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.

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.

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.

Impact of rheumatoid arthritis on sexuality: adaptation and validation of the Qualisex questionnaire for use in Spain.

Patients with rheumatoid arthritis (RA) have a significantly increased risk of sexual dysfunction. However, it is not properly included in commonly used questionnaires to assess health-related quality of life in RA. Qualisex is a questionnaire developed in France to assess the impact of RA on patients´ sexual function. Our aim was to adapt and validate this questionnaire for use with Spanish RA patients. Two independent translations and a backward translation were obtained. The final version was tested in a pilot study with 10 RA patients to detect any aspects that could hinder interpretation. The validity and reliability of the linguistically validated questionnaire were studied in a multicenter cross-sectional study, with a longitudinal component for reliability estimation. 125 RA patients were included. The response process, discrimination, internal consistency, internal structure, convergent validity (correlation with MGH-SFQ questionnaire, DAS-28, physician global assessment, patient global health assessment, RAID, HAQ, HADS and SF-12©) and reliability were analyzed. The inclusion of two extra items was proposed in the pilot study. The validity analysis detected responses for item 10 that were not coherent with responses for the rest of items. The Cronbach alpha coefficient was 0.971. The highest correlation (0.665) was obtained with MGH-SFQ (questionnaire measuring sexual functioning), followed by RAID (0.516). The intra-class correlation was 0.880 (95% CI 0.815; 0.923), higher than 0.85, which indicates excellent reliability. All parameters used to assess this questionnaire show highly acceptable values. Qualisex allows for a global score of RA patients' sexual functioning and can be self-administered.

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.

Postoperative Psychosocial Factors in Health Functioning and Health-Related Quality of Life After Knee Arthroplasty: A 6-Month Follow up Prospective Observational Study.

OBJECTIVE: Knee arthroplasty (KA) is an effective and cost-effective treatment for end-stage knee osteoarthritis. Despite high surgical success rates, as many as 25% of patients report compromised postoperative functioning, persistent pain, and reduced quality of life. The purpose of this study was to assess the predictive value of psychological factors in health functioning and quality of life, during a 6-month period after KA. DESIGN: A prospective observational study. SETTING: Surgery at two hospitals and follow-up was carried out through the domiciliary rehabilitation service. SUBJECTS: In total, 89 patients (age 70.27 ± 7.99 years) met the inclusion criteria. METHOD: A test battery composed of Health functioning associated with osteoarthritis (WOMAC), Health-related quality of life (EQ-5D-5L), Anxiety and Depression (HADS), Pain attitudes (SOPA-B), Pain catastrophizing (PCS), and Fear of Movement (TSK-11) was assessed at 1 week, and 1, 3, and 6 months after surgery. A mixed effects linear model was used to estimate the effect of time and covariates. An exploratory factor analysis was used to identify the number of dimensions underlying the group of psychological measurements. RESULTS: In WOMAC model, anxiety level (F = 120.8), PCS (F = 103.9), depression level (F = 93.6) and pain score (F = 72.8) were the most influential variables. Regarding EQ-5D-5L model, anxiety level (F = 98.5), PCS (F = 79.8), depression level (F = 78.3) and pain score (F = 45) were the most influential variables. Pain score and the psychosocial variables of PCS, TSK, HADS-A, HADS-D, SOPA-B Emotion, SOPA-B Harm and SOPA-B Disability loaded in one single dimension. CONCLUSIONS: Postoperative acute pain and psychosocial factors of pain catastrophizing, anxiety, depression, and pain attitudes might influence health functioning and quality of life during KA rehabilitation. Such factors could be gathered into one single dimension defined as pain-related psychologic distress.

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.

Habitat suitability of Rhincodon typus in three localities of the Gulf of California: Environmental drivers of seasonal aggregations.

The whale shark is an endangered species that usually feeds in coastal areas of highly productive seas such as the Gulf of California, Mexico. This study aims to describe the effect of sea surface temperature, chlorophyll a, bathymetry and slope on the habitat suitability of whale sharks in three important aggregation sites of the Gulf of California. A total of 2396 records of occurrence of whale sharks were obtained from international databases and scientific literature between 1996 and 2018. These records were used for the creation of a species distribution model using MaxEnt for each of the three aggregation sites. The concentration of chlorophyll a explained 71% of the habitat suitability, followed by bathymetry and slope with a combined 17%, and sea surface temperature constituting 10% of the model. Habitat suitability was related to areas where nontargeted fisheries may impact whale sharks through bycatch, entanglement and ship strikes. The implications for the conservation of whale sharks should be considered for management decisions in terms of marine protected areas, fishing refugees or bans, and other regulations regarding fisheries activities.

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.

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).

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.

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.

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.

Mapping of the Gastrointestinal Short Form Questionnaire (GSF-Q) into EQ-5D-3L and SF-6D in patients with gastroesophageal reflux disease.

BACKGROUND: The short, self-administered Gastroesophageal Reflux Disease (GERD) Symptom Frequency Questionnaire (GSFQ) is a specific Quality of Life (QoL) instrument which measures the impact of GERD symptoms on QoL. This study aims to map the specific scores in GSFQ into two generic instruments: SF-6D and EQ-5D-3 L, in order to obtain utility estimates derived from the GERD condition. METHOD: A national representative sample of GERD patients was selected, stratified by gender, age (< 45, ≥45 years) and GERD severity (0-I, II-IV Savary-Miller score) for validation purposes. Age, gender, BMI, GERD diagnose, GERD severity, associated comorbidities and risk factors were recorded. GSFQ, SF-6D, EQ-5D-3 L, and the HRQoL Visual Analogue Scale (VAS) were answered by patients. Several mapping methods were estimated, regression using dummy variables, and linear, quadratic and cubic regression using optimal factor scores. The use of a GERD aggregated summary severity derived from the GSFQ was dimed the best predictor. Overall Mean Absolute Error (MAE), overall Mean Absolute Percentage Error (MAPE) were used as goodness-of-fit (GOF) indexes to compare models. RESULTS: A total of 3405 patients were recruited by 490 clinicians. Mean age was 49 (±14.4) years and 49.8% were women. Reported comorbidities were clustered in 6 antecedents and 15 concomitant pathologies. Aggregation of levels for the frequency of symptoms items was found more suitable for estimation. Regression weights were found to follow a monotonous progressive pattern. Overall MAE ranged from 0.092 to 0.094 for SF-6D utility prediction and from 0.008 to 0.08 for EQ-5D-3 L, while MAPE values ranged from 27.9 to 29% for SF-6D and from 36.8 to 38.4% for EQ-5D-3 L. Cubic regression GOF demonstrated a better fit. CONCLUSIONS: It is possible to translate specific GSFQ scores assessing GERD condition into generic SF-6D and EQ-5D-3 L utility values. Although regression using dummy variables is a suitable mapping procedure, other alternative mapping methods convey better fit, in particular cubic regression.

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.

Role of the different eyes in the visual odometry in the wolf spider Lycosa tarantula (Araneae, Lycosidae).

The wolf spider Lycosa tarantula returns home by means of path integration. Previous studies demonstrated: (i) that the angular component of the outbound run is measured using a polarized-light compass associated with the anterior median eyes; (ii) changes in direction of the substratum are detected by the anterior lateral eyes (ALEs); and (iii) in relation to the linear component of the outbound run, an increase of optic flow, in either the lateral or ventral fields of view, caused spiders to search for the burrow at a point nearer to the goal. However, the role of the secondary eyes [ALEs, posterior lateral eyes (PLEs) and posterior median eyes (PMEs)] in the perception of this optic flow and the importance of them for gauging the distance walked is still unknown. In this study, lateral or ventral gratings of wavelength λ=1 cm were used, with two groups of spiders in each setup: (1) PLEs+PMEs covered and (2) ALEs covered. The largest reduction in the distance walked to return to the burrow was observed with the ventral grating/ALEs covered. These results show the importance of the previously neglected ALEs for the visual behavior of these spiders. The possibility of gathering information for locomotion from the three pairs of secondary eyes in the mushroom bodies is discussed.

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.