Cyclometalated phosphine-based pincer complexes: Mechanistic insight in catalysis, coordination, and bond activation

s of Papers, 221st ACS National Meeting, San Diego, CA, April 1-5, 2001; American Chemical Society:Washington, DC, 2001; INOR287. (b) Dijkstra, H. P.; Slagt, M. Q.; McDonald, A.; Kruithof, C. A.; Kreiter, R.; Mills, A. M.; Lutz, M.; Spek, A. L.; Klopper, W.; van Klink, G. P. M.; van Koten, G. Eur. J. Inorg. Chem. 2003, 830. (c) Mehendale, N. C.; Bezemer, C.; van Walree, C. A.; Klein Gebbink, R. J. M.; van Koten, G. J. Mol. Catal. A 2006, 257, 167. (d)Mehendale, N. C.; Sietsma, J. R. A.; de Jong, K. P.; vanWalree, C. A.; Gebbink, R. J. M. K.; van Koten, G. Adv. Synth. Catal. 2007, 349, 2619. (e) Mehendale, N. C.; Lutz, M.; Spek, A. L.; Klein Gebbink, R. J. M.; van Koten, G. J. Organomet. Chem. 2008, 693, 2971. (f)McDonald, A. R.; Dijkstra, H. P.; Suijkerbuijk, B.M. J. M.; van Klink, G. P. M.; van Koten, G.Organometallics 2009, 28, 4689. (g) McDonald, A. R.; Franssen, N.; van Klink, G. P. M.; van Koten, G. J. Organomet. Chem. 2009, 694, 2153. (h) O’Leary, P.; vanWalree, C. A.; Mehendale, N. C.; Sumerel, J.; Morse, D. E.; Kaska, W. C.; van Koten, G.; Klein Gebbink, R. J. M. Dalton Trans. 2009, 4289. (164) Gimenez, R.; Swager, T. M. J. Mol. Catal. A 2001, 166, 265. (165) Poyatos, M.; Marquez, F.; Peris, E.; Claver, C.; Fernandez, E. New J. Chem. 2003, 27, 425. (166) Yu, K.; Sommer, W.; Weck, M.; Jones, C. W. J. Catal. 2004, 226, 101. (167) Sommer,W. J.; Yu, K.; Sears, J. S.; Ji, Y.; Zheng, X.; Davis, R. J.; Sherrill, C. D.; Jones, C. W.; Weck, M. Organometallics 2005, 24, 4351. (168) Brookhart, M.; Huang, Z.; MacArthur, A. H.; Carson, E. C.; Goldman, A.; Scott, S. L.; Vicente, B. C. Abstracts of Papers, 239th ACS National Meeting, San Francisco, CA, March 21-25, 2010; American Chemical Society: Washington, DC, 2010; CATL-79. (169) del Pozo, C.; Corma, A.; Iglesias, M.; Sanchez, F. Organometallics 2010, 29, 4491.

Dehydrogenation and related reactions catalyzed by iridium pincer complexes

Metal-ligand cooperation (MLC) has become an important concept in catalysis by transition metal complexes both in synthetic and biological systems. MLC implies that both the metal and the ligand are directly involved in bond activation processes, by contrast to "classical" transition metal catalysis where the ligand (e.g. phosphine) acts as a spectator, while all key transformations occur at the metal center. In this Review, we will discuss examples of MLC in which 1) both the metal and the ligand are chemically modified during bond activation and 2) bond activation results in immediate changes in the 1st coordination sphere involving the cooperating ligand, even if the reactive center at the ligand is not directly bound to the metal (e.g. via tautomerization). The role of MLC in enabling effective catalysis as well as in catalyst deactivation reactions will be discussed.

Metal–Ligand Cooperation

ed by an internal site in intramolecular heterolytic splitting, intermolecular activation requires an external base. Such intramolecular heterolytic splitting is also applicable to C−H or other heteroatom−H bond activation as is frequently observed with ruthenium pincer complexes and discussed in this section. 3.1. Activation of the H−H Bond As shown in Scheme 4b, formation of a dihydride complex such as [(PNP)Ru(H)2(H2)] 20 is a result of dihydrogen activation by oxidative addition due to the electron-rich ruthenium center as discussed above. Gunnnoe and co-workers reported a five-coordinate amido complex (PCP)Ru(CO)(NH2) 71, which heterolytically activates H2, as 71 has the required vacant coordination site for H2 coordination and a basic amido ligand, which abstracts intramolecularly a proton from coordinated H2, followed by dissociation of the formed ammonia (BDERu−NH3 = 12.6 kcal/mol), providing the complex (PCP)RuH(CO) 72 (Scheme 23). The dearomatized pincer complexes 3a−5a developed by Milstein react with molecular hydrogen at room temperature, undergoing rearomatization to provide the trans-dihydride complexes of 3b−5b, respectively, upon heterolysis of dihydrogen (Scheme 24). In the H NMR spectra, the magnetically equivalent trans-dihydrides of 3b and 4b resonate as a triplet at δ = −4.96 ppm (JPH = 20.0 Hz) and δ = −4.90 ppm (JPH = 17.0 Hz), respectively, whereas they display a doublet at δ = −4.06 ppm (JPH = 17.0 Hz) for complex 5b. Further, the structure of the trans-dihydride complex 5b was determined by a single-crystal X-ray analysis (Figure 2). The trans-dihydride complexes 3b−5b slowly lose H2 at room temperature to regenerate complexes 3a−5a, respectively, setting the stage for several catalytic processes (see below) including the production of molecular hydrogen from biorenewable sources. As discussed in the MLC section, the acridine pincer complex 9 also heterolytically activates dihydrogen (Scheme 16). The amido ruthenium pincer complex 73 is in equilibrium with complexes 74 and 75. Formation of amino trans-dihydride complex 74 results from the reversible heterolysis of dihydrogen (Scheme 25). The trans-dihydrides of 74, which resonate at δ = −8.00 and δ = −8.52 ppm, are magnetically inequivalent (JPH = 16.7−24.3 Hz), due to the proximity of one of the hydrides to the backbone amino proton. As observed in heterolysis of hydrogen by Ir pincer complexes, DFT studies suggest that proton transfer from ruthenium to the amido nitrogen is facilitated by the presence of water, which forms a hydrogen bond with both amido nitrogen and H2, leading to a six-membered transition state and lowering the barrier for proton transfer. Complex 73 was found to be an active dehydrogenation catalyst for ammoniaborane and hydrogenation reactions as discussed below. The heterolytic activation of dihydrogen by NH/H2 MLC was reported by Fryzuk and co-workers in 1987 with pincer Ir and Rh complexes. Using the pincer complex [RuCl(PPh3)Scheme 22. Oxidative Addition versus Heterolytic Cleavage of H−H and H−X Bonds Scheme 23. Heterolytic Activation of Hydrogen Scheme 24. Heterolytic Activation of Hydrogen by Aromatization−Dearomatization Process Figure 2. X-ray structure of complex 5b (50% probability level). Hydrogen atoms (except hydrides) are omitted for clarity. Reproduced with permission from ref 100. Copyright 2011 Nature Publishing Group. Chemical Reviews Review dx.doi.org/10.1021/cr5002782 | Chem. Rev. XXXX, XXX, XXX−XXX K (N(SiMe2CH2PPh2)2)], they reported in 1991 that reaction with H2 resulted in a mixture of Ru−H complexes, albeit the reversibility of the reaction was not observed. Recently, Koridze and co-workers reported that a metallocene-derived PCP pincer ruthenium complex also activates molecular hydrogen heterolytically. 3.2. Activation of C−H Bonds While many PCP-type ruthenium pincer complexes were formed as a result of C−H activation or even double C−H activation of the ligand, there are only a few examples of intraor intermolecular C−H activations by ruthenium pincer complexes, as discussed in this section. C−H activation of arenes is widespread with Ir-pincer PNP and PCP complexes. However, such sp C−H activation by Rupincer complexes is rarely encountered. An example of intramolecular C−H activation in a Ru pincer complex was reported by Fryzuk and co-workers. Gunnnoe and co-workers reported that the five-coordinate complexes [(PCP)Ru(CO)(NH2)] 71 and [(PCP)Ru(CO)(CH3)] 76 liberate ammonia and methane, respectively, to generate the cyclometalated PCP ruthenium pincer complex 77 as a result of intramolecular sp C−H activation (Scheme 26). The conversion rate of the methyl complex 76 to 77 is approximately 5 times faster (Kobs = 3.2(1) × 10 −4 s−1 at 50 °C) than the analogous conversion with the amido complex 71 (Kobs = 6.0(3) × 10 −5 s−1 at 50 °C). However, attempted intermolecular C−H activation of methane by complex 71 was not successful and led only to intramolecular C−H activation to provide 77. Gusev and co-workers reported a double C−H activation reaction in a pincer complex. Caulton’s square-planar Ru(II) pincer complex 63a reacted with 1 equiv of MeLi at −78 °C to afford the hydrido−carbene complex 79 as a result of double C−H activation of a single methyl group (Scheme 27). Apart from the characteristic spectroscopic features, DFT calculations indicate that the Ru−C bond length (2.08 Å) in complex 78 decreases to 1.84 Å in 79, in line with formation of a Ru− carbene. The intermediate complex 78 facilitates the C−H agostic interaction and the observed loss of methane. The hydrido−carbene complex 79 reacts with excess of pyridine, immediately forming the diamagnetic η-pyridyl complex 80 as a result of ortho sp C−H activation. Recently, Milstein reported the intramolecular sp C−H activation of expanded PNN ruthenium pincer complexes. Upon deprotonation of the saturated Ru(II) PNN pincer complexes (7 and 8), containing alkyl or cycloalkyl groups on one of the methylene arms, the dearomatized pincer complexes 7a and 8a were formed (Scheme 28). Attempted synthesis of 7a also resulted in intramolecular C−H activation and quantitative formation of the cyclometalated 7b after 4 h. Independent synthesis of 7a was possible using the base KHMDS (potassium hexamethyldisilazide) at −35 °C in toluene-d8, although upon workup only 7b was obtained as a single diastereoisomer, implying that 7a is indeed an intermediate that undergoes cyclometalation and concomitant aromatization to provide 7b. The X-ray structure of 7b exhibits a highly distorted octahedron with the PNC donors coordinated in a pseudomeridional manner (Figure 3). The PNN complex 8a, analogous to 7a, was relatively stable due to steric rigidity, and the conversion to cyclometalated aromatized complex 8b occurred slowly over 5 days. Dearomatized pincer complexes, particularly the bipyridine derived [(PNN)Ru(H)(CO)] 6a and its parent complex 6, are involved in the sp CH activation/exchange of αand βpositions of alcohols with D2O, as will be discussed in section 4.3.1. 3.3. Activation of N−H Bonds As in H2 and C−H activation reactions, MLC of pyridinederived pincer complexes also enables N−H activation of amines and ammonia. As described by Milstein, upon reaction of the dearomatized PNP complex 4a with electron-poor anilines, the unsaturated ligand arm was protonated, and the pyridine ring underwent rearomatization as a result of N−H activation (Scheme 29). The saturated amide complexes 82a Scheme 25. Heterolytic Activation of Hydrogen by Amide−Amine Interconversion Scheme 26. Intramolecular Activation of sp C−H Bonds Scheme 27. Double C−H Activation Leading to the Formation of a Hydrido Carbene Complex Chemical Reviews Review dx.doi.org/10.1021/cr5002782 | Chem. Rev. XXXX, XXX, XXX−XXX L and 82b were obtained in pure form from the reaction of complex 4a with 4-nitroaniline and 2-chloro-4-nitroaniline, respectively, and their symmetrical structures were evident from the P NMR (single signal for each complex) and H NMR spectra. However, the reaction of 2-bromoaniline and 3,4dichloroaniline with complex 4a provided equilibrium mixtures of aromatized N−H activated amide complexes 82c and 82d, and the starting 4a, despite the presence of excess of haloanilines. This observation of reversible N−H bond activation at room temperature was unique, and indicated the low barrier for these reactions. For electron-rich amines and ammonia, the amine-coordinated unsaturated complexes of type 81 are thermodynamically favored. Upon reaction of complex 4a with ND3, formation of the deuterated complex 83 was observed after 5 min at room temperature, showing N−D activation (Scheme 30). The H NMR spectrum of 83 confirmed that deuteration at the methylene arm is stereospecific as only one of the two CH2 arm protons disappeared. No exchange occurred with vinylic protons, and such high selectivity indicated that the activation process on these types of pincer systems occurs only intramolecularly on one face of the ligand with the coordinated ND3 ligand. This observation indicated that other activation processes could also be stereoselective. The trend observed in the experiment was in agreement with DFT studies carried out on the N−H activation reactions (Figure 4). In the reaction of 2-bromoaniline with 4a, the unbound state (I) and the activated state (III) have similar energies with a connecting barrier of 20 kcal/mol. The N−H activated complex of isopropylamine is 16.8 kcal mol−1 above the unbound state, and experimentally it reacted with complex 4a upon warming to 80 °C, whereas in the case of the amines that underwent irreversible N−H activation at room temperature the calculated activated complexes (III) are energetically below the unbound state (I) as expected; barriers for the exchange between amine coordinated (II) and activated (III) states are accessible at room temperature. PNP Rh(I) pincer complexes also activate N−H bonds by similar MLC. N−H bond acti

Bond Activation and Catalysis by Ruthenium Pincer Complexes

Coordination chemistry and catalysis with hemilabile oxygen-phosphorus ligands

IrCl3 reacts with But2P[CH2]5PBut2 to give [[graphic omitted]] which loses dihydrogen reversibly to give [[graphic omitted]], the structure of which has been determined by X-ray diffraction.

Synthesis and X-ray structure of an unusual iridium ylide or carbene complex

Treatment of But2P(CH2)5PBut2, with iridium trichloride gives a mixture of the 16-atom ring dihydride [lr2H2Cl4{But2P(CH2)5PBut2}2], a co-ordinatively saturated cyclometallated hydride, [[graphic omitted]But2)])(1b), which is non-fluxional, and an unidentified complex. A better route to the cyclometallated hydride (1b) is to treat [Ir2Cl2(C8H14)4](C8H14= cyclo-octene) with the diphosphine. Complex (1b) takes up carbon monoxide to give the six-co-ordinate [[graphic omitted]But2)] and loses dihydrogen on heating [ca. 200 °C (15 mmHg)] to give the very dark carbene/ylide complex [[graphic omitted]But2)](3)/(4). This carbene/ylide complex takes up dihydrogen at 20 °C (1 atm) to give back (1b). The diphosphine But2PCH2CH2CHMeCH2CH2PBut2 reacts with IrCl3 to give the 16-atom ring chelate [Ir2H2Cl4(But2PCH2CH2CHMeCH2CH2 PBut2)2], no cyclometallated product being detected. However, the complex [[graphic omitted]But2)], can be prepared from [Ir2Cl2(C8H14)4] and the diphosphine. Hydrogen-1, 13C, and 31P n.m.r. and i.r. data are reported. The crystal structures of (1b) and of the carbene/ylide (3)/(4) have been determined. Cell dimensions are, for (1b), a= 1 231.8(3), b= 1 435.9(3), c= 1 485.4(3) pm, and β= 104.82(2)° and for (3)/(4), a= 1 232.6(3), b= 1 436.2(3), c= 1 480.7(3) pm, and β= 104.87(2)°. The structures are isomorphous, with space group P21/c and Z= 4.

Transition metal–carbon bonds. Part 52. Large ring and cyclometallated complexes formed from But2PCH2CH2CHRCH2CH2PBut2(R H or Me) and IrCl3, or [Ir2Cl4(cyclo-octene)4] : crystal structures of the cyclometallated hydride, [IrHCl(But2PCH2CH2CHCH2CH2PBut2)], and the carbene complex [IrCl(But2PCH2CH2CCH2CH2PBut2)]

Treatment of [PdCl2(NCPh)2] with But2 PCH2CH2CHMeCH2CH2PBut2(Q) gives the binuclear complex [Pd2Cl4(But2PCH2CH2CHMeCH2CH2PBut2)2]. The crystal structure of this 16-atom ring complex shows that the two methyl substituents on the ring occupy ‘corner positions’ and the C5 chains are not in the extended conformation. The crystals are monoclinic, space group Pn, with unit-cell dimensions a= 8.616(2), b= 28.485(5), c= 12.127(2)A, β= 109.35(2)°, and Z= 2, final R= 0.07. A variable-temperature 31P n.m.r. study shows the ring to be fluxional. With [PtCl2(NCPh)2], Q gives a complex [(PtCl2Q)x](also fluxional) and a cyclometallated complex [graphic omitted]But2)] abbreviated to [PtCl(P–C–P)], [PtCl2Q] with CF3COOH gives [Pt(OOCCF3)(P–C–P)], and [PtCl(P–C–P)] with Na[BH4] gives [PtH(P–C–P)]. Infrared and 1H and 31P n.m.r. data are given.

Formation of large chelate rings and cyclometallated complexes from But2PCH2CH2CHMeCH2CH2PBut2 and platinum and palladium chlorides. Crystal structure of [Pd2Cl4{But2PCH2CH2CHMeCH2CH2PBUt2}2]

The compound PBut2[C6H3(OMe)2-2,6] reacts with iridium trichloride in propan-2-ol to give the purple five-co-ordinate hydride [[graphic omitted]But2-2)}2](1). This hydride in solution is converted by air into the red paramagnetic iridium(II) complex [[graphic omitted]But2-2)}2](3) which can be converted back to (1) when treated with Na[BH4]. The hydride (1) takes up small ligands (L) such as pyridine or carbon monoxide reversibly to give colourless adducts [[graphic omitted]But2-2)}2]. Complex (3) takes up dioxygen reversibly to give a purple complex, probably [[graphic omitted]But2-2)}2], reacts with NO to give brown diamagnetic [[graphic omitted]But2-2)}2] and with CO to give a pale green complex which in air becomes intensely blue, then red, and finally gives the colourless C-cyclometallated iridium(III) complex [[graphic omitted]}{OC6H3(OMe-3)(PBut2-2)}](7; L = CO). The dioxygen adduct is slowly converted into the purple, co-ordinatively unsaturated, C-cyclometallated complex [[graphic omitted]But2-2)}](8). Complex (8) takes up small ligands such as CO, pyridine, or MeNC more strongly than (1) to give six-co-ordinate species. The structure of the title complex (7; L = MeNC) has been determined by X-ray diffraction. The crystals are monoclinic, space group P21/c, with a= 13.471 (2), b= 16.043(3), c= 16.690(3)A, and β= 104.22(1)°. The complex has a five-membered IrPC2O chelate ring bound to a highly strained four-membered IrPC2 ring. Complex (8) also takes up PMe2Ph; this addition is reversed on heating and the 31P n.m.r. spectrum at 300 K shows that rapid PMe2Ph exchange occurs (at 233 K exchange does not occur). Treatment of iridium carbonyl chloride solution with PBut2[C6H3(OMe)2-2,6] and PBut2[C6H3(OMe)2-2,3] gives yellow complexes of the type [[graphic omitted]But2-2)}2], isomeric and much more stable than the one described above. Hydrogen-1, 13C, and 31P n.m.r. and i.r. data are given.

Some unusual iridium complexes formed from (2,6-dimethoxyphenyl) and (2,3-dimethoxyphenyl)-di-t-butylphosphine: crystal structure of [2-di-t-butylphosphino-3-methoxyphenoxo-OP]{2-[(2-hydroxy-6-methoxyphenyl)t-butylphosphino]-2-methylpropanato(2—)-C1PO2}-(methyl isocyanide)iridium(III)

Michael C. Norton

Papers

Synthesis and X-ray structure of an unusual iridium ylide or carbene complex

Formation of large chelate rings and cyclometallated complexes from But2PCH2CH2CHMeCH2CH2PBut2 and platinum and palladium chlorides. Crystal structure of [Pd2Cl4{But2PCH2CH2CHMeCH2CH2PBUt2}2]

Some unusual iridium complexes formed from (2,6-dimethoxyphenyl) and (2,3-dimethoxyphenyl)-di-t-butylphosphine: crystal structure of [2-di-t-butylphosphino-3-methoxyphenoxo-OP]{2-[(2-hydroxy-6-methoxyphenyl)t-butylphosphino]-2-methylpropanato(2—)-C1PO2}-(methyl isocyanide)iridium(III)