P–C, P–N, and M–N Bond Formation Processes in Reactions of Heterometallic Phosphinidene-Bridged MoMn and MoRe Complexes with Diazoalkanes and Organic Azides to Build Three- to Five-Membered Phosphametallacycles

Reactions of the heterometallic MoRe complex [MoReCp(μ-PR*)(CO)6] and its MoMn analogue with some small molecules having N–N multiple bonds, such as diazoalkanes and organic azides, were investigated (R* = 2,4,6-C6H2tBu3). Reactions with excess ethyl diazoacetate proceeded slowly and with concomitant denitrogenation to give complexes [MoMCp(μ-η2P,C:κ2P,O-PR*CHCO2Et)(CO)5], which display a bridging phosphaalkene ligand in a novel μ-η2:κ2 coordination mode, while reactions with other diazoalkanes resulted only in the decomposition of the organic reagent. The MoRe complex reacted with benzyl- or p-tolyl azide at room temperature to give the green complexes [MoReCp(μ-η2P,N:κP,N′2-PR*N3R)(CO)6] [R = Bn, p-tol], which display bridging phosphatriazadiene ligands in a novel 6-electron donor coordination mode as a result of a formal [2 + 1] cycloaddition of the terminal N atom of the azide to the Mo–P double bond of the parent complex, followed by coordination of the distal NR nitrogen to the rhenium center. Denitrogenation was only observed for the p-tolyl azide derivative, which upon heating at 333 K yielded [MoReCp{μ-κP:κN-PR*N(p-tol)}(CO)6], a molecule displaying a bridging phosphaimine ligand in a rare κP:κN coordination mode. Analogous reactions of the MoMn phosphinidene complex proceeded similarly at 273 K to give the phosphatriazadiene-bridged derivatives [MoMnCp(μ-η2P,N:κ2P,N′-PR*N3R)(CO)6], but these were thermally unstable and degraded at room temperature to give the mononuclear triazenylphosphanyl complexes [Mn2(κP,N-PR*NHNNR)(CO)3] as major products, along with small amounts of the phosphaimine-bridged complex [MoMnCp{μ-κP:κN-PR*N(p-tol)}(CO)6] in the case of the p-tolyl azide derivative. The structure of the new complexes was analyzed in light of spectroscopic data and single-crystal diffraction studies on selected examples of each type of complex.


■ INTRODUCTION
Reactions of mononuclear metal complexes bearing terminal phosphinidene ligands (PR) with small organic molecules have proved to be a very successful and largely exploitable strategy to build a great variety of organophosphorus molecules on the coordination sphere of metal atoms. 1,2 In contrast, only more recently this sort of reactivity has been extended to binuclear complexes featuring bridging PR ligands, to show that the particular coordination mode of the ligand (A to C in Chart 1) greatly influences the result of these reactions. 3 The latter work, however, focused mostly on homometallic complexes, but the synergic and cooperative effects that the combination of distinct metals with different coordination surroundings can induce, as found in heterometallic complexes, 4 have not been explored for phosphinidene-bridged complexes. Following our recent preparation of the novel heterometallic complex [MoReCp(μ-PR*)(CO) 6 ] (1a), 5 we found that, in spite of the isoelectronic nature of the Mo and Re fragments, the πbonding metal−phosphorus interaction in this molecule is essentially located at the Mo−P junction, whereas bonding of P with the group 7 metal atom can be essentially described as a donor single bond, all of it accounting for a new coordination mode of the bridging phosphinidene ligand (D in Chart 1) deserving some studies about the chemical behavior derived from it. Preliminary studies on the reactivity of 1a revealed, among other features, a defined trend of this complex to undergo cycloaddition processes at the Mo−P double bond when reacting with organic molecules having C−C or C−N triple bonds, such as alkynes and isocyanides. 5 In this paper, we analyze the reactivity of 1a and that of its manganese analogue [MoMnCp(μ-PR*)(CO) 6 ] (1b) 6 toward some small molecules having N−N multiple bonds, such as diazoalkanes and organic azides.
Previous studies on reactions of homometallic PR-bridged complexes with diazoalkanes and organic azides are scarce, yet they indicate that both the coordination mode of the PR ligand and the particular metals involved in each case would have a significant influence on the output of these reactions, not only on the coordination mode of the newly generated organophosphorus ligands, but also on the denitrogenation processes that might follow at the complexes first formed in these reactions. The type A trigonal phosphinidene complexes [Mn 2 (μ-PN i Pr 2 )(CO) 8 ] and [Co 2 (μ-PN i Pr 2 )(CO) 4 (μ-Ph 2 PCH 2 PPh 2 )] yielded phosphadiazadiene-, phosphaalkeneor phosphaimine-bridged derivatives upon reaction with diazoalkanes and azides, depending on the particular metal and reagent 7 (Scheme 1). Phosphadiazadiene and phosphaalkene-bridged complexes were also formed in the reactions of the type A ditungsten complex [W 2 (μ-PCp*)(CO) 10 ] with diazoalkanes, 8 but no denitrogenation took place in reactions with azides, these yielding triazaphosphete-bridged complexes instead. 9 As for complexes of type B, only reactions of the dimolybdenum complex [Mo 2 Cp(μ-κ 1 :κ 1 ,η 5 -PC 5 H 4 )-(CO) 2 (η 6 -R*H)] with diazoalkanes have been investigated, these invariably resulting in spontaneous denitrogenation at room temperature to yield phosphaalkene-bridged products, which can be viewed as resulting from a formal [2 + 1] cycloaddition of the corresponding carbene to the Mo−P double bond of the parent complex (Scheme 2). 10 In contrast, denitrogenation seems to be much less favored in reactions with complexes bearing pyramidal phosphinidene ligands (type C). Thus, the diiron complexes [Fe 2 Cp 2 (μ-PR)(μ-CO)(CO) 2 ] (R = Cy, Ph, R*) reacted with different diazoalkanes and benzyl azide to give isolable κ 1 P :κ 1 Pphosphadiazadiene-and phosphatriazadiene-bridged deriva-tives, respectively, with denitrogenation being only induced in the latter case upon heating (Scheme 3). 11−13 In the same line, we reported recently that the dimolybdenum complex [Mo 2 Cp(μ-κ 1 :κ 1 ,η 5 -PC 5 H 4 )(CO) 2 (η 6 -R*H)(PMe 3 )] reacts with different diazoalkanes and organic azides at low temperature to give the corresponding κ 1 P :κ 1 P -phosphadiazadiene-and phosphatriazadiene-bridged derivatives, which, however, were quite unstable and could be only isolated as solid materials after protonation or methylation steps. Once again, denitrogenation was only observed in some of the azide derivatives. 14 As we will discuss below, the reactions of the heterometallic complexes 1a,b with diazoalkanes and organic azides reported here not only bear some similarities with the ones discussed above but also reflect a relevant role of the heterometallic center, whereby rare or new coordination modes of phosphaalkene, phosphatriazadiene, phosphaimine, and triazenylphosphanyl ligands are unveiled.

■ RESULTS AND DISCUSSION
Reactions with Diazoalkanes. The rhenium complex 1a reacted slowly with a slight excess of ethyl diazoacetate at room temperature to give the phosphaalkene-bridged complex [MoReCp(μ-η 2 P,C :κ 2 P,O -PR*CHCO 2 Et)(CO) 5 ] (2a) (Scheme 4) in modest yield (ca. 20% after chromatographic workup). Unfortunately, the use of less activated diazoalkanes led to no new complexes; thus, the reaction of 1a with N 2 CHSiMe 3 at room temperature just resulted in decomposition of the diazoalkane, whereas reaction with N 2 CPh 2 only proceeded in refluxing toluene, and then led to decomposition of both the metal complex and the added diazoalkane. The manganese complex 1b seemed less reactive than its rhenium analogue, Scheme 1. Diazoalkane and Azide Derivatives of Phosphinidene Complexes of type A a a Mn−Mn = Mn 2 (CO) 8 ; Co−Co = Co 2 (CO) 4 (μ-Ph 2 PCH 2 PPh 2 ); W = W(CO) 5 ; X = Cp* or NR 2 , with Cp* = C 5 Me 5 and R = i Pr; R′= SiMe 3 , SnMe 3 , Ph, adamantyl; R″ = Cy, Hex. since its reaction with ethyl diazoacetate only proceeded at a significant rate upon warming the solution up to ca. 333 K, then needing several additions of the reagent to counterbalance the decomposition of the latter. Eventually, however, the corresponding phosphaalkene-bridged complex [MoMnCp(μη 2 P,C :κ 2 P,O -PR*CHCO 2 Et)(CO) 5 ] (2b) could be isolated in medium yield (ca. 50% after chromatographic workup).
The formation of complexes 2 formally follows from a [2 + 1] cycloaddition of the carbene CHCO 2 Et to the Mo−P double bond of the parent complexes 1, as observed in the reactions of the type B phosphinidene complex mentioned in the Introduction (Scheme 2), this now being followed by coordination of the carbonyl group of the reagent to block the vacant coordination position left by the spontaneous decarbonylation of the M(CO) 4 fragment. The actual mechanism of this process, however, might actually be more complex and likely would involve first the formation of a P−N bond to give undetected phosphadiazadiene intermediates (cf. Scheme 3) that would rapidly evolve through denitrogenation, as actually observed in the reactions of 1a with azides to be discussed later on, and then through a decarbonylation step that would force the formation of a new O−Re/Mn bond.
The structure of the rhenium complex 2a in the crystal ( Figure 1 and Table 1) can be derived from that of the parent compound 1a by adding the carbenic carbon to the Mo−P double bond of the precursor through a direction perpendicular to the MoPRe plane, thus maximizing interaction with the π and π* frontier orbitals of 1a, 5 while the C�O oxygen atom in the carbene substituent binds the Re atom trans to a carbonyl ligand, thus defining a little twisted RePCCO fivemembered ring. The resulting phosphaalkene ligand can thus be considered as contributing with two electrons to the Mo center (η 2 coordination) and with four electrons to the rhenium center (κ 2 P,O coordination). This yields a 34-electron complex for which a single Mo−Re bond has to be proposed according to the 18 electron rule, which is in agreement with the Mo−Re distance of 3.1579(3) Å, very similar to the distance of 3.1745(6) Å measured in the parent compound 1a. 5 We note that no other heterometallic complex with κ 1 :η 2bridging phosphaalkene ligands appears to have been crystallographically characterized so far, 15 and the additional coordination of the oxygen atom to render a 6-electron donor μ-κ 2 :η 2 coordination mode is also unprecedented for a phosphaalkene ligand.
Spectroscopic data for compounds 2a and 2b in solution are consistent with the solid-state structure of 2a. The IR spectra display, in each case, a high-frequency C−O stretch at ca. 2020 cm −1 of high intensity, as expected from the presence of pyramidal M(CO) 3 oscillators, 16 while evidence for the coordination of the carboxylate group is given by the significant red shift of the corresponding C�O stretch, from ca. 1700 cm −1 observed in uncoordinated groups to ca. 1550 cm −1 in complexes 2. This is also consistent with the C−ORe distance of 1.250(3) Å measured for 2a in the solid state, slightly enlarged when compared to the reference value of ca. 1.21 Å for a double bond between these atoms. 17 The formation of the three-membered phosphametallacycle found in compounds 2 is denoted by the dramatic shielding of its 31 P resonance, which moves from ca. 600 ppm (for the parent compounds 1) to ca. 100 ppm ( Table 2). As expected, the resonance of the Re compound appears some 50 ppm more shielded than the one of its Mn analogue, a difference typically observed when comparing chemical shifts of P atoms bound to heavier metals within the same group. 18 Finally, we note that the methylenic group of the MoPC ring gives rise to considerably shielded 13 C (δ C ca. 25 ppm) and 1 H (δ H ca. 2 ppm) NMR resonances, which is consistent with the strong η 2 coordination observed in the solid state, as deduced from the values of the Mo−C and C−P distances (2.296(3) and 1.780(3) Å respectively), which are close to the expected figures for single bonds between the C(sp 2 ) and Mo or P atoms (2.27 and 1.80 Å). 19 Reactions of the Rhenium Complex 1a with Organic Azides. Compound 1a reacted with benzyl-or p-tolyl azide smoothly at room temperature in toluene solution to give the green complexes [MoReCp(μ-η 2 P,N :κ 2 P,N′ 2 -PR*N 3 R)(CO) 6 ] [R = Bn (3a.1), p-tol (3a.2)] in good yields (ca. 80% after chromatographic workup), which display bridging phosphatriazadiene ligands in a novel 6-electron donor μ-κ 2 :η 2 coordination mode (Scheme 5). 20 Compounds 3a formally   (3) follow from a [2 + 1] cycloaddition of the terminal N atom of the azide to the Mo−P double bond of the parent complex, this being followed by the coordination of the distal NR nitrogen to the rhenium center without decarbonylation. As a result of the latter coordination, the intermetallic interaction is vanished in the resulting 36 electron complexes. The contrast with the diazoalkane reactions of 1a,b discussed above is thus evident, since no spontaneous denitrogenation takes place here at room temperature. In fact, the benzyl azide derivative 3a.1 could be heated in refluxing toluene solution without significant transformation. However, the p-tolyl azide derivative 3a.2 underwent clean denitrogenation upon heating in toluene solution at 333 K to yield the orange complex [MoReCp{μ-κ P :κ N -PR*N(p-tol)}(CO) 6 ] (4a) in good yield (ca. 70% yield after chromatographic workup). The latter displays a bridging phosphaimine (or iminophosphinidene) ligand in a rare κ P :κ N coordination mode (Scheme 5), previously identified only in the rhenium complex [Re 2 (μ-Br) 2 {μ-κ P :κ N -P(N i Pr 2 )N( t Bu)}(CO) 6 ]. 21 We note the specific ligation of P to the Mo atom and the NR nitrogen to the Re atom, thus retaining most of the connections in the parent compound 3a.2. No evidence for the formation of an alternative isomer of 4a (with P-binding of the bridging ligand to Re, and N-binding to Mo) was obtained in this denitrogenation reaction. From the above differences between the thermal evolution of compounds 3a.1 and 3a.2, we may conclude that their phosphatriazadiene ligands are more prone to denitrogenation when having an electron-withdrawing aryl substituent at the N atom rather than an electron-releasing alkyl one. This is in line with our previous studies on the reactions of the dimolybdenum complex of type C [Mo 2 Cp(μ-κ 1 :κ 1 ,η 5 -PC 5 H 4 )(CO) 2 (η 6 -R*H)(PMe 3 )] with different organic azides. 14 Thus, it seems that denitrogenation processes in bridging phosphatriazadiene ligands are largely influenced by the nature of the substituent at the N atom (electronwithdrawing or electron-releasing ones) and less by the exact nature of the dimetal site to which they are bound.
Structure of Phosphatriazadiene Complexes 3a. The molecule of the p-tolyl azide derivative 3a.2 in the crystal ( Figure 2 and Table 3) can be derived from that of the parent compound upon [2 + 1] cycloaddition of the terminal N atom of the azide to the Mo−P double bond of the parent compound, expectedly from a direction perpendicular to the former MoPRe plane, as discussed above. The coordination of the distal NR atom to the Re center removes the intermetallic interaction (Mo1···Re1 ca. 4.36 Å) and increases the coordination number of this metal atom, which now displays a local octahedral geometry, whereas the conformation of the resulting PNNNRe five-membered ring is essentially planar.     17,19 even if the pyramidal environment around the bridgehead N1 atom would seem to disfavor any delocalization of the N2−N3 π interaction. We should finally remark that compound 3a.2 provides the first structural characterization of the μ-η 2 P,N :κ P (and μ-η 2 P,N :κ 2 P,N′ ) coordination mode for a bridging phosphatriazadiene ligand. As concluded from the above geometrical analysis, the η 2 interaction of the P�N bond of this ligand with the Mo atom is strong enough to get close to the "metallacyclopropane" extreme of [2 + 1] cycloadditions.
Spectroscopic data for compounds 3a.1 and 3a.2 in solution are consistent with the solid-state structure of 3a.2. In particular, the IR spectra of these compounds display, in each case, six C−O stretches with a pattern indicative of the presence of vibrationally independent cisoid Mo(CO) 2 and disphenoidal M(CO) 4 oscillators, as expected for molecules having these fragments not connected through a metal−metal bond. 16 In addition, the 31 P NMR resonances of these complexes appear strongly shielded (δ P ca. −20 ppm), with a chemical shift some 100 ppm below the one measured for the phosphaalkene-bridged complex 2a, which likely is another spectroscopic feature derived from the absence of a metal− metal bond connecting the metal fragments in these molecules. 18 Other spectroscopic parameters of these complexes are not unusual and deserve no detailed comments.
Structure of the Phosphaimine Complex 4a. The molecule of this complex in the crystal (Figure 3 and Table 4) is built from cisoid MoCp(CO) 2 and disphenoidal Re(CO) 4 fragments connected via a 4-electron donor phosphaimine ligand, which is P-bound to the Mo atom and N-bound to the Re atom, and defines an almost flat MoReNP central ring. The coordination sphere of the metal atoms is completed with an intermetallic single bond, as expected for a 34-electron complex. The corresponding length of 3.0968(2) Å is a bit shorter than the ones in compounds 1a or 2a but otherwise is not unusual for a single bond between these metal atoms (cf. 3.1307(8) Å in [MoRe(μ-η 5 :κ 1 P -C 5 H 4 PCy 2 )(CO) 7 ]). 22 As for the coordination of the bridging ligand, we note that the Re−N separation of 2.205(2) Å is close to the reference figure of ca. 2.22 Å for a single bond between these atoms, 19 actually very close to the corresponding distance measured in the mentioned complex [Re 2 (μ-Br) 2 {μ-κ P :κ N -P(N i Pr 2 )N-( t Bu)}(CO) 6 ] (2.21(2) Å). 21 In contrast, the Mo−P distance of 2.3081 (7) 24 a molecule for which a Mo−P bond order of 1.5 should be proposed. At the same time, the P−N distance of 1.603(2) Å is somewhat longer than the reference value of 1.57 Å for a double bond between these atoms or the distance of 1.56(2) Å measured in the mentioned dirhenium complex. All of this indicates that for our heterometallic complex 4a.2 (but not for the mentioned Re 2 complex), the interaction of the phosphaimine ligand with the heterometallic center cannot be just described using conventional single-donor bonds (canonical form F1 in Chart 2). Instead, the above geometrical parameters suggest that there must also be a significant contribution of the interaction represented by canonical form F2, involving a Mo−P double bond and a P−N single bond.
Spectroscopic data for 4a in solution imply a symmetry higher than the one found in the crystal, thus suggesting the presence of dynamic effects. Its IR spectrum displays six C−O stretches, and the medium intensity of the most energetic band at 2072 cm −1 is characteristic of M(CO) 4 fragments with local disphenoidal geometry. 16 On the other hand, its 31 P NMR spectrum displays a substantially deshielded resonance, with a chemical shift (δ P 289.6 ppm) comparable to the one measured for the mononuclear phosphanyl complex syn-[MoCp(PR*Cl)(CO) 2 ] (δ P 266.8 ppm), 5 in any case consistent with the trigonal environment of the P atom of the ligand. However, the 13 C and 1 H NMR spectra of 4a display single resonances for each of the pairs of Mo-bound carbonyls, two Re-bounds carbonyls, ring protons, and ortho-t Bu protons of the supermesityl group (see the   25 and not investigated here. Reactions of the Manganese Complex 1b with Organic Azides. Compound 1b turned out to be more reactive toward organic azides than its Re analogue 1a, as it was able to react with benzyl or p-tolyl azide, even at 273 K, to give the corresponding phosphatriazadiene-bridged derivatives [MoMnCp(μ-η 2 P,N :κ 2 P,N′ -PR*N 3 R)(CO) 6 ] [R = Bn (3b.1), ptol (3b.2)] as major products, respectively (Scheme 6). The latter complexes could be isolated as green solids in ca. 55% yield upon chromatographic purification as long as all manipulations were carried out at low temperatures, as they were thermally unstable, and their spectroscopic data (Table 2 and Experimental Section) were analogous to those of the rhenium complexes 3a.1,2, thus indicating that they all display the same structure.
Upon standing in solution at room temperature, the benzyl azide derivative 3b.1 fully degraded in a few hours to give the mononuclear phosphanyl complex [Mn(κ 2 P,N -PR*NHNNBn)-(CO) 3 ] (5.1) as a major product, which could be isolated in 58% yield upon chromatographic workup. The p-tolyl azide derivative 3b.2 behaved similarly and yielded the related complex [Mn{κ 2 P,N -PR*NHNN(p-tol)}(CO) 3 ] (5.2) as a major product (44% yield after purification), but in this case, small amounts of the phosphaimine-bridged complex [MoMnCp{μ-κ P :κ N -PR*N(p-tol)}(CO) 6 ] (4b) were also formed. Compound 4b obviously follows from a minor denitrogenation pathway of 3b.2 that was dominant for its rhenium analogue 3a.2 and is also taking place for the azide derivative having the electron-withdrawing aryl substituent. Spectroscopic data for this product are analogous to those of the rhenium complex 4a and deserve no particular comment, except for the observation that its 31 P chemical shift of 292.6 ppm is almost identical to the one measured for 4a (δ P 289.6 ppm). This indicates that the coordination mode of the phosphaimine ligand also involves, in this case, the selective coordination of phosphorus to the Mo atom.
The formation of compounds 5 requires the cleavage of Mo−P and Mo−N bonds in the parent complexes 3b. The latter cleavage would generate MoCp(CO) 2 and Mn-(CO) 4 (RPPN 3 R) radicals that would evolve differently. The Mo fragment appears to just decompose, as no likely derivatives of it ([Mo 2 Cp 2 (CO) n ], with n = 4, 6, or [MoCpH(CO) 3 ]) were identified in the corresponding reaction mixtures. As for the Mn fragment, it would undergo decarbonylation and H atom abstraction (from the solvent or trace amounts of water present in the solvent), both of them being well-established reactions of organometallic radicals. 26 The abstraction process would occur selectively at the P-bound nitrogen of the phosphatriazadiene group to eventually render a triazenylphosphanyl ligand, although the exact sequence of events (degradation/decarbonylation/abstraction) is unknown. Under this view, the fact that the related rhenium complexes 3a are not degrading thermally into similar mononuclear complexes can possibly be attributed to the higher reluctance of the Re(CO) 4 fragment (compared to the Mn(CO) 4 one) to undergo decarbonylation, likely at some of the early stages preceding degradation into mononuclear fragments.
Structure of Triazenylphosphanyl Complexes 5. In the crystal (Figure 4 and Table 5), the benzyl azide derivative 5.1 displays a distorted trigonal bipyramidal environment for the manganese atom, with three carbonyl ligands occupying two equatorial and one axial position, while the bidentate triazenylphosphanyl ligand binds the metal atom through its phosphanyl group at the remaining equatorial site, and through the distal NBn nitrogen at the remaining axial site, trans to a carbonyl ligand (C3−Mn1−N3 ca. 170°). The ligand thus configures an almost perfectly flat five-membered MnPN 3 ring that bisects the Mn(CO) 3 fragment and defines a trigonal planar environment around the P atom but with angles   . We note that no other complex with a chelating, 5-electron donor triazenylphospanyl ligand appears to have been structurally characterized so far, although we have reported previously examples of a similar ligand bridging molybdenum atoms in a μ-κ 1 P :κ 2 P,N fashion. 14 The corresponding Mn−N length of 1.994(2) Å in 5.1 falls on the short side of the range of distances measured in imine and related carbonyl complexes of manganese (1.95−2.15 Å), 27 while the short Mn−P distance of 2.1168(6) Å is consistent with the formulation of a double bond for the interaction of this three-electron donor group with the manganese atom, this being slightly shorter than the value of 2.1414(8) Å measured in the MoMn complex [MoMnCp(μ-κ 1 :κ 1 ,η 6 -PR*)(CO) 4 ], 28 and falling in the upper part of the range of ca. 2.06−2.12 Å found for the few mononuclear complexes of type [Mn(PX 2 )-(CO) 4 ] structurally characterized to date (X = R, OR, NR 2 substituent). 29,30 As for other distances within the phosphametallacyclic ring, we note that the P1−N1 separation of 1.704(2) Å is below the reference value for a P−N single bond (ca. 1.78 Å), while the N1−N2 and N2−N3 separations (1.325(2) and 1.297(2) Å, respectively) have values close to each other and intermediate between the reference values for single and double bonds between N atoms (1.42 and 1.25 Å respectively), 17,19 all of this suggesting significant delocalization of π-bonding interactions along the PN 3 chain.
Spectroscopic data for compounds 5.1 and 5.2 in solution are consistent with the solid-state structure of 5.1. Thus, their IR spectra display, in each case, two strong C−O stretches characteristic of pyramidal M(CO) 3 oscillators in a highsymmetry local enviroment, 16 while the presence of a N-bound hydrogen is revealed by a weak N−H stretch at 3329 cm −1 in the solid-state spectrum of 5.1 and by 1 H NMR resonances at ca. 11 ppm in both cases. Both compounds display quite deshielded 31 P NMR resonances at ca. 253 ppm, indicative of the retention of the trigonal environment for the P atom observed in the solid state (cf. 246 ppm for [Mn{P-(RNC 2 H 2 NR)}(CO) 4 ], with R = 2,6-C 6 H 3 i Pr 2 ). 30c We finally note that rather than the separate resonances expected for the equatorial and axial carbonyls of these molecules, the 13 C NMR spectra of compounds 5.1,2 displayed single-carbonyl resonances at ca 227 ppm in each case when recorded at room temperature or 253 K. This reveals the operation of a fast (on the NMR time scale) carbonyl exchange process within the Mn(CO) 3 fragment, quite common in carbonyl complexes having pyramidal M(CO) 3 fragments, which was not further investigated.
X-ray Structure Determination of Compounds 2a and 5.1. Data collection for these compounds was performed at 100 K on a Bruker D8 Venture Photon III 14 κ-geometry diffractometer, using Mo Kα radiation. Structure solution and refinements were performed following general procedures described before 5,6 to give the residuals shown in Table S1. In compound 2a, two independent but otherwise similar molecules were present in the unit cell; both of them had a disordered t Bu group, satisfactorily modeled over two sites with 0.70/ 0.30 and 0.75/0.25 occupancies, respectively. The disordered carbon atoms were refined isotropically, and this caused B-level alerts in the corresponding checkcif file. For compound 5.1, there was a disordered t Bu group too, satisfactorily modeled over two sites with 0.65/0.35 occupancies in this case. There was also a toluene molecule (one per two molecules of the complex) placed on an inversion center, which caused symmetry-imposed disorder (50% occupancies), which could be modeled while applying restraints on the C−C bond lengths and the ring planarity. The disordered carbon atoms were refined isotropically, and this again caused the appearance of B-level alerts in the corresponding checkcif file.
X-ray Structure Determination of Compounds 3a.2 and 4a. Data collection for these compounds was performed at ca. 150 K on an Oxford Diffraction Xcalibur Nova single-crystal diffractometer using Cu Kα radiation Structure solution, and refinements were performed following general procedures described before 5,6 to give the residuals shown in Table S1. ■ ASSOCIATED CONTENT