Документ взят из кэша поисковой машины. Адрес оригинального документа : http://www.enzyme.chem.msu.ru/ryabov/pdf/O_98.pdf Дата изменения: Wed Aug 2 12:56:34 2000 Дата индексирования: Mon Oct 1 21:29:48 2012 Кодировка:

Organometallics 1998, 17, 3615-3618

3615

Notes
Access to Planar Chirality through Cycloplatination of ((Dimethylamino)methyl)ferrocene by cis-[PtCl2(SOMeAr)2] (Ar ) Phenyl, p-Tolyl)
Alexander D. Ryabov,*,, Irina M. Panyashkina, Vladimir A. Polyakov,§ Judith A. K. Howard,| Lyudmila G. Kuz'mina, Michael S. Datt,# and Cheryl Sacht#
Department of Chemistry, M. V. Lomonosov Moscow State University, 119899, Moscow, Russia, Division of Chemistry, G. V. Plekhanov Russian Economic Academy, Stremyanny per. 28, 113054 Moscow, Russia, D. I. Mendeleev Moscow Academy of Chemical Technology, Miusskaya sq. 9, 125820 Moscow, Russia, Department of Chemistry, University of Durham, South Road, Durham DH1 31E, England, N. S. Kurnakov Institute of General and Inorganic Chemistry RAS, Leninsky prosp. 31, 117907 Moscow, Russia, and Department of Chemistry, Rhodes University, P.O. Box 94, Grahamstown 6140, South Africa Received December 8, 1997 Summary: A reaction between ((dimethylamino)methyl)ferrocene and the enantiomerically pure complex cis[PtCl2(S-SOMeC6H4Me-p)2] affords the two easily separable cycloplatinated SSRP and SSSP diastereoisomers 4 and 5, respectively. The absolute configuration of 4 was established by an X-ray study. Diastereomers 4 and 5 react with PPh3 to give enantiomers with the planar chirality only. Introduction Cyclometalation has been so well refined1-10 that a new but standard report in this area seems rather ordinary. However, the knowledge gained by numerous groups of workers is now being used in solving more advanced tasks compared with routine syntheses of new metallacycles. One such task includes the further development of the asymmetric cyclometalation pioneered by Sokolov and co-workers.11 Surprisingly, after nearly 3 decades from the appearance of the first
* To whom correspondence should be addressed at M. V. Lomonosov Moscow State University. M. V. Lomonosov Moscow State University. G. V. Plekhanov Russian Economic Academy. § D. I. Mendeleev Moscow Academy of Chemical Technology. | University of Durham. N. S. Kurnakov Institute of General and Inorganic Chemistry RAS. # Rhodes University. (1) Dehand, J.; Pfeffer, M. Coord. Chem. Rev. 1976, 18, 327. (2) Bruce, M. I. Angew. Chem., Int. Ed. Engl. 1977, 16, 73. (3) Omae, I. Chem. Rev. 1979, 79, 287. (4) Constable, E. C. Polyhedron 1984, 3, 1037. (5) Ryabov, A. D. Synthesis 1985, 233. (6) Newkome, G. R.; Puckett, W. E.; Gupta, V. K.; Kiefer, G. Chem. Rev. 1986, 86, 451. (7) Omae, I. Organometallic Intramolecular-coordination Compounds; Elsevier Science: Amsterdam, New York, 1986. (8) Dunina, V. V.; Zalevskaya, O. A.; Potapov, V. M. Usp. Khim. 1988, 57, 434. (9) Ryabov, A. D. Chem. Rev. 1990, 90, 403. (10) Canty, A. J. In Comprehensive Organometallic Chemistry II: A Review of the Literature 1982-1994; Abel, E. F., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, New York, 1995; Vol. 9, p 225. (11) Sokolov, V. I. J. Organomet. Chem. 1995, 500, 299.

optically active cyclopalladated and cycloplatinated compounds, their number remains limited and, to our knowledge, only the Sokolov approach (palladium(II) salt with an N-protected amino acid) provides direct access to enantiomerically enriched metallacycles.12 In addition to the recently emphasized virtue of planar chiral ferrocenes in various fields of chemistry,13 studies in this area are undoubtedly a great challenge. The recent progress in using the platinum(II) complex cis[PtCl2(dmso)2] as a cyclometalating agent for sp2 C-H bonds14-17 suggested a synthetic approach to asymmetrically cycloplatinated ferrocenes using PtII coordinated to enantiomerically pure sulfoxides of the type SOMeAr. The fact that the sulfoxide remains bound to PtII in the reaction product, unlike amino acid derivatives used as asymmetric inductors by Sokolov, gave hope for their utility in asymmetric cycloplatination and/ or subsequent resolution of the planar chiral species formed. In this communication, we present evidence that a platinum(II) complex with enantiomerically pure sulfoxide reacts with a ferrocene derivative to afford a pair of cycloplatinated diastereomers which are extremely easy to separate and can be converted into individual enantiomers with planar chirality. Results and Discussion To ensure that PtII complexes with sulfoxides bulkier than dmso are capable of cycloplatinating ((dimethy(12) Sokolov, V. I.; Troitskaya, L. L.; Reutov, O. A. J. Organomet. Chem. 1979, 182, 537. (13) Togni, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 1475. (14) Ranatunge-Bandarage, P. R. R.; Robinson, B. H.; Simpson, J. Organometallics 1994, 13, 500. (15) Annunziata, R.; Cenini, S.; Demartin, F.; Palmisano, G.; Tollari, S. J. Organomet. Chem. 1995, 496, C1. (16) Wu, Y. J.; Ding, L.; Wang, H. X.; Liu, Y. H.; Yuan, H. Z.; Mao, X. A. J. Organomet. Chem. 1997, 535, 49. (17) Ryabov, A. D.; Kazankov, G. M.; Panyashkina, I. M.; Grozovsky, O. V.; Dyachenko, O. G.; Polyakov, V. A.; Kuz'mina, L. G. J. Chem. Soc., Dalton Trans. 1997, 4385.

S0276-7333(97)01076-5 CCC: $15.00 © 1998 American Chemical Society Publication on Web 07/03/1998


3616 Organometallics, Vol. 17, No. 16, 1998

Notes

lamino)methyl)ferrocene (1), the reaction of the latter with cis-[PtCl2(rac-SOMePh)2] was performed under the conditions elaborated by Ranatunge-Bandarage et al.14 Among the other ferrocene derivatives tested, viz. acetylferrocene and (aminocarbonyl)ferrocene oximes, 1 provided the highest yield in the reaction with cis-[PtCl2(dmso)2]. According to TLC, the interaction between 1 and cis-[PtCl2(rac-SOMePh)2] afforded two major products which were separated and thoroughly characterized. The 1H NMR spectra were consistent with their formulation as a pair of racemic diastereomeric cycloplatinated compounds with different orientations of the sulfoxide ligand with respect to the iron and/or nonmetalated cyclopentadienyl ring; i.e., the sulfoxide phenyl ring was directed toward and opposite the C5H5 ring in the cases of 2 and 3, respectively. The proof comes from the 1H NMR spectra of 2 and 3. A singlet from the C5H5 ring in 2 is seen at 3.60, which is 0.59 ppm upfield compared to that in 3, due to the ring current effect from the sulfoxide phenyl group. There is no shielding for the corresponding singlet in 3, since the C5H5 and phenyl rings are spatially separated. According to the 1H NMR spectral data, compounds 2 and 3 have no tendency to rearrange into each other in a d8-toluene solution in the temperature range 230316 °C.

Figure 1. Crystal structure of complex 3. Thermal ellipsoids are drawn at the 30% probability level.

Figure 2. Crystal structure of complex 4. Thermal ellipsoids are drawn at the 30% probability level.

The cycloplatination of 1 by the enantiomerically pure complex cis-[PtCl2(S-SOMeC6H4Me-p)2] (the absolute configuration of sulfur is indicated for the coordinated ligand) was carried out in the same way as for the racemic complex to afford diastereomers 4 and 5 in 21 and 16.5% yields, respectively. Remarkably, the diastereomerically pure compound 4 crystallized from the reaction solution and no TLC was needed to isolate it. Its 1H NMR spectrum, which had only one set of signals, indicated that complex 4 is structurally similar to 2, since the singlet from the C5H5 ligand appeared at 3.62. In the mother liquor, diastereomer 5, which is analogous to 3, was found and recovered using preparative TLC. It should be pointed out that that the 1H NMR spectrum of 5 consisted of two sets of signals. The material was presumably contaminated by either 4 and/ or an analogue of 5 in which the tolyl group is directed at the C5H5 ring, provided the rotational barrier around the Pt-S bond is large at least for steric reasons in this case. The geometry of the complexes discussed above was supported by X-ray structural studies of 3 and 4 (Figures 1 and 2, respectively). The key conclusions are

as follows. (i) The absolute configuration of the sulfoxide sulfur remains unchanged during the course of cycloplatination. (ii) Whereas complex 3 is racemic, comprising of RSRP (as in Figure 1) and SSSP stereoisomers, complex 4 is stereochemically pure and only a SSRP stereoisomer is present. (iii) Diastereomers 2/3 and 4/5 have differently oriented sulfoxide aryl groups, and the X-ray and 1H NMR data are in perfect agreement. (iv) The fact that the p-tolyl ring is directed at the C5H5 group, providing an H(10),,,C(19) distance of 2.939 е (a sum of the van der Waals radii) in 4, accounts for a 20° staggered conformation of the Cp rings. The opposite orientation of the phenyl ring in 3 is accompanied by an eclipsed configuration, as observed for other cycloplatinated ferrocene derivatives.14,16-19 The platinum center has a square-planar environment. The bond lengths and angles in molecules 3 and 4 are in the same range as recently reported.14,16-19 The Pt-C bond distances equal 1.990(4) and 1.975(8) е, and the Pt-Cl bond distances are 2.4061(9) and 2.395(2) е for 3 and 4, respectively. Structural features of the coordinated sulfoxide also seem to be normal.20 Platinacycles 2, 4, and 5 were treated with a 5% excess of PPh3 in benzene at 70 °C for 1 h to afford the
(18) Headford, C. E. L.; Mason, R.; Ranatunge-Bandarage, P. R. R.; Robinson, B. H.; Simpson, J. J. Chem. Soc., Chem. Commun. 1990, 601. (19) Ranatunge-Bandarage, P. R. R.; Duffy, N. V.; Johnston, S. M.; Robinson, B. H.; Simpson, J. Organometallics 1994, 13, 511. (20) Calligaris, M.; Carugo, O. Coord. Chem. Rev. 1996, 153, 83.


Notes

Organometallics, Vol. 17, No. 16, 1998 3617

complexes (RP,SP)-6, (RP)-6, and (SP)-6 with [R]D (c 0.4, CHCl3) equal to 0, +43.7, and -23.7°, respectively, with the coordinated achiral phosphine instead of asymmetric sulfoxides (eq 1). The structure of 6 was established

cycloplatination is not very stereoselective by itself and the process reported is a successful combination of less stereoselective cyclometalation and much more efficient resolution of enantiomers. In conclusion, we have shown an easy entry to both enantiomers of a planar chiral compound which is based on cycloplatination of ferrocenes with a chelate arm by enantiomerically pure platinum(II) sulfoxide complexes of the type cis-[PtCl2(SOMeAr)2]. Unfortunately, neither we nor other workers14,16,19 have been able yet to develop a successful functionalization procedure for cycloplatinated ferrocenes. However, our first preliminary results show that the chemistry reported here can be extended to palladium(II) compounds, which are recognized starting materials in fine organic synthesis.5,21 Experimental Section
The starting complexes were prepared according to Price et al.22 A 3-fold excess of the sulfoxide (R)-methyl p-tolyl sulfoxide or methyl phenyl sulfoxide (Aldrich) was added to a solution of K2PtCl4 in 5 mL of water and the mixture stirred for 48 h to form a white precipitate (90%). (Note that the sign of the sulfoxide changes upon complexation.) Satisfactory C, H, S anaylsis was obtained. IR (KBr, cm-1): cis-[PtCl2(racSOMePh)2] 1145 and 1155; cis-[PtCl2(S-SOMeC6H4Me-p)2] 1150 (s, sh, SdO). [R]D25 ) -160° (c ) 0.283, acetone). cis[PtCl2(rac-SOMePh)2] was a mixture of meso and RR/SS stereoisomers in a 0.33:1 ratio (1H NMR); cis-[PtCl2(SSOMeC6H4Me-p)2] was a single stereoisomer. Complexes 2 and 3. 1 (99 mg, 0.4 mmol) and [PtCl2(racSOMePh)2] (231.5 mg, 0.42 mmol) were mixed in 16 mL of absolute MeOH and refluxed for 4 h. The yellow heterogeneous mixture turned into a crimson solution after 1 h, from which an orange material began to precipitate. Two products were observed by TLC (Silufol) with Rf 0.7 and 0.5 (C6H6/ acetone 9.5:0.5). After the reaction was completed, the precipitate was filtered off and dried to give 80.7 mg of mostly the product with Rf 0.5. The mother liquor contained mostly the product with Rf 0.7. Both fractions were purified by preparative TLC on SiO2 with benzene/acetone (9:1) as eluent. The products with Rf 0.7 and 0.5 were washed off from SiO2 with acetone and CHCl3, respectively; with solvents removed, 50.2 (25%) and 31.5 mg (16%) of the compounds with Rf 0.5 and 0.7, respectively, were obtained. Analytically pure samples were obtained on recrystallization from C6H6/petroleum ether and MeOH, respectively. 2 (Rf 0.5): mp 193 °C; 1H NMR (CDCl3, , J in Hz) 3.03 (s, NCH3, J 33), 3.27 (s, NCH3, J 31), 3.60 (bs, NCH2, J 29.2), 3.60 (s, C5H5), 3.64 (s, SCH3, J 21.2), 4.01 and 4.02 (s, H(3) and H(4)), 4.41 (s, H(5)), 7.60-7.66 (m, 3H, Ph), 8.28-8.32 (m, 2H, Ph). Anal. Found: C, 39.04, 38.81; H, 4.07, 4.04; N, 2.24. Calcd for C20H24NSOClFePt: C, 39.20; H, 3.95; N, 2.29. 3 (Rf ) 0.7): mp 183 °C; 1H NMR (CDCl3, , J in Hz) 2.91 (s, NCH3, J 33.6), 3.28 (s, NCH3, J 31.8), 3.65 (s, SCH3, J 20.5), 4.01 (bs, NCH2), 4.19 (s, C5H5), 4.41 (s, H(5)), 7.49-7.50 (m, 3H, Ph), 8.10-8.16 (m, 2H, Ph). Complexes 4 and 5. 1 (81.5 mg, 0.335 mmol) and [PtCl2(SOSMeC6H4Me-p)2] (206 mg, 0.358 mmol) were refluxed in 15 mL of MeOH as above. Brownish red crystals started to form after 1 h. The TLC analysis (benzene/acetone 9:1) showed two products with Rf 0.65 and 0.45. The reaction mixture was kept at +5 °C for 3 days to afford brownish red crystals, which were washed with hexane and dried; Rf 0.45 (43.8 mg, 21%). The product 5 with Rf 0.65 (34.8 mg, 16.5%) was recovered from the mother liquor by TLC. 4 (Rf 0.45): mp 103 °C; 1H NMR
(21) Pfeffer, M. Recl. Trav. Chim. Pays-Bas 1990, 109, 567. (22) Price, J. H.; Williamson, A. N.; Schramm, R. F.; Wayland, B. B. Inorg. Chem. 1972, 11, 1280.

on the basis of the 1H NMR and IR data. No sulfoxides were coordinated to platinum in 6 (abscence of strong SdO bands in the region 1140-1130 cm-1), whereas the Pt-N bond was preserved (4JPH ) 2.3 Hz at the NCH3 signals). The CD spectra of 6 showed that a sample derived from 2 is racemic, as expected, whereas those from 4 and 5 are enantiomerically enriched. The spectra of the last two mirror each other, and in the case of (RP)-6, in particular, the strongly positive and negative CD effects are observed around 470 and 335 nm, respectively, together with a crossover point at 357 nm. A comparison of the [R]D values for (RP)-6 and (SP)-6 allows us to estimate the enantiomeric purity of (SP)-6. Taking into account that (RP)-6 was derived from a diastereomerically homogeneous material and assuming that the optical purity of the "planar chiral" center is unaffected by reaction 1, it follows that the enantiomeric purity of (SP)-6 equals 54% ee. The X-ray data reported here and elsewhere17 together with the CD measurements allow us to understand the origin of different orientations of the aryl groups of the coordinated sulfoxide with respect to the C5H5 ring observed by 1H NMR. It has recently been indicated17 that the oxygen atom of dmso is involved in hydrogen bonding with the hydrogen of the C-H bond of the platinated Cp ring (O(1) and H(5) atoms in Figure 2). This bonding should retard an easy rotation around the Pt-S bond, implying that the p-tolyl group must be directed toward and opposite the C5H5 ring in the cases of 4 and 5, respectively. There is an interesting observation that throws light on the mechanism of the cycloplatination. It should first be indicated that 4 and 5 are isolated in similar yields, viz. 21 and 16.5%, respectively. Second, the X-ray data reveal that platination by cis-[PtCl2(rac-SOMePh)2] and cis-[PtCl2(S-SOMeC6H4Me-p)2] affords species with different planar chirality, the central sulfur chirality being the same. In particular, 4 is a SSRP compound (Figure 2) and, if the cycloplatination were in fact distereospecific, the product with the same "planar" configuration (RP) should be SS configured at sulfur. As seen in Figure 1, one of the enantiomers of racemic complex 3 is, however, a RSRP diastereomer rather than the expected SSRP one. Therefore, it seems likely that the


3618 Organometallics, Vol. 17, No. 16, 1998
(CDCl3, , J in Hz) 2.45 (s, CH3), 3.02 (s, NCH3, J 34), 3.25 (s, NCH3, J 31), 3.50 (bs, NCH2, J 30.6), 3.62 (s, C5H5), 3.61 (s, SCH3, J 20.2), 4.01 and 4.06 (s, H(3) and H(4)), 4.45 (s, H(5)), 7.41, 7.45, 8.14, and 8.18 (AABB, C6H4). Found: C, 39.95, 39.93; H, 4.31; N, 2.23. Calcd for C21H26NSOClFePt: C, 40.24; H, 4.18, N, 2.23. Crystal Structure Analyses. A Siemens SMART diffractometer was used, with Mo KR radiation (graphite monochromator, ) 0.710 73 е, T ) 150 K). 3: light brown crystals, crystal dimensions 0.56 в 0.10 в 0.08 mm, C20H24ClFeNOPtS, Mr ) 612.85, a ) 30.5504(6) е, b ) 30.5504(6) е, c ) 11.1282(6) е, V ) 8994.8(2) е3; hexagonal, space group R3, Z ) 18, h Fcalcd ) 2.037 g cm-3, µ ) 7.964 mm-1, 4247 independent reflections with 1.33e e 26.75°. The structure was solved by full-matrix least squares on F2 (SHELXL-93).23 All H atoms were found from difference Fourier synthesis and refined with isotropic thermal parameters. Final R indices (I > 2(I)) R1 ) 0.0228 and wR2 ) 0.0484. Selected bond distances: (е): Pt-C(1), 1.990(4); Pt-N, 2.136(3); Pt-S, 2.1973(9), Pt-Cl, 2.4061(9); S-O, 1.473(3). Selected bond angles (deg): C(1)Pt-N, 82.35(14); C(1)-Pt-S 93.12(11); N-Pt-S, 175.25(9); N-Pt-Cl, 90.72(9); S-Pt-Cl, 93.89(4). 4: brownish red crystals, crystal dimensions 0.55 в 0.16 в 0.07 mm; C21H26ClFeNOPtS, Mr ) 626.88, a ) 10.4742(2) е, b ) 9.5587(2) е, c ) 10,8507(2) е, ) 101.3693(3)°, V ) 1065.07(4) е3; monoclinic, space group P21, Z ) 2, Fcalcd ) 1.955 g cm-3, µ )
(23) Sheldrick, G. M. SHELXL-93, Program for Crystal Structure Refinement; University of Gottingen: Gottingen, Germany, 1993. Ё Ё

Notes
7.476 mm-1, 4553 independent reflections with 1.91e e 25.57°. The structure was solved by full-matrix least squares on F2 (SHELXL-93).23 All H atoms were calculated in ideal positions and refined using the riding model with B(iso) ) 1.5B(eq) of the parent carbon atom. Final R indices (I > 2(I)) R1 )0.0424 and wR2 ) 0.1055. Selected bond distances: (е): Pt-C(1), 1.975(8); Pt-N, 2.141(7); Pt-S, 2.197(2); PtCl, 2.395(2); S-O, 1.473(6). Selected bond angles (deg): C(1)Pt-N, 82.9(3); C(1)-Pt-S, 92.9(2); N-Pt-S, 175.8(2); N-PtCl, 91.2(2); S-Pt-Cl, 92.95(8). Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication No. CCDC-100667.

Acknowledgment. We are grateful to the Russian Foundation for Fundamental Research for financial support (Grant 95-03-09633) and Dr. G. M. Kazankov for his interest in this work. C.S. and M.S.D. gratefully acknowledge financial assistance from Rhodes University and the Foundation for Research Development.
Supporting Information Available: Tables of X-ray experimental details, positional and thermal parameters, bond lengths, and bond angles for the crystal structures of 3 and 4 (14 pages). Ordering information is given on any current masthead page. OM971076F