMR spectrum of [Cp*Fe(dppe)SEt2]PF6 in the aromatic region in CDCl3 solution. The asterisk denote the signal of CDCl3 and of the CH2Cl2 of crystallization.

in shown the 1H-NMR spectrum of [CpFe(dppe) (SEt2)]PF6. On the other hand their 31P-NMR spectrum exhibits the dppe signal shifted at 28.95 ppm respect to the normal position for Cp*Fe dppe X or [Cp*Fe(dppe) L]PF6 around 90 ppm [2a]. The signal of PF6 appears very weak (due to broadening probably) at - 142 ppm The rare paramagnetism exhibit by 18 electron [Cp*Fe(dppe)L]+ species in solution have been attributed to the equilibrium.

[Cp*Fe (dppe) L]+ [Cp*Fe(dppe)]+ + L

(1)

to generate the 16e specie Cp*Fe(dppe)+ which is known to be paramagnetic [8]. Recent theoretical calculation [9] found a tripet ground state for Cp*Fe(dppe)+ species. However the solid state paramagnetism exhibit by the 18e complexes [Cp*Fe(dppe)SEt2]PF6 and [Cp*Fe(dppe)PPh3]PF6, neither the previously reported [Cp*Fe(dppe)OCMe2]PF6 and Cp*Fe(dppe)OSO2CF3 can not be explained by the theoretical results. The paramagnetic behavior exhibit by the complexes [Cp*Fe(dppe)PPh3]PF6 and [Cp*Fe(dppe)SEt2]PF6 in solution can be explained by the equilibrium (eq.1); however the origin of the paramagnetism in solid state is not clear. The paramagnetism exhibited by these species it appears to be associated in same unclear manner to the presence of pentamethylcyclopentadienyl groups because [CpFe(dppe)L]PF6 complexes are generally diamagnetic. Consistently with this, the complex [CpFe(dippe)NCCH3]PF6 is diamagnetic while the complex [Cp*Fe(dippe)NCCH3]+ is paramagnetic dippe ¾ 1,2 Bis (diisopropylphosphine) ethane.

The high magnetic moment exhibits by the complex [Cp*Fe(dppe)SCH2C6H5 ]PF6 can be due to a ground state of Fe(III) high spin situation. In contrast the complexes [Cp Fe(dppe)SR]PF6 are paramagnetic (m =1,6-2.4BM) with a low spin ground state Fe(III). Most detailed temperature variable susceptibility measurements for all the paramagnetic complexes are in course.

Uv-visible spectra of the complexes (2)-(7) exhibit a similar absorption patterns to that Cp*Fe(PMe3)2CH3 and Cp*Fe(PMe3)2Cl previously assigned [2e], however a less defined maximal were observed.The band around 450nm and some unresolved band in the range 450-600nm were observed.

Comparison of the CpFe(dppe) and Cp*Fe(dppe) fragments.

Several experimental evidences have pointed the most electron donor character of the C5Me5 ring than the C5H5, leading to most electron rich character to C5Me5Fe(dppe)+ fragment than C5H5Fe(dppe)+. In fact as is shows in Table I the half wave potential oxidation is lower for the C5Me5 series than the unsubstituted C5H5, indicating an iron with greatest electron density.

T A B L E I

Comparison of Oxidation Potential for CpFe(dppe)+ and their Methylated
Analogue Cp*Fe(dppe)+

On the other, hand Mössbauer data also indicate a most high electron density on the iron atom for the Cp* derivative compared with their Cp counter parts. As shown in Table II, the Cp* derivative produces a most lower isomeric shifts which can be interpreted as a most high electron density around the iron atom.

T A B L E II

For to confirm this we have performed extended Hückel (EH) calculation on the models Cp*Fe(PH3 )2+ and CpFe(PH3)2+. As in shown in figure 2 the main changes on going from Cp to Cp* iron derivatives are the increasing in the HOMO - LUMO level, the HOMO-LUMO gap as well as the increasing of the electron density from - 0.5 to - 1.4.


Figure 2. OM diagram and atomic charges for the fragment models CpFe(PH3)2 and Cp*Fe(PH3)2+

EXPERIMENTAL

All reactions were carried out under purified N2 or Ar using standard Schlenk techniques and the solvent used (methanol, dichloromethane, diethyl ether and n-hexane) were appropriately distilled and dried before use. [Cp*Fe(CO)2]2 (Strem), I2, [NBu4]PF6, NH4PF6 and dppe (Aldrich) were used as received. TlPF6 (caution! Thallous salts are very poisonous and should be handled with precaution) was prepared from Tl2CO3 and HPF6. IR spectra were recorded as KBr pellets on a FT-Bruker 66V spectrometer. NMR spectra were run in CD2Cl2 or (CD2)2C0 solution at room temperature on a Bruker AMX 300 spectrometer with TMS(H) d = 0.0 ppm as internal standard or 85% H3PO4 and downfield positive to the reference as external standard for the 31P measurements. UV-Visible spectra were run on a Varian DMS-9 spectrophotometer with 1 cm optical path cuvettes.. Magnetic measurements were carried out by a Gouy`s method at room temperature (25ºC) using a Johnson Matthey Balance, using mercury tetrathiocyanate cobaltate(II) as calibrant.

Reaction of [Cp*Fe(CO)2]2 with I2 in CH2Cl2.

A mixture of 0.5 g (1.0 mmol) of [Cp*Fe(CO)2]2 and I2 1.0 g (3.9 mmol) in 50 ml dichloromethane was stirred at room temperature for 1h. The solution was filtered and washed three twice with an aqueous solution of Na2S2O3 (2.5g in 50ml H2O) and the organic phase was treated with anhydrous Na2SO4 and filtered through celite.The red solution was then evaporated to dried under reduced pressure. The resulting solid was recrystallized from of a n-hexane-diethyl ether 1:1 mixture to give (2) as red-dark crystal . Yield 0.69 g; 91%. Anal. Found. : C 37.42, H 3.93. Calc.for C12H21O2IFe C 38.52, H 4.01.

Ir(Kbr,pellets): n(CO):2000,1953

Reaction of Cp*Fe(CO)2I with dppe in Toluene.

A solution of Cp*Fe(CO)2I 0.5 g (1.33mmol) and dppe 0.6 g (0.15mmol) were irradiated in toluene(50ml) for 8hr.After this, the solution was filtered through celite and the solution evaporated to dried in a rotavapor. The resulting red dark solid was redisolved in a n-hexane-diethyl ether 1:1 mixture and placed in the freezer for overnitgh to give (3) as red-brown solid. Yield 0.62 g, 72%.The complex Cp*Fe(dppe)I was characterized by Ir and NMR spectroscopy by comparison with an authentically sample [2a].

Reaction of Cp*Fe(dppe)I with CH3CN in presence of NH4PF6.

Cp*Fe(dppe)I 0.08 g (011 mmol) was stirred with 10ml of a mixture CH3CN/CH2Cl2 in presence of NH4PF6 0.04 g (0.2 mmol) were stirred for 22h. at room temperature. The solution was evaporated under vacuum and the solid residue extracted with dichloromethane and filtered through Celite. Then the solution was evaporated and the red solid washed with diethyl ether. and dried under reduced pressure. Yield 0.05g 63%.The complex [Cp*Fe(dppe)(CH3CN)]PF6 was characterized by Ir and NMR spectroscopy by comparison with an authentically sample [2a,b].

Reaction of Cp*Fe(dppe)I with CH3CN in presence of TlPF6.

Cp*Fe(dppe)I 0.08 g (011 mmol) was stirred with 10ml of CH3CN in presence of TlPF6 0.08g (0.22 mmol) were stirred for 27h. at room temperature. The solution was filtered through Celite and the solvent was evaporated to dried .The red solid washed with diethyl ether. and dried under reduced pressure. Yield 0.05g 63%.The complex [Cp*Fe(dppe)(CH3CN)]PF6 was characterized by Ir and NMR spectroscopy by comparison with an authentically sample [2a,b]

Reaction of Cp*Fe(dppe)I with PPh3 in presence of NH4PF6.

Cp*Fe(dppe)I 0.11g (0.15 mmol) and 0.08g (0.3mmol) PPh3 in presence of NH4PF6 0.02 g (0.24 mmol) in CH3OH (20 ml) were stirred for 21 h. The solvent was evaporated under vacuum and the solid residue extracted with CH2Cl2 and filtered through celite. The solvent was eliminated and the solid residue washed with ether and dried under reduced pressure give (5) as a red _brown solid. Yield 0.08g 53% meff=1.58 BM . Anal. Found. : C 62.72, H 4.96. Calc. for C61H54F6P4 Fe•3CH2Cl2 C 61.41, H 4.79.

Ir(KBr, pellets): 1117 d(CH)ip : 695 d(CH)op : 843 (PF6).

Reaction of Cp*Fe(dppe)I with PPh3 in presence of TlPF6.

Cp*Fe(dppe)I 0.14g (0.19 mmol) and 0.08g (0.3mmol) PPh3 in presence of TlPF6 0.14 g (0.4 mmol) in CH2Cl2 (20 ml) were stirred for 19 h.The solution was filtered through celite and the solvent was evaporated under vacuum and the solid residue washed with ether and dried under reduced pressure. Yield 0.08g, 53%. Spectroscopic data were similar to that obtained for the complex [Cp*Fe(dppe)PPh3][PF6] obtained by the above method.

Reaction of Cp*Fe(dppe)I with S(C2H5)2 in presence of TlPF6.

Cp*Fe(dppe)I 0.10g (013mmol) and 0.08g (0.93mmol) S(C2H5)2 in presence of TlPF6 0.14 g (0.4 mmol) in CH2Cl2 (20 ml) were stirred for 22 h.The red solution was filtered through celite and the solvent was evaporated under vacuum and the solid residue washed with ether and dried under reduced pressure to,give (6) as brown solid. Yield 0.05g 56%. meff=1.34 BM . Anal. Found. : C 50.57, H4.51. Calc. for C40H49F6S P3Fe • 2CH2Cl2 C 50.72, H 4.93.

Ir(KBr, pellets): 1120 d(CH)ip , 695 d(CH)op , 843 (PF6).

Reaction of Cp*Fe(dppe)I with S2(CH2-C6H5 )2 in presence of TlPF6.

. Cp*Fe(dppe)I 0.1g (0.14 mmol) and 0.05g (0.2 mmol) S2(CH2-C6H5 )2 in presence of TlPF6 0.02 g (0.28 mmol) in CH2Cl2 (20 ml) were stirred for 22 h at room temperature. The solution was filtered through celite, and the solvent eliminated in vacuum. The solid residue was washed with ether and dried under reduced pressure, to give (6) as a gray-brown solid. Yield 0.09 g, 75%.meff= 6.36 BM Ir(Kbr, pellets) 1123 d(CH)ip , 695 d(CH)op , 843 (PF6).

Calculations. EH. MO calculations were carried out using the modified Wolfsberg -Helmholz formula [13]. The atomic parameters for the elements involved in our calculations have been previously reported [14]. The bonding distances used in the models CpFe(PH3)2 3+ and Cp*Fe(PH3)2+ were similar to those for the crystal structure of [CpFe(dppe)L]+ as well as [Cp*Fe(dppe)]+ derivatives [8,9]. For the two fragments the basic parameters were: bond distances Fe-P 2.17 Å, Fe-C 2.08 Å, bond angle P-Fe-P 98.9°. MO drawing were generated with the use of the program CACAO [15].

ACKNOWLEDGEMENTS

The authors thanks to FONDECYT(1000672) the financial support.

REFERENCES

1. Comprehensive Organometallic Chemistry; Wilkinson G, Stone F.G., Abel, E.W., Eds., Pergamon. London 1982; Chapters 19-43.         [ Links ]

2. (a) Ch. Roger, P. Hamon, L. Toupet, H. Rabaa, J. Y. Saillard, , J. R. Hamon, C. Lapinte, Organometallics 10, 1045 (1991)         [ Links ]

(b) J.Morrow, D. Catheline, M. Desbois ,J.M.Manriquez ,J.Ruiz ,D. Astruc. Organometallics, 6, 2605 (1987)         [ Links ]

(c) M.L. Green, L.L. Wong, J.Chem. Soc. Chem. Commun. 1442 (1984)         [ Links ]

(d) E.E. Bunnel, L.. Valle, J.M. Manríquez , Organometallics 4, 1680 (1985)         [ Links ]

(e) R.G. Bray, J.E. Bercaw, H.B. Gray, M.D. Hopkins, R.A. Paciello, Organometallics, 6, 922 (1987)         [ Links ]

(f) H. Lehmkuhl, G. Mehler, Bi. Benn, A. Rufunka, G. Schroth, C. Krüger, E. Raabe, Chem. Ber. 120, 1987 (1987)         [ Links ]

(g) Ch. Roger, R. Marseill, Ch. Salus, J.R. Hamon, C. Lapinte, J. Organomet. Chem. 336, C13 (1987)         [ Links ]

3. (a) C. Díaz., R. Latorre, Bol. Soc. Chil. Quím. 37, 211 (1992)         [ Links ]

(b) G, Barrado, G.A. Carriedo, C. Díaz, V. Riera, Inorg. Chem. 30, 4416 (1991)         [ Links ]

4. (a) C. Díaz, A. Arancibia, Polyhedron 13, 117 (1994)         [ Links ]

(b) C. Díaz, C. Leal, Polyhedron 15, 2825 (1996)         [ Links ]

(c) G.A. Carriedo, A. Arancibia, C. Diaz ,N. Yutronic, E. Pérez Carreño, S.G Granda J, Organomet. Chem. 508, 23 (1996)         [ Links ]

5. F. Coat, M.A. Guillaume, L. Toupet, F. Paul , C. Lapinte. Organometallics 16, 588 (1997)         [ Links ]

6. M.Akita, M. Terada, S. Oyama, Y. Moro-Oka, Organometallics 9, 816 (1990) However a detailed synthesis description of Cp* Fe (CO)2 I is not give.         [ Links ]

7. J.M. Manríquez, D. Astruc. Bol. Soc. Chil. Quím. 31, 161 (1986)         [ Links ]

8. P. Hamon, L. Toupet, J.R. Hamon , C. Lapinte. Organometallic 15, 588 (1996)         [ Links ]

9. K. Costuas, I.Y. Saillard, Organometallic 18, 2505 (1999)         [ Links ]

10. P.M. Treichel, D.C. Molzahn, K.P. Wagner. J. Organomet. Chem. 174, 191 (1979)         [ Links ]

11. N.G. Connelly, M.P. Gamasa, J.Gimero, C. Lapinte, E. Lastra, J.P. Maher, N-Le Narvor; A. Rieger, P.H. Rieger, J. Chem. Soc. Dalton Trans. 2575 (1993).         [ Links ]

12. For a comparison of Cp with Cp* or the most bulky R5C5 R = Ph, i-Pr, (Me3Si)3H2, PhCH2 see : Ch. Janiak, H. Schumann, Adv. in Organomet. Chem. 33, 291 (1991) ; C. Lapinte. Coord. Chem. Rev. 178-180, 431 (1998).         [ Links ]

13.- J.H.Ammeter , H.B.Burgi , J.C.Thibeault ,R. Hoffmann, J. Am.Chem. Soc. 100 ,368(1978)         [ Links ]

14.- C. Diaz , I. Izquierdo ,F.Mendizabal, N.Yutronic ,Inorg. Chim. Acta 294, 20 (1999)         [ Links ]

15.- C. Mealli ,M. Proserpio J. Chem. Educ. ,67, 399 (1990)         [ Links ]