C≡N and N≡O Bond Cleavages of Acetonitrile and Nitrosyl Ligands at a Dimolybdenum Center to Render Ethylidyne and Acetamidinate Ligands.

Extended reduction of [Mo2Cp2(µ-Cl)(µ-PtBu2)(NO)2] (1) with Na(Hg) in acetonitrile (MeCN) at room temperature resulted in an unprecedented full cleavage of the C≡N bond of a coordinated MeCN molecule to yield the vinylidene derivative Na[Mo2Cp2(µ-PtBu2)(µ-CCH2)(NO)2], which upon protonation with (NH4)PF6 gave the ethylidyne complex [Mo2Cp2(µ-PtBu2)(µ-CMe)(NO)2] [Mo1-Mo2 = 2.9218(2) Å] in a selective and reversible way. Controlled reduction of 1 at 273 K yielded instead, after protonation, the 30-electron acetamidinate complex [Mo2Cp2(µ-PtBu2)(µ-κN:κN'-HNCMeNH)(µ-NO)]PF6 [Mo1-Mo2 = 2.603(2) Å], in a process thought to stem from the paramagnetic MeCN-bridged intermediate [Mo2Cp2(µ-PtBu2)(µ-NCMe)(NO)2], followed by a complex sequence of elementary steps including cleavage of the N≡O bond of a nitrosyl ligand.

E-H Bond Cleavage Processes in Reactions of Heterometallic Phosphinidene-Bridged MoRe and MoMn Complexes with Hydrogen and p-Block Element Hydrides.

Reactions of complexes [MoMCp(µ-PMes*)(CO)6] with H2 and several p-block element (E) hydrides mostly resulted in the cleavage of E-H bonds under mild conditions [M = Re (1a) and Mn (1b); Mes* = 2,4,6-C6H2tBu3]. The reaction with H2 (ca. 4 atm) proceeded even at 295 K to give the hydrides [MoMCp(µ-H)(µ-PHMes*)(CO)6]. The same result was obtained in the reactions with H3SiPh and, for 1a, upon reduction with Na(Hg) followed by protonation of the resulting anion [MoReCp(µ-PHMes*)(CO)6]-. The latter reacted with [AuCl{P(p-tol)3}] to yield the related heterotrimetallic cluster [MoReAuCp(µ-PHMes*)(CO)6{P(p-tol)3}]. The reaction of 1a with thiophenol gave the thiolate-bridged complex [MoReCp(µ-PHMes*)(µ-SPh)(CO)6], which evolved readily to the pentacarbonyl derivative [MoReCp(µ-PHMes*)(µ-SPh)(CO)5]. In contrast, no P-H bond cleavage was observed in reactions of complexes 1a,b with PHCy2, which just yielded the substituted derivatives [MoMCp(µ-PMes*)(CO)5(PHCy2)]. Reactions with HSnPh3 again resulted in E-H bond cleavage, but now with the stannyl group terminally bound to M, while 1a reacted with BH3·PPh3 to give the hydride-bridged derivatives [MoReCp(µ-H)(µ-PHMes*)(CO)5(PPh3)] and [MoReCp(µ-H){µ-P(CH2CMe2)C6H2tBu2}(CO)5(PPh3)], which follow from hydrogenation, C-H cleavage, and CO/PPh3 substitution steps. Density functional theory calculations on the PPh-bridged analogue of 1a revealed that hydrogenation likely proceeds through the addition of H2 to the Mo=P double bond of the complex, followed by rearrangement of the Mo fragment to drive the resulting terminal hydride into a bridging position.

Cycloaddition and C-S Bond Cleavage Processes in Reactions of Heterometallic Phosphinidene-Bridged MoRe and MoMn Complexes with Alkynes and Phenyl Isothiocyanate.

Reactions of [MoReCp(µ-PMes*)(CO)6] with internal alkynes RC≡CR yielded the phosphapropenylidene-bridged complexes [MoReCp(µ-κ2P,C:η3-PMes*CRCR)(CO)5] (Mes* = 2,4,6-C6H2tBu3; R = CO2Me, Ph). Terminal alkynes HC≡CR1 gave mixtures of isomers [MoReCp(µ-κ2P,C:η3-PMes*CHCR1)(CO)5] and [MoReCp(µ-κ2P,C:η3-PMes*CR1CH)(CO)5], with the first isomer being major (R1 = CO2Me) or unique (R1 = tBu), indicating the relevance of steric repulsions during the [2 + 2] cycloaddition step between Mo=P and C≡C bonds in these reactions. Similar reactions were observed for [MoMnCp(µ-PMes*)(CO)6]. Addition of ligands to these complexes promoted rearrangement of the phosphapropenylidene ligand into the allyl-like µ-η3:κ1C mode, as shown by the reaction of [MoReCp(µ-κ2P,C:η3-PMes*CHC(CO2Me)}(CO)5] with CN(p-C6H4OMe) to give [MoReCp{µ-η3:κ1C-PMes*CHC(CO2Me)}(CO)5{CN(p-CH4OMe)}2]. The MoRe phosphinidene complex reacted with S=C=NPh to give as major products the phosphametallacyclic complex [MoReCp{µ-κ2P,S:κ2P,S-PMes*C(NPh)S}(CO)5] and its thiophosphinidene-bridged isomer [MoReCp(µ-η2:κ1S-SPMes*)(CO)5(CNPh)]. The first product follows from a [2 + 2] cycloaddition between Mo=P and C=S bonds, with specific formation of P-C bonds, whereas the second one would arise from the alternative cycloaddition involving the formation of P-S bonds, more favored on steric grounds. The prevalence of the µ-η2:κ1S coordination mode of the SPMes* ligand over the µ-η2:κ1p mode was investigated theoretically to conclude that steric congestion favors the first mode, while the kinetic barrier for interconversion between isomers is low in any case.

Reactions of Heterometallic Phosphinidene-Bridged MoMn and MoRe Complexes with Sulfur and Selenium: From Chalcogenophosphinidene- to Trithiophosphonate-Bridged Derivatives.

Reactions of [MoReCp(µ-PR*)(CO)6] with S8 were strongly dependent on experimental conditions (R* = 2,4,6-C6H2tBu3). When using 1 equiv of sulfur, complex [MoReCp(µ-η2:κ1S-SPR*)(CO)6] was slowly formed at 313 K, with a thiophosphinidene ligand unexpectedly bridging the dimetal center in the novel µ-κ1S:η2 coordination mode, as opposed to the µ-κ1P:η2 mode usually found in related complexes. The latter underwent fast decarbonylation at 363 K to give [MoReCp(µ-η2:η2-SPR*)(CO)5], with a six-electron donor thiophosphinidene ligand rearranged into the rare µ-η2:η2 coordination mode. Depending on reaction conditions, reactions with excess sulfur involved the addition of two or three S atoms to the phosphinidene ligand to give new complexes identified as the dithiophosphinidene-bridged complex [MoReCp(µ-η2:κ2S,S'-S2PR*)(CO)5], its dithiophosphonite-bridged isomer [MoReCp(µ-κ2S,S':κ2S,S'-S2PR*)(CO)5], or the trithiophosphonate-bridged derivative [MoReCp(µ-κ2S,S':κ2S,S'-S3PR*)(CO)5], all of them displaying novel coordination modes of their PRS2 and PRS3 ligands, as determined by X-ray diffraction studies. In contrast, the related MoMn complex yielded [MoMnCp(µ-η2:η2-SPR*)(CO)5] under most conditions. A similar output was obtained in reactions with gray selenium for either MoRe or MoMn phosphinidene complexes, which under different conditions only gave the pentacarbonyl complexes [MoMCp(µ-η2:η2-SePR*)(CO)5] (M = Re, Mn), these providing a new coordination mode for selenophosphinidene ligands.

Portion control tableware differentially impacts eating behaviour in women with and without overweight.

Portion control tableware has been described as a potentially effective approach for weight management, however the mechanisms by which these tools work remain unknown. We explored the processes by which a portion control (calibrated) plate with visual stimuli for starch, protein and vegetable amounts modulates food intake, satiety and meal eating behaviour. Sixty-five women (34 with overweight/obesity) participated in a counterbalanced cross-over trial in the laboratory, where they self-served and ate a hot meal including rice, meatballs and vegetables, once with a calibrated plate and once with a conventional (control) plate. A sub-sample of 31 women provided blood samples to measure the cephalic phase response to the meal. Effects of plate type were tested through linear mixed-effect models. Meal portion sizes (mean ± SD) were smaller for the calibrated compared with the control plate (served: 296 ± 69 vs 317 ± 78 g; consumed: 287 ± 71 vs 309 ± 79 g respectively), especially consumed rice (69 ± 24 vs 88 ± 30 g) (p < 0.05 for all comparisons). The calibrated plate significantly reduced bite size (3.4 ± 1.0 vs 3.7 ± 1.0 g; p < 0.01) in all women and eating rate (32.9 ± 9.5 vs 33.7 ± 9.2 g/min; p < 0.05), in lean women. Despite this, some women compensated for the reduced intake over the 8 h following the meal. Pancreatic polypeptide and ghrelin levels increased post-prandially with the calibrated plate but changes were not robust. Plate type had no influence on insulin, glucose levels, or memory for portion size. Meal size was reduced by a portion control plate with visual stimuli for appropriate amounts of starch, protein and vegetables, potentially because of the reduced self-served portion size and the resulting reduced bite size. Sustained effects may require the continued use of the plate for long-term impact.

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.

Chemistry of a Nitrosyl Ligand κ:η-Bridging a Ditungsten Center: Rearrangement and N-O Bond Cleavage Reactions.

The novel nitrosyl-bridged complex [W2Cp2(µ-PtBu2)(µ-κ:η-NO)(CO)(NO)](BAr4) [Ar = 3,5-C6H3(CF3)2] was prepared in a multistep procedure starting from the hydride [W2Cp2(µ-H)(µ-PtBu2)(CO)4] and involving the new complexes [W2Cp2(µ-PtBu2)(CO)4](BF4), [W2Cp2(µ-PtBu2)(CO)2(NO)2](BAr4), and [W2(µ-κ:η5-C5H4)Cp(µ-PtBu2)(CO)(NO)2] as intermediates, which follow from reactions with HBF4·OEt2, NO, and Me3NO·2H2O, respectively. The nitrosyl-bridged cation easily added chloride upon reaction with [N(PPh3)2]Cl, with concomitant NO rearrangement into the terminal coordination mode, to give [W2ClCp2(µ-PtBu2)(CO)(NO)2], and underwent N-O and W-W bond cleavages upon the addition of CNtBu to give the mononuclear phosphinoimido complex [WCp(NPtBu2)(CNtBu)2](BAr4). Another N-O bond cleavage was induced upon photochemical decarbonylation at 243 K, which gave the oxo- and phosphinito-bridged nitrido complex [W2Cp2(N)(µ-O)(µ-OPtBu2)(NO)](BAr4), likely resulting from a N-O bond cleavage step following decarbonylation.

Electronic Structure and Donor Ability of an Unsaturated Triphosphorus-Bridged Dimolybdenum Complex.

The triphosphorus complex [Mo2Cp2(µ-η3:η3-P3)(µ-PtBu2)] was prepared in 83% yield by reacting the methyl complex [Mo2Cp2(µ-κ1:η2-CH3)(µ-PtBu2)(µ-CO)] with P4 at 333 K, a process also giving small amounts of the methyldiphosphenyl complex [Mo2Cp2(µ-η2:η2-P2Me)(µ-PtBu2)(CO)2]. The latter could be better prepared by first reacting the anionic complex Na[Mo2Cp2(µ-PtBu2)(µ-CO)2] with P4 to give the diphosphorus derivative Na[Mo2Cp2(µ-η2:η2-P2)(µ-PtBu2)(CO)2] and further reaction of the latter with MeI. Density functional theory calculations on the title complex revealed that its triphosphorus group can be viewed as an allylic-like P3- ligand acting as a six-electron donor via the external P atoms, while coordination of the internal P atom involves donation from the π orbital of the ligand and back-donation to its π* orbital, both interactions having a weakening effect on the Mo-Mo and P-P connections. The reactivity of the title compound is dominated by the electron-donor ability associated with the lone pairs located at the P atoms. Its reaction with CF3SO3Me gave [Mo2Cp2(µ-η3:η3-P3Me)(µ-PtBu2)](CF3SO3) as a result of methylation at an external atom of the P3 ligand, while its reaction with [Fe2(CO)9] enabled the addition of one, two, or three Fe(CO)4 fragments at these P atoms, but only the diiron derivative [Mo2Fe2Cp2(µ-η3:η3:κ1:κ1-P3)(µ-PtBu2)(CO)8] could be isolated. This complex bears a Fe(CO)4 fragment at each of the external atoms of the P3 ligand, and the central P atom of the latter displays the lowest 31P chemical shift reported to date (δP -721.8 ppm). The related complexes [Mo2M2Cp2(µ-η3:η3:κ1:κ1-P3)(µ-PtBu2)(CO)10] (M = Mo, W) were prepared by reacting the title compound with the corresponding [M(CO)5(THF)] complexes in toluene, while reaction with [Mo(CO)4(THF)2] also enabled the formation of the heptanuclear derivative [Mo7Cp4(µ-η3:η3:κ1:κ1-P3)2(µ-PtBu2)2(CO)14]. The interatomic distances in the above compounds indicate that the central Mo2P3 skeleton of these molecules is little modified by the attachment of 16-electron M(CO)n fragments at the external atoms of the P3 ligand.

Impact of Portion Control Tools on Portion Size Awareness, Choice and Intake: Systematic Review and Meta-Analysis.

Portion control utensils and reduced size tableware amongst other tools, have the potential to guide portion size intake but their effectiveness remains controversial. This review evaluated the breadth and effectiveness of existing portion control tools on learning/awareness of appropriate portion sizes (PS), PS choice, and PS consumption. Additional outcomes were energy intake and weight loss. Published records between 2006-2020 (n = 1241) were identified from PubMed and WoS, and 36 publications comparing the impact of portion control tools on awareness (n = 7 studies), selection/choice (n = 14), intake plus related measures (n = 21) and weight status (n = 9) were analyzed. Non-tableware tools included cooking utensils, educational aids and computerized applications. Tableware included mostly reduced-size and portion control/calibrated crockery/cutlery. Overall, 55% of studies reported a significant impact of using a tool (typically smaller bowl, fork or glass; or calibrated plate). A meta-analysis of 28 articles confirmed an overall effect of tool on food intake (d = -0.22; 95%CI: -0.38, -0.06; 21 comparisons), mostly driven by combinations of reduced-size bowls and spoons decreasing serving sizes (d = -0.48; 95%CI: -0.72, -0.24; 8 comparisons) and consumed amounts/energy (d = -0.22; 95%CI: -0.39, -0.05, 9 comparisons), but not by reduced-size plates (d = -0.03; 95%CI: -0.12, 0.06, 7 comparisons). Portion control tools marginally induced weight loss (d = -0.20; 95%CI: -0.37, -0.03; 9 comparisons), especially driven by calibrated tableware. No impact was detected on PS awareness; however, few studies quantified this outcome. Specific portion control tools may be helpful as potentially effective instruments for inclusion as part of weight loss interventions. Reduced size plates per se may not be as effective as previously suggested.

Efficient Synthesis and Multisite Reactivity of a Phosphinidene-Bridged Mo-Re Complex. A Platform Combining Nucleophilic and Electrophilic Features.

The heterometallic complex [MoReCp(µ-PR*)(CO)6] (3) was prepared in 60% overall yield from syn-[MoCp(PHR*)(CO)2] via a three-step procedure involving complexes syn-[MoCp(PClR*)(CO)2] and [MoReCp(µ-PR*)(CO)7] as intermediate species (R* = 2,4,6-C6H2tBu3). The PR* ligand in 3 displays a novel asymmetric interaction with the dimetal center, involving a double bond with one atom (Mo) and a dative single bond with the other one (Re). Compound 3 underwent thermal isomerization involving a C-H bond cleavage to yield the hydride [MoReCp(µ-H){µ-P(CH2CMe2)C6H2tBu2}(CO)6] and reacted with I2 to give [MoReCpI2(µ-PR*)(CO)6], which displays a symmetrical phosphinidene bridge. Its reaction with methyl propiolate at 293 K proceeded with [2 + 2] cycloaddition of the alkyne and decarbonylation to yield the phosphapropenylidene-bridged complex [MoReCp{µ-κ2P,C:η3-PR*CHC(CO2Me)}(CO)5] as the major product, whereas its reaction with excess CN(4-C6H4OMe) at 273 K proceeded with formal [2 + 1] cycloaddition of the isocyanide and further isocyanide addition at the Re site to yield the complex [MoReCp{µ-η2P,C:κ1P-PR*CN(4-C6H4OMe)}(CO)6{CN(4-C6H4OMe)}], which displays an azaphosphaallene ligand in a novel bridging coordination mode.

P-N and N-Mo Bond Formation Processes in the Reactions of a Pyramidal Phosphinidene-Bridged Dimolybdenum Complex with Diazoalkanes and Organic Azides.

The reactivity of the complex [Mo2Cp(µ-κ1:κ1,η5-PC5H4)(CO)2(η6-HMes*)(PMe3)] (1) toward different diazoalkanes and organic azides was investigated. The pyramidal phosphinidene ligand in 1 displayed a strong nucleophilicity, enabling these reactions to proceed rapidly even below room temperature. Thus, 1 reacted rapidly at 253 K with different diazoalkanes N2CRR' (R,R' = H,H, Ph,Ph, H,CO2Et) to give the corresponding P:P-bridged phosphadiazadiene derivatives as major products which, however, could not be isolated. Reaction of the latter with [H(OEt2)2](BAr'4) yielded the corresponding cationic derivatives [Mo2Cp{µ-κ1P:κ1P,η5-P(NHNCRR')C5H4}(η6-HMes*)(CO)2(PMe3)](BAr'4), which were isolated in ca. 70% yield. The related species [Mo2Cp{µ-κ1P:κ1P,η5-P(NMeNCHCO2Et)C5H4}(η6-HMes*)(CO)2(PMe3)](BAr'4) was isolated upon reaction of the ethyl diazoacetate derivative with MeI and subsequent anion exchange with Na(BAr'4). Reaction of 1 with aryl azides (4-C6H4Me)N3 and (4-C6H4F)N3 proceeded rapidly at low temperature to give possibly the corresponding P:P-bridged phosphaimine derivatives as major products, which could be neither isolated. Protonation of these products with [H(OEt2)2](BAr'4) gave the corresponding aminophosphanyl complexes [Mo2Cp{µ-κ1P:κ1P,η5-P(NHR)C5H4}(η6-HMes*)(CO)2(PMe3)](BAr'4), isolated in ca. 75% yield. In contrast, the result of reactions of 1 with benzyl azide was strongly dependent on temperature, including the temperature in the subsequent methylation step that gave isolable cationic derivatives. By a careful choice of experimental conditions, different complexes having methylated phosphatriazadiene ligands were isolated, such as [Mo2Cp{µ-κ1P:κ1P,η5-P(NNNMeCH2Ph)C5H4}(η6-HMes*)(CO)2(PMe3)](BAr'4) and the metallacyclic derivatives syn- and anti-[Mo2Cp{µ-κ2P,N:κ1P,η5-P(NMeNNCH2Ph)C5H4}(η6-HMes*)(CO)(PMe3)](BAr'4). Density functional theory calculations, along with NMR monitoring experiments, revealed that the formation of the latter products stemmed from different and kinetically favored phosphatriazadiene intermediates, thermodynamically disfavored with respect to the denitrogenation process, otherwise yielding phosphaimine derivatives.

Coordination and Dehydrogenation of Diphosphine-Borane Ph2PCH2PPh2·BH3 at a Heterometallic MoRe Center to Give an Agostic Boryl-Bridged Derivative.

The coordination chemistry of the title diphosphine-borane adduct at heterometallic MoRe centers was examined through its reactions with the hydride complex [MoReCp(µ-H)(µ-PCy2)(CO)5(NCMe)] (Cp = η5-C5H5). The latter reacted rapidly with stoichiometric amounts of dppm·BH3 (dppm = Ph2PCH2PPh2) in refluxing toluene solution, with displacement of the nitrile ligand, to give [MoReCp(µ-H)(µ-PCy2)(CO)5(κ1P-dppm·BH3)], with a P-bound diphosphine-borane ligand arranged trans to the PCy2 group. Decarbonylation of the latter complex was accomplished rapidly upon irradiation with visible-UV light in toluene solution at 263 K, to give the agostic derivative [MoReCp(µ-H)(µ-PCy2)(CO)4(κ1P,η2-dppm·BH3)] as major product (Mo-Re = 3.2075(5) Å), along with small amounts of the diphosphine-bridged complex [MoReCp(µ-H)(µ-PCy2)(CO)4(µ-dppm)]. Extended photolysis of the agostic complex at 288 K promoted an unprecedented dehydrogenation process involving the borane group and the hydride ligand, to give the diphosphine-boryl complex [MoReCp(µ-η2:κ2P,B-H2B·dppm)(µ-PCy2)(CO)4] (Mo-Re = 3.075(1) Å). The latter displayed a boryl ligand in a novel bridging coordination mode, it being σ-bound to one of the metal atoms (B-Re = 2.38(2) Å) while interacting with the second metal atom via a strong side-on tricentric B-H-M interaction (B-Mo = 2.31(1); H-Mo = 1.9(1) Å). The overall dehydrogenation process was endergonic by 43 kJ/mol, according to density functional theory calculations.

One-step synthesis and P-H bond cleavage reactions of the phosphanyl complex syn-[MoCp{PH(2,4,6-C6H2tBu3)}(CO)2] to give heterometallic phosphinidene-bridged derivatives.

Photolysis of [Mo2Cp2(CO)6] and PH2R* (R* = 2,4,6-C6H2tBu3) yielded the title complex, which turned out to be a versatile precursor of novel heterometallic phosphinidene-bridged complexes via three different P-H bond activation processes: photolysis, deprotonation and reduction. In this way the new complexes [MoReCp(µ-PR*)(CO)n] (n = 6,7), [MoFeCp2(µ-PR*)(CO)m], (m = 3, 4) and [MoAuCp(µ-PR*)(CO)2{P(p-tol)3}] were prepared.

N-O Bond Activation and Cleavage Reactions of the Nitrosyl-Bridged Complexes [M2Cp2(µ-PCy2)(µ-NO)(NO)2] (M = Mo, W).

The title complexes (1a,b) were prepared in two steps by first reacting the hydrides [M2Cp2(µ-H)(µ-PCy2)(CO)4] with [NO](BF4) in the presence of Na2CO3 to give dinitrosyls [M2Cp2(µ-PCy2)(CO)2(NO)2](BF4), which were then fully decarbonylated upon reaction with NaNO2 at 323 K. An isomer of the Mo2 complex having a cisoid arrangement of the terminal ligands ( cis-1a) was prepared upon irradiation of toluene solutions of 1a with visible-UV light at 288 K. The structure of these trinitrosyl complexes was investigated using X-ray diffraction and density functional theory (DFT) calculations, these revealing a genuine pyramidalization of the bridging NO that might be associated in part to an increase of charge at the N atom and anticipated a weakening of the N-O bond upon reaction with bases or reducing reagents. Complexes 1a,b reacted with [FeCp2](BF4) to give first the radicals [M2Cp2(µ-PCy2)(µ-NO)(NO)2](BF4) according to CV experiments, which then underwent H-abstraction to yield the nitroxyl-bridged complexes [M2Cp2(µ-PCy2)(µ-κ1:η2-HNO)(NO)2](BF4), alternatively prepared upon protonation with HBF4·OEt2. The novel coordination mode of the nitroxyl ligand in these products was thermodynamically favored over its tautomeric hydroximido form, according to DFT calculations, and similar nitrosomethane-bridged cations [M2Cp2(µ-PCy2)( µ-κ1:η2-MeNO)(NO)2]+ were prepared by reacting 1a,b with CF3SO3Me or [Me3O]BF4. Complexes 1 reacted with M(Hg) (M = Zn, Na) in tetrahydrofuran to give the amido-bridged derivatives [M2Cp2(µ-PCy2)(µ-NH2)(NO)2] with retention of stereochemistry, a transformation also induced by using mild O atom scavengers such as CO and phosphites in the presence of water. In the absence of water, phosphites accomplished a deoxygenation of the bridging NO of the Mo2 complexes to yield the phosphoraniminato-bridged derivatives [Mo2Cp2(µ-PCy2){µ-NP(OR)3}(NO)2] (R = Et, Ph), also with retention of stereochemistry.

Dehydrogenation, Methyl Elimination and Insertion Reactions of the Agostic Methyl-Bridged Complex [Mo2 Cp2 (µ-κ1 :η2 -CH3 )(µ-PtBu2 )(µ-CO)].

The high unsaturation of the title complex enabled it to react with a wide variety of molecules under mild conditions, whereby the agostic methyl ligand underwent unusual or unprecedented processes. Methane elimination occurred in the reactions with PPh2 H and SiPh2 H2 , this being followed in the latter case by Si-H bond oxidative addition to give the hydride silylene derivative [Mo2 Cp2 H(µ-PtBu2 )(µ-SiPh2 )(CO)]. Dehydrogenation, however, was the dominant process in the room temperature reaction with [Fe2 (CO)9 ], to give the unsaturated methylidyne cluster [Mo2 FeCp2 (µ3 -CH)(µ-PtBu2 )(CO)5 ] (Mo-Mo=2.6770(8) Å). In contrast, PMe elimination took place in the reaction with P4 , to give the unsaturated triphosphorus complex [Mo2 Cp2 (µ-η3 :η3 -P3 )(µ-PtBu2 )] (Mo-Mo=2.6221(3) Å). Yet a most remarkable reaction occurred with BH3 ⋅THF, involving insertion of two BH3 units and dehydrogenation to yield [Mo2 Cp2 (µ-B2 H4 Me)(µ-PtBu2 )(CO)], with the novel methyldiboranyl ligand acting as a 5-electron donor due to the presence of two 3-centre, 2-electron B-H-Mo interactions, according to spectroscopic data and DFT calculations (Mo-Mo ca. 2.65 Å).

E-H Bond Activation and Insertion Processes in the Reactions of the Unsaturated Hydride [W2Cp2(µ-H)(µ-PPh2)(NO)2].

The reactions of the title complex (1) with different p-block element (E) molecules was examined. Compound 1 reacted with BH3·THF at room temperature to give the trihydride [W2Cp2(µ-H)H2(µ-PPh2)(NO)2], which formally results from hydrogenation of 1, a reaction that actually does not take place when neat dihydrogen is used. Clean E-H bond oxidative addition, however, took place when 1 was reacted with HSnPh3, to give the related dihydride stannyl derivative [W2Cp2(µ-H)H(µ-PPh2)(NO)2(SnPh3)]. In contrast, the reaction of 1 with HSPh involved H2 elimination to give the thiolate-bridged complex [W2Cp2(µ-SPh)(µ-PPh2)(NO)2], while that with (p-tol)C(O)H resulted in insertion of the aldehyde to yield the related alkoxide complex [W2Cp2{µ-OCH2(p-tol)}(µ-PPh2)(NO)2]. Insertion also prevailed in the reactions of 1 with CNtBu, which, however, involved the competitive formation of new C-H or N-H bonds, to give a mixture of formimidoyl and aminocarbyne derivatives, [W2Cp2(µ-κ1:η2-HCNtBu)(µ-PPh2)(NO)2] (W-W = 3.0177(2) Å) and [W2Cp2{µ-C(NHtBu)}(µ-PPh2)(NO)2] (W-W = 2.9010(4) Å), respectively, even though the latter was thermodynamically preferred, according to density functional theory calculations. The former represents the first structurally characterized complex displaying a formimidoyl or iminoacyl ligand in the alkenyl-like µ-κ1:η2 coordination mode. The reaction of 1 with diazomethane proceeded with N2 elimination and C-H coupling to yield the agostic methyl-bridged complex [W2Cp2(µ-κ1:η2-CH3)(µ-PPh2)(NO)2] (calculated W-W = 2.923 Å), whereas the reaction with N2CH(SiMe3) proceeded with insertion of the diazoalkane to give the corresponding hydrazonide complex [W2Cp2{µ-NH(NCHSiMe3)}(µ-PPh2)(NO)2] (W-W = 2.8608(4) Å). The latter was converted under alkaline conditions to the methyldiazenide derivative [W2Cp2{µ-N(NMe)}(µ-PPh2)(NO)2] (W-W = 2.8730(2) Å), in a process involving hydrolysis of the C-Si bond coupled with a 1,3-H shift from N to C.

Phosphinidene-Bridged MoMn Derivatives of the Thiophosphinidene Complex [Mo2Cp2(µ-κ2:κ1,η6-SPMes*)(CO)2] (Mes* = 2,4,6-C6H2tBu3).

The title complex (1) reacted with [Mn2(CO)10] under visible-UV irradiation (toluene solution and quartz glassware) to give a mixture of the phosphinidene complex [MnMoCp(µ-κ1:κ1,η6-PMes*)(CO)4], the cluster [Mn2Mo2Cp2(µ-κ1:κ1,η6-PMes*)(µ3-S)(CO)8], and the thiophosphinidene complex [MnMoCp(µ-κ2:κ1,η4-SPMes*)(CO)5], in yields of ca. 60, 20, and 10% respectively (Mes* = 2,4,6-C6H2tBu3). The major product follows from formal replacement of the SMoCp(CO)2 fragment in 1 with a Mn(CO)4 fragment, and displayed multiple bonding to phosphorus (Mn-P = 2.1414(8) Å); the tetranuclear cluster results from formal insertion of a Mn2(CO)6 fragment in 1, with cleavage of P-S and P-Mo bonds, to render a µ3-S bridged Mn2Mo core bearing an exocyclic phosphinidene ligand involved in multiple bonding to one of the Mn atoms (Mn-P = 2.140(2) Å); the thiophosphinidene complex (Mn-P = 2.294(1) Å) formally results from addition of sulfur and carbon monoxide to the major MnMo product, a transformation which actually could be performed stepwise, via the MnMo thiophosphinidene complex [MnMoCp(µ-κ2:κ1,η6-SPMes*)(CO)4]. When the photolysis of 1 and [Mn2(CO)10] was performed in tetrahydrofuran solution and using conventional glassware, then the V-shaped cluster [Mn2MoCp{µ-κ1:κ1:κ1,η5-P(C6H3tBu3)}(CO)8] was obtained selectively (Mo-Mn = 3.2910(5) Å, Mn-Mn = 2.9223(5) Å), which unexpectedly displays a cyclohexadienylidene-phosphinidene ligand resulting from H atom abstraction at the aryl ring of the precursor. Density functional theory calculations on the complexes [LnM(µ-κ1:κ1,η6-PMes*)MoCp] (MLn = MoCp(CO)2, Mn(CO)4, Co(CO)3) revealed that the degree of delocalization of the metal-phosphorus π-bonding interaction over the Mo-P-M chain is significantly conditioned by the heterometal fragment MLn, it being increased in the order Mn ≤ Mo < Co.

Acetonitrile Adduct [MoReCp(µ-H)(µ-PCy2)(CO)5(NCMe)]: A Surrogate of an Unsaturated Heterometallic Hydride Complex.

The title compound was prepared upon irradiation of acetonitrile solutions of the readily available hexacarbonyl [MoReCp(µ-H)(µ-PCy2)(CO)6]. The acetonitrile ligand in this compound could be replaced easily by donor molecules or displaced upon two-electron reduction. In most cases, the substitution step was followed by additional processes such as insertion into the M-H bonds, E-H bond cleavage, H2 elimination, and other transformations.

Structural and Chemical Effects of the PtBu2 Bridge at Unsaturated Dimolybdenum Complexes Having Hydride and Hydrocarbyl Ligands.

A high-yield synthetic route for the preparation of the unsaturated anion [Mo2Cp2(µ-PtBu2)(µ-CO)2]- (2) was implemented, via two-electron reduction of the chloride complex [Mo2Cp2(µ-Cl)(µ-PtBu2)(CO)2] (1). Reaction of 2 with [NH4][PF6] led to the formation of the 30-electron complex [Mo2Cp2(H)(µ-PtBu2)(CO)2] (3), in which the hydride ligand adopts an uncommon terminal disposition. DFT analysis of the electronic structure of 3 gave support to the presence of a M≡M triple bond in this complex following from a σ2δ2δ2 configuration, a view also supported by the high electron density accumulated at the corresponding Mo-Mo bond critical point. In contrast, reactions of 2 with IMe or ClCH2Ph gave the alkyl-bridged complexes [Mo2Cp2(µ-κ1:η2-CH2R)(µ-PtBu2)(CO)2] (R = H (4a), Ph (4b)), which in solution display agostic Mo-H-C interactions. Decarbonylation of 4a took place rapidly under photochemical conditions to give the 30-electron complex [Mo2Cp2(µ-κ1:η2-CH3)(µ-PtBu2)(µ-CO)] (7), with a stronger agostic coordination of its methyl ligand. In contrast, irradiation of 4b led to the formation of the benzylidyne derivative [Mo2Cp2(µ-CPh)(µ-PtBu2)(µ-CO)] (9), following from fast decarbonylation and dehydrogenation of the bridging benzyl ligand. Low-temperature photochemistry allowed for the NMR characterization of an intermediate preceding the hydrogen elimination, identified as the carbene hydride [Mo2Cp2(H)(µ-CHPh)(µ-PtBu2)(CO)] (10), a product which evolves slowly by H2 elimination to the benzylidyne derivative. Analogous dehydrogenation of the methyl ligand in 7 could be accomplished upon moderate heating, to yield the corresponding methylidyne derivative [Mo2Cp2(µ-CH)(µ-PtBu2)(µ-CO)] (9). A complete reaction mechanism accounting for these photochemical reactions was elaborated, based on the reaction intermediates identified experimentally and on extensive DFT calculations. Surprisingly, for both systems the C-H bond activation steps are relatively easy thermal processes occurring with modest activation energies after photochemical ejection of CO, with a rate-determining step involving the formation of agostic carbenes requiring also a strong structural reorganization of the central Mo2PC rings of these molecules.

C-C and C-N Couplings Following Hydride Addition on Isocyanide Cyclopolyenyl Dimolybdenum Complexes to Give Tethered Aldimine and Aminocarbene Derivatives.

Reaction of [Mo2 Cp2 (µ-κ1 :κ1 ,η6 -PMes*)(CO)2 ] with S or Se followed by protonation with [H(OEt2 )2 ](BAr'4 ) gave the cationic derivatives [Mo2 Cp2 {µ-κ2P,E :κ1P ,η5 -EP(C6 H3 tBu3 )}(CNR)(CO)2 ](BAr'4 ) (E=S; R=tBu, iPr, Ph, 4-C6 H4 OMe, Xyl; or E=Se; R=tBu; Ar'=3,5-C6 H3 (CF3 )2 ). Reaction of the latter with K[BHsBu3 ] yielded the aldimine complexes [Mo2 Cp2 {µ-κ2P,E :κ2P,N ,η4 -SP(C6 H3 tBu3 (CHNR))}(CO)2 ] and their aminocarbene isomers [Mo2 Cp2 {µ-κ2P,E :κ2P,C ,η4 -SP(C6 H3 tBu3 (NRCH))}(CO)2 ] (R ≠ Xyl), following C-C and C-N couplings, respectively. Monitoring of these reactions revealed that the initial H- attack takes place at a Cp ligand to give cyclopentadiene intermediates [Mo2 Cp{µ-κ2P,S :κ1P ,η5 -SP(C6 H3 tBu3 )}(η4 -C5 H6 )(CNR)(CO)2 ], which then undergo C-H oxidative addition to give the hydride isomers [Mo2 Cp2 {µ-κ2P,S :κ1P ,η3 -SP(C6 H3 tBu3 )}(H)(CNR)(CO)2 ]. In turn, the latter rearrange to give the aldimine and aminocarbene complexes. DFT calculations revealed that the hydride intermediates first undergo migratory insertion of the isocyanide ligand into the Mo-H bond to give unobservable formimidoyl intermediates, which then evolve either by nucleophilic attack of the N atom on the C6 ring (C-N coupling) or by migratory insertion of the formimidoyl ligand into the C6 ring (C-C coupling). Our data suggest that increasing the size of the substituent R at the isocyanide ligand destabilizes the aldimine isomer to a greater extent, thus favoring formation of the aminocarbene complex.